| scholarly article | Q13442814 |
| P50 | author | Andrew Singleton | Q4758591 |
| John Anthony Hardy | Q6237755 | ||
| P2860 | cites work | Initial sequencing and analysis of the human genome | Q21045365 |
| Genetic variation in an individual human exome | Q21145035 | ||
| The Sequence of the Human Genome | Q22065842 | ||
| The complete genome of an individual by massively parallel DNA sequencing | Q22122226 | ||
| Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol | Q22337068 | ||
| Genome sequencing in microfabricated high-density picolitre reactors | Q24544260 | ||
| Complement factor H polymorphism in age-related macular degeneration | Q24553334 | ||
| Strong association of de novo copy number mutations with autism | Q24633543 | ||
| A haplotype map of the human genome | Q24679827 | ||
| CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration | Q24681526 | ||
| Mutation in the alpha-synuclein gene identified in families with Parkinson's disease | Q27860459 | ||
| alpha-Synuclein locus triplication causes Parkinson's disease | Q27860533 | ||
| Complement factor H variant increases the risk of age-related macular degeneration | Q28239239 | ||
| A genome-wide association study identifies novel risk loci for type 2 diabetes | Q28287727 | ||
| The future of genetic studies of complex human diseases | Q29547215 | ||
| Large-scale analysis of the human and mouse transcriptomes | Q29547360 | ||
| Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin | Q29547423 | ||
| Common genetic variation and human traits | Q29614445 | ||
| Genetics of gene expression and its effect on disease | Q29614591 | ||
| A HapMap harvest of insights into the genetics of common disease | Q29614875 | ||
| Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma | Q29614903 | ||
| Complement factor H polymorphism and age-related macular degeneration | Q29614931 | ||
| Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin | Q29615684 | ||
| Gene expression analysis by massively parallel signature sequencing (MPSS) on microbead arrays | Q29615937 | ||
| A genome-wide investigation of SNPs and CNVs in schizophrenia | Q33406258 | ||
| The future of genetic analysis of neurological disorders | Q33900133 | ||
| Mapping determinants of human gene expression by regional and genome-wide association | Q34421244 | ||
| Genome-wide association studies: theoretical and practical concerns | Q34555195 | ||
| Effect of 17q21 variants and smoking exposure in early-onset asthma | Q34857209 | ||
| Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms | Q35752480 | ||
| MicroRNA target site polymorphisms and human disease | Q37263538 | ||
| The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcripts | Q40194429 | ||
| Molecular medicine. The cholesterol quartet | Q43613380 | ||
| The minisatellite in the diabetes susceptibility locus IDDM2 regulates insulin transcription. | Q46033146 | ||
| Drinking from the fire hose--statistical issues in genomewide association studies | Q47838945 | ||
| An utter refutation of the "fundamental theorem of the HapMap". | Q51950798 | ||
| A survey of genetic human cortical gene expression | Q57272923 | ||
| alpha-synuclein gene haplotypes are associated with Parkinson's disease | Q57905836 | ||
| Structural variation in the human genome | Q79953699 | ||
| Enrichment of super-sized resequencing targets from the human genome | Q81524359 | ||
| Genetic risk prediction--are we there yet? | Q83658297 | ||
| Genomewide association studies--illuminating biologic pathways | Q83658310 | ||
| P433 | issue | 17 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 10 | |
| P304 | page(s) | 1759-1768 | |
| P577 | publication date | 2009-04-15 | |
| P1433 | published in | The New England Journal of Medicine | Q582728 |
| P1476 | title | Genomewide association studies and human disease | |
| P478 | volume | 360 |
| Q36450351 | 'Location, Location, Location': a spatial approach for rare variant analysis and an application to a study on non-syndromic cleft lip with or without cleft palate |
| Q45361290 | A 7-gene signature of the recipient predicts the progression of fibrosis after liver transplantation for hepatitis C virus infection |
| Q34335418 | A Follow-up Association Study of Genetic Variants for Bone Mineral Density in a Korean Population. |
| Q34072975 | A KRAS-variant in ovarian cancer acts as a genetic marker of cancer risk |
| Q28477617 | A New Methodology to Associate SNPs with Human Diseases According to Their Pathway Related Context |
| Q38604266 | A Weighted SNP Correlation Network Method for Estimating Polygenic Risk Scores |
