| meta-analysis | Q815382 |
| scholarly article | Q13442814 |
| P50 | author | Joel Hirschhorn | Q56277942 |
| John Ioannidis | Q6251482 | ||
| Cristen J. Willer | Q37389746 | ||
| Orestis A. Panagiotou | Q42589634 | ||
| P2860 | cites work | Consistency of genome-wide associations across major ancestral groups | Q44515366 |
| Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis | Q44921278 | ||
| Comparison of effect sizes associated with biomarkers reported in highly cited individual articles and in subsequent meta-analyses | Q46207178 | ||
| What should the genome-wide significance threshold be? Empirical replication of borderline genetic associations | Q46543455 | ||
| Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides | Q46809732 | ||
| A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits | Q47936547 | ||
| Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits | Q51009301 | ||
| Screening of 134 single nucleotide polymorphisms (SNPs) previously associated with type 2 diabetes replicates association with 12 SNPs in nine genes | Q51482486 | ||
| The Emergence of Networks in Human Genome Epidemiology | Q56828411 | ||
| Optimal designs for two-stage genome-wide association studies | Q56879653 | ||
| Genomewide association studies--illuminating biologic pathways | Q83658310 | ||
| Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size | Q21092465 | ||
| Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis | Q21144992 | ||
| Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability | Q21563383 | ||
| Potential etiologic and functional implications of genome-wide association loci for human diseases and traits | Q22066284 | ||
| Finding the missing heritability of complex diseases | Q22122198 | ||
| Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease | Q22251069 | ||
| Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease | Q22337234 | ||
| Replication in Genome-Wide Association Studies | Q24288830 | ||
| High-resolution whole-genome association study of Parkinson disease. | Q24535861 | ||
| Genome-wide association studies for complex traits: consensus, uncertainty and challenges | Q24550632 | ||
| Common variants at 30 loci contribute to polygenic dyslipidemia | Q24598765 | ||
| A common variant of HMGA2 is associated with adult and childhood height in the general population | Q24603211 | ||
| Five years of GWAS discovery | Q24610574 | ||
| A map of human genome variation from population-scale sequencing | Q24617794 | ||
| Biological, clinical and population relevance of 95 loci for blood lipids | Q24622541 | ||
| Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk | Q24630394 | ||
| Hundreds of variants clustered in genomic loci and biological pathways affect human height | Q24630979 | ||
| From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus | Q24633183 | ||
| Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans | Q24643492 | ||
| Six new loci associated with body mass index highlight a neuronal influence on body weight regulation | Q24646434 | ||
| Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes | Q24651119 | ||
| A second generation human haplotype map of over 3.1 million SNPs | Q24651939 | ||
| A haplotype map of the human genome | Q24679827 | ||
| Measuring inconsistency in meta-analyses | Q27860655 | ||
| Meta-analysis in clinical trials | Q27860779 | ||
| Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease | Q27860821 | ||
| Newly identified loci that influence lipid concentrations and risk of coronary artery disease | Q28264535 | ||
| Identification of ten loci associated with height highlights new biological pathways in human growth | Q28275237 | ||
| Many sequence variants affecting diversity of adult human height | Q28275246 | ||
| The mystery of missing heritability: Genetic interactions create phantom heritability | Q28732355 | ||
| Improving the assessment of the outcome of nonsynonymous SNVs with a consensus deleteriousness score, Condel. | Q34768428 | ||
| Schizophrenia Genetics: Where Next? | Q34830762 | ||
| Validating, augmenting and refining genome-wide association signals | Q34976245 | ||
| Imputation aware meta-analysis of genome-wide association studies | Q35007657 | ||
| Random-Effects Model Aimed at Discovering Associations in Meta-Analysis of Genome-wide Association Studies | Q35136958 | ||
| Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians | Q35172107 | ||
| Genome-wide association study of body height in African Americans: the Women's Health Initiative SNP Health Association Resource (SHARe) | Q35674693 | ||
| Estimation of effect size distribution from genome-wide association studies and implications for future discoveries | Q36191121 | ||
| A network of investigator networks in human genome epidemiology | Q36193157 | ||
| zCall: a rare variant caller for array-based genotyping: genetics and population analysis | Q36294014 | ||
| Genome-wide significant associations for variants with minor allele frequency of 5% or less--an overview: A HuGE review | Q36480665 | ||
| A gene-centric approach to genome-wide association studies | Q36626619 | ||
| Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits | Q36670925 | ||
| Non-replication and inconsistency in the genome-wide association setting | Q36841272 | ||
| Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation | Q37088889 | ||
| Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis | Q37089998 | ||
| Genetic variation in GPR133 is associated with height: genome wide association study in the self-contained population of Sorbs | Q37411795 | ||
| Genotyping technologies for genetic research | Q37488213 | ||
| Rare Variant Association Analysis Methods for Complex Traits | Q37806780 | ||
| Methods for meta-analyses of genome-wide association studies: critical assessment of empirical evidence | Q37994668 | ||
