| scholarly article | Q13442814 |
| P356 | DOI | 10.1111/J.0006-341X.1999.00997.X |
| P3181 | OpenCitations bibliographic resource ID | 257431 |
| P698 | PubMed publication ID | 11315092 |
| P5875 | ResearchGate publication ID | 12019938 |
| P894 | zbMATH Open document ID | 1059.62640 |
| P2093 | author name string | Devlin B | |
| Roeder K | |||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P6104 | maintained by WikiProject | WikiProject Mathematics | Q8487137 |
| P304 | page(s) | 997-1004 | |
| P577 | publication date | 1999-12-01 | |
| P1433 | published in | Biometrics | Q2025724 |
| P1476 | title | Genomic control for association studies | |
| P478 | volume | 55 |
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| Q47581804 | A genome-wide association analysis identifies PDE1A|DNAJC10 locus on chromosome 2 associated with idiopathic pulmonary arterial hypertension in a Japanese population |
| Q33579535 | A genome-wide association analysis of serum iron concentrations |
| Q29417059 | A genome-wide association meta-analysis identifies new childhood obesity loci |
| Q24653943 | A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project |
| Q37056239 | A genome-wide association study (GWAS) for bronchopulmonary dysplasia |
| Q28943418 | A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy |
| Q35909380 | A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex |
| Q58707050 | A genome-wide association study for natural antibodies measured in blood of Canadian Holstein cows |
| Q28943430 | A genome-wide association study identifies an osteoarthritis susceptibility locus on chromosome 7q22 |
| Q47188914 | A genome-wide association study identifies genomic loci associated with backfat thickness, carcass weight, and body weight in two commercial pig populations |
| Q28943542 | A genome-wide association study identifies locus at 10q22 associated with clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients in Japanese |
| Q29417009 | A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. |
| Q28287727 | A genome-wide association study identifies novel risk loci for type 2 diabetes |
| Q47546322 | A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth |
| Q28264861 | A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population |
| Q24655759 | A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder |
| Q28943536 | A genome-wide association study in 574 schizophrenia trios using DNA pooling |
| Q35187404 | A genome-wide association study in large white and landrace pig populations for number piglets born alive |
| Q28943372 | A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma |
| Q33716853 | A genome-wide association study meta-analysis of clinical fracture in 10,012 African American women |
| Q35816887 | A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13. |
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| Q33812108 | A genome-wide association study of serum uric acid in African Americans |
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| Q28741024 | Accounting for population stratification in practice: a comparison of the main strategies dedicated to genome-wide association studies |
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| Q52936701 | Adjusting for population structure in admixed populations. |
| Q35749711 | Adjusting heterogeneous ascertainment bias for genetic association analysis with extended families |
| Q34588543 | Adjustment for local ancestry in genetic association analysis of admixed populations |
| Q33307544 | Admixture mapping provides evidence of association of the VNN1 gene with hypertension |
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| Q34699776 | All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs |
| Q43157779 | Allele and haplotype frequency distribution in PTPN22 gene across variable ethnic groups: Implications for genetic association studies for autoimmune diseases |
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| Q40617466 | Allowing for population stratification in case-only studies of gene-environment interaction, using genomic control |
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| Q56681114 | An Icelandic example of the impact of population structure on association studies |
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| Q33315564 | Analysis and application of European genetic substructure using 300 K SNP information |
| Q52005896 | Analysis of SNPs in pooled DNA: a decision theoretic model. |
| Q36055011 | Analysis of case-control association studies with known risk variants |
| Q44693607 | Analysis of genetic variations of protein tyrosine kinase fyn and their association with alcohol dependence in two independent cohorts |
| Q42612701 | Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk |
| Q42796366 | Analysis of rare variant population structure in Europeans explains differential stratification of gene-based tests. |
| Q34672061 | Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls |
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| Q33348850 | Analytical approaches to detect maternal/fetal genotype incompatibilities that increase risk of pre-eclampsia |
| Q34953548 | Analyze multivariate phenotypes in genetic association studies by combining univariate association tests |
| Q42404864 | Analyzing genetic association studies with an extended propensity score approach |
| Q47604685 | Ancestral haplotype-based association mapping with generalized linear mixed models accounting for stratification |
| Q42690314 | Ancestry inference using principal component analysis and spatial analysis: a distance-based analysis to account for population substructure |
| Q34804773 | Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America |
| Q92445764 | Ancestry-specific association mapping in admixed populations |
| Q33809374 | Application of a new method for GWAS in a related case/control sample with known pedigree structure: identification of new loci for nephrolithiasis |
| Q37190463 | Application of association mapping to understanding the genetic diversity of plant germplasm resources |
| Q34107682 | Application of genetic/genomic approaches to allergic disorders |
| Q33519282 | Application of seventeen two-locus models in genome-wide association studies by two-stage strategy |
| Q38674308 | Application of t-SNE to human genetic data |
| Q42697286 | Applying meta-analysis to genotype-tissue expression data from multiple tissues to identify eQTLs and increase the number of eGenes |
| Q38650976 | Approaches to detect genetic effects that differ between two strata in genome-wide meta-analyses: Recommendations based on a systematic evaluation |
| Q33519304 | Armitage's trend test for genome-wide association analysis: one-sided or two-sided? |
| Q35552640 | Artifact due to differential error when cases and controls are imputed from different platforms |
| Q35587787 | Assessing the Probability that a Finding Is Genuine for Large-Scale Genetic Association Studies. |
| Q34185496 | Assessing the accuracy of observer-reported ancestry in a biorepository linked to electronic medical records |
| Q39870473 | Assessing the impact of population stratification on association studies of rare variation |
| Q22337235 | Assessing the impact of population stratification on genetic association studies |
| Q34143219 | Assessing the joint effect of population stratification and sample selection in studies of gene-gene (environment) interactions |
| Q42562411 | Assessment of Population Structure and Its Effects on Genome-Wide Association Studies |
| Q36952959 | Assessment of cumulative evidence on genetic associations: interim guidelines |
| Q36322116 | Assessment of osteoarthritis candidate genes in a meta-analysis of nine genome-wide association studies |
| Q34980182 | Association analysis between polymorphisms in the conserved dopamine neurotrophic factor (CDNF) gene and cocaine dependence |
| Q42923785 | Association analysis between polymorphisms in the myo-inositol monophosphatase 2 (IMPA2) gene and bipolar disorder |
| Q34060004 | Association analysis of frost tolerance in rye using candidate genes and phenotypic data from controlled, semi-controlled, and field phenotyping platforms |
| Q61796185 | Association between DNA methylation in obesity-related genes and body mass index percentile in adolescents |
| Q33705559 | Association between a common immunoglobulin heavy chain allele and rheumatic heart disease risk in Oceania |
| Q44392668 | Association between a promoter dopamine D2 receptor gene variant and the personality trait detachment |
| Q51115874 | Association between antinuclear antibodies and the HLA class II locus and heterogeneous characteristics of staining patterns: the Nagahama study. |
| Q43639148 | Association between glutamic acid decarboxylase genes and anxiety disorders, major depression, and neuroticism |
| Q34530457 | Association between polymorphisms in the metallophosphoesterase (MPPE1) gene and bipolar disorder |
| Q49028093 | Association between polymorphisms in the vesicle-associated membrane protein-associated protein A (VAPA) gene on chromosome 18p and bipolar disorder. |
| Q28296326 | Association between the SERPING1 gene and age-related macular degeneration: a two-stage case-control study |
| Q36973407 | Association between the catechol-O-methyltransferase Val158Met polymorphism and cocaine dependence |
| Q87383260 | Association mapping and genetic dissection of nitrogen use efficiency-related traits in rice (Oryza sativa L.). |
| Q37156218 | Association mapping and significance estimation via the coalescent |
| Q33903172 | Association mapping in structured populations |
| Q40016412 | Association mapping of complex trait loci with context-dependent effects and unknown context variable |
| Q33728311 | Association mapping of insecticide resistance in wild Anopheles gambiae populations: major variants identified in a low-linkage disequilbrium genome |
| Q39014231 | Association mapping of morphological traits in wild and captive zebra finches: reliable within, but not between populations |
| Q95822812 | Association mapping of partitioning loci in barley |
| Q37630239 | Association mapping of yield-related traits and SSR markers in wild soybean (Glycine soja Sieb. and Zucc.). |
| Q74737426 | Association mapping, using a mixture model for complex traits |
| Q34569326 | Association mapping: where we've been, where we're going |
| Q55040266 | Association of BET1L and TNRC6B with uterine leiomyoma risk and its relevant clinical features in Han Chinese population. |
| Q48891651 | Association of HPA axis genes with suicidal behaviour in schizophrenia. |
| Q33645915 | Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies. |
| Q35588451 | Association of SSR markers with functional traits from heat stress in diverse tall fescue accessions |
| Q28214098 | Association of a 5-HT(5A) receptor polymorphism, Pro15Ser, to schizophrenia |
| Q36141781 | Association of alpha4beta2 nicotinic receptor and heavy smoking in schizophrenia |
| Q37156204 | Association of genetic variants at 3q22 with nephropathy in patients with type 1 diabetes mellitus |
| Q34997022 | Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals |
| Q91902230 | Association of imputed prostate cancer transcriptome with disease risk reveals novel mechanisms |
| Q34660856 | Association of the HSPG2 gene with neuroleptic-induced tardive dyskinesia |
| Q28943399 | Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases |
| Q36143063 | Association of variants in innate immune genes with asthma and eczema |
| Q24646663 | Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants |
| Q24802474 | Association studies for asthma and atopic diseases: a comprehensive review of the literature |
| Q35934138 | Association studies for finding cancer-susceptibility genetic variants |
| Q58047109 | Association studies for quantitative traits in structured populations |
| Q47224991 | Association studies of WD repeat domain 3 and chitobiosyldiphosphodolichol beta-mannosyltransferase genes with schizophrenia in a Japanese population |
| Q61822090 | Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use |
| Q34186026 | Association study designs for complex diseases |
| Q34235895 | Association study of 182 candidate genes in anorexia nervosa |
| Q36108124 | Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophrenia |
| Q48810649 | Association study of H2AFZ with schizophrenia in a Japanese case-control sample. |
| Q42697241 | Association testing of bisulfite-sequencing methylation data via a Laplace approximation |
| Q43480058 | Association tests for a censored quantitative trait and candidate genes in structured populations with multilevel genetic relatedness |
| Q36273072 | Assocplots: a Python package for static and interactive visualization of multiple-group GWAS results. |
| Q34482054 | Asthma genetics 2006: the long and winding road to gene discovery. |
| Q36279538 | Asthma in Hispanics |
| Q37273821 | Attempted replication of reported chronic obstructive pulmonary disease candidate gene associations |
| Q35057796 | Attenuated monocyte apoptosis, a new mechanism for osteoporosis suggested by a transcriptome-wide expression study of monocytes |
| Q49334627 | BAYESIAN LARGE-SCALE MULTIPLE REGRESSION WITH SUMMARY STATISTICS FROM GENOME-WIDE ASSOCIATION STUDIES. |
| Q24625454 | BDNF Val66Met is associated with introversion and interacts with 5-HTTLPR to influence neuroticism |
| Q34303965 | BLUP genotype imputation for case-control association testing with related individuals and missing data |
| Q27853316 | BRCA1/2 mutations associated with progression-free survival in ovarian cancer patients in the AGO-OVAR 16 study. |
| Q24618859 | Basic statistical analysis in genetic case-control studies |
| Q64060882 | Bayesian Inference for Mixed Model-Based Genome-Wide Analysis of Expression Quantitative Trait Loci by Gibbs Sampling |
| Q35582333 | Bayesian Spatial Modeling of Haplotype Associations |
| Q47693227 | Bayesian analysis of multilocus association in quantitative and qualitative traits |
| Q42908217 | Bayesian association-based fine mapping in small chromosomal segments. |
| Q33867602 | Bayesian semiparametric copula estimation with application to psychiatric genetics |
| Q31010545 | Behavior of QQ-plots and genomic control in studies of gene-environment interaction |
| Q35951033 | Benzene Uptake and Glutathione S-transferase T1 Status as Determinants of S-Phenylmercapturic Acid in Cigarette Smokers in the Multiethnic Cohort |
| Q64911704 | Beyond the traditional simulation design for evaluating type 1 error control: From the "theoretical" null to "empirical" null. |
| Q39121793 | Bias correction to secondary trait analysis with case-control design. |
| Q40250955 | BinomiRare: A robust test of the association of a rare variant with a disease for pooled analysis and meta-analysis, with application to the HCHS/SOL. |
| Q42173729 | Binomial mixture model-based association tests under genetic heterogeneity |
| Q40276166 | Bivariate genomic analysis identifies a hidden locus associated with bacteria hypersensitive response in Arabidopsis thaliana. |
| Q37040432 | Blood lipids influence DNA methylation in circulating cells |
| Q51798489 | Boar taint in entire male pigs: a genomewide association study for direct and indirect genetic effects on androstenone. |
| Q33813557 | Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1. |
| Q57023926 | Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data |
| Q33705604 | CAPL: a novel association test using case-control and family data and accounting for population stratification |
| Q36151217 | CERAMIC: Case-Control Association Testing in Samples with Related Individuals, Based on Retrospective Mixed Model Analysis with Adjustment for Covariates. |
| Q45972181 | CMPK1 and RBP3 are associated with corneal curvature in Asian populations. |
| Q33572328 | COL4A1 is associated with arterial stiffness by genome-wide association scan |
| Q52317581 | CXCR4 involvement in neurodegenerative diseases. |
| Q47661053 | Calibrating Population Stratification in Association Analysis. |
| Q37636600 | Candidate gene association study of coronary artery calcification in chronic kidney disease: findings from the CRIC study (Chronic Renal Insufficiency Cohort). |
| Q37459384 | Candidate gene polymorphisms for diabetes mellitus, cardiovascular disease and cancer are associated with longevity in Koreans |
| Q34281187 | Candidate gene studies of bipolar disorder |
| Q46340423 | Candidate-gene association study of mothers with pre-eclampsia, and their infants, analyzing 775 SNPs in 190 genes |
| Q35095358 | Capitalizing on admixture in genome-wide association studies: a two-stage testing procedure and application to height in African-Americans |
| Q40615674 | Cardiometabolic risk loci share downstream cis- and trans-gene regulation across tissues and diseases. |
| Q84092139 | Carotenoid biosynthesis genes provide evidence of geographical subdivision and extensive linkage disequilibrium in the carrot |
| Q80175794 | Case-control association studies with matching and genomic controlling |
| Q37464245 | Case-control association testing in the presence of unknown relationships |
| Q34769893 | Case-control association testing of common variants from sequencing of DNA pools |
| Q36542324 | Case-control studies in the genomic era: a clinician's guide |
| Q37003743 | Catechol-O-methyltransferase contributes to genetic susceptibility shared among anxiety spectrum phenotypes |
| Q52931795 | Caught in the trio trap? Potential selection bias inherent to association studies using parent-offspring trios. |
| Q99571954 | Causal inference in genetic trio studies |
| Q51949093 | Centralizing the non-central chi-square: A new method to correct for population stratification in genetic case-control association studies. |
| Q98188474 | Chances and challenges of machine learning-based disease classification in genetic association studies illustrated on age-related macular degeneration |
| Q44892899 | Changes in food reward following smoking cessation: a pharmacogenetic investigation |
| Q37003617 | Characteristics of a spina bifida population including North American Caucasian and Hispanic individuals |
| Q24810869 | Characterization of a likelihood based method and effects of markers informativeness in evaluation of admixture and population group assignment |