| Q38498148 | A database of annotated promoters of genes associated with common respiratory and related diseases |
| Q33897363 | A first step towards inferring levels of long‐distance dispersal during past expansions |
| Q35230158 | A generalizable hypothesis for the genetic architecture of disease: pleomorphic risk loci |
| Q35532916 | A genome-wide association study identifies a region at chromosome 12 as a potential susceptibility locus for restenosis after percutaneous coronary intervention |
| Q42704966 | A genome-wide association study identifies susceptibility loci of silica-related pneumoconiosis in Han Chinese |
| Q38068788 | A global "imaging'' view on systems approaches in immunology. |
| Q24595378 | A high-coverage genome sequence from an archaic Denisovan individual |
| Q30435297 | A high-resolution association mapping panel for the dissection of complex traits in mice |
| Q36790023 | A likelihood ratio-based Mann-Whitney approach finds novel replicable joint gene action for type 2 diabetes. |
| Q50293790 | A method for integrating neuroimaging into genetic models of learning performance |
| Q53320826 | A methodology based on molecular interactions and pathways to find candidate genes associated to diseases: its application to schizophrenia and Alzheimer's disease |
| Q37378112 | A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia |
| Q35080521 | A post-GWAS replication study confirming the PTK2 gene associated with milk production traits in Chinese Holstein |
| Q38011259 | A review of family history of cardiovascular disease: risk factor and research tool |
| Q37585898 | A systematic review of cancer GWAS and candidate gene meta-analyses reveals limited overlap but similar effect sizes |
| Q35950161 | A two-SNP IL-6 promoter haplotype is associated with increased lung cancer risk |
| Q34529478 | A vertex similarity-based framework to discover and rank orphan disease-related genes |
| Q33999506 | ABO blood group and other genetic variants associated with pancreatic cancer |
| Q34334093 | Advances in the genetics of endometriosis |
| Q37506586 | An Overview of Genetic Polymorphisms and Pancreatic Cancer Risk in Molecular Epidemiologic Studies |
| Q34686828 | An efficient algorithm to perform multiple testing in epistasis screening. |
| Q37039893 | An information-gain approach to detecting three-way epistatic interactions in genetic association studies |
| Q26774805 | Analytical Complexity in Detection of Gene Variant-by-Environment Exposure Interactions in High-Throughput Genomic and Exposomic Research |
| Q34163075 | Application of statistical and functional methodologies for the investigation of genetic determinants of coronary heart disease biomarkers: lipoprotein lipase genotype and plasma triglycerides as an exemplar. |
| Q38063617 | Applying In Silico Integrative Genomics to Genetic Studies of Human Disease |
| Q44810056 | Association and cumulative effects of GWAS‐identified genetic variants for nonsyndromic orofacial clefts in a Chinese population |
| Q34429937 | Association between vitamin D receptor gene polymorphisms (Fok1 and Bsm1) and osteoporosis: a systematic review |
| Q37823646 | Association genetics of complex traits in plants |
| Q30495629 | Association mapping of spot blotch resistance in wild barley |
| Q35389741 | Association of ADIPOR2 gene variants with cardiovascular disease and type 2 diabetes risk in individuals with impaired glucose tolerance: the Finnish Diabetes Prevention Study |
| Q48312604 | Association of GWAS-Supported Variants rs2200733 and rs6843082 on Chromosome 4q25 with Ischemic Stroke in the Southern Chinese Han Population |
| Q38121860 | Association of MeCP2 (rs2075596, rs2239464) genetic polymorphisms with systemic lupus erythematosus: a meta-analysis |
| Q50682448 | Association of a single nucleotide polymorphism in HOXB9 with developmental dysplasia of the hip: a case-control study |
| Q39573029 | Association of angiotensin II type 1 receptor-associated protein gene polymorphism with increased mortality in septic shock* |
| Q36903321 | Association of the AIRE gene with susceptibility to rheumatoid arthritis in a European population: a case control study |
| Q37930954 | Bariatric surgery, adipose tissue and gut microbiota |
| Q37989838 | Behavioural Genetics of Childhood Disorders |
| Q30884486 | Biodemographic Analyses of Longitudinal Data on Aging, Health, and Longevity: Recent Advances and Future Perspectives |
| Q24622541 | Biological, clinical and population relevance of 95 loci for blood lipids |
| Q38826375 | Biomarkers in cardiovascular disease: Statistical assessment and section on key novel heart failure biomarkers |
