| scholarly article | Q13442814 |
| P50 | author | Frank Dudbridge | Q60878633 |
| P2093 | author name string | Arief Gusnanto | |
| P2860 | cites work | Evaluating coverage of genome-wide association studies | Q46423138 |
| Betting odds and genetic associations. | Q52001328 | ||
| Rank truncated product of P-values, with application to genomewide association scans. | Q52007500 | ||
| Modeling household transmission of American trypanosomiasis. | Q52058263 | ||
| Evaluating and improving power in whole-genome association studies using fixed marker sets. | Q53255191 | ||
| Why most published research findings are false | Q21092395 | ||
| Population structure and eigenanalysis | Q21145248 | ||
| A Bayesian measure of the probability of false discovery in genetic epidemiology studies | Q24289227 | ||
| Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls | Q24550675 | ||
| Sequential tests for the detection of linkage | Q24676543 | ||
| A haplotype map of the human genome | Q24679827 | ||
| A new multipoint method for genome-wide association studies by imputation of genotypes | Q29547209 | ||
| The future of genetic studies of complex human diseases | Q29547215 | ||
| Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results | Q29547377 | ||
| Empirical threshold values for quantitative trait mapping | Q29615044 | ||
| Assessing the probability that a positive report is false: an approach for molecular epidemiology studies | Q29616285 | ||
| Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies | Q30946038 | ||
| Genomics, prior probability, and statistical tests of multiple hypotheses. | Q35789924 | ||
| Empirical bayes methods and false discovery rates for microarrays | Q46277377 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 227-34 | |
| P577 | publication date | 2008-04-01 | |
| P1433 | published in | Genetic Epidemiology | Q5532864 |
| P1476 | title | Estimation of significance thresholds for genomewide association scans | |
| P478 | volume | 32 |
| Q52317485 | A Comprehensive Analysis of Nuclear-Encoded Mitochondrial Genes in Schizophrenia. |
| Q50120171 | A Genome-Wide Association Study Identifies a Candidate Gene Associated With Atazanavir Exposure Measured in Hair. |
| Q36066687 | A Joint Location-Scale Test Improves Power to Detect Associated SNPs, Gene Sets, and Pathways |
| Q35558848 | A cis-eQTL in PFKFB2 is associated with diabetic nephropathy, adiposity and insulin secretion in American Indians |
| Q36664721 | A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults. |
| Q35528453 | A comparison of whole genome sequencing with exome sequencing for family-based association studies |
| Q40906978 | A family-based, genome-wide association study of young-onset breast cancer: inherited variants and maternally mediated effects. |
| Q42203515 | A general framework for two-stage analysis of genome-wide association studies and its application to case-control studies |
| Q36594318 | A genome-wide association study for corneal curvature identifies the platelet-derived growth factor receptor α gene as a quantitative trait locus for eye size in white Europeans. |
| Q37536395 | A genome-wide association study for reading and language abilities in two population cohorts. |
| Q24642266 | A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose |
| Q28943398 | A genome-wide association study in American Indians implicates DNER as a susceptibility locus for type 2 diabetes |
| Q24625579 | A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality |
| Q28597255 | A genome-wide association study of antidepressant response in Koreans |
| Q29417101 | A genome-wide association study of attempted suicide. |
| Q36013881 | A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor |
| Q28943500 | A genome-wide association study of female sexual dysfunction |
| Q28943460 | A genome-wide association study of host genetic determinants of the antibody response to Anthrax Vaccine Adsorbed |
| Q34585466 | A genome-wide association study of self-rated health |
| Q43711913 | A genome-wide search for type 2 diabetes susceptibility genes in an extended Arab family. |
| Q30494112 | A global in vivo Drosophila RNAi screen identifies NOT3 as a conserved regulator of heart function. |
| Q38558394 | A guide on gene prioritization in studies of psychiatric disorders. |
| Q28293885 | A large-scale, consortium-based genomewide association study of asthma |
| Q38375836 | A new approach to account for the correlations among single nucleotide polymorphisms in genome: wide association studies |
| Q33728642 | A novel adaptive method for the analysis of next-generation sequencing data to detect complex trait associations with rare variants due to gene main effects and interactions |