| Q57673367 | Characterizing the Extent of Human Genetic Variation for Performance-Related Traits |
| Q37696685 | Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue |
| Q36830876 | Chromosome painting in silico in a bacterial species reveals fine population structure |
| Q36482639 | Chronic obstructive pulmonary disease in Hispanics |
| Q27014915 | Clinical review: Genome-wide association studies of skeletal phenotypes: what we have learned and where we are headed |
| Q30982184 | Cluster analysis and association study of structured multilocus genotype data |
| Q33767014 | Clustering by genetic ancestry using genome-wide SNP data |
| Q46922584 | Clustering of pedigrees using marker allele frequencies: impact on linkage analysis |
| Q34570951 | Coalescent-based association mapping and fine mapping of complex trait loci |
| Q38598293 | Coherent synthesis of genomic associations with phenotypes and home environments. |
| Q28751965 | Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts |
| Q28606497 | Collaborative Cross and Diversity Outbred data resources in the Mouse Phenome Database |
| Q33743947 | Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture |
| Q28924378 | Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci |
| Q33352742 | Combined haplotype relative risk (CHRR): a general and simple genetic association test that combines trios and unrelated case-controls |
| Q34176788 | Combining effects from rare and common genetic variants in an exome-wide association study of sequence data |
| Q37201519 | Combining genetic association study designs: a GWAS case study |
| Q43262217 | Comment on a simple and improved correction for population stratification |
| Q35639599 | Common NOTCH3 Variants and Cerebral Small-Vessel Disease |
| Q45737025 | Common and low-frequency variants associated with genome-wide recombination rate |
| Q57426309 | Common and rare genetic markers of lipid variation in subjects with type 2 diabetes from the ACCORD clinical trial |
| Q34028001 | Common and rare variant analysis in early-onset bipolar disorder vulnerability |
| Q36018506 | Common and rare variants associated with kidney stones and biochemical traits |
| Q36548818 | Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase |
| Q29417063 | Common body mass index-associated variants confer risk of extreme obesity |
| Q84347026 | Common genetic variants in pre-microRNAs and risk of gallbladder cancer in North Indian population |
| Q34458961 | Common genetic variants influence human subcortical brain structures |
| Q37325815 | Common genetic variation and human disease |
| Q36468817 | Common genetic variation and survival after colorectal cancer diagnosis: a genome-wide analysis |
| Q55088883 | Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison's disease in Sweden. |
| Q30414536 | Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: a genome-wide association study of 13,372 participants. |
| Q21143760 | Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies |
| Q21091170 | Common polymorphisms influencing serum uric acid levels contribute to susceptibility to gout, but not to coronary artery disease |
| Q34572775 | Common variants associated with general and MMR vaccine-related febrile seizures |
| Q34355379 | Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways |
| Q37173595 | Common variants at 12q15 and 12q24 are associated with infant head circumference |
| Q37338403 | Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations |
| Q28943518 | Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis |
| Q35816788 | Common variants at VRK2 and TCF4 conferring risk of schizophrenia |
| Q37240241 | Common variants at ten loci influence QT interval duration in the QTGEN Study |
| Q34289629 | Common variants at ten loci modulate the QT interval duration in the QTSCD Study |
| Q34298428 | Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus |
| Q24614376 | Common variants conferring risk of schizophrenia |
| Q37604461 | Common variants in polygenic schizophrenia. |
| Q30435234 | Common variants in the GDF5-UQCC region are associated with variation in human height |
| Q37147155 | Common variants in the region around Osterix are associated with bone mineral density and growth in childhood |
| Q35569618 | Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma |
| Q36956625 | Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis |
| Q42442996 | Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits |
| Q36878530 | Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations |
| Q34631785 | Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer |
| Q33920653 | Common variants spanning PLK4 are associated with mitotic-origin aneuploidy in human embryos |
| Q37369101 | Common variation contributes to the genetic architecture of social communication traits. |
| Q24627043 | Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer |
| Q34561066 | Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration |
| Q30587939 | Common variation near ROBO2 is associated with expressive vocabulary in infancy. |
| Q24631241 | Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects |
| Q35804142 | Comparative genome-wide association studies of a depressive symptom phenotype in a repeated measures setting by race/ethnicity in the Multi-Ethnic Study of Atherosclerosis |
| Q91968924 | Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data |
| Q34328116 | Comparing population structure as inferred from genealogical versus genetic information |
| Q57245709 | Comparison of SSRs and SNPs in assessment of genetic relatedness in maize |
| Q33519277 | Comparison of a unified analysis approach for family and unrelated samples with the transmission-disequilibrium test to study associations of hypertension in the Framingham Heart Study |
| Q39481029 | Comparison of gene-based rare variant association mapping methods for quantitative traits in a bovine population with complex familial relationships |
| Q33519221 | Comparison of methods for correcting population stratification in a genome-wide association study of rheumatoid arthritis: principal-component analysis versus multidimensional scaling |
| Q30836933 | Comparison of methods to account for relatedness in genome-wide association studies with family-based data |
| Q33688537 | Comparison of multimarker logistic regression models, with application to a genomewide scan of schizophrenia. |
| Q33375723 | Comparison of population-based association study methods correcting for population stratification |
| Q37289097 | Comparison of statistical methods for estimating genetic admixture in a lung cancer study of African Americans and Latinos |
| Q45955672 | Comparison of three methods to estimate genetic ancestry and control for stratification in genetic association studies among admixed populations. |
| Q36078055 | Complex trait mapping in isolated populations: Are specific statistical methods required? |
| Q36272449 | Complexities in psychiatric genetics |
| Q34020703 | Complexity and power in case-control association studies |
| Q36670925 | Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits |
| Q28742726 | Conditional random fields for fast, large-scale genome-wide association studies |
| Q34285669 | Conditions under which genome-wide association studies will be positively misleading. |
| Q37236347 | Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. |
| Q36764953 | Confounding and heterogeneity in genetic association studies with admixed populations |
| Q21092505 | Confounding from cryptic relatedness in case-control association studies |
| Q60638541 | Confounding from cryptic relatedness in haplotype-based association studies |
| Q92741170 | Confounding of linkage disequilibrium patterns in large scale DNA based gene-gene interaction studies |
| Q36875722 | Conserved Genetic Architecture Underlying Individual Recombination Rate Variation in a Wild Population of Soay Sheep (Ovis aries) |
| Q22337167 | Control of confounding of genetic associations in stratified populations |
| Q35051003 | Control of population stratification by correlation-selected principal components |
| Q35720573 | Controlling Population Structure in Human Genetic Association Studies with Samples of Unrelated Individuals |
| Q37611099 | Controlling bias and inflation in epigenome- and transcriptome-wide association studies using the empirical null distribution |
| Q38670517 | Controlling false discoveries in genome scans for selection |
| Q36182654 | Controlling for P-value inflation in allele frequency change in experimental evolution and artificial selection experiments |
| Q36983683 | Convergent genomic studies identify association of GRIK2 and NPAS2 with chronic fatigue syndrome |
| Q30435913 | Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples |
| Q34381880 | Converging genetic and functional brain imaging evidence links neuronal excitability to working memory, psychiatric disease, and brain activity |
| Q35857407 | Correcting for Population Stratification in Genomewide Association Studies |
| Q30939859 | Correcting for cryptic relatedness by a regression-based genomic control method |
| Q33894110 | Correcting for cryptic relatedness in population-based association studies of continuous traits |
| Q46259406 | Correcting for differential genotyping error in genetic association analysis |
| Q35034503 | Correcting for population structure and kinship using the linear mixed model: theory and extensions |
| Q33448503 | Correcting for relatedness in Bayesian models for genomic data association analysis. |
| Q33706425 | Correcting population stratification in genetic association studies using a phylogenetic approach |
| Q34151779 | Correction for hidden confounders in the genetic analysis of gene expression |
| Q33314841 | Correction of population stratification in large multi-ethnic association studies |
| Q36953199 | Correlation of population parameters leading to power differences in association studies with population stratification. |
| Q91688790 | Correlations between relatives: From Mendelian theory to complete genome sequence |
| Q73091243 | Cost of linkage versus association methods |
| Q42739774 | Covariate-modulated local false discovery rate for genome-wide association studies |
| Q38837306 | Critical Issues in the Inclusion of Genetic and Epigenetic Information in Prevention and Intervention Trials |
| Q34577720 | CrypticIBDcheck: an R package for checking cryptic relatedness in nominally unrelated individuals. |
| Q21563360 | Cuba: exploring the history of admixture and the genetic basis of pigmentation using autosomal and uniparental markers |
| Q35247767 | Current gene discovery strategies for ocular conditions |
| Q35608483 | D-HaploDB: a database of definitive haplotypes determined by genotyping complete hydatidiform mole samples |
| Q34988384 | DNA Pooling: a tool for large-scale association studies |
| Q48041910 | DNA methylation as a mediator of the association between prenatal adversity and risk factors for metabolic disease in adulthood. |
| Q64095904 | DNA methylation signature of smoking in lung cancer is enriched for exposure signatures in newborn and adult blood |
| Q28250903 | DNA pooling: a comprehensive, multi-stage association analysis of ACSL6 and SIRT5 polymorphisms in schizophrenia |
| Q43759682 | DNA-Methylation and Body Composition in Preschool Children: Epigenome-Wide-Analysis in the European Childhood Obesity Project (CHOP)-Study |
| Q57757087 | DNAH5 is associated with total lung capacity in chronic obstructive pulmonary disease |
| Q51565168 | DNMT3B -579 G>T promoter polymorphism and risk of gallbladder carcinoma in North Indian population. |
| Q93190239 | Data in support of genetic architecture of glucosinolate variations in Brassica napus |
| Q51020220 | Deciphering the Genic Basis of Yeast Fitness Variation by Simultaneous Forward and Reverse Genetics. |
| Q74115794 | Deconstructing maize population structure |
| Q90658220 | Deconstructing the sources of genotype-phenotype associations in humans |
| Q57418313 | Demonstrating stratification in a European American population |
| Q24633290 | Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis |
| Q58910969 | Design and Statistical Analysis of Pooled Next Generation Sequencing for Rare Variants |
| Q42130054 | Designing penalty functions in high dimensional problems: The role of tuning parameters |
| Q37270473 | Designing pharmacogenetic projects in industry: practical design perspectives from the Industry Pharmacogenomics Working Group |
| Q34235532 | Detailed analysis of Japanese population substructure with a focus on the southwest islands of Japan |
| Q52967299 | Detect and adjust for population stratification in population-based association study using genomic control markers: an application of Affymetrix Genechip Human Mapping 10K array. |
| Q28601596 | Detecting adaptive evolution based on association with ecological gradients: orientation matters! |
| Q36489228 | Detecting and exploiting etiologic heterogeneity in epidemiologic studies |
| Q34105619 | Detecting association in a case-control study while correcting for population stratification |
| Q47600019 | Detecting association of rare and common variants by testing an optimally weighted combination of variants |
| Q37598393 | Detecting association of rare variants by testing an optimally weighted combination of variants for quantitative traits in general families |
| Q28750109 | Detecting natural selection by empirical comparison to random regions of the genome |
| Q34248911 | Detecting rare variant associations by identity-by-descent mapping in case-control studies |
| Q41108346 | Detecting the footprints of divergent selection in oaks with linked markers |
| Q39404555 | Determination of the genetic architecture of seed size and shape via linkage and association analysis in soybean (Glycine max L. Merr.). |
| Q35072505 | Development and application of genomic control methods for genome-wide association studies using non-additive models |
| Q28972484 | Development of a Panel of Genome-Wide Ancestry Informative Markers to Study Admixture Throughout the Americas |
| Q43030977 | Development of a novel aluminum tolerance phenotyping platform used for comparisons of cereal aluminum tolerance and investigations into rice aluminum tolerance mechanisms |
| Q42054812 | Differential confounding of rare and common variants in spatially structured populations |
| Q51920848 | Differential dropout among SNP genotypes and impacts on association tests. |
| Q34081990 | Differentiating population stratification from genotyping error using family data |
| Q33315561 | Discerning the ancestry of European Americans in genetic association studies |
| Q28546045 | Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation |
| Q36358432 | Discovery and fine mapping of serum protein loci through transethnic meta-analysis |
| Q30252943 | Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations |
| Q28661470 | Discovery and refinement of loci associated with lipid levels |
| Q96431750 | Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis |
| Q90101893 | Discovery of shared genomic loci using the conditional false discovery rate approach |
| Q33395678 | Distinct genetic loci control plasma HIV-RNA and cellular HIV-DNA levels in HIV-1 infection: the ANRS Genome Wide Association 01 study |
| Q24644398 | Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease |
| Q44411863 | Dopamine D2 receptor gene Ser311Cys variant and schizophrenia: association study and meta-analysis |
| Q34730588 | Dosage transmission disequilibrium test (dTDT) for linkage and association detection |
| Q36486361 | Double genomic control is not effective to correct for population stratification in meta-analysis for genome-wide association studies |
| Q28550578 | Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium |
| Q37154348 | Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval |
| Q24621951 | EDNRA variants associate with smooth muscle mRNA levels, cell proliferation rates, and cystic fibrosis pulmonary disease severity |
| Q37159866 | EGFR and SYNE2 are associated with p21 expression and SYNE2 variants predict post-operative clinical outcomes in HBV-related hepatocellular carcinoma |
| Q34596089 | ETHNOPRED: a novel machine learning method for accurate continental and sub-continental ancestry identification and population stratification correction |
| Q57309121 | EVI5 is a risk gene for multiple sclerosis |
| Q36107681 | Early gestation as the critical time-window for changes in the prenatal environment to affect the adult human blood methylome. |
| Q27305178 | Ectopic KIT copy number variation underlies impaired migration of primordial germ cells associated with gonadal hypoplasia in cattle (Bos taurus) |
| Q57363076 | Effect of linkage disequilibrium between markers in linkage and association analyses |
| Q34176552 | Effect of population stratification analysis on false-positive rates for common and rare variants |
| Q92719088 | Effect of population stratification on SNP-by-environment interaction |
| Q52971046 | Effect of population stratification on case-control association studies. II. False-positive rates and their limiting behavior as number of subpopulations increases. |
| Q30975979 | Effect of population stratification on the identification of significant single-nucleotide polymorphisms in genome-wide association studies |
| Q42174946 | Effect of population structure corrections on the results of association mapping tests in complex maize diversity panels |
| Q31102613 | Effect of sample stratification on dairy GWAS results |
| Q47825022 | Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritability. |
| Q35057499 | Effective sample size: Quick estimation of the effect of related samples in genetic case-control association analyses |
| Q33742044 | Effectively identifying regulatory hotspots while capturing expression heterogeneity in gene expression studies |
| Q83208707 | Effects of a neuregulin 1 variant on conversion to schizophrenia and schizophreniform disorder in people at high risk for psychosis |
| Q34094442 | Effects of endotoxin exposure on childhood asthma risk are modified by a genetic polymorphism in ACAA1 |
| Q38797998 | Effects of gene action, marker density, and time since selection on the performance of landscape genomic scans of local adaptation. |
| Q33858783 | Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations |
| Q33232701 | Effects of population structure on genetic association studies |
| Q30622171 | Efficient Bayesian mixed-model analysis increases association power in large cohorts. |
| Q45000788 | Efficient approximation of P-value of the maximum of correlated tests, with applications to genome-wide association studies |
| Q40992352 | Efficient calculation of P-value and power for quadratic form statistics in multilocus association testing |
| Q36515832 | Efficient control of population structure in model organism association mapping |
| Q34041665 | Efficient genome-wide association testing of gene-environment interaction in case-parent trios |
| Q34956942 | Efficient inference of local ancestry |
| Q31038287 | Efficient study designs for test of genetic association using sibship data and unrelated cases and controls |
| Q33775580 | Efficient utilization of rare variants for detection of disease-related genomic regions |
| Q39797372 | EigenGWAS: finding loci under selection through genome-wide association studies of eigenvectors in structured populations |
| Q28477763 | Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms |
| Q58696739 | Empirical Comparisons of Different Statistical Models To Identify and Validate Kernel Row Number-Associated Variants from Structured Multi-parent Mapping Populations of Maize |
| Q31108294 | Empirical estimation of genome-wide significance thresholds based on the 1000 Genomes Project data set |
| Q39564678 | Enabling Privacy-Preserving GWASs in Heterogeneous Human Populations |
| Q30432415 | Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium |
| Q35906170 | Environmental Association Analyses Identify Candidates for Abiotic Stress Tolerance in Glycine soja, the Wild Progenitor of Cultivated Soybeans |
| Q115031569 | Environmental response in gene expression and DNA methylation reveals factors influencing the adaptive potential of Arabidopsis lyrata |
| Q30489866 | Epigenetic Signatures of Cigarette Smoking |
| Q64243405 | Epigenetic findings in periodontitis in UK twins: a cross-sectional study |
| Q46690173 | Epigenome-wide association studies without the need for cell-type composition |
| Q103803412 | Epigenome-wide meta-analysis of DNA methylation differences in prefrontal cortex implicates the immune processes in Alzheimer's disease |
| Q34620473 | Epistasis between polymorphisms in COMT, ESR1, and GCH1 influences COMT enzyme activity and pain |
| Q36582532 | Estimating Effect Sizes and Expected Replication Probabilities from GWAS Summary Statistics |
| Q34085599 | Estimating and adjusting for ancestry admixture in statistical methods for relatedness inference, heritability estimation, and association testing |
| Q36096091 | Estimating kinship in admixed populations |
| Q37149387 | Estimating local ancestry in admixed populations |
| Q33332851 | Estimating the number and size of the main effects in genome-wide case-control association studies |
| Q33754531 | Estimating the total number of susceptibility variants underlying complex diseases from genome-wide association studies. |
| Q33929681 | Estimation of allele frequency and association mapping using next-generation sequencing data |
| Q44876533 | Estimation of cis-eQTL effect sizes using a log of linear model. |
| Q21092502 | European population substructure: clustering of northern and southern populations |
| Q35097760 | Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples |
| Q35708043 | Evaluation of an approximation method for assessment of overall significance of multiple-dependent tests in a genomewide association study |
| Q33519338 | Evaluation of an optimal receiver operating characteristic procedure |
| Q34020842 | Evaluation of candidate genes in case-control studies: a statistical method to account for related subjects |
| Q36271926 | Evaluation of logistic regression models and effect of covariates for case-control study in RNA-Seq analysis |
| Q96827219 | Evaluation of population stratification adjustment using genome-wide or exonic variants |
| Q37257592 | Evidence for association between polycystic ovary syndrome (PCOS) and TCF7L2 and glucose intolerance in women with PCOS and TCF7L2. |
| Q40387551 | Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder |
| Q30275016 | Evidence for large-scale gene-by-smoking interaction effects on pulmonary function. |
| Q34319297 | Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion |
| Q37650437 | Exome chip analyses in adult attention deficit hyperactivity disorder. |
| Q33810009 | Exome localization of complex disease association signals. |
| Q92157836 | Exome sequences and multi-environment field trials elucidate the genetic basis of adaptation in barley |
| Q27027055 | Exome sequencing and complex disease: practical aspects of rare variant association studies |
| Q37056084 | Exome sequencing and the genetic basis of complex traits |
| Q35622119 | Expanding the range of ZNF804A variants conferring risk of psychosis |
| Q28387512 | Exploring the Major Sources and Extent of Heterogeneity in a Genome-Wide Association Meta-Analysis |
| Q38799740 | Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease |
| Q34117615 | Extent of height variability explained by known height-associated genetic variants in an isolated population of the Adriatic coast of Croatia |
| Q39549689 | Extracting actionable information from genome scans |
| Q46667102 | Extreme-phenotype genome-wide association study (XP-GWAS): a method for identifying trait-associated variants by sequencing pools of individuals selected from a diversity panel |
| Q41882858 | Extremely low-coverage sequencing and imputation increases power for genome-wide association studies |
| Q33565486 | FAM-MDR: a flexible family-based multifactor dimensionality reduction technique to detect epistasis using related individuals |
| Q36588857 | FTO genotype is associated with phenotypic variability of body mass index |
| Q46661213 | FaST linear mixed models for genome-wide association studies |
| Q86659834 | FaST-LMM-Select for addressing confounding from spatial structure and rare variants |
| Q36148601 | Factors affecting statistical power in the detection of genetic association |
| Q37737040 | False discovery rates: a new deal |
| Q37495697 | Familial young-onset diabetes, pre-diabetes and cardiovascular disease are associated with genetic variants of DACH1 in Chinese |
| Q37371260 | Family-based association testing strongly implicates DRD2 as a risk gene for schizophrenia in Han Chinese from Taiwan. |
| Q36492206 | Family-based association tests for genomewide association scans |
| Q57077220 | Family-based association tests for quantitative traits using pooled DNA |
| Q34096126 | Family-based association tests using genotype data with uncertainty |
| Q30941221 | Family-based bivariate association tests for quantitative traits |
| Q37883023 | Family-based designs for genome-wide association studies |
| Q30995743 | Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data |
| Q37389487 | Family-based genome-wide association studies |
| Q37150639 | Family-based samples can play an important role in genetic association studies |
| Q33253242 | Family-based versus unrelated case-control designs for genetic associations |
| Q34285337 | Fast and accurate imputation of summary statistics enhances evidence of functional enrichment |
| Q64265989 | Fast and flexible linear mixed models for genome-wide genetics |
| Q31056324 | FastPop: a rapid principal component derived method to infer intercontinental ancestry using genetic data |
| Q37030631 | Fc receptor genes and the systemic lupus erythematosus diathesis |
| Q64917597 | Finding associated variants in genome-wide association studies on multiple traits. |
| Q37538006 | Finding common susceptibility variants for complex disease: past, present and future |
| Q34671087 | Finding genes underlying human disease |
| Q51958506 | Fine mapping by linkage and association in nuclear family and case-control designs. |
| Q34007867 | Fine mapping in 94 inbred mouse strains using a high-density haplotype resource |
| Q36695139 | Fine mapping of eight psoriasis susceptibility loci |
| Q34019187 | Fine-mapping QTLs in advanced intercross lines and other outbred populations |
| Q56910517 | Fine-mapping analysis of a chromosome 2 region linked to resistance to Mycobacterium tuberculosis infection in Uganda reveals potential regulatory variants |
| Q57295524 | Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps |
| Q33232817 | Fine-mapping using the weighted average method for a case-control study |
| Q40505706 | Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans |
| Q46964301 | Fine-scale genetic structure in a wild bird population: the role of limited dispersal and environmentally based selection as causal factors |
| Q46584231 | Fine-scale recombination rate differences between sexes, populations and individuals |
| Q35168433 | First genome-wide association study in an Australian aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetes |
| Q53585636 | Folate metabolic gene polymorphisms and childhood acute lymphoblastic leukemia: a case-control study. |
| Q30988891 | Forward-time simulation of realistic samples for genome-wide association studies |
| Q64882781 | Frequentist p-values for large-scale-single step genome-wide association, with an application to birth weight in American Angus cattle. |
| Q33954528 | From SNPs to genes: disease association at the gene level |
| Q36813721 | From single-SNP to wide-locus: genome-wide association studies identifying functionally related genes and intragenic regions in small sample studies |
| Q90567439 | Functional Genomics of the Retina to Elucidate its Construction and Deconstruction |
| Q44984247 | Functional SNPs are enriched for schizophrenia association signals |
| Q53317555 | Functional SNPs in CD244 increase the risk of rheumatoid arthritis in a Japanese population. |
| Q47763855 | Functional polymorphisms of the cyclooxygenase (PTGS2) gene and risk for gallbladder cancer in a North Indian population |
| Q38602733 | Further investigations of the W-test for pairwise epistasis testing |
| Q36906421 | G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetes |
| Q28741872 | GATES: a rapid and powerful gene-based association test using extended Simes procedure |
| Q64064642 | GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study |
| Q33698621 | GPFrontend and GPGraphics: graphical analysis tools for genetic association studies |
| Q90636085 | GRK5 Is Associated with the Regulation of Methadone Dosage in Heroin Dependence |
| Q33521158 | GWAF: an R package for genome-wide association analyses with family data |
| Q33590114 | GWAMA: software for genome-wide association meta-analysis |
| Q24289119 | GWAS of 126,559 individuals identifies genetic variants associated with educational attainment |
| Q37380173 | GWAS of human bitter taste perception identifies new loci and reveals additional complexity of bitter taste genetics |
| Q91995911 | GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI |
| Q90214149 | GWASpro: a high-performance genome-wide association analysis server |
| Q33808898 | Gallbladder cancer predisposition: a multigenic approach to DNA-repair, apoptotic and inflammatory pathway genes |
| Q30497912 | Gene by sex interaction for measures of obesity in the framingham heart study |
| Q36787564 | Gene discovery in diabetic nephropathy |
| Q33780246 | Gene expression and genetic variation data implicate PCLO in bipolar disorder |
| Q37385974 | Gene-alcohol interactions identify several novel blood pressure loci including a promising locus near SLC16A9. |
| Q37026772 | Gene-centric association study of acute chest syndrome and painful crisis in sickle cell disease patients |
| Q94554869 | Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci |
| Q34407923 | Gene-environment interactions in human diseases |
| Q28303293 | Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk |
| Q58786918 | Genes associated with anhedonia: a new analysis in a large clinical trial (GENDEP) |
| Q37623634 | Genetic Analysis of Association Between Calcium Signaling and Hippocampal Activation, Memory Performance in the Young and Old, and Risk for Sporadic Alzheimer Disease |
| Q35814969 | Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders |
| Q57437605 | Genetic Diversity among Wheat Accessions from the USDA National Small Grains Collection |
| Q36473454 | Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos |
| Q35901532 | Genetic Geostatistical Framework for Spatial Analysis of Fine-Scale Genetic Heterogeneity in Modern Populations: Results from the KORA Study |
| Q61480160 | Genetic Variants Associated with Circulating Fibroblast Growth Factor 23 |
| Q38785985 | Genetic Variants Associated with Circulating Parathyroid Hormone |
| Q37009894 | Genetic Variation in the IL-6 and HLA-DQB1 Genes Is Associated with Spontaneous Clearance of Hepatitis C Virus Infection |
| Q43531843 | Genetic analysis and characterization of a new maize association mapping panel for quantitative trait loci dissection |
| Q30625643 | Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease |
| Q37495182 | Genetic and methylation variation in the CYP2B6 gene is related to circulating p,p'-dde levels in a population-based sample |
| Q35563817 | Genetic approaches to stature, pubertal timing, and other complex traits |
| Q37469593 | Genetic architecture of nonadditive inheritance in Arabidopsis thaliana hybrids. |
| Q42055852 | Genetic architecture of plant stress resistance: multi-trait genome-wide association mapping |
| Q36343939 | Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus. |
| Q36234313 | Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans. |
| Q33211937 | Genetic association analysis using data from triads and unrelated subjects |
| Q58614131 | Genetic association and differential expression of PITX2 with acute appendicitis |
| Q21092470 | Genetic association and expression studies indicate a role of toll-like receptor 8 in pulmonary tuberculosis |
| Q34526866 | Genetic association mapping at the crossroads: which test and why? Overview and practical guidelines |
| Q36591396 | Genetic association of cyclic AMP signaling genes with bipolar disorder |
| Q30357928 | Genetic association of left ventricular mass assessed by M-mode and two-dimensional echocardiography. |
| Q35222770 | Genetic association of recovery from eating disorders: the role of GABA receptor SNPs |
| Q36267276 | Genetic association studies |
| Q36142031 | Genetic association studies of complex neurological diseases |
| Q33516997 | Genetic association tests: a method for the joint analysis of family and case-control data |
| Q86905588 | Genetic association with multiple traits in the presence of population stratification |
| Q30277642 | Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function |
| Q31074202 | Genetic associations in preterm birth: a primer of marker selection, study design, and data analysis |
| Q37724733 | Genetic associations with intimate partner violence in a sample of hazardous drinking men in batterer intervention programs |
| Q36925317 | Genetic associations with schizophrenia: meta-analyses of 12 candidate genes. |
| Q37251803 | Genetic background comparison using distance-based regression, with applications in population stratification evaluation and adjustment |
| Q38602403 | Genetic correlations between intraocular pressure, blood pressure and primary open-angle glaucoma: a multi-cohort analysis |
| Q37350436 | Genetic determinants of circulating sphingolipid concentrations in European populations |
| Q28254206 | Genetic determinants of hair, eye and skin pigmentation in Europeans |
| Q37214302 | Genetic epidemiology in aging research |
| Q36244624 | Genetic epidemiology of osteoporosis: past, present, and future |
| Q35600184 | Genetic epidemiology of type 1 diabetes |
| Q34558523 | Genetic evidence for ubiquitin-specific proteases USP24 and USP40 as candidate genes for late-onset Parkinson disease |
| Q34501150 | Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci |
| Q28601322 | Genetic imaging consortium for addiction medicine: From neuroimaging to genes |
| Q30313100 | Genetic loci associated with heart rate variability and their effects on cardiac disease risk |
| Q34775960 | Genetic loci for retinal arteriolar microcirculation |
| Q29614943 | Genetic mapping in human disease |
| Q35804226 | Genetic model selection in two-phase analysis for case-control association studies |
| Q49608512 | Genetic modifiers of Mendelian disease: Huntington's disease and the trinucleotide repeat disorders. |
| Q39965012 | Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors |
| Q29417094 | Genetic polymorphisms of the human PNPLA3 gene are strongly associated with severity of non-alcoholic fatty liver disease in Japanese |
| Q37139308 | Genetic predictors of depressive symptoms in cardiac patients |
| Q28943368 | Genetic predictors of medically refractory ulcerative colitis |
| Q46051862 | Genetic predictors of response to antidepressants in the GENDEP project |
| Q31061507 | Genetic relatedness analysis: modern data and new challenges |
| Q24635370 | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis |
| Q28732735 | Genetic signatures of exceptional longevity in humans |
| Q33594845 | Genetic signatures of high-altitude adaptation in Tibetans |
| Q21143785 | Genetic structure of Europeans: a view from the North-East |
| Q24644546 | Genetic structure of the Han Chinese population revealed by genome-wide SNP variation |
| Q22305005 | Genetic studies of body mass index yield new insights for obesity biology |
| Q96610280 | Genetic study of the Arctic CPT1A variant suggests that its effect on fatty acid levels is modulated by traditional Inuit diet |
| Q34997411 | Genetic substructure of Kuwaiti population reveals migration history |
| Q34309196 | Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease |
| Q35064459 | Genetic susceptibility to peripheral arterial disease: a dark corner in vascular biology |
| Q33575138 | Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept |
| Q91796279 | Genetic variability in response to amyloid beta deposition influences Alzheimer's disease risk |
| Q38760182 | Genetic variants affecting cross-sectional lung function in adults show little or no effect on longitudinal lung function decline |