| Q35212736 | Cancer GAMAdb: database of cancer genetic associations from meta-analyses and genome-wide association studies |
| Q33653672 | Cardiovascular drug discovery: a perspective from a research-based pharmaceutical company |
| Q37877282 | Celiac disease: moving from genetic associations to causal variants |
| Q47587631 | Cerebrospinal fluid and blood biomarkers for neurodegenerative dementias: An update of the Consensus of the Task Force on Biological Markers in Psychiatry of the World Federation of Societies of Biological Psychiatry |
| Q49830216 | Characterization of viral RNA splicing using whole-transcriptome datasets from host species |
| Q34017084 | Characterizing genetic interactions in human disease association studies using statistical epistasis networks |
| Q37688994 | Child and adolescent psychiatric genetics |
| Q28647429 | Choosing blindly but wisely: differentially private solicitation of DNA datasets for disease marker discovery |
| Q35857520 | Chromosome 4p16.3 variant modify bladder cancer risk in a Chinese population |
| Q60957690 | Clinical Implications of Single Nucleotide Polymorphisms in Diagnosis of Asthma and its Subtypes |
| Q64087689 | Clusterin in Alzheimer's Disease: Mechanisms, Genetics, and Lessons From Other Pathologies |
| Q47345621 | Coalitional game theory as a promising approach to identify candidate autism genes. |
| Q28394555 | Commentary: The Year in Endocrine Genetics for Basic Scientists |
| Q36946406 | Common and specific liability to addiction: Approaches to association studies of opioid addiction |
| Q33937980 | Common variants in cardiac ion channel genes are associated with sudden cardiac death |
| Q35721674 | Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration |
| Q33950989 | Comparative analysis of methods for detecting interacting loci |
| Q37823792 | Complex systems in pulmonary medicine: a systems biology approach to lung disease |
| Q34860129 | Construction of gene clusters resembling genetic causal mechanisms for common complex disease with an application to young-onset hypertension |
| Q37379477 | Control of fetal hemoglobin: new insights emerging from genomics and clinical implications |
| Q37615360 | Controversies surrounding the diagnosis of schizophrenia and other psychoses |
| Q55007510 | Correlation between prostate stem cell antigen gene expression and oral squamous cell carcinoma. |
| Q35640566 | Correlation of rare coding variants in the gene encoding human glucokinase regulatory protein with phenotypic, cellular, and kinetic outcomes |
| Q64118172 | Cumulative evidence for association between genetic polymorphisms and esophageal cancer susceptibility: A review with evidence from meta-analysis and genome-wide association studies |
| Q41962387 | DTC-and-Me: Patient, Provider, Proteins and Regulators |
| Q53119815 | Defining the role of pharmacology in the emerging world of translational research |
| Q41930852 | Destabilizing the autoinhibitory conformation of Zap70 induces up-regulation of inhibitory receptors and T cell unresponsiveness |
| Q35630175 | Detecting genome-wide epistases based on the clustering of relatively frequent items. |
| Q42912914 | Detecting new neurodegenerative disease genes: does phenotype accuracy limit the horizon? |
| Q38685285 | Developmental mechanisms underlying variation in craniofacial disease and evolution. |
| Q24604314 | Different differences: The use of ‘genetic ancestry’ versus race in biomedical human genetic research |
| Q84745208 | Different roles of two novel susceptibility loci for nonsyndromic orofacial clefts in a Chinese Han population |
| Q41889353 | Digging up the human genome: current progress in deciphering adverse drug reactions. |
| Q61806769 | Dissecting closely linked association signals in combination with the mammalian phenotype database can identify candidate genes in dairy cattle |
| Q36130888 | Dissection of complex adult traits in a mouse synthetic population. |
| Q37644444 | Drosophila and genome-wide association studies: a review and resource for the functional dissection of human complex traits |
| Q34853856 | Ecological genetics and genomics of plant defences: evidence and approaches |
| Q40178869 | Effect of Human Genetic Variability on Gene Expression in Dorsal Root Ganglia and Association with Pain Phenotypes. |
| Q37216430 | Efficiently identifying significant associations in genome-wide association studies |
| Q85050714 | Electrochemical detection of insertion/deletion mutations based on enhanced flexibility of bulge-containing duplexes on electrodes |
| Q35151858 | Epigenetic regulation by heritable RNA. |