| Genome-wide association analysis of imputed rare variants: application to seven common complex diseases | Q41820122 | ||
| Multiple regions within 8q24 independently affect risk for prostate cancer | Q42038345 | ||
| A combined functional annotation score for non-synonymous variants | Q42227205 | ||
| Laboratory mouse models for the human genome-wide associations | Q28748647 | ||
| Practical aspects of imputation-driven meta-analysis of genome-wide association studies | Q28749837 | ||
| Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project | Q28943291 | ||
| Genome-wide association study of blood pressure and hypertension | Q28943443 | ||
| Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm | Q29547194 | ||
| Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels | Q29547214 | ||
| METAL: fast and efficient meta-analysis of genomewide association scans | Q29547217 | ||
| Integrating common and rare genetic variation in diverse human populations | Q29547220 | ||
| Common SNPs explain a large proportion of the heritability for human height | Q29547221 | ||
| Prediction of deleterious human alleles | Q29614367 | ||
| Genome-wide association study identifies eight loci associated with blood pressure | Q29614414 | ||
| Common genetic variation and human traits | Q29614445 | ||
| Genome-wide association analysis identifies 20 loci that influence adult height | Q29614583 | ||
| Genotype imputation | Q29614590 | ||
| A HapMap harvest of insights into the genetics of common disease | Q29614875 | ||
| Quantitative Synthesis in Systematic Reviews | Q29614894 | ||
| Systematic localization of common disease-associated variation in regulatory DNA | Q29614895 | ||
| Estimation of the multiple testing burden for genomewide association studies of nearly all common variants | Q29614917 | ||
| Replicating genotype-phenotype associations | Q29614919 | ||
| Genetic mapping in human disease | Q29614943 | ||
| Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts | Q29614946 | ||
| Rare variants create synthetic genome-wide associations | Q29614955 | ||
| Replication validity of genetic association studies | Q29615456 | ||
| On the allelic spectrum of human disease | Q29616298 | ||
| Common variants in the GDF5-UQCC region are associated with variation in human height | Q30435234 | ||
| Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study | Q30539203 | ||
| Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry | Q31036626 | ||
| Optimal tests for rare variant effects in sequencing association studies | Q31065241 | ||
| Meta-analysis in genome-wide association datasets: strategies and application in Parkinson disease | Q33276409 | ||
| Heterogeneity in meta-analyses of genome-wide association investigations | Q33297003 | ||
| Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data | Q33359015 | ||
| Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions | Q33474863 | ||
| Discovery properties of genome-wide association signals from cumulatively combined data sets | Q33508966 | ||
| Prioritizing GWAS results: A review of statistical methods and recommendations for their application | Q33571786 | ||
| Synthetic associations are unlikely to account for many common disease genome-wide association signals | Q33803713 | ||
| The False-positive to False-negative Ratio in Epidemiologic Studies | Q34178142 | ||
| Problems of reporting genetic associations with complex outcomes | Q34184173 | ||
| Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9. | Q34385127 | ||
| On the relative efficiency of using summary statistics versus individual-level data in meta-analysis | Q34437384 | ||
| Prediction of individual genetic risk to disease from genome-wide association studies | Q34676890 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | meta-analysis | Q815382 |
| genome-wide association study | Q1098876 | ||
| P304 | page(s) | 441-65 | |
| P577 | publication date | 2013-01-01 | |
| P1433 | published in | Annual Review of Genomics and Human Genetics | Q567360 |
| P1476 | title | The power of meta-analysis in genome-wide association studies | |
| P478 | volume | 14 |
| Q35177444 | A genome-wide pleiotropy scan for prostate cancer risk |
| Q89661625 | A novel estimator of between-study variance in random-effects models |
| Q35489723 | A review of study designs and statistical methods for genomic epidemiology studies using next generation sequencing |
| Q38287451 | A systematic appraisal of field synopses in genetic epidemiology: a HuGE review |
| Q48158524 | Beyond genomics: understanding exposotypes through metabolomics |
| Q63738935 | Biomedical informatics and machine learning for clinical genomics |
| Q49587994 | Cross-Phenotype Association Analysis Using Summary Statistics from GWAS. |
| Q30366188 | Design and Implementation of the International Genetics and Translational Research in Transplantation Network |
| Q24288911 | Diverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factors |
| Q40233002 | Exposure-wide epidemiology: revisiting Bradford Hill |
| Q50950355 | Four Genome-Wide Association Studies Identify New Extreme Longevity Variants |
| Q34468469 | GACT: a Genome build and Allele definition Conversion Tool for SNP imputation and meta-analysis in genetic association studies |
| Q57392986 | GWAS for BMI: a treasure trove of fundamental insights into the genetic basis of obesity |
| Q30277642 | Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function |
| Q36542738 | Genetic studies of major depressive disorder: why are there no genome-wide association study findings and what can we do about it? |
| Q100528967 | Genetic variation in the body mass index of adult survivors of childhood acute lymphoblastic leukemia: A report from the Childhood Cancer Survivor Study and the St. Jude Lifetime Cohort |
| Q89737463 | Genetically Determined Height and Risk of Non-hodgkin