| Q34692085 | Genetic variants associated with increased risk of malignant pleural mesothelioma: a genome-wide association study. |
| Q33904459 | Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes |
| Q36828742 | Genetic variants in the cocaine- and amphetamine-regulated transcript gene (CARTPT) and cocaine dependence |
| Q37477713 | Genetic variants influencing circulating lipid levels and risk of coronary artery disease |
| Q24622351 | Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration |
| Q35870147 | Genetic variation and association mapping for 12 agronomic traits in indica rice |
| Q30275184 | Genetic variation at 16q24.2 is associated with small vessel stroke |
| Q64234977 | Genetic variation in is associated with white matter hyperintensities (n = 11,226) |
| Q64899769 | Genetic variations for egg quality of chickens at late laying period revealed by genome-wide association study. |
| Q47137616 | Genetically defined elevated homocysteine levels do not result in widespread changes of DNA methylation in leukocytes |
| Q38379199 | Genetics and brain morphology |
| Q35978336 | Genetics and drug use as a complex phenotype |
| Q28255432 | Genetics in geographically structured populations: defining, estimating and interpreting F(ST) |
| Q37033774 | Genetics moderate alcohol and intimate partner violence treatment outcomes in a randomized controlled trial of hazardous drinking men in batterer intervention programs: A preliminary investigation |
| Q36110574 | Genetics of Crohn disease, an archetypal inflammatory barrier disease |
| Q61676903 | Genetics of Susceptibility and Resistance to Infection |
| Q34846313 | Genetics of callous-unemotional behavior in children |
| Q28394588 | Genetics of healthy aging and longevity |
| Q48632226 | Genetics of postoperative complications following thoracic surgery. |
| Q35744021 | Genetics of posttraumatic stress disorder. |
| Q35173640 | Genetics of preeclampsia: what are the challenges? |
| Q28744518 | Genetics of venous thrombosis: insights from a new genome wide association study |
| Q36466472 | Genetics, transcriptomics, and proteomics of Alzheimer's disease |
| Q34064863 | Genome scans for detecting footprints of local adaptation using a Bayesian factor model. |
| Q35247899 | Genome wide association studies using a new nonparametric model reveal the genetic architecture of 17 agronomic traits in an enlarged maize association panel |
| Q55314023 | Genome-Wide Association Analysis of Age-Dependent Egg Weights in Chickens. |
| Q40604431 | Genome-Wide Association Identifies TBX5 as Candidate Gene for Osteochondrosis Providing a Functional Link to Cartilage Perfusion as Initial Factor |
| Q37781545 | Genome-Wide Association Studies in Nephrology Research |
| Q57294902 | Genome-Wide Association Study of Susceptibility Loci for Radiation-Induced Brain Injury |
| Q35774006 | Genome-Wide Association Study on Resistance to Stalk Rot Diseases in Grain Sorghum. |
| Q38733565 | Genome-Wide Association and Replication Study of Hepatotoxicity Induced by Antiretrovirals Alone or with Concomitant Anti-Tuberculosis Drugs |
| Q28392110 | Genome-Wide Meta-Analysis of Sciatica in Finnish Population |
| Q30353876 | Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes. |
| Q38621394 | Genome-wide Association Studies for Female Fertility Traits in Chinese and Nordic Holsteins |
| Q91529384 | Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals |
| Q38657925 | Genome-wide Association Study of Susceptibility to Particulate Matter-Associated QT Prolongation |
| Q33894025 | Genome-wide SNP associations with rubella-specific cytokine responses in measles-mumps-rubella vaccine recipients |
| Q36915435 | Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait |
| Q46950679 | Genome-wide admixture and association study of subclinical atherosclerosis in the Women's Interagency HIV Study (WIHS). |
| Q37613249 | Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders |
| Q54108240 | Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma. |
| Q37352439 | Genome-wide analyses of aggressiveness in attention-deficit hyperactivity disorder |
| Q35393713 | Genome-wide analysis of attention deficit hyperactivity disorder in Norway |
| Q34254081 | Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma |
| Q58705577 | Genome-wide analysis of polymorphism × sodium interaction effect on blood pressure identifies a novel 3'-BCL11B gene desert locus |
| Q37172364 | Genome-wide and candidate gene association studies of placental abruption |
| Q55437423 | Genome-wide assessment of gene-by-smoking interactions in COPD. |
| Q35601164 | Genome-wide association analyses for boar taint components and testicular traits revealed regions having pleiotropic effects |
| Q33417654 | Genome-wide association analyses identify SPOCK as a key novel gene underlying age at menarche |
| Q46530826 | Genome-wide association analyses identify variants in developmental genes associated with hypospadias |
| Q34434235 | Genome-wide association analyses of genetic, phenotypic, and environmental risks in the age-related eye disease study. |
| Q30437542 | Genome-wide association analyses suggested a novel mechanism for smoking behavior regulated by IL15 |
| Q37725795 | Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation |
| Q28305142 | Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype |
| Q28297287 | Genome-wide association analysis identifies 13 new risk loci for schizophrenia |
| Q29614583 | Genome-wide association analysis identifies 20 loci that influence adult height |
| Q37698113 | Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension |
| Q36915419 | Genome-wide association analysis identifies genetic variations in subjects with myalgic encephalomyelitis/chronic fatigue syndrome |
| Q30408891 | Genome-wide association analysis identifies six new loci associated with forced vital capacity |
| Q28943462 | Genome-wide association analysis in primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4 |
| Q92620659 | Genome-wide association analysis of egg production performance in chickens across the whole laying period |
| Q41820122 | Genome-wide association analysis of imputed rare variants: application to seven common complex diseases |
| Q33549937 | Genome-wide association analysis of total cholesterol and high-density lipoprotein cholesterol levels using the Framingham heart study data |
| Q92527797 | Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure |
| Q34555458 | Genome-wide association and admixture analysis of glaucoma in the Women's Health Initiative |
| Q34220999 | Genome-wide association and functional follow-up reveals new loci for kidney function |
| Q28943526 | Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption |
| Q30427183 | Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. |
| Q28943449 | Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry |
| Q37156094 | Genome-wide association and replication studies identified TRHR as an important gene for lean body mass |
| Q36145491 | Genome-wide association and replication study of anti-tuberculosis drugs-induced liver toxicity |
| Q37280609 | Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo |
| Q36049128 | Genome-wide association for milk production and female fertility traits in Canadian dairy Holstein cattle |
| Q36031664 | Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration |
| Q24635872 | Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes |
| Q24816825 | Genome-wide association mapping in Arabidopsis identifies previously known flowering time and pathogen resistance genes |
| Q84941070 | Genome-wide association mapping of agronomic and morphologic traits in highly structured populations of barley cultivars |
| Q34411292 | Genome-wide association mapping to candidate polymorphism resolution in the unsequenced barley genome |
| Q35336192 | Genome-wide association mapping unravels the genetic control of seed germination and vigor in Brassica napus |
| Q33332893 | Genome-wide association mapping using mixed-models: application to GAW15 Problem 3. |
| Q29248524 | Genome-wide association meta-analyses identified 1q43 and 2q32.2 for hip Ward's triangle areal bone mineral density |
| Q36895545 | Genome-wide association meta-analyses to identify common genetic variants associated with hallux valgus in Caucasian and African Americans |
| Q52319652 | Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability. |
| Q33904445 | Genome-wide association of anthropometric traits in African- and African-derived populations |
| Q30417624 | Genome-wide association of body fat distribution in African ancestry populations suggests new loci |
| Q30426500 | Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions. |
| Q33838241 | Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE |
| Q21142620 | Genome-wide association of lipid-lowering response to statins in combined study populations |
| Q35827026 | Genome-wide association of serum uric acid concentration: replication of sequence variants in an island population of the Adriatic coast of Croatia |
| Q24608568 | Genome-wide association scan for five major dimensions of personality |
| Q30487416 | Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci |
| Q35150554 | Genome-wide association scan for variants associated with early-onset prostate cancer |
| Q21092459 | Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution |
| Q33699542 | Genome-wide association scan of attention deficit hyperactivity disorder |
| Q28943415 | Genome-wide association scan of trait depression |
| Q29614593 | Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits |
| Q28658449 | Genome-wide association studies and beyond |
| Q37339440 | Genome-wide association studies for atherosclerotic vascular disease and its risk factors |
| Q29615822 | Genome-wide association studies for common diseases and complex traits |
| Q30420166 | Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction |
| Q36500755 | Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference |
| Q98222355 | Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels |
| Q21145019 | Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae |
| Q33814805 | Genome-wide association studies in cancer--current and future directions |
| Q33516266 | Genome-wide association studies of family data in pharmacogenetics: a case study |
| Q30433126 | Genome-wide association studies of the PR interval in African Americans |
| Q33519299 | Genome-wide association studies using single-nucleotide polymorphisms versus haplotypes: an empirical comparison with data from the North American Rheumatoid Arthritis Consortium |
| Q37292889 | Genome-wide association studies: implications for multiethnic samples |
| Q34555195 | Genome-wide association studies: theoretical and practical concerns |
| Q61811322 | Genome-wide association study and a post replication analysis revealed a promising genomic region and candidate genes for chicken eggshell blueness |
| Q37695742 | Genome-wide association study and meta-analysis of intraocular pressure |
| Q35800154 | Genome-wide association study dissects genetic architecture underlying longitudinal egg weights in chickens. |
| Q57269424 | Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus |
| Q28681381 | Genome-wide association study for birth weight in Nellore cattle points to previously described orthologous genes affecting human and bovine height |
| Q28943344 | Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA |
| Q28714390 | Genome-wide association study heterogeneous cohort homogenization via subject weight knock-down |
| Q36928764 | Genome-wide association study identified UQCC locus for spine bone size in humans |
| Q21144987 | Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis |
| Q28943502 | Genome-wide association study identifies HLA-DP as a susceptibility gene for pediatric asthma in Asian populations |
| Q46798900 | Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos |
| Q46332214 | Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24. |
| Q28943557 | Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm |
| Q29614414 | Genome-wide association study identifies eight loci associated with blood pressure |
| Q24629653 | Genome-wide association study identifies five loci associated with lung function |
| Q28248384 | Genome-wide association study identifies five new schizophrenia loci |
| Q28943484 | Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population |
| Q34165031 | Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients |
| Q28943387 | Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot |
| Q35014321 | Genome-wide association study identifies major loci for carcass weight on BTA14 in Hanwoo (Korean cattle). |
| Q24645441 | Genome-wide association study identifies novel breast cancer susceptibility loci |
| Q28943488 | Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1 |
| Q46584350 | Genome-wide association study identifies quantitative trait loci affecting hematological traits in an F2 intercross between Landrace and Korean native pigs |
| Q36241862 | Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure |
| Q36442663 | Genome-wide association study identifies three key loci for high mesocarp oil content in perennial crop oil palm. |
| Q37736430 | Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy. |
| Q34477629 | Genome-wide association study identifies two major loci affecting calving ease and growth-related traits in cattle |
| Q37154259 | Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation |
| Q24612662 | Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease |
| Q28943289 | Genome-wide association study implicates PARD3B-based AIDS restriction |
| Q29417097 | Genome-wide association study in German patients with attention deficit/hyperactivity disorder |
| Q29416988 | Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease |
| Q47251063 | Genome-wide association study in Han Chinese identifies three novel loci for human height |
| Q28943533 | Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP |
| Q28281906 | Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci |
| Q29417149 | Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder |
| Q24289047 | Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region |
| Q34504872 | Genome-wide association study of 107 phenotypes in Arabidopsis thaliana inbred lines. |
| Q24550675 | Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls |
| Q29417042 | Genome-wide association study of Alzheimer's disease with psychotic symptoms |
| Q30484496 | Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study |
| Q33772170 | Genome-wide association study of PR interval |
| Q28943413 | Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe |
| Q29417061 | Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3 |
| Q28943321 | Genome-wide association study of alcohol dependence |
| Q28943324 | Genome-wide association study of ancestry-specific TB risk in the South African Coloured population |
| Q35575555 | Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci |
| Q24612100 | Genome-wide association study of antibody response to smallpox vaccine |
| Q36073692 | Genome-wide association study of antipsychotic-induced QTc interval prolongation |
| Q24628870 | Genome-wide association study of bipolar disorder in European American and African American individuals |
| Q29417122 | Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension |
| Q35674693 | Genome-wide association study of body height in African Americans: the Women's Health Initiative SNP Health Association Resource (SHARe) |
| Q42267178 | Genome-wide association study of chronic hepatitis B virus infection reveals a novel candidate risk allele on 11q22.3. |
| Q44670236 | Genome-wide association study of co-occurring anxiety in major depression |
| Q28943353 | Genome-wide association study of coronary artery disease in the Japanese |
| Q40161459 | Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts. |
| Q33815554 | Genome-wide association study of homocysteine levels in Filipinos provides evidence for CPS1 in women and a stronger MTHFR effect in young adults |
| Q24630663 | Genome-wide association study of intracranial aneurysm identifies three new risk loci |
| Q34453062 | Genome-wide association study of kidney function decline in individuals of European descent |
| Q34729737 | Genome-wide association study of lung function phenotypes in a founder population |
| Q37222748 | Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16. |
| Q36162221 | Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults |
| Q47172157 | Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics |
| Q50767477 | Genome-wide association study of osteochondrosis in the tarsocrural joint of Dutch Warmblood horses identifies susceptibility loci on chromosomes 3 and 10. |
| Q30389438 | Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium |
| Q35875163 | Genome-wide association study of plasma levels of polychlorinated biphenyls disclose an association with the CYP2B6 gene in a population-based sample |
| Q33400334 | Genome-wide association study of plasma polyunsaturated fatty acids in the InCHIANTI Study |
| Q28943558 | Genome-wide association study of recurrent early-onset major depressive disorder |
| Q57323019 | Genome-wide association study of recurrent major depressive disorder in two European case–control cohorts |
| Q34653028 | Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions |
| Q34580862 | Genome-wide association study of retinopathy in individuals without diabetes |
| Q33519381 | Genome-wide association study of rheumatoid arthritis by a score test based on wavelet transformation |
| Q40051668 | Genome-wide association study of sporadic brain arteriovenous malformations |
| Q47889975 | Genome-wide association study of the five-factor model of personality in young Korean women |
| Q35116111 | Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence |
| Q35882587 | Genome-wide association study of toxic metals and trace elements reveals novel associations |
| Q21143786 | Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan |
| Q35854195 | Genome-wide association study reveals a locus for nasal carriage of Staphylococcus aureus in Danish crossbred pigs |
| Q33535894 | Genome-wide association study reveals multiple loci associated with primary tooth development during infancy |
| Q24652468 | Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia |
| Q37322218 | Genome-wide association study suggested copy number variation may be associated with body mass index in the Chinese population |
| Q37209075 | Genome-wide association study to identify novel loci associated with therapy-related myeloid leukemia susceptibility |
| Q58796205 | Genome-wide association study using haplotype alleles for the evaluation of reproductive traits in Nelore cattle |
| Q34488758 | Genome-wide associations and functional genomic studies of musculoskeletal adverse events in women receiving aromatase inhibitors |
| Q34678968 | Genome-wide associations for birth weight and correlations with adult disease |
| Q34075548 | Genome-wide copy number variation association study suggested VPS13B gene for osteoporosis in Caucasians |
| Q37156061 | Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis |
| Q37640853 | Genome-wide detection of genetic markers associated with growth and fatness in four pig populations using four approaches |
| Q61804392 | Genome-wide gene-based analyses of weight loss interventions identify a potential role for NKX6.3 in metabolism |
| Q38960024 | Genome-wide genetic heterogeneity discovery with categorical covariates |
| Q40400164 | Genome-wide genetic homogeneity between sexes and populations for human height and body mass index |
| Q36184615 | Genome-wide genetic investigation of serological measures of common infections |
| Q90183136 | Genome-wide identification of DNA methylation QTLs in whole blood highlights pathways for cardiovascular disease |
| Q57587870 | Genome-wide linkage and association scans for pulse pressure in Chinese twins |
| Q45138496 | Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux |
| Q33960326 | Genome-wide local ancestry approach identifies genes and variants associated with chemotherapeutic susceptibility in African Americans |
| Q55341981 | Genome-wide mapping of quantitative trait loci in admixed populations using mixed linear model and Bayesian multiple regression analysis. |
| Q47248078 | Genome-wide meta-analyses identifies novel taxane-induced peripheral neuropathy-associated loci |
| Q24597886 | Genome-wide meta-analyses identify multiple loci associated with smoking behavior |
| Q64066365 | Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals |
| Q29417047 | Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci |
| Q39489732 | Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations |
| Q92586755 | Genome-wide meta-analysis of SNP and antihypertensive medication interactions on left ventricular traits in African Americans |
| Q30360969 | Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke. |
| Q34214974 | Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci |
| Q34994543 | Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease |
| Q91736532 | Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry |
| Q36435865 | Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans |
| Q37058633 | Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence |
| Q34502635 | Genome-wide patterns of selection in 230 ancient Eurasians |
| Q33926334 | Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. |
| Q33610252 | Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults |
| Q91971036 | Genome-wide scan highlights the role of candidate genes on phenotypic plasticity for age at first calving in Nellore heifers |
| Q37200992 | Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations |
| Q37148239 | Genome-wide screen for asthma in Puerto Ricans: evidence for association with 5q23 region |
| Q34796363 | Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk |
| Q37563079 | Genome-wide strategies for discovering genetic influences on cognition and cognitive disorders: methodological considerations |
| Q41174649 | Genome-wide studies of von Willebrand factor propeptide identify loci contributing to variation in propeptide levels and von Willebrand factor clearance. |
| Q29417007 | Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility |
| Q57249723 | Genomewide Association Study of an AIDS‐Nonprogression Cohort Emphasizes the Role Played byHLAGenes (ANRS Genomewide Association Study 02) |
| Q28659652 | Genomewide association for schizophrenia in the CATIE study: results of stage 1 |
| Q28742939 | Genomewide association scan of suicidal thoughts and behaviour in major depression |
| Q34982913 | Genomewide association studies in allergy and the influence of ethnicity |
| Q40720335 | Genomewide association study of liver abscess in beef cattle. |
| Q35946334 | Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan |
| Q58047101 | Genomic Control to the extreme |
| Q49644807 | Genomic Prediction and Association Mapping of Curd-Related Traits in Gene Bank Accessions of Cauliflower. |
| Q31096966 | Genomic Profiles of Diversification and Genotype-Phenotype Association in Island Nematode Lineages. |
| Q49399965 | Genomic Region Containing Toll-Like Receptor Genes Has a Major Impact on Total IgM Antibodies Including KLH-Binding IgM Natural Antibodies in Chickens. |
| Q58761912 | Genomic analysis reveals genes affecting distinct phenotypes among different Chinese and western pig breeds |
| Q45985294 | Genomic and genealogical investigation of the French Canadian founder population structure. |
| Q57148357 | Genomic associations with bill length and disease reveal drift and selection across island bird populations |
| Q37466190 | Genomic dissection of population substructure of Han Chinese and its implication in association studies |
| Q35108650 | Genomic inflation factors under polygenic inheritance |
| Q57398166 | Genomic profiling of interpopulation diversity guides prioritization of candidate-genes for autoimmunity |
| Q30991447 | Genomic screening and replication using the same data set in family-based association testing |
| Q36094457 | Genomics, genetic epidemiology, and genomic medicine |
| Q29614590 | Genotype imputation |
| Q36133326 | Genotype-Based Score Test for Association Testing in Families |
| Q37320894 | Genotype-based matching to correct for population stratification in large-scale case-control genetic association studies |
| Q50114444 | Geographical and environmental determinants of the genetic structure of wild barley in southeastern Anatolia. |
| Q37176308 | Geographical structure and differential natural selection among North European populations |
| Q28392728 | Germ line variants predispose to both JAK2 V617F clonal hematopoiesis and myeloproliferative neoplasms |
| Q30979536 | Global Individual Ancestry Using Principal Components for Family Data |
| Q33322404 | Goldsurfer2 (Gs2): a comprehensive tool for the analysis and visualization of genome wide association studies |
| Q34222307 | Grasping nettles: cellular heterogeneity and other confounders in epigenome-wide association studies |
| Q33357910 | HAPSIMU: a genetic simulation platform for population-based association studies. |
| Q37523930 | HEFT: eQTL analysis of many thousands of expressed genes while simultaneously controlling for hidden factors |
| Q35954773 | HLA class II locus and susceptibility to podoconiosis |
| Q37368122 | HLA class II sequence variants influence tuberculosis risk in populations of European ancestry |
| Q34320612 | HSD3B and gene-gene interactions in a pathway-based analysis of genetic susceptibility to bladder cancer |
| Q34182879 | HTreeQA: Using Semi-Perfect Phylogeny Trees in Quantitative Trait Loci Study on Genotype Data |
| Q36439328 | HYST: a hybrid set-based test for genome-wide association studies, with application to protein-protein interaction-based association analysis |
| Q35073303 | Haplotype analysis in population genetics and association studies |
| Q81436606 | Haplotype analysis of the preprotachykinin-1 (TAC1) gene in multiple sclerosis |
| Q34569687 | Haplotype structure and phenotypic associations in the chromosomal regions surrounding two Arabidopsis thaliana flowering time loci |
| Q36698785 | Haplotype thinking in lung disease |
| Q34437899 | Haplotypes with copy number and single nucleotide polymorphisms in CYP2A6 locus are associated with smoking quantity in a Japanese population |
| Q38001919 | Harnessing genomics and genome biology to understand malaria biology |
| Q35583245 | Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence |
| Q36355207 | High gene flow despite opposite chirality in hybrid zones between enantiomorphic door snails |
| Q31139643 | High-resolution SNP scan of chromosome 6p21 in pooled samples from patients with complex diseases |
| Q33358669 | High-resolution mapping of gene expression using association in an outbred mouse stock |
| Q24535861 | High-resolution whole-genome association study of Parkinson disease. |
| Q49484498 | Homocysteine levels associate with subtle changes in leukocyte DNA methylation: an epigenome-wide analysis. |
| Q34107976 | How to deal with the early GWAS data when imputing and combining different arrays is necessary |
| Q38953773 | Human Birth Weight and Reproductive Immunology: Testing for Interactions between Maternal and Offspring KIR and HLA-C Genes |
| Q93036777 | Human exposure to trichloroethylene is associated with increased variability of blood DNA methylation that is enriched in genes and pathways related to autoimmune disease and cancer |
| Q35164673 | Human population structure and genetic association studies |
| Q24630979 | Hundreds of variants clustered in genomic loci and biological pathways affect human height |
| Q33438460 | IL10 Haplotype Associated with Tuberculin Skin Test Response but Not with Pulmonary TB |
| Q29614896 | IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapy |
| Q33858333 | IMPROVING POPULATION-SPECIFIC ALLELE FREQUENCY ESTIMATES BY ADAPTING SUPPLEMENTAL DATA: AN EMPIRICAL BAYES APPROACH. |
| Q35207735 | IREB2 and GALC are associated with pulmonary artery enlargement in chronic obstructive pulmonary disease |
| Q61805919 | Identification of 12 genetic loci associated with human healthspan |
| Q30419116 | Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. |
| Q29417010 | Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies |
| Q36891119 | Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility |
| Q34127757 | Identification of Diabetic Retinopathy Genes through a Genome-Wide Association Study among Mexican-Americans from Starr County, Texas |
| Q21134736 | Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study |
| Q33367562 | Identification of PLCL1 gene for hip bone size variation in females in a genome-wide association study |
| Q40534911 | Identification of Susceptibility Loci for Cutaneous Squamous Cell Carcinoma |
| Q92830041 | Identification of a 1p21 independent functional variant for abdominal obesity |
| Q35560469 | Identification of a Novel Mucin Gene HCG22 Associated With Steroid-Induced Ocular Hypertension |
| Q28943257 | Identification of a candidate gene for astigmatism |
| Q34506471 | Identification of a short region on chromosome 6 affecting direct calving ease in Piedmontese cattle breed |
| Q33954488 | Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals |
| Q28943285 | Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study |
| Q35031906 | Identification of associated SSR markers for yield component and fiber quality traits based on frame map and Upland cotton collections |
| Q84918997 | Identification of chromosomal locations associated with tail biting and being a victim of tail-biting behaviour in the domestic pig (Sus scrofa domesticus) |
| Q36792668 | Identification of common variants associated with human hippocampal and intracranial volumes |
| Q35190649 | Identification of fat4 and tsc22d1 as novel candidate genes for spontaneous pulmonary adenomas |
| Q29417130 | Identification of loci associated with schizophrenia by genome-wide association and follow-up |
| Q35692714 | Identification of new susceptibility loci for IgA nephropathy in Han Chinese. |
| Q33954423 | Identification of nine novel loci associated with white blood cell subtypes in a Japanese population |
| Q90091185 | Identification of novel breast cancer susceptibility loci in meta-analyses conducted among Asian and European descendants |
| Q36147462 | Identification of novel germline polymorphisms governing capecitabine sensitivity. |
| Q34457014 | Identification of novel single nucleotide polymorphisms associated with acute respiratory distress syndrome by exome-seq |
| Q30490128 | Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolates |
| Q89705331 | Identification of novel variants and candidate genes associated with porcine bone mineral density using genome-wide association study |
| Q57249724 | Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scans |
| Q96136701 | Identification of type 2 diabetes loci in 433,540 East Asian individuals |
| Q58896057 | Identifying QTLs and Epistasis in Structured Plant Populations Using Adaptive Mixed LASSO |
| Q35079924 | Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach |
| Q57464769 | Identifying loci affecting trait variability and detecting interactions in genome-wide association studies |
| Q91743420 | Identifying loci with breeding potential across temperate and tropical adaptation via EigenGWAS and EnvGWAS |
| Q39450044 | Identifying outlier loci in admixed and in continuous populations using ancestral population differentiation statistics. |
| Q38610509 | Identifying pleiotropic genes in genome-wide association studies from related subjects using the linear mixed model and Fisher combination function. |
| Q30948190 | Identifying the susceptibility gene(s) in a set of trait-linked genes using genotype data |
| Q36440915 | Imaging phenotypes and genotypes in schizophrenia |
| Q36791694 | Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance |
| Q40045602 | Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis. |
| Q34077316 | Impact of female cigarette smoking on circulating B cells in vivo: the suppressed ICOSLG, TCF3, and VCAM1 gene functional network may inhibit normal cell function |
| Q36474856 | Impact of human population history on distributions of individual-level genetic distance |
| Q44469372 | Impact of population substructure on trend tests for genetic case-control association studies |
| Q35055247 | Impacts of population structure and analytical models in genome-wide association studies of complex traits in forest trees: a case study in Eucalyptus globulus |
| Q34362378 | Implications of correlations between skin color and genetic ancestry for biomedical research. |
| Q52576545 | Improved Use of Small Reference Panels for Conditional and Joint Analysis with GWAS Summary Statistics. |
| Q36865877 | Improved ancestry inference using weights from external reference panels |
| Q80413781 | Improved correction for population stratification in genome-wide association studies by identifying hidden population structures |
| Q34342469 | Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate |
| Q34325802 | Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors |
| Q91968660 | Improved detection of common variants in coronary artery disease and blood pressure using a pleiotropy cFDR method |
| Q30942462 | Improved integrative framework combining association data with gene expression features to prioritize Crohn's disease genes |
| Q57057122 | Improving Imputation Accuracy by Inferring Causal Variants in Genetic Studies |
| Q33502372 | Improving power in genetic-association studies via wavelet transformation |
| Q33895016 | Improving the power of GWAS and avoiding confounding from population stratification with PC-Select |
| Q61443957 | Imputation to whole-genome sequence using multiple pig populations and its use in genome-wide association studies |
| Q34114536 | Imputation without doing imputation: a new method for the detection of non-genotyped causal variants |
| Q38616956 | In silico phenotyping via co-training for improved phenotype prediction from genotype |
| Q38375854 | Including additional controls from public databases improves the power of a genome-wide association study |
| Q48220907 | Inconsistent designs of association studies: a missed opportunity |
| Q40592888 | Increased Power for Detection of Parent-of-Origin Effects via the Use of Haplotype Estimation |
| Q89601889 | Increased circulating levels of Factor H-Related Protein 4 are strongly associated with age-related macular degeneration |
| Q34505622 | Increased power of mixed models facilitates association mapping of 10 loci for metabolic traits in an isolated population |
| Q36024232 | Inference of kinship using spatial distributions of SNPs for genome-wide association studies |
| Q29615942 | Inference of population structure using multilocus genotype data: dominant markers and null alleles |
| Q38851560 | Inference on the Genetic Basis of Eye and Skin Color in an Admixed Population via Bayesian Linear Mixed Models |
| Q36268143 | Inferences from genomic models in stratified populations |
| Q36730128 | Influence of common genetic variation on blood lipid levels, cardiovascular risk, and coronary events in two British prospective cohort studies |
| Q33362603 | Influence of genotyping error in linkage mapping for complex traits--an analytic study |
| Q34372353 | Inheritance beyond plain heritability: variance-controlling genes in Arabidopsis thaliana. |
| Q64461691 | Insight into the genetic architecture of back pain and its risk factors from a study of 509,000 individuals |
| Q95730181 | Insights into the genetic basis of retinal detachment |
| Q31031864 | Integrated analysis of genetic data with R. |
| Q36260421 | Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies |
| Q34961828 | Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes |
| Q35038043 | Integrating epidemiology and genetic association: the challenge of gene-environment interaction |
| Q36214438 | Integrating mean and variance heterogeneities to identify differentially expressed genes |
| Q36545157 | Integration of cell line and clinical trial genome-wide analyses supports a polygenic architecture of Paclitaxel-induced sensory peripheral neuropathy |
| Q30278644 | Integrative pathway genomics of lung function and airflow obstruction |
| Q59806150 | Interethnic analyses of blood pressure loci in populations of East Asian and European descent |
| Q36087896 | International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways |
| Q35082735 | Interpretation of genetic association studies in complex disease |