| Q35814809 | Equine clinical genomics: A clinician's primer. |
| Q28750293 | Ethical data release in genome-wide association studies in developing countries |
| Q37981666 | Evidence for a genetic role in varicose veins and chronic venous insufficiency. |
| Q34267484 | Evidence that Gsta4 modifies susceptibility to skin tumor development in mice and humans |
| Q37739741 | Exome Sequence Analysis of 14 Families With High Myopia. |
| Q37380039 | Expression sensitivity analysis of human disease related genes |
| Q34179460 | FGFR2 and other loci identified in genome-wide association studies are associated with breast cancer in African-American and younger women. |
| Q36860474 | Finding risk in all the right places |
| Q22122198 | Finding the missing heritability of complex diseases |
| Q39263959 | From genetic single candidate gene studies to complex genomics of GvHD. |
| Q88911128 | From genome-wide associations to candidate causal variants by statistical fine-mapping |
| Q37928504 | Frontotemporal dementia: from Mendelian genetics towards genome wide association studies |
| Q35110769 | Functional Genomics Applied to Cardiovascular Medicine |
| Q52665776 | Functional Validation of Candidate Genes Detected by Genomic Feature Models |
| Q36393304 | Functional dyadicity and heterophilicity of gene-gene interactions in statistical epistasis networks |
| Q34978355 | Functional evaluation of TNFAIP3 (A20) in rheumatoid arthritis |
| Q34301870 | Future health applications of genomics: priorities for communication, behavioral, and social sciences research |
| Q42906338 | GIP: No Longer the Neglected Incretin Twin? |
| Q35304041 | GWAS Integrator: a bioinformatics tool to explore human genetic associations reported in published genome-wide association studies |
| Q38526092 | Gene-Environment Interactions in Asthma: Genetic and Epigenetic Effects |
| Q33790213 | Gene-environment interactions in asthma and allergy: the end of the beginning? |
| Q37676313 | GenePANDA-a novel network-based gene prioritizing tool for complex diseases |
| Q36998001 | Genes and epigenetic processes as prospective pain targets |
| Q37483043 | Genetic Contributions of Inflammation to Depression |
| Q26782062 | Genetic Diversity and Societally Important Disparities |
| Q45358008 | Genetic Factors and Hepatitis C Virus Infection |
| Q38115496 | Genetic Profiles in Ischaemic Stroke |
| Q47717219 | Genetic Variations of COL4A1 gene and Intracerebral Hemorrhage risk: A case-control Study in Chinese Han Population |
| Q36450465 | Genetic and epigenetic variants influencing the development of nonalcoholic fatty liver disease |
| Q35915818 | Genetic determinants of risk and progression in multiple sclerosis |
| Q37863139 | Genetic determinants of susceptibility and severity in nonalcoholic fatty liver disease |
| Q37658863 | Genetic polymorphism of inosine-triphosphate-pyrophosphatase influences mercaptopurine metabolism and toxicity during treatment of acute lymphoblastic leukemia individualized for thiopurine-S-methyl-transferase status. |
| Q90088035 | Genetic polymorphisms and gastric cancer risk: a comprehensive review synopsis from meta-analysis and genome-wide association studies |
| Q38783258 | Genetic polymorphisms associated with overweight and obesity in uncontrolled Type 2 diabetes mellitus |
| Q36402309 | Genetic predictors of the response to the treatment of hepatitis C virus infection |
| Q43897330 | Genetic predisposition to sarcoidosis: another brick in the wall |
| Q26863517 | Genetic psychophysiology: advances, problems, and future directions |
| Q34109845 | Genetic studies of IgA nephropathy: past, present, and future. |
| Q34129582 | Genetic variability at the PARK16 locus |
| Q33538000 | Genetic variability in CLU and its association with Alzheimer's disease |
| Q34398489 | Genetic variability in the regulation of gene expression in ten regions of the human brain |
| Q34648887 | Genetic variant rs7758229 in 6q26-q27 is not associated with colorectal cancer risk in a Chinese population |
| Q30559534 | Genetic variants in platelet factor 4 modulate inflammatory and platelet activation biomarkers |
| Q55360400 | Genetic variation affecting exon skipping contributes to brain structural atrophy in Alzheimer's disease. |
| Q29147442 | Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge |
| Q38324392 | Genetic variation in T-box binding element functionally affects SCN5A/SCN10A enhancer |
| Q36250066 | Genetic variations in STAT4,C2,HLA-DRB1 and HLA-DQ associated with risk of hepatitis B virus-related liver cirrhosis |
| Q59399481 | Genetics of Alzheimer's disease |