| Q34737151 | A novel colorectal cancer risk locus at 4q32.2 identified from an international genome-wide association study |
| Q90955290 | A simple and accurate method to determine genomewide significance for association tests in sequencing studies |
| Q39760459 | A simple yet accurate correction for winner's curse can predict signals discovered in much larger genome scans |
| Q36643809 | A simulation study of permutation, bootstrap, and gene dropping for assessing statistical significance in the case of unequal relatedness |
| Q52372349 | A tutorial on conducting genome-wide association studies: Quality control and statistical analysis. |
| Q35559052 | A twin study of breastfeeding with a preliminary genome-wide association scan |
| Q24632742 | A weighted false discovery rate control procedure reveals alleles at FOXA2 that influence fasting glucose levels |
| Q29417099 | ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology |
| Q35102393 | Addressing population-specific multiple testing burdens in genetic association studies |
| Q44055564 | Allowing for sex differences increases power in a GWAS of multiplex Autism families |
| Q37801363 | Alzheimer's disease genetics: current knowledge and future challenges |
| Q42037133 | An Efficient Multiple-Testing Adjustment for eQTL Studies that Accounts for Linkage Disequilibrium between Variants. |
| Q52560100 | An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder. |
| Q30435869 | An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits |
| Q34469246 | Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2. |
| Q48473885 | Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis? |
| Q47627545 | Assessing the Heritability of Complex Traits in Humans: Methodological Challenges and Opportunities |
| Q33588013 | Association analyses of the vitamin D receptor gene in 1654 families with type I diabetes |
| Q38341815 | Association between TCF4 and schizophrenia does not exert its effect by common nonsynonymous variation or by influencing cis-acting regulation of mRNA expression in adult human brain |
| Q24273315 | Association claims in the sequencing era |
| Q60914196 | Association of Genetic Variation at Locus with Vascular Depression |
| Q35891516 | Association of PDE4B Polymorphisms with Susceptibility to Schizophrenia: A Meta-Analysis of Case-Control Studies |
| Q56774769 | Association of angiotensin type 2 receptor gene polymorphisms with ureteropelvic junction obstruction in Brazilian patients |
| Q36247629 | Association of β-defensin copy number and psoriasis in three cohorts of European origin. |
| Q92546032 | At the interface |
| Q34779086 | BR-squared: a practical solution to the winner's curse in genome-wide scans |
| Q24618859 | Basic statistical analysis in genetic case-control studies |
| Q30497403 | Bayes factors in complex genetics |
| Q91865303 | Benefits and limitations of genome-wide association studies |
| Q64911704 | Beyond the traditional simulation design for evaluating type 1 error control: From the "theoretical" null to "empirical" null. |
| Q35528600 | Bivariate linear mixed model analysis to test joint associations of genetic variants on systolic and diastolic blood pressure |
| Q33813557 | Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1. |
| Q37185215 | Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study. |
| Q35714414 | COGENT (COlorectal cancer GENeTics) revisited |
| Q36750746 | CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk |
| Q34085418 | Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder |
| Q42399753 | Challenges in Rare Variant Association Studies for Complex Kidney Traits: CFHR5 and IgA Nephropathy |
| Q21145310 | Chapter 11: Genome-wide association studies |
| Q34008978 | Characterisation of genome-wide association epistasis signals for serum uric acid in human population isolates |
| Q34438637 | Clinical outcomes and genome-wide association for a brain methylation site in an antidepressant pharmacogenetics study in Mexican Americans |
| Q34288646 | Common genetic variation in and near the melanocortin 4 receptor gene (MC4R) is associated with body mass index in American Indian adults and children |
| Q21143760 | Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies |
| Q37236291 | Common variation in SIM1 is reproducibly associated with BMI in Pima Indians |
| Q21144905 | Comparison of family history and SNPs for predicting risk of complex disease |
| Q33688537 | Comparison of multimarker logistic regression models, with application to a genomewide scan of schizophrenia. |
| Q44016780 | Comparisons of power of statistical methods for gene-environment interaction analyses |
| Q28943364 | Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study |
| Q37864684 | Correcting away the hidden heritability |
| Q34807118 | Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. |