| Q34313660 | Interrogating local population structure for fine mapping in genome-wide association studies. |
| Q24288726 | Investigating the role of mitochondrial haplogroups in genetic predisposition to meningococcal disease |
| Q93079302 | Investigation of Maternal Effects, Maternal-Fetal Interactions, and Parent-of-Origin Effects (Imprinting) for Candidate Genes Positioned on Chromosome 18q21, in Probands with Schizophrenia and their First-Degree Relatives |
| Q34511692 | Investigation of maternal effects, maternal-fetal interactions and parent-of-origin effects (imprinting), using mothers and their offspring |
| Q44199896 | Investigation of the fine structure of European populations with applications to disease association studies |
| Q39861509 | Involvement of SMARCA2/BRM in the SWI/SNF chromatin-remodeling complex in schizophrenia |
| Q24288730 | Is replication the gold standard for validating genome-wide association findings? |
| Q51976715 | Issues in association analysis: error control in case-control association studies for disease gene discovery. |
| Q24657654 | Japanese population structure, based on SNP genotypes from 7003 individuals compared to other ethnic groups: effects on population-based association studies |
| Q61805692 | Joint Analysis of Multiple Phenotypes in Association Studies based on Cross-Validation Prediction Error |
| Q35948043 | Joint Analysis of Multiple Traits Using "Optimal" Maximum Heritability Test |
| Q36813570 | Joint Analysis of Multiple Traits in Rare Variant Association Studies |
| Q31026573 | Joint analysis for genome-wide association studies in family-based designs |
| Q34320527 | Joint linkage-linkage disequilibrium mapping is a powerful approach to detecting quantitative trait loci underlying drought tolerance in maize |
| Q52676895 | Joint study of two genome-wide association meta-analyses identified 20p12.1 and 20q13.33 for bone mineral density. |
| Q36254149 | Key concepts in genetic epidemiology |
| Q35831121 | LD Score regression distinguishes confounding from polygenicity in genome-wide association studies |
| Q34748177 | LDL-cholesterol concentrations: a genome-wide association study |
| Q92321993 | LEI: A Novel Allele Frequency-Based Feature Selection Method for Multi-ancestry Admixed Populations |
| Q30499949 | Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies |
| Q58529972 | Lack of association between the corticotropin-releasing hormone locus and rheumatoid arthritis |
| Q93254970 | Landscape genomics provides evidence of climate-associated genetic variation in Mexican populations of Quercus rugosa |
| Q30941054 | Laplacian eigenfunctions learn population structure |
| Q34432345 | Large-scale SNP analysis reveals clustered and continuous patterns of human genetic variation |
| Q29417023 | Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease |
| Q28272915 | Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes |
| Q24596652 | Large-scale candidate gene analysis of spontaneous clearance of hepatitis C virus |
| Q29417143 | Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 |
| Q29416989 | Large-scale genotyping identifies 41 new loci associated with breast cancer risk |
| Q30502442 | Large-scale in silico mapping of complex quantitative traits in inbred mice |
| Q38948366 | Leaf Growth Response to Mild Drought: Natural Variation in Arabidopsis Sheds Light on Trait Architecture. |
| Q33289961 | Leveraging hierarchical population structure in discrete association studies |
| Q53648320 | Leveraging population information in family-based rare variant association analyses of quantitative traits. |
| Q33910261 | Linkage analysis of a complex disease through use of admixed populations. |
| Q47182807 | Linkage analysis of adult height in a large pedigree from a Dutch genetically isolated population |
| Q35789952 | Linkage analysis without defined pedigrees |
| Q35046494 | Linkage disequilibrium analysis of the renin-angiotensin system genes. |
| Q33793490 | Linkage disequilibrium mapping of the chromosome 6q21-22.31 bipolar I disorder susceptibility locus |
| Q28752440 | Linkage disequilibrium mapping of the replicated type 2 diabetes linkage signal on chromosome 1q |
| Q39576724 | Linking Alzheimer's disease and type 2 diabetes: Novel shared susceptibility genes detected by cFDR approach. |
| Q37519086 | Liver Enzymes and Risk of Ischemic Heart Disease and Type 2 Diabetes Mellitus: A Mendelian Randomization Study |
| Q36439846 | Local ancestry corrects for population structure in Saccharomyces cerevisiae genome-wide association studies |
| Q35119731 | Local and global ancestry inference and applications to genetic association analysis for admixed populations |
| Q36853815 | Loci influencing blood pressure identified using a cardiovascular gene-centric array |
| Q43198448 | Logistic regression protects against population structure in genetic association studies |
| Q34010750 | Longitudinal analysis is more powerful than cross-sectional analysis in detecting genetic association with neuroimaging phenotypes |
| Q34468561 | Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease |
| Q48168326 | Loss-of-function variants in ATM confer risk of gastric cancer |
| Q29547217 | METAL: fast and efficient meta-analysis of genomewide association scans |
| Q36416257 | Major regulatory genes in maize contribute to standing variation in teosinte (Zea mays ssp. parviglumis). |
| Q51580308 | Mapping QTLs for improving grain yield using the USDA rice mini-core collection. |
| Q28087013 | Mapping asthma-associated variants in admixed populations |
| Q34348337 | Mapping genes that predict treatment outcome in admixed populations |
| Q28601618 | Mapping the genomic architecture of adaptive traits with interspecific introgressive origin: a coalescent-based approach |
| Q42086468 | Marbled inflation from population structure in gene-based association studies with rare variants |
| Q33909653 | Matching strategies for genetic association studies in structured populations |
| Q36015303 | Maternal Smoking during Pregnancy and DNA-Methylation in Children at Age 5.5 Years: Epigenome-Wide-Analysis in the European Childhood Obesity Project (CHOP)-Study |
| Q36569421 | Maternal plasma folate impacts differential DNA methylation in an epigenome-wide meta-analysis of newborns |
| Q35952214 | Maximizing the Power of Genome-Wide Association Studies: A Novel Class of Powerful Family-Based Association Tests |
| Q24682611 | Measuring European population stratification with microarray genotype data |
| Q34376788 | Measuring and using admixture to study the genetics of complex diseases |
| Q36950890 | Mechanisms of disease: The genetic basis of coronary heart disease. |
| Q22252418 | Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder |
| Q34142739 | Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution |
| Q28943527 | Meta-analysis identifies a MECOM gene as a novel predisposing factor of osteoporotic fracture |
| Q35785297 | Meta-analysis identifies common variants associated with body mass index in east Asians |
| Q45807411 | Meta-analysis identifies loci affecting levels of the potential osteoarthritis biomarkers sCOMP and uCTX-II with genome wide significance |
| Q36764466 | Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error |
| Q29417150 | Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1. |
| Q30669834 | Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity |
| Q29417079 | Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22 |
| Q35172107 | Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians |
| Q30277235 | Meta-analysis of genome-wide association studies identifies three novel loci for saturated fatty acids in East Asians |
| Q34555532 | Meta-analysis of genome-wide association studies identifies two loci associated with circulating osteoprotegerin levels |
| Q30411328 | Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes |
| Q34211781 | Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index |
| Q35152820 | Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci |
| Q34851773 | Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants |
| Q37757136 | Methodological and statistical issues in pharmacogenomics |
| Q28681049 | Methodological challenges of genome-wide association analysis in Africa |
| Q37807426 | Methodological issues of genetic association studies |
| Q37999301 | Methods for detecting and correcting for population stratification |
| Q22337164 | Methods for high-density admixture mapping of disease genes |
| Q30617964 | Methods for meta-analysis of genetic data |
| Q37707119 | Methods for optimizing statistical analyses in pharmacogenomics research |
| Q34604581 | MethylPCA: a toolkit to control for confounders in methylome-wide association studies |
| Q28742733 | MicroRNA expression in abdominal and gluteal adipose tissue is associated with mRNA expression levels and partly genetically driven |
| Q21562568 | Mitochondrial DNA haplogroup D4a is a marker for extreme longevity in Japan |
| Q59192511 | Mixed Ancestry and Disease Risk Transferability |
| Q40408225 | Mixed Model Association with Family-Biased Case-Control Ascertainment |
| Q34097144 | Mixed linear model approach adapted for genome-wide association studies |
| Q41042554 | Mixed model with correction for case-control ascertainment increases association power |
| Q33772072 | Model-based multifactor dimensionality reduction for detecting epistasis in case-control data in the presence of noise |
| Q34629056 | Modulation of cystic fibrosis lung disease by variants in interleukin-8. |
| Q35691688 | Molecular genetic studies of gene identification for osteoporosis: a 2004 update |
| Q34756545 | Molecular genetic studies of schizophrenia: challenges and insights |
| Q28673414 | Molecular reclassification of Crohn's disease: a cautionary note on population stratification |
| Q62477920 | Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions |
| Q57073078 | Multi-Environmental Trials Reveal Genetic Plasticity of Oat Agronomic Traits Associated With Climate Variable Changes |
| Q54234994 | Multi-locus Test and Correction for Confounding Effects in Genome-Wide Association Studies. |
| Q46899641 | Multi-locus candidate gene polymorphisms and risk of myocardial infarction: a population-based, prospective genetic analysis |
| Q33896238 | Multi-population GWA mapping via multi-task regularized regression |
| Q35808621 | Multicohort genomewide association study reveals a new signal of protection against HIV-1 acquisition |
| Q34468692 | Multifactor dimensionality reduction for detecting gene-gene and gene-environment interactions in pharmacogenomics studies |
| Q30815413 | Multilocus statistics to uncover epistasis and heterogeneity in complex diseases: revisiting a set of multiple sclerosis data |
| Q37283463 | Multiple Loci within the major histocompatibility complex confer risk of psoriasis |
| Q47746680 | Multiple genes influence BMI on chromosome 7q31-34: the NHLBI Family Heart Study |
| Q46937467 | Multiple hypothesis testing in genomics. |
| Q37276573 | Multiple imputation to correct for measurement error in admixture estimates in genetic structured association testing |
| Q24655591 | Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium |
| Q34378679 | Multistage analysis strategies for genome-wide association studies: summary of group 3 contributions to Genetic Analysis Workshop 16. |
| Q37619295 | Multistage genome-wide association meta-analyses identified two new loci for bone mineral density |
| Q40054832 | Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation |
| Q31018434 | Myelin basic protein as a novel genetic risk factor in rheumatoid arthritis--a genome-wide study combined with immunological analyses |
| Q38404295 | NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality |
| Q37306237 | NQO1 polymorphisms and de novo childhood leukemia: a HuGE review and meta-analysis |
| Q39479443 | Nationwide Genomic Study in Denmark Reveals Remarkable Population Homogeneity |
| Q35517391 | Natural CMT2 variation is associated with genome-wide methylation changes and temperature seasonality |
| Q36163079 | Natural variation in Arabidopsis. How do we find the causal genes? |
| Q33818067 | Neuronal genes for subcutaneous fat thickness in human and pig are identified by local genomic sequencing and combined SNP association study |
| Q37765137 | New approaches to population stratification in genome-wide association studies |
| Q35909375 | New gene functions in megakaryopoiesis and platelet formation |
| Q44613289 | New genetic evidence for involvement of the dopamine system in migraine with aura |
| Q28270700 | New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk |
| Q35114362 | New genetic loci link adipose and insulin biology to body fat distribution |
| Q36708957 | New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism |
| Q24630646 | New loci associated with kidney function and chronic kidney disease |
| Q30844089 | New statistical approaches exploit the polygenic architecture of schizophrenia--implications for the underlying neurobiology |
| Q24654340 | Newly identified genetic risk variants for celiac disease related to the immune response |
| Q28264535 | Newly identified loci that influence lipid concentrations and risk of coronary artery disease |
| Q37330353 | No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis |
| Q39142200 | No association between NRG1 and ErbB4 genes and psychopathological symptoms of schizophrenia |
| Q52148454 | No association between schizophrenia susceptibility variants and macroscopic structural brain volume variation in healthy subjects. |
| Q34796836 | No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects |
| Q52011683 | No evidence for phenotypic variation between probands in case-control versus family-based association studies of schizophrenia. |
| Q36851908 | Non-replication of association studies: "pseudo-failures" to replicate? |
| Q37260633 | Nonmetric multidimensional scaling corrects for population structure in association mapping with different sample types |
| Q33942281 | Nonparametric tests of association of multiple genes with human disease |
| Q35579884 | Nonreplication in Genetic Association Studies of Obesity and Diabetes Research |
| Q47150554 | Novel Common Variants Associated with Obesity and Type 2 Diabetes Detected Using a cFDR Method |
| Q33349442 | Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women |
| Q33906355 | Novel case-control test in a founder population identifies P-selectin as an atopy-susceptibility locus |
| Q35603770 | Novel genetic matching methods for handling population stratification in genome-wide association studies |
| Q36939452 | Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects |
| Q36615898 | Novel loci and pathways significantly associated with longevity |
| Q30416016 | Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts |
| Q36966054 | Novel methods for detecting epistasis in pharmacogenomics studies |
| Q39063443 | Novel probabilistic models of spatial genetic ancestry with applications to stratification correction in genome-wide association studies |
| Q47858538 | OPATs: Omnibus P-value association tests. |
| Q64287594 | OSCA: a tool for omic-data-based complex trait analysis |
| Q37485550 | On Robust Association Testing for Quantitative Traits and Rare Variants. |
| Q52947036 | On a semiparametric test to detect associations between quantitative traits and candidate genes using unrelated individuals. |
| Q37570009 | On association analysis of rare variants under population substructure: an approach for the detection of subjects that can cause bias in the analysis--T opt: an outlier detection method |
| Q33392516 | On combining triads and unrelated subjects data in candidate gene studies: an application to data on testicular cancer |
| Q41665474 | On the adjustment for covariates in genetic association analysis: a novel, simple principle to infer direct causal effects |
| Q30944833 | On the analysis of genome-wide association studies in family-based designs: a universal, robust analysis approach and an application to four genome-wide association studies |
| Q57398172 | On the applicability of a haplotype map to un-assayed populations |
| Q33576480 | On the association analysis of CNV data: a fast and robust family-based association method |
| Q90261614 | On the differences between mega- and meta-imputation and analysis exemplified on the genetics of age-related macular degeneration |
| Q33905080 | On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit. |
| Q47116107 | On the impact of relatedness on SNP association analysis |
| Q36718825 | On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants |
| Q36235583 | On the validity of the likelihood ratio test and consistency of resulting parameter estimates in joint linkage and linkage disequilibrium analysis under improperly specified parametric models |
| Q33332834 | One-stage design is empirically more powerful than two-stage design for family-based genome-wide association studies |
| Q42400210 | Optimizing the power of genome-wide association studies by using publicly available reference samples to expand the control group |
| Q33323356 | Osteopontin and systemic lupus erythematosus association: a probable gene-gender interaction |
| Q40477448 | Overdispersion of allele frequency differences between populations: implications for meta-analyses of genotypic disease associations. |
| Q34573373 | Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses |
| Q33632115 | Overview of techniques to account for confounding due to population stratification and cryptic relatedness in genomic data association analyses. |
| Q33300136 | PCA-correlated SNPs for structure identification in worldwide human populations |
| Q24614975 | PKCα is genetically linked to memory capacity in healthy subjects and to risk for posttraumatic stress disorder in genocide survivors |
| Q24677407 | PLINK: a tool set for whole-genome association and population-based linkage analyses |
| Q30653367 | PUMA: a unified framework for penalized multiple regression analysis of GWAS data |
| Q37102209 | Parental origin of sequence variants associated with complex diseases |
| Q88508400 | Parenting stress and DNA methylation among African Americans in the InterGEN Study |
| Q33961554 | Pathway-based association analyses identified TRAIL pathway for osteoporotic fractures |