| Q37834045 | Genetics of Liver Injury and Fibrosis |
| Q35157607 | Genetics of common polygenic ischaemic stroke: current understanding and future challenges |
| Q26775633 | Genetics of ischaemic stroke in young adults |
| Q34569552 | Genome reassembly with high-throughput sequencing data |
| Q34388219 | Genome wide assessment of young onset Parkinson's disease from Finland |
| Q35845762 | Genome wide association and genomic prediction for growth traits in juvenile farmed Atlantic salmon using a high density SNP array |
| Q34147463 | Genome wide association identifies PPFIA1 as a candidate gene for acute lung injury risk following major trauma |
| Q35076098 | Genome wide association studies in presence of misclassified binary responses |
| Q27022629 | Genome-Wide Association Studies of Allergic Diseases |
| Q34545632 | Genome-Wide Association Studies of Sleep Disorders |
| Q28714390 | Genome-Wide Association Study Heterogeneous Cohort Homogenization via Subject Weight Knock-Down |
| Q35769777 | Genome-wide Association Study on Platinum-induced Hepatotoxicity in Non-Small Cell Lung Cancer Patients |
| Q34817128 | Genome-wide association studies in diverse populations |
| Q38195863 | Genome-wide association studies of atopic dermatitis |
| Q26825851 | Genome-wide association studies of chronic kidney disease: what have we learned? |
| Q24273247 | Genome-wide association studies: a primer |
| Q34271719 | Genome-wide association studies: hypothesis-"free" or "engaged"? |
| Q34165031 | Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients |
| Q57030060 | Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese |
| Q37118492 | Genome-wide association study of 8 carcass traits in Jinghai Yellow chickens using specific-locus amplified fragment sequencing technology |
| Q89273205 | Genome-wide association study of body weight in Wenshang Barred chicken based on the SLAF-seq technology |
| Q47425743 | Genome-wide association study of myelosuppression in non-small-cell lung cancer patients with platinum-based chemotherapy |
| Q38000445 | Genome-wide association study of skin complex diseases |
| Q36585419 | Genome-wide association study reveals the genetic architecture of flowering time in rapeseed (Brassica napus L.). |
| Q37830958 | Genome-wide association: from confounded to confident. |
| Q34268288 | Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture |
| Q34994543 | Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease |
| Q34271734 | Genomic convergence of genome-wide investigations for complex traits |
| Q28296883 | Genomics: In search of rare human variants |
| Q41630600 | Genotype imputation in a coalescent model with infinitely-many-sites mutation |
| Q24273285 | Genotyping sleep disorders patients |
| Q42416318 | Given the complexity of the human genome, can 'personalised medicine' or 'individualised drug therapy' ever be achieved? |
| Q50986179 | Giving and withholding of information following genomic screening: challenges identified in a study of primary care physicians in Estonia |
| Q60960404 | Global Expression Profiling Identifies a Novel Hyaluronan Synthases 2 Gene in the Pathogenesis of Lower Extremity Varicose Veins |
| Q37708392 | Guilt by rewiring: gene prioritization through network rewiring in genome wide association studies. |
| Q33976828 | Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants. |
| Q28280647 | Hereditary and familial colon cancer |
| Q39537322 | Hierarchical Generalized Linear Models for Multiple Groups of Rare and Common Variants: Jointly Estimating Group and Individual-Variant Effects |
| Q34713944 | High-resolution genetic mapping in the diversity outbred mouse population identifies Apobec1 as a candidate gene for atherosclerosis |
| Q34031894 | Homozygosity mapping on homozygosity haplotype analysis to detect recessive disease-causing genes from a small number of unrelated, outbred patients |
| Q93047901 | Host Genetic Determinants of Hepatitis B Virus Infection |
| Q36166473 | How Genes Influence Life Span: The Biodemography of Human Survival |
| Q35077860 | How genome-wide SNP-SNP interactions relate to nasopharyngeal carcinoma susceptibility |
| Q39015956 | Human aging in the post-GWAS era: further insights reveal potential regulatory variants |
| Q36878088 | Human genome epidemiology, progress and future |
| Q35131979 | Human leukocyte antigen in primary biliary cirrhosis: An old story now reviving |
| Q37376994 | Human leukocyte antigens and epstein-barr virus-associated nasopharyngeal carcinoma: old associations offer new clues into the role of immunity in infection-associated cancers. |