| Q51285929 | Cumulative meta-analysis for genetic association: when is a new study worthwhile? |
| Q38126836 | Deciphering the complex: methodological overview of statistical models to derive OMICS-based biomarkers |
| Q41844886 | Design and analysis of multiple diseases genome-wide association studies without controls |
| Q42276967 | Detecting Gene-Environment Interactions for a Quantitative Trait in a Genome-Wide Association Study |
| Q34570218 | Detecting differentially methylated loci for Illumina Array methylation data based on human ovarian cancer data |
| Q34248911 | Detecting rare variant associations by identity-by-descent mapping in case-control studies |
| Q33392518 | Deviations from hardy-weinberg equilibrium in parental and unaffected sibling genotype data |
| Q33795085 | Discussion on common data analysis strategies used in MS-based proteomics. |
| Q38583222 | Dissecting Complex and Multifactorial Nature of Alzheimer's Disease Pathogenesis: a Clinical, Genomic, and Systems Biology Perspective. |
| Q36691602 | Dissecting direct and indirect genetic effects on chronic obstructive pulmonary disease (COPD) susceptibility. |
| Q24288911 | Diverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factors |
| Q38021404 | Does familial clustering of risk factors for long-term diabetic complications leave any place for genes that act independently? |
| Q36582532 | Estimating Effect Sizes and Expected Replication Probabilities from GWAS Summary Statistics |
| Q41486298 | Estimating genome-wide significance for whole-genome sequencing studies |
| Q50770651 | Estimating the heritability of reporting stressful life events captured by common genetic variants. |
| Q33680062 | Estimation and partition of heritability in human populations using whole-genome analysis methods. |
| Q46263944 | Estimation of a significance threshold for epigenome-wide association studies |
| Q35886287 | Evaluating the effective numbers of independent tests and significant p-value thresholds in commercial genotyping arrays and public imputation reference datasets |
| Q57233959 | Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases |
| Q34237671 | Evaluation of A2BP1 as an obesity gene |
| Q39785284 | Evaluation of risk loci for schizophrenia derived from genome-wide association studies in a German population |
| Q59801708 | Examining the current standards for genetic discovery and replication in the era of mega-biobanks |
| Q33810009 | Exome localization of complex disease association signals. |
| Q35620463 | Experimental designs for robust detection of effects in genome-wide case-control studies |
| Q56243461 | Exploring the association of genetic factors with participation in the Avon Longitudinal Study of Parents and Children |
| Q41897152 | Exploring the potential benefits of stratified false discovery rates for region-based testing of association with rare genetic variation |
| Q83751936 | Factors affecting the effective number of tests in genetic association studies: a comparative study of three PCA-based methods |
| Q28943341 | Family-based genome-wide association scan of attention-deficit/hyperactivity disorder |
| Q40041080 | FastLSU: a more practical approach for the Benjamini-Hochberg FDR controlling procedure for huge-scale testing problems |
| Q35920852 | Filtering genetic variants and placing informative priors based on putative biological function. |
| Q36107288 | Fine mapping a major obesity locus (jObes1) using a Berlin Fat Mouse × B6N advanced intercross population |
| Q30278976 | Fine mapping analysis of HLA-DP/DQ gene clusters on chromosome 6 reveals multiple susceptibility loci for HBV infection |
| Q37571848 | Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder |
| 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 |
| Q33954528 | From SNPs to genes: disease association at the gene level |
| Q36276884 | GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway |
| Q89748027 | GWAS significance thresholds for deep phenotyping studies can depend upon minor allele frequencies and sample size |
| Q28652698 | GWATCH: a web platform for automated gene association discovery analysis |
| Q24273353 | Gene Prioritization for Imaging Genetics Studies Using Gene Ontology and a Stratified False Discovery Rate Approach |
| Q36470865 | Gene-set and multivariate genome-wide association analysis of oppositional defiant behavior subtypes in attention-deficit/hyperactivity disorder |
| 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 |
| Q55399312 | Genetic Polymorphism Predisposing to Differentiated Thyroid Cancer: A Review of Major Findings of the Genome-Wide Association Studies. |
| Q64102762 | Genetic association and transcriptome integration identify contributing genes and tissues at cystic fibrosis modifier loci |