| Q33636681 | Pathway-based genome-wide association analysis identified the importance of EphrinA-EphR pathway for femoral neck bone geometry |
| Q35157827 | Pathway-based genome-wide association analysis identified the importance of regulation-of-autophagy pathway for ultradistal radius BMD. |
| Q40344929 | Pathway-based variant enrichment analysis on the example of dilated cardiomyopathy. |
| Q41811636 | Patterns of methylation heritability in a genome-wide analysis of four brain regions. |
| Q47282078 | Perceived Racial Discrimination and DNA Methylation Among African American Women in the InterGEN Study |
| Q36833380 | Periconceptional folate consumption is associated with neonatal DNA methylation modifications in neural crest regulatory and cancer development genes |
| Q41908748 | Permutation testing in the presence of polygenic variation |
| Q36105218 | Permutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis |
| Q41201745 | Perturbation analysis: a simple method for filtering SNPs with erroneous genotyping in genome-wide association studies |
| Q41559949 | Pharmacodynamic genome-wide association study identifies new responsive loci for glucocorticoid intervention in asthma |
| Q36120821 | Pharmacogenetic studies of response to risperidone and other newer atypical antipsychotics |
| Q35038056 | Pharmacogenetics in drug development |
| Q34155796 | Pharmacogenetics of antidepressant response |
| Q34575636 | Pharmacogenomics and schizophrenia: clinical implications |
| Q36221718 | Phenotypic variance explained by local ancestry in admixed African Americans |
| Q37877244 | Planning a genome-wide association study: points to consider |
| Q28943512 | Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis |
| Q35067424 | Platelet CD36 surface expression levels affect functional responses to oxidized LDL and are associated with inheritance of specific genetic polymorphisms |
| Q34085504 | PlatinumCNV: a Bayesian Gaussian mixture model for genotyping copy number polymorphisms using SNP array signal intensity data |
| Q36351680 | Polygenic Scores in Epidemiology: Risk Prediction, Etiology, and Clinical Utility |
| Q35212317 | Polygenic risk for externalizing disorders: Gene-by-development and gene-by-environment effects in adolescents and young adults |
| Q58462183 | Polygenic risk for schizophrenia and season of birth within the UK Biobank cohort |
| Q43011482 | Polymorphisms in ERCC2, MSH2, and OGG1 DNA repair genes and gallbladder cancer risk in a population of Northern India |
| Q28295248 | Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment |
| Q35152765 | Polymorphisms in HLA-DPB1 are associated with differences in rubella virus-specific humoral immunity after vaccination |
| Q35229951 | Polymorphisms in predicted miRNA binding sites and osteoporosis |
| Q36295787 | Polymorphisms in the serum- and glucocorticoid-inducible kinase 1 gene are associated with blood pressure and renin response to dietary salt intake. |
| Q35232346 | Pooled sequencing and rare variant association tests for identifying the determinants of emerging drug resistance in malaria parasites |
| Q36681034 | Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's disease |
| Q50087966 | Population Stratification in Genetic Association Studies. |
| Q37307521 | Population admixture associated with disease prevalence in the Boston Puerto Rican health study |
| Q34611980 | Population admixture: detection by Hardy-Weinberg test and its quantitative effects on linkage-disequilibrium methods for localizing genes underlying complex traits. |
| Q57317080 | Population differences in the International Multi-Centre ADHD Gene Project |
| Q35098240 | Population stratification and patterns of linkage disequilibrium |
| Q28211105 | Population stratification and spurious allelic association |
| Q46550987 | Population stratification confounds genetic association studies among Latinos |
| Q21145248 | Population structure and eigenanalysis |
| Q60932187 | Population structure in genetic studies: Confounding factors and mixed models |
| Q29614945 | Population structure, differential bias and genomic control in a large-scale, case-control association study |
| Q33348644 | Population substructure and control selection in genome-wide association studies |
| Q34922527 | Population-specific haplotype association of the postsynaptic density gene DLG4 with schizophrenia, in family-based association studies |
| Q44714343 | Possible association between a haplotype of the GABA-A receptor alpha 1 subunit gene (GABRA1) and mood disorders |
| Q43683512 | Postassociation cleaning using linkage disequilibrium information |
| Q35818791 | Posterior predictive checks to quantify lack-of-fit in admixture models of latent population structure |
| Q35711847 | Potential genetic risk factors for chronic TMD: genetic associations from the OPPERA case control study |
| Q37217339 | Power calculations for genetic association studies using estimated probability distributions |
| Q41201653 | Power consequences of linkage disequilibrium variation between populations |
| Q38865539 | Power considerations for λ inflation factor in meta-analyses of genome-wide association studies. |
| Q80713092 | Power of transmission/disequilibrium tests in admixed populations |
| Q64117497 | Powerful testing via hierarchical linkage disequilibrium in haplotype association studies |
| Q28749837 | Practical aspects of imputation-driven meta-analysis of genome-wide association studies |
| Q49053095 | Practical capability and cost effectiveness of a DNA pool-based genome-wide association study using BovineSNP50 array in a cattle population. |
| Q57418932 | Practical population group assignment with selected informative markers: Characteristics and properties of Bayesian clustering via STRUCTURE |
| Q37807916 | Pre-operative pulmonary assessment for patients with hip fracture |
| Q41654260 | Principal component regression and linear mixed model in association analysis of structured samples: competitors or complements? |
| Q27860975 | Principal components analysis corrects for stratification in genome-wide association studies |
| Q33519218 | Principal-component-based population structure adjustment in the North American Rheumatoid Arthritis Consortium data: impact of single-nucleotide polymorphism set and analysis method |
| Q36180606 | Priorities and standards in pharmacogenetic research |
| Q64945658 | Prioritizing Crohn's disease genes by integrating association signals with gene expression implicates monocyte subsets. |
| Q33541240 | ProbABEL package for genome-wide association analysis of imputed data |
| Q36951986 | Probability that a two-stage genome-wide association study will detect a disease-associated snp and implications for multistage designs |
| Q88571278 | Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes |
| Q34537519 | Progress and promise of genome-wide association studies for human complex trait genetics |
| Q63977115 | Promotor genotype of the platelet-derived growth factor receptor-alpha gene shows population stratification but not association with spina bifida meningomyelocele |
| Q34799461 | Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder |
| Q51977908 | Properties of structured association approaches to detecting population stratification. |
| Q34386501 | Proposal for a telehealth concept in the translational research model |
| Q102055043 | Prospecting genomic regions associated with milk production traits in Egyptian buffalo |
| Q21144712 | Prospective study of one million deaths in India: rationale, design, and validation results |
| Q22337163 | Prospects for admixture mapping of complex traits |
| Q42708956 | Prospects for association mapping in classical inbred mouse strains |
| Q34151113 | QTL for white spot syndrome virus resistance and the sex-determining locus in the Indian black tiger shrimp (Penaeus monodon) |
| Q52011034 | Qualitative semi-parametric test for genetic associations in case-control designs under structured populations. |
| Q28656219 | Quality control and conduct of genome-wide association meta-analyses |
| Q30498925 | Quality control and quality assurance in genotypic data for genome-wide association studies |
| Q34732931 | Quality control procedures for genome-wide association studies |
| Q41924730 | Quantification of population structure using correlated SNPs by shrinkage principal components |
| Q34044615 | Quantitative similarity-based association tests using population samples |
| Q40996264 | Quantitative trait Loci association mapping by imputation of strain origins in multifounder crosses |
| Q91989992 | Quick assessment for systematic test statistic inflation/deflation due to null model misspecifications in genome-wide environment interaction studies |
| Q30564266 | RNA-Seq optimization with eQTL gold standards |
| Q33645960 | ROADTRIPS: case-control association testing with partially or completely unknown population and pedigree structure |
| Q35136958 | Random-effects model aimed at discovering associations in meta-analysis of genome-wide association studies |
| Q33432685 | Rapid and accurate multiple testing correction and power estimation for millions of correlated markers |
| Q33539723 | Rapid assessment of genetic ancestry in populations of unknown origin by genome-wide genotyping of pooled samples |
| Q51322861 | Rapid variance components-based method for whole-genome association analysis. |
| Q34306378 | Rare and low frequency variant stratification in the UK population: description and impact on association tests. |
| Q34682478 | Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease |
| Q26852733 | Rare-variant association analysis: study designs and statistical tests |
| Q34448299 | Recent advances in computational genomics |
| Q90574779 | Reduced neonatal brain-derived neurotrophic factor is associated with autism spectrum disorders |
| Q52327404 | Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. |
| Q31120147 | Region-based association analysis of human quantitative traits in related individuals |
| Q33255347 | Regional admixture mapping and structured association testing: conceptual unification and an extensible general linear model |
| Q37378123 | Replication of celiac disease UK genome-wide association study results in a US population |
| Q41963101 | Replication of genetic associations as pseudoreplication due to shared genealogy |
| Q34051756 | Replication study of candidate genes/loci associated with osteoporosis based on genome-wide screening |
| Q44000393 | Replication study of novel risk variants in six genes with type 2 diabetes and related quantitative traits in the Han Chinese lean individuals |
| Q33184110 | Reporting, appraising, and integrating data on genotype prevalence and gene-disease associations |
| Q30841474 | Reproduction and In-Depth Evaluation of Genome-Wide Association Studies and Genome-Wide Meta-analyses Using Summary Statistics |
| Q52373466 | Research Techniques Made Simple: Using Genome-Wide Association Studies to Understand Complex Cutaneous Disorders. |
| Q34482919 | Results of a "GWAS plus:" general cognitive ability is substantially heritable and massively polygenic |
| Q46686237 | Results of a haplotype-based GWAS for recurrent laryngeal neuropathy in the horse |
| Q24657564 | Revealing the architecture of gene regulation: the promise of eQTL studies |
| Q30492697 | Review and evaluation of methods correcting for population stratification with a focus on underlying statistical principles |
| Q48133826 | Risk estimation model for nonalcoholic fatty liver disease in the Japanese using multiple genetic markers. |
| Q51570163 | Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. |
| Q35748549 | Robust and Powerful Affected Sibpair Test for Rare Variant Association |
| Q51921994 | Robust genomic control and robust delta centralization tests for case-control association studies. |
| Q34398890 | Robust genomic control for association studies |
| Q36813187 | Robust inference of population structure for ancestry prediction and correction of stratification in the presence of relatedness |
| Q44355927 | Robust linear regression methods in association studies. |
| Q34677850 | Robust methods for population stratification in genome wide association studies |
| Q35830576 | Role of angiotensin II type I (AT1 A1166C) receptor polymorphism in susceptibility of left ventricular dysfunction |
| Q39650084 | Role of common sarcomeric gene polymorphisms in genetic susceptibility to left ventricular dysfunction |
| Q36246589 | SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypes |
| Q45965746 | SNP-based analysis of genetic substructure in the German population. |
| Q33423394 | SNPit: a federated data integration system for the purpose of functional SNP annotation |
| Q33300170 | Sample matching by inferred agonal stress in gene expression analyses of the brain |
| Q47445341 | Sample size calculations for population- and family-based case-control association studies on marker genotypes |
| Q35126150 | Sardinians genetic background explained by runs of homozygosity and genomic regions under positive selection. |
| Q28652647 | Scalable privacy-preserving data sharing methodology for genome-wide association studies |
| Q29616281 | Score tests for association between traits and haplotypes when linkage phase is ambiguous |
| Q36310868 | Screening for interaction effects in gene expression data |
| Q53010655 | Search for low penetrance alleles for colorectal cancer through a scan of 1467 non-synonymous SNPs in 2575 cases and 2707 controls with validation by kin-cohort analysis of 14 704 first-degree relatives. |
| Q37179785 | Searching for disease susceptibility variants in structured populations |
| Q36834152 | Searching for genes underlying susceptibility to osteoporotic fracture: current progress and future prospect |
| Q22337300 | Searching for genetic determinants in the new millennium |
| Q33232696 | Selecting cases from nuclear families for case-control association analysis |
| Q37626196 | Selection against variants in the genome associated with educational attainment |
| Q37009636 | Selective estrogen receptor modulators and pharmacogenomic variation in ZNF423 regulation of BRCA1 expression: individualized breast cancer prevention |
| Q34669917 | Self-reported ethnicity, genetic structure and the impact of population stratification in a multiethnic study |
| Q41917642 | Semi-supervised spectral clustering with application to detect population stratification |
| Q28478141 | Sensitivity of genome-wide-association signals to phenotyping strategy: the PROP-TAS2R38 taste association as a benchmark |
| Q47138654 | Sequence data and association statistics from 12,940 type 2 diabetes cases and controls |
| Q35964294 | Sequence variant on 8q24 confers susceptibility to urinary bladder cancer |
| Q34112069 | Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior |
| Q34829535 | Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption |
| Q33786392 | Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis |
| Q44808056 | Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility |
| Q28943501 | Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density |
| Q36511060 | Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures |
| Q34743856 | Sequence variants in the RNF212 gene associate with genome-wide recombination rate |
| Q39162678 | Sequencing and expression analyses of the synaptic lipid raft adapter gene PAG1 in schizophrenia |
| Q24628995 | Serotonin Receptor 2A (HTR2A) Gene Polymorphisms Are Associated with Blood Pressure, Central Adiposity, and the Metabolic Syndrome |
| Q36336558 | Serotonin gene polymorphisms and bipolar I disorder: focus on the serotonin transporter |
| Q39696405 | Serotonin receptor 2A (HTR2A) gene polymorphism predicts treatment response to venlafaxine XR in generalized anxiety disorder |
| Q36291621 | Serotonin transporter polymorphism and borderline or antisocial traits among low-income young adults |
| Q29416998 | Seven new loci associated with age-related macular degeneration |
| Q48317391 | Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31. |
| Q35824202 | Severity of Mitral Valve Degeneration Is Associated with Chromosome 15 Loci in Whippet Dogs |
| Q34765317 | Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits |
| Q37240605 | Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms |
| Q34342875 | Sherlock: detecting gene-disease associations by matching patterns of expression QTL and GWAS |
| Q34355228 | Shifting paradigms in gene-mapping methodology for complex traits |
| Q46294943 | Signatures of polygenic adaptation associated with climate across the range of a threatened fish species with high genetic connectivity. |
| Q92873138 | Significance testing and genomic inflation factor using high-density genotypes or whole-genome sequence data |
| Q42816435 | Simultaneously accounting for population structure, genotype by environment interaction, and spatial variation in marker-trait associations in sugarcane |
| Q36430788 | Simultaneously correcting for population stratification and for genotyping error in case-control association studies |
| Q36094770 | Single Nucleotide Polymorphism Clustering in Systemic Autoimmune Diseases |
| Q33835639 | Single nucleotide polymorphism and haplotype effects associated with somatic cell score in German Holstein cattle |
| Q35030943 | Single nucleotide polymorphisms in innate immunity genes: abundant variation and potential role in complex human disease |
| Q37462074 | Single-nucleotide polymorphism bioinformatics: a comprehensive review of resources |
| Q91014086 | Single-nucleotide polymorphisms in a cohort of significantly obese women without cardiometabolic diseases |
| Q36392496 | Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation |
| Q90053897 | Sketching algorithms for genomic data analysis and querying in a secure enclave |
| Q44812227 | Socio-economic status covaries with central nervous system serotonergic responsivity as a function of allelic variation in the serotonin transporter gene-linked polymorphic region |
| Q91845288 | Some statistical consideration in transcriptome-wide association studies |
| Q34775103 | Special considerations in prognostic research in cancer involving genetic polymorphisms |
| Q58554313 | Species-Wide Variation in Shoot Nitrate Concentration, and Genetic Loci Controlling Nitrate, Phosphorus and Potassium Accumulation in L |