| Q42739783 | HyperModules: identifying clinically and phenotypically significant network modules with disease mutations for biomarker discovery |
| Q36783894 | Identification of SPOCK2 as a susceptibility gene for bronchopulmonary dysplasia |
| Q83591768 | Identification of genes affecting apolipoprotein B secretion following siRNA-mediated gene knockdown in primary human hepatocytes |
| Q36347919 | Identification of shared genetic susceptibility locus for coronary artery disease, type 2 diabetes and obesity: a meta-analysis of genome-wide studies |
| Q33563269 | Identification of type 2 diabetes-associated combination of SNPs using support vector machine |
| Q37010357 | Identifying Darwinian selection acting on different human APOL1 variants among diverse African populations. |
| Q33719613 | Identifying disease polymorphisms from case–control genetic association data |
| Q35233885 | Identifying functional single nucleotide polymorphisms in the human CArGome |
| Q34989308 | Identifying genetic interactions associated with late-onset Alzheimer's disease |
| Q37683472 | Identifying genetic relatives without compromising privacy |
| Q30652067 | Improving data and knowledge management to better integrate health care and research. |
| Q36487017 | Inflammatory gene variants in the Tsimane, an indigenous Bolivian population with a high infectious load |
| Q36625970 | Initial assessment of the pathogenic mechanisms of the recently identified Alzheimer risk Loci |
| Q37922222 | Insights into the genetics of osteoporosis from recent genome-wide association studies |
| Q35413415 | Integrating omics technologies to study pulmonary physiology and pathology at the systems level |
| Q33773021 | Integrating pathway analysis and genetics of gene expression for genome-wide association studies |
| Q34506746 | Interactive association of five candidate polymorphisms in Apelin/APJ pathway with coronary artery disease among Chinese hypertensive patients |
| Q36011868 | Interleukin-10 Genotype Correlated to Deficiency Syndrome in Hepatitis B Cirrhosis |
| Q34187048 | Interpreting meta-analyses of genome-wide association studies |
| Q52324550 | Intragenic transcriptional interference regulates the human immune ligand MICA. |
| Q36944836 | Introduction to the Special Section on Genomics |
| Q24602526 | Joint influence of small-effect genetic variants on human longevity |
| Q34427355 | Lactase Persistence and Lipid Pathway Selection in the Maasai |
| Q43598248 | Leucyl/Cystinyl Aminopeptidase Gene Variants in Septic Shock |
| Q28704307 | Leveraging models of cell regulation and GWAS data in integrative network-based association studies |
| Q45891500 | Likelihood Approach for Detecting Imprinting and In Utero Maternal Effects Using General Pedigrees from Prospective Family‐Based Association Studies |
| Q33576732 | Liver and adipose expression associated SNPs are enriched for association to type 2 diabetes |
| Q92452836 | Locus-specific DNA methylation prediction in cord blood and placenta |
| Q37471784 | MDA5 and PTPN2, two candidate genes for type 1 diabetes, modify pancreatic beta-cell responses to the viral by-product double-stranded RNA. |
| Q26824221 | Mechanisms of granulin deficiency: lessons from cellular and animal models |
| Q34329119 | Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy |
| Q33761835 | Methods for investigating gene-environment interactions in candidate pathway and genome-wide association studies |
| Q37707119 | Methods for optimizing statistical analyses in pharmacogenomics research |
| Q33632915 | Methylation potential associated with diet, genotype, protein, and metabolite levels in the Delta Obesity Vitamin Study |
| Q37882589 | Milestones in PD genetics |
| Q41670529 | Mimvec: a deep learning approach for analyzing the human phenome |
| Q33772072 | Model-based multifactor dimensionality reduction for detecting epistasis in case-control data in the presence of noise |
| Q37722954 | Molecular epidemiology and its current clinical use in cancer management |
| Q28383483 | Molecular epidemiology of DNA repair gene polymorphisms and head and neck cancer |
| Q37594580 | Molecular networks as sensors and drivers of common human diseases |
| Q36285002 | Multiple quantitative trait loci for cortical and trabecular bone regulation map to mid-distal mouse chromosome 4 that shares linkage homology to human chromosome 1p36 |
| Q26824094 | Natural history and clinical response: “It’s the virus, stupid, or is it the host?” |
| Q35695044 | Networks of intergenic long-range enhancers and snpRNAs drive castration-resistant phenotype of prostate cancer and contribute to pathogenesis of multiple common human disorders |