| Q33853712 | Genetic association of FTO/IRX region with obesity and overweight in the Polish population |
| Q34076218 | Genetic association signal near NTN4 in Tourette syndrome |
| Q36472889 | Genetic association test for multiple traits at gene level |
| Q37350436 | Genetic determinants of circulating sphingolipid concentrations in European populations |
| Q93035719 | Genetic influences on susceptibility to rheumatoid arthritis in African-Americans |
| Q40108507 | Genetic loci associated with an earlier age at onset in multiplex schizophrenia. |
| Q28484419 | Genetic predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysis |
| Q38056803 | Genetic regulation of vitamin D levels |
| Q35023117 | Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study |
| Q53833569 | Genetic risk factors for orofacial clefts in Central Africans and Southeast Asians. |
| Q34109845 | Genetic studies of IgA nephropathy: past, present, and future. |
| Q33575138 | Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept |
| Q38379199 | Genetics and brain morphology |
| Q24600995 | Genetics of Sjögren's syndrome in the genome-wide association era |
| Q35775223 | Genetics of breast cancer: a topic in evolution |
| Q34846313 | Genetics of callous-unemotional behavior in children |
| Q34085844 | Genetics of obsessive-compulsive disorder and related disorders |
| Q22252693 | Genetics of psychosis; insights from views across the genome |
| Q35722688 | Genome Wide Association Study for Predictors of Progression Free Survival in Patients on Capecitabine, Oxaliplatin, Bevacizumab and Cetuximab in First-Line Therapy of Metastatic Colorectal Cancer |
| Q35374597 | Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder |
| Q28554877 | Genome-Wide Association of Heroin Dependence in Han Chinese |
| Q58728978 | Genome-Wide Expression Quantitative Trait Loci Analysis Using Mixed Models |
| Q36159275 | Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer |
| Q39032868 | Genome-Wide Interaction Analysis of Air Pollution Exposure and Childhood Asthma with Functional Follow-up |
| Q50248511 | Genome-wide analysis identifies an african-specific variant in SEMA4D associated with body mass index. |
| Q34254081 | Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma |
| Q33798453 | Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease |
| Q24632119 | Genome-wide and fine-resolution association analysis of malaria in West Africa |
| Q34138007 | Genome-wide approaches to schizophrenia |
| Q34718106 | Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster |
| Q33549937 | Genome-wide association analysis of total cholesterol and high-density lipoprotein cholesterol levels using the Framingham heart study data |
| Q35138418 | Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin. |
| Q57277952 | Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error |
| Q36108378 | Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis |
| Q24597781 | Genome-wide association meta-analysis identifies new endometriosis risk loci |
| Q33699542 | Genome-wide association scan of attention deficit hyperactivity disorder |
| Q28943421 | Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations |
| Q37175234 | Genome-wide association studies in ADHD. |
| Q21145019 | Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae |
| Q37968670 | Genome-wide association studies in the hunt for genes causing primary open-angle glaucoma: a review |
| Q37831225 | Genome-wide association studies of alcohol dependence and substance use disorders |
| Q35074796 | Genome-wide association studies of antidepressant outcome: a brief review |
| Q35065065 | Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium |
| Q27012711 | Genome-wide association studies of late-onset cardiovascular disease |
| Q34924529 | Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium |
| Q29416999 | Genome-wide association study identifies BICD1 as a susceptibility gene for emphysema |
| Q57083838 | Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23 |
| Q28248384 | Genome-wide association study identifies five new schizophrenia loci |
| Q33740363 | Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels |
| Q29417149 | Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder |
| Q23936582 | Genome-wide association study of Tourette's syndrome |
| Q36315528 | Genome-wide association study of a quantitative disordered gambling trait |
| Q28943321 | Genome-wide association study of alcohol dependence |
| Q35679930 | Genome-wide association study of antidepressant treatment-emergent suicidal ideation |
| Q44670236 | Genome-wide association study of co-occurring anxiety in major depression |
| Q34373206 | Genome-wide association study of handedness excludes simple genetic models |