| Q35185164 | Statistical Optimization of Pharmacogenomics Association Studies: Key Considerations from Study Design to Analysis |
| Q26799032 | Statistical analysis for genome-wide association study |
| Q51927030 | Statistical analysis for haplotype-based matched case-control studies. |
| Q79202441 | Statistical analysis of the GAMES studies |
| Q37279970 | Statistical distributions of test statistics used for quantitative trait association mapping in structured populations |
| Q36391069 | Statistical genetic issues for genome-wide association studies |
| Q30798286 | Statistical power to detect genetic (co)variance of complex traits using SNP data in unrelated samples. |
| Q36252211 | Statistical tools for linkage analysis and genetic association studies |
| Q34137330 | Straightforward inference of ancestry and admixture proportions through ancestry-informative insertion deletion multiplexing. |
| Q40651600 | Strategies to improve the performance of rare variant association studies by optimizing the selection of controls |
| Q37115935 | Study designs for genome-wide association studies |
| Q33292908 | Subarachnoid hemorrhage: tests of association with apolipoprotein E and elastin genes |
| Q38087425 | Substance use disorders: a theory-driven approach to the integration of genetics and neuroimaging |
| Q52007503 | Sum statistics for the joint detection of multiple disease loci in case-control association studies with SNP markers. |
| Q90227989 | SumHer better estimates the SNP heritability of complex traits from summary statistics |
| Q45022135 | Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12-16 October 2014. |
| Q35008595 | Summary of results and discussions from the gene-based tests group at Genetic Analysis Workshop 18. |
| Q35532894 | Susceptibility loci revealed for bovine respiratory disease complex in pre-weaned holstein calves |
| Q55374314 | Susceptibility to corticosteroid-induced adrenal suppression: a genome-wide association study. |
| Q34291615 | Susceptibility to leprosy is associated with PARK2 and PACRG. |
| Q34615542 | Syndrome-causing mutations of the BLM gene in persons in the Bloom's Syndrome Registry |
| Q33917269 | Synthesis of 53 tissue and cell line expression QTL datasets reveals master eQTLs |
| Q35211167 | Systematic permutation testing in GWAS pathway analyses: identification of genetic networks in dilated cardiomyopathy and ulcerative colitis. |
| Q42377141 | Systematic removal of outliers to reduce heterogeneity in case-control association studies |
| Q35169046 | Systemic sclerosis: the susceptible host (genetics and environment). |
| Q40487943 | TESS3: fast inference of spatial population structure and genome scans for selection. |
| Q24657292 | TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study |
| Q33847792 | Testing for an unusual distribution of rare variants |
| Q42613826 | Testing for association based on excess allele sharing in a sample of related cases and controls |
| Q51851098 | Testing for genetic association in the presence of population stratification in genome-wide association studies. |
| Q41141623 | Testing for genetic associations in arbitrarily structured populations |
| Q29399910 | Testing for non-random mating: evidence for ancestry-related assortative mating in the Framingham heart study |
| Q39883188 | Testing for polygenic effects in genome-wide association studies. |
| Q40725291 | Testing for population subdivision and association in four case-control studies |
| Q37394166 | Tests of association for quantitative traits in nuclear families using principal components to correct for population stratification |
| Q47677767 | The Analysis of Ethnic Mixtures |
| Q35766836 | The Bayesian revolution in genetics |
| Q48294110 | The CRP and GDNF genes do not contribute to apnea-hypopnea index or risk of obstructive sleep apnea |
| Q91386056 | The DNA methylome in panic disorder: a case-control and longitudinal psychotherapy-epigenetic study |
| Q48850972 | The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl. |
| Q37223768 | The GABA transporter 1 (SLC6A1): a novel candidate gene for anxiety disorders |
| Q28685216 | The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation |
| Q34673513 | The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study |
| Q58618177 | The Joint Null Criterion for Multiple Hypothesis Tests |
| Q24569609 | The NCBI dbGaP database of genotypes and phenotypes |
| Q36915440 | The Population Reference Sample, POPRES: a resource for population, disease, and pharmacological genetics research |
| Q36469964 | The Quantitative-MFG Test: A Linear Mixed Effect Model to Detect Maternal-Offspring Gene Interactions |
| Q33600077 | The Relation Between Inflation in Type-I and Type-II Error Rate and Population Divergence in Genome-Wide Association Analysis of Multi-Ethnic Populations |
| Q53572756 | The SERPINE2 gene is associated with chronic obstructive pulmonary disease in two large populations. |
| Q91713761 | The accuracy of LD Score regression as an estimator of confounding and genetic correlations in genome-wide association studies |
| Q36622794 | The analysis of ethnic mixtures |
| Q38105252 | The benefits of selecting phenotype-specific variants for applications of mixed models in genomics |
| Q42674445 | The bias introduced by population stratification in IBD based linkage analysis |
| Q87221623 | The challenge of causal inference in gene-environment interaction research: leveraging research designs from the social sciences |
| Q37090601 | The complex genetics of multiple sclerosis: pitfalls and prospects |
| Q36847577 | The concerted impact of domestication and transposon insertions on methylation patterns between dogs and grey wolves |
| Q37483891 | The confounding effect of cryptic relatedness for environmental risks of systolic blood pressure on cohort studies |
| Q57294388 | The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype |
| Q35608194 | The effect of rare variants on inflation of the test statistics in case-control analyses |
| Q22337233 | The effects of human population structure on large genetic association studies |
| Q91236067 | The evolution of polymorphism in the warning coloration of the Amazonian poison frog Adelphobates galactonotus |
| Q34261341 | The genetic architecture of economic and political preferences |
| Q90421903 | The genetic architecture of socially-affected traits: a GWAS for direct and indirect genetic effects on survival time in laying hens showing cannibalism |
| Q29583824 | The genetic architecture of type 2 diabetes |
| Q35541559 | The genetic basis of population fecundity prediction across multiple field populations of Nilaparvata lugens |
| Q35010190 | The genetics of variation in gene expression |
| Q37766201 | The genome-wide association study--a new era for common polygenic disorders |
| Q28754746 | The genome-wide patterns of variation expose significant substructure in a founder population |
| Q41827047 | The genomic distribution of population substructure in four populations using 8,525 autosomal SNPs. |
| Q24813001 | The impact of HLA-DRB1 genes on extra-articular disease manifestations in rheumatoid arthritis |
| Q92862394 | The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change |
| Q21090210 | The impact of divergence time on the nature of population structure: an example from Iceland |
| Q42623786 | The importance of genealogy in determining genetic associations with complex traits |
| Q30428393 | The landscape of recombination in African Americans |
| Q34462958 | The major histocompatibility complex conserved extended haplotype 8.1 in AIDS-related non-Hodgkin lymphoma |
| Q34372347 | The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits |
| Q24288699 | The molecular genetic architecture of self-employment |
| Q85485630 | The nature of confounding in genome-wide association studies |
| Q57251838 | The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG) |
| Q34793225 | The novel atherosclerosis locus at 10q11 regulates plasma CXCL12 levels |
| Q37207832 | The possible role of chromosome X variability in hypertensive familiarity |
| Q33686851 | The potential for enhancing the power of genetic association studies in African Americans through the reuse of existing genotype data |
| Q34390708 | The power of genomic control |
| Q42534447 | The power of the Transmission Disequilibrium Test in the presence of population stratification |
| Q57591592 | The role of Self-Defined Race/Ethnicity in Population Structure Control |
| Q37364693 | The role of local ancestry adjustment in association studies using admixed populations |
| Q33986970 | The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease |
| Q40072966 | The use of common mitochondrial variants to detect and characterise population structure in the Australian population: implications for genome-wide association studies |
| Q33700373 | Theoretical formulation of principal components analysis to detect and correct for population stratification |
| Q24656270 | Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene |
| Q35898478 | Three missense variants of metabolic syndrome-related genes are associated with alpha-1 antitrypsin levels |
| Q33370082 | Tracing sub-structure in the European American population with PCA-informative markers |
| Q91677361 | Tracing the ancestry of modern bread wheats |
| Q33563018 | Traffic-related air pollution, oxidative stress genes, and asthma (ECHRS) |
| Q30276011 | Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity |
| Q28596552 | Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin |
| Q34270911 | Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A. |
| Q60921869 | Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies |
| Q40040676 | Trans-ethnic meta-regression of genome-wide association studies accounting for ancestry increases power for discovery and improves fine-mapping resolution |
| Q40287055 | Transethnic meta-analysis identifies GSDMA and PRDM1 as susceptibility genes to systemic sclerosis. |
| Q30415336 | Trps1 differentially modulates the bone mineral density between male and female mice and its polymorphism associates with BMD differently between women and men. |
| Q97692972 | Tutorial: a guide to performing polygenic risk score analyses |
| Q24609915 | Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis |
| Q24289320 | Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies |
| Q41520420 | Two Rare Mutations in the COL1A2 Gene Associate With Low Bone Mineral Density and Fractures in Iceland |
| Q37120830 | Two independent alleles at 6q23 associated with risk of rheumatoid arthritis |
| Q61447372 | Two novel genomic regions associated with fearfulness in dogs overlap human neuropsychiatric loci |
| Q56968912 | Two variants on chromosome 17 confer prostate cancer risk and the one in TCF2 protects against type 2 diabetes |
| Q36339854 | Two-Variance-Component Model Improves Genetic Prediction in Family Datasets. |
| Q35837634 | UGT1A1 is a major locus influencing bilirubin levels in African Americans |
| Q39960259 | Ulcerative Colitis Is Under Dual (Mitochondrial and Nuclear) Genetic Control. |
| Q24643514 | Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study |
| Q36198251 | Ultraconserved elements in the human genome: association and transmission analyses of highly constrained single-nucleotide polymorphisms |
| Q34469169 | Unbiased methods for population-based association studies |
| Q26748550 | Uncovering the Genetic Architectures of Quantitative Traits |
| Q33620811 | Underestimation of heritability using a mixed model with a polygenic covariance structure in a genome-wide association study for complex traits |
| Q34367715 | Understanding the population structure of North American patients with cystic fibrosis |
| Q37220757 | Unified tests for fine-scale mapping and identifying sparse high-dimensional sequence associations |
| Q33490138 | Univariate/multivariate genome-wide association scans using data from families and unrelated samples |
| Q35065389 | Unraveling the genetic architecture of subtropical maize (Zea mays L.) lines to assess their utility in breeding programs |
| Q34490929 | Unraveling the genetic basis of seed tocopherol content and composition in rapeseed (Brassica napus L.). |
| Q30969809 | Use of unphased multilocus genotype data in indirect association studies |
| Q28397316 | Using DNA fingerprints to infer familial relationships within NHANES III households |
| Q35670900 | Using Network Methodology to Infer Population Substructure |
| Q57393096 | Using Penalised Logistic Regression to Fine Map HLA Variants for Rheumatoid Arthritis |
| Q27330547 | Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies |
| Q36511667 | Using ancestry-informative markers to define populations and detect population stratification |
| Q34215665 | Using ancestry-informative markers to identify fine structure across 15 populations of European origin |
| Q37669579 | Using association mapping to dissect the genetic basis of complex traits in plants |
| Q41754041 | Using biological networks to search for interacting loci in genome-wide association studies |
| Q43464396 | Using evidence for population stratification bias in combined individual- and family-level genetic association analyses of quantitative traits |
| Q30423046 | Using family-based imputation in genome-wide association studies with large complex pedigrees: the Framingham Heart Study |
| Q30458056 | Using previously genotyped controls in genome-wide association studies (GWAS): application to the Stroke Genetics Network (SiGN) |
| Q90580816 | Using whole genome scores to compare three clinical phenotyping methods in complex diseases |
| Q42603532 | Utilizing graph theory to select the largest set of unrelated individuals for genetic analysis |
| Q31034686 | Utilizing the Jaccard index to reveal population stratification in sequencing data: a simulation study and an application to the 1000 Genomes Project |
| Q35017923 | Validation of a small set of ancestral informative markers for control of population admixture in African Americans. |
| Q46264193 | Validation of an updated Associative Transcriptomics platform for the polyploid crop species Brassica napus by dissection of the genetic architecture of erucic acid and tocopherol isoform variation in seeds. |
| Q37501520 | Validation of associations for female fertility traits in Nordic Holstein, Nordic Red and Jersey dairy cattle |
| Q43722416 | Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorder |
| Q46313387 | Variability of grain quality in sorghum: association with polymorphism in Sh2, Bt2, SssI, Ae1, Wx and O2. |
| Q34971144 | Variance component model to account for sample structure in genome-wide association studies |
| Q30813514 | Variant association tools for quality control and analysis of large-scale sequence and genotyping array data |
| Q28943517 | Variant in the sequence of the LINGO1 gene confers risk of essential tremor |
| Q92461020 | Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos |
| Q24632704 | Variants at 6q21 implicate PRDM1 in the etiology of therapy-induced second malignancies after Hodgkin's lymphoma |
| Q35230234 | Variants for HDL-C, LDL-C, and triglycerides identified from admixture mapping and fine-mapping analysis in African American families |
| Q33820794 | Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight |
| Q34669975 | Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma |
| Q53532459 | Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus. |
| Q43510887 | Variants in the 1q21 risk region are associated with a visual endophenotype of autism and schizophrenia. |
| Q34655360 | Variants in the GH-IGF axis confer susceptibility to lung cancer |
| Q45149880 | Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population |
| Q38719386 | Variants in the fetal genome near FLT1 are associated with risk of preeclampsia |
| Q93064046 | Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration |
| Q24646034 | Variants of the serotonin transporter gene and NEO-PI-R Neuroticism: No association in the BLSA and SardiNIA samples |
| Q48013134 | Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's disease. |
| Q34364719 | Variation and genetic control of gene expression in primary immunocytes across inbred mouse strains |
| Q36041812 | Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome |
| Q30441439 | Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels |
| Q47705456 | Vitamin D receptor (VDR) gene polymorphism influences the risk of osteoporosis in postmenopausal women of Northwest India |
| Q33848659 | WNT3A gene polymorphisms are associated with bone mineral density variation in postmenopausal mestizo women of an urban Mexican population: findings of a pathway-based high-density single nucleotide screening. |
| Q21092440 | Web-based, participant-driven studies yield novel genetic associations for common traits |
| Q28652300 | Where is the friend's home? |
| Q45324472 | Whole Exome Sequencing reveals new candidate genes in host genomic susceptibility to Respiratory Syncytial Virus Disease. |
| Q60913135 | Whole genome variant association across 100 dogs identifies a frame shift mutation in DISHEVELLED 2 which contributes to Robinow-like syndrome in Bulldogs and related screw tail dog breeds |
| Q36895709 | Whole-exome sequencing of over 4100 men of African ancestry and prostate cancer risk |
| Q57702196 | Whole-genome association study for fatty acid composition of oleic acid in Japanese Black cattle |
| Q47226678 | Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis |
| Q96136673 | Whole-genome sequencing of a sporadic primary immunodeficiency cohort |
| Q37146968 | XM: association testing on the X-chromosome in case-control samples with related individuals |
| Q51773783 | c-MET pathway involvement in chronic rhinosinusitis: a genetic association analysis. |
| Q39093452 | easyGWAS: A Cloud-Based Platform for Comparing the Results of Genome-Wide Association Studies. |
| Q99420252 | locStra: Fast analysis of regional/global stratification in whole-genome sequencing studies |
| Q39416393 | pcadapt: an R package to perform genome scans for selection based on principal component analysis. |
| Q60907889 | sim1000G: a user-friendly genetic variant simulator in R for unrelated individuals and family-based designs |
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