| Q64104680 | New Insights Into Monogenic Causes of Osteoporosis |
| Q37560444 | New genes and new insights from old genes: update on Alzheimer disease |
| Q37499291 | New tools for functional genomic analysis. |
| Q35157201 | New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis. |
| Q27026914 | New virologic tools for management of chronic hepatitis B and C |
| Q34222296 | Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations |
| Q37789759 | Occupational toxicology of asbestos-related malignancies |
| Q30244335 | Omic studies reveal the pathogenic lipid droplet proteins in non-alcoholic fatty liver disease |
| Q38523018 | On optimal pooling designs to identify rare variants through massive resequencing |
| Q37482173 | On the simultaneous association analysis of large genomic regions: a massive multi-locus association test |
| Q38037294 | Opportunities and challenges associated with clinical diagnostic genome sequencing: a report of the Association for Molecular Pathology. |
| Q37190694 | Overview of Behavioral Genetics Research for Family Researchers |
| Q38686298 | PCOS in 2015: New insights into the genetics of polycystic ovary syndrome |
| Q34044630 | PTPN2, a candidate gene for type 1 diabetes, modulates pancreatic β-cell apoptosis via regulation of the BH3-only protein Bim. |
| Q34117595 | Pathway-based analysis of a melanoma genome-wide association study: analysis of genes related to tumour-immunosuppression |
| Q38029641 | Personalized Medicine: the Impact on Chemistry |
| Q24621065 | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score |
| Q91633083 | Pharmacogenetics of Pediatric Asthma: Current Perspectives |
| Q37770487 | Pharmacogenetics of drug-induced liver injury |
| Q36166448 | Polygenic Effects of Common Single-Nucleotide Polymorphisms on Life Span: When Association Meets Causality |
| Q28681745 | Population genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) Consortium |
| Q31129426 | Predicting disease risk using bootstrap ranking and classification algorithms |
| Q83445215 | Prediction of fibrosis progression in hepatitis C infection: Are genetics ready for clinical use? |
| Q37643740 | Predictive genetic testing for coronary artery disease |
| Q33571786 | Prioritizing GWAS results: A review of statistical methods and recommendations for their application |
| Q34537519 | Progress and promise of genome-wide association studies for human complex trait genetics |
| Q36051664 | Progress of cancer genomics |
| Q34163437 | Quantitative analyses link modulation of sonic hedgehog signaling to continuous variation in facial growth and shape |
| Q63359102 | Quantitative trait loci for electrocardiographic parameters and arrhythmia in the mouse |
| Q55339749 | RETRACTED: Dissecting closely linked association signals in combination with the mammalian phenotype database can identify candidate genes in dairy cattle. |
| Q35646732 | Race and ancestry in the age of inclusion: technique and meaning in post-genomic science |
| Q35136958 | Random-Effects Model Aimed at Discovering Associations in Meta-Analysis of Genome-wide Association Studies |
| Q34630019 | Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses |
| Q38116806 | Recent advances in Parkinson’s disease genetics. |
| Q36353087 | Relationship of Genetic Polymorphisms of the Chemokine, CCL5, and Its Receptor, CCR5, with Coronary Artery Disease in Taiwan |
| Q51899355 | Replication of two novel susceptibility loci for non-syndromic orofacial clefts in a Chinese population |
| Q46946218 | Replication study of three functional polymorphisms associated with bone mineral density in a cohort of Spanish women. |
| Q41902413 | Reporting and evaluating genetic association studies |
| Q34026195 | Reverse-engineering human regulatory networks |
| Q30829290 | Review of statistical methodologies for the detection of parent-of-origin effects in family trio genome-wide association data with binary disease traits |
| Q60310012 | Role of SH2B3 R262W gene polymorphism and risk of coronary heart disease: A PRISMA-compliant meta-analysis |
| Q33957829 | SPOT: a web-based tool for using biological databases to prioritize SNPs after a genome-wide association study |
| Q34293847 | Scientific imperatives, clinical implications, and theoretical underpinnings for the investigation of the relationship between genetic variables and patient-reported quality-of-life outcomes |
| Q21092453 | Sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates MMP20 in human kidney aging |
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