| Q49024786 | Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. |
| Q34322551 | Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid. |
| Q51873167 | Genome-wide association study of motor coordination problems in ADHD identifies genes for brain and muscle function. |
| Q34445418 | Genome-wide association study of obsessive-compulsive disorder. |
| Q37525681 | Genome-wide association study of proneness to anger |
| Q28943558 | Genome-wide association study of recurrent early-onset major depressive disorder |
| Q29417072 | Genome-wide association study of smoking behaviours in patients with COPD |
| Q30590832 | Genome-wide association study of spontaneous resolution of hepatitis C virus infection: data from multiple cohorts |
| Q28943428 | Genome-wide association study of the child behavior checklist dysregulation profile |
| Q46071753 | Genome-wide association study of working memory brain activation |
| Q37446213 | Genome-wide association study on detailed profiles of smoking behavior and nicotine dependence in a twin sample |
| Q34469412 | Genome-wide association study to identify the genetic determinants of otitis media susceptibility in childhood |
| Q34531401 | Genome-wide association study using whole-genome sequencing rapidly identifies new genes influencing agronomic traits in rice. |
| Q37226294 | Genome-wide association uncovers shared genetic effects among personality traits and mood states |
| Q64119866 | Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder |
| Q29417001 | Genome-wide diet-gene interaction analyses for risk of colorectal cancer |
| Q92860871 | Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank |
| Q33638413 | Genome-wide identification of expression quantitative trait loci (eQTLs) in human heart |
| Q24597886 | Genome-wide meta-analyses identify multiple loci associated with smoking behavior |
| Q33641349 | Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene |
| Q34214974 | Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci |
| Q37563079 | Genome-wide strategies for discovering genetic influences on cognition and cognitive disorders: methodological considerations |
| Q28742939 | Genomewide association scan of suicidal thoughts and behaviour in major depression |
| Q34606096 | Genomewide association studies: history, rationale, and prospects for psychiatric disorders |
| Q29417034 | Genomewide association study for onset age in Parkinson disease |
| Q30425270 | Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease |
| Q36931805 | Genomics in cardiovascular disease |
| Q40200164 | Global measures of peripheral blood-derived DNA methylation as a risk factor in the development of mature B-cell neoplasms |
| Q64055372 | Guidance for DNA methylation studies: statistical insights from the Illumina EPIC array |
| Q52645939 | Heritability and Genome-Wide Association Analyses of Serum Uric Acid in Middle and Old-Aged Chinese Twins. |
| Q59327149 | Heritability and Genome-Wide Association Study of Plasma Cholesterol in Chinese Adult Twins |
| Q34486620 | Hope for GWAS: relevant risk genes uncovered from GWAS statistical noise. |
| Q89705989 | Human genetics of leishmania infections |
| Q43116230 | IL6 and IL10 are genetic susceptibility factors of periodontal disease |
| Q29416993 | Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis |
| Q36783894 | Identification of SPOCK2 as a susceptibility gene for bronchopulmonary dysplasia |
| Q36844565 | Identification of genetic variation that determines human trehalase activity and its association with type 2 diabetes |
| Q37316697 | Identifying rare variants associated with complex traits via sequencing |
| Q34331816 | Identity-by-descent mapping to detect rare variants conferring susceptibility to multiple sclerosis |
| Q91891350 | Improving the odds of drug development success through human genomics: modelling study |
| Q36636532 | In vitro screening for population variability in toxicity of pesticide-containing mixtures |
| Q37464371 | Independent test assessment using the extreme value distribution theory |
| Q92016259 | Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies |
| Q48875894 | Jointly determining significance levels of primary and replication studies by controlling the false discovery rate in two-stage genome-wide association studies. |
| Q24273406 | Jumping on the Train of Personalized Medicine: A Primer for Non-Geneticist Clinicians: Part 2. Fundamental Concepts in Genetic Epidemiology |
| Q51272269 | Large scale association analysis for drug addiction: results from SNP to gene. |
| Q30252611 | Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. |
| Q22252418 | Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder |
| Q38105261 | Meta-analysis methods for genome-wide association studies and beyond |
| Q21092458 | Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations |
| Q90776533 | Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia |
| Q55423202 | Meta-analysis of GABRB2 polymorphisms and the risk of schizophrenia combined with GWAS data of the Han Chinese population and psychiatric genomics consortium. |
| Q34761012 | Meta-analysis of genetic association studies and adjustment for multiple testing of correlated SNPs and traits |
| Q38670978 | Meta-analysis of genome-wide SNP- and pathway-based associations for facets of neuroticism |
| Q29417150 | Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1. |
| Q35212724 | Meta-analysis of genome-wide association for migraine in six population-based European cohorts |
| Q37202305 | Meta-analysis of genome-wide association studies for personality. |
| Q35670184 | Meta-analysis of new genome-wide association studies of colorectal cancer risk |
| Q28681049 | Methodological challenges of genome-wide association analysis in Africa |
| Q33359015 | Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data |
| Q92228662 | Methods for the Analysis and Interpretation for Rare Variants Associated with Complex Traits |
| Q38795760 | Microbial genome-wide association studies: lessons from human GWAS. |
| Q45386905 | Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries |
| Q41232448 | Multiple Testing in the Context of Gene Discovery in Sickle Cell Disease Using Genome-Wide Association Studies. |
| Q30426239 | Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis |
| Q24608614 | Multiple common variants for celiac disease influencing immune gene expression |
| Q42682842 | Multiple testing corrections for imputed SNPs |
| Q37955708 | MyelomA Genetics International Consortium |
| Q21284775 | NCK2 is significantly associated with opiates addiction in African-origin men |
| Q31033001 | Network-assisted analysis of primary Sjögren's syndrome GWAS data in Han Chinese |
| Q34924165 | Neuroimaging measures as endophenotypes in Alzheimer's disease |
| Q33856171 | New Genetic Findings in Schizophrenia: Is there Still Room for the Dopamine Hypothesis of Schizophrenia? |
| Q37374232 | New findings from genetic association studies of schizophrenia |
| Q35237172 | New findings in the genetics of major psychoses |
| Q47436767 | New insights into the pharmacogenomics of antidepressant response from the GENDEP and STAR*D studies: rare variant analysis and high-density imputation. |
| Q37225243 | New susceptibility locus for coronary artery disease on chromosome 3q22.3. |
| Q47805269 | Next generation sequencing applications for cardiovascular disease |
| Q45928430 | No evidence that rare coding variants in ZNF804A confer risk of schizophrenia. |
| Q28751388 | Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies |
| Q35221561 | Novel rank-based approaches for discovery and replication in genome-wide association studies. |
| Q26782027 | Obesity genetics in mouse and human: back and forth, and back again |
| Q44974812 | On optimal gene-based analysis of genome scans |
| Q55186690 | P values in display items are ubiquitous and almost invariably significant: A survey of top science journals. |
| Q34864222 | Penalized multimarker vs. single-marker regression methods for genome-wide association studies of quantitative traits |
| Q28647065 | Pleiotropy analysis of quantitative traits at gene level by multivariate functional linear models |
| Q45002205 | Population genomics of Populus trichocarpa identifies signatures of selection and adaptive trait associations |
| Q34337027 | Power and predictive accuracy of polygenic risk scores. |
| Q28749837 | Practical aspects of imputation-driven meta-analysis of genome-wide association studies |
| Q62659444 | Presidential address: Six open questions to genetic epidemiologists |
| Q37765631 | REVIEW: Genome-wide findings in schizophrenia and the role of gene-environment interplay. |
| Q24305127 | RING finger protein RNF207, a novel regulator of cardiac excitation |
| Q33432685 | Rapid and accurate multiple testing correction and power estimation for millions of correlated markers |
| Q47195417 | Rationale and design of GENEiUS: a prospective observational study on the genetic and environmental determinants of body mass index evolution in Canadian undergraduate students |
| Q35082533 | Rationale for an international consortium to study inherited genetic susceptibility to childhood acute lymphoblastic leukemia |
| Q57178026 | Re-assessment of multiple testing strategies for more efficient genome-wide association studies |
| Q36984772 | Replication of a rare protective allele in the noradrenaline transporter gene and ADHD. |
| Q33941069 | Replication of putative susceptibility loci from genome-wide association studies associated with coronary atherosclerosis in Chinese Han population |
| Q41972613 | Reply to: Is a microRNA-328 binding site in PAX6 associated with Rolandic epilepsy? |
| Q38781016 | Resetting the bar: Statistical significance in whole-genome sequencing-based association studies of global populations. |
| Q91337965 | Rigor and reproducibility in genetic research on eating disorders |
| Q35136955 | Risk prediction of complex diseases from family history and known susceptibility loci, with applications for cancer screening |
| Q34444807 | Role of genomics in cardiovascular medicine |
| Q37483078 | Schizophrenia genetics: new insights from new approaches |
| Q50974272 | Searching new signals for production traits through gene-based association analysis in three Italian cattle breeds. |
| Q41987411 | Shrinkage estimation of effect sizes as an alternative to hypothesis testing followed by estimation in high-dimensional biology: applications to differential gene expression |
| Q92873138 | Significance testing and genomic inflation factor using high-density genotypes or whole-genome sequence data |
| Q24289462 | Six persistent research misconceptions |
| Q57591377 | Statistical challenges in high-dimensional molecular and genetic epidemiology |
| Q38205106 | Statistical power and significance testing in large-scale genetic studies |
| Q44996911 | Statistical properties of single-marker tests for rare variants |
| Q40651600 | Strategies to improve the performance of rare variant association studies by optimizing the selection of controls |
| Q41844748 | Strategy to control type I error increases power to identify genetic variation using the full biological trajectory |
| Q48248036 | TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies |
| Q42685838 | Testing for association in case-control genome-wide association studies with shared controls |
| Q41141623 | Testing for genetic associations in arbitrarily structured populations |
| Q26798159 | The Current and Future Use of Ridge Regression for Prediction in Quantitative Genetics |
| Q41301586 | The Machado-Joseph disease-associated mutant form of ataxin-3 regulates parkin ubiquitination and stability |
| Q24282612 | The Use of Multiplicity Corrections, Order Statistics and Generalized Family-Wise Statistics with Application to Genome-Wide Studies |
| Q34924454 | The association of previously reported polymorphisms for microvascular complications in a meta-analysis of diabetic retinopathy. |
| Q64997169 | The evidential statistical paradigm in genetics. |
| Q37403131 | The future for genetic studies in reproduction. |
| Q35012899 | The genetics of Tourette syndrome: a review. |
| Q61451298 | The harmonic mean -value for combining dependent tests |
| Q40039328 | The more you test, the more you find: The smallest P-values become increasingly enriched with real findings as more tests are conducted. |
| Q24617186 | The neuronal transporter gene SLC6A15 confers risk to major depression |
| Q33813262 | The nuclear transcription factor PKNOX2 is a candidate gene for substance dependence in European-origin women |
| Q33680855 | The null distributions of test statistics in genomewide association studies |
| Q42361578 | The performance of a new local false discovery rate method on tests of association between coronary artery disease (CAD) and genome-wide genetic variants. |
| Q28748800 | The role of genetics in the etiology of schizophrenia |
| Q38203024 | The synapse in schizophrenia |
| Q35230162 | Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour |
| Q60619265 | Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders |
| Q33735365 | Utility of the pooling approach as applied to whole genome association scans with high-density Affymetrix microarrays |
| Q91834804 | Validation of 46 loci associated with female fertility traits in cattle |
| Q34971144 | Variance component model to account for sample structure in genome-wide association studies |
| Q28943328 | Variants in several genomic regions associated with asperger disorder |
| Q24601340 | Variation near complement factor I is associated with risk of advanced AMD |
| Q36281464 | Weighted multiple testing procedures for genomic studies |
| Q33612076 | Were genome-wide linkage studies a waste of time? Exploiting candidate regions within genome-wide association studies |
| Q30928632 | What is the impact of genome-wide supported risk variants for schizophrenia and bipolar disorder on brain structure and function? A systematic review |
| Q34837985 | Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism. |
| Q30827085 | Whole-genome analyses of whole-brain data: working within an expanded search space |
| Q36594535 | Whole-genome sequencing suggests a chemokine gene cluster that modifies age at onset in familial Alzheimer's disease. |
Search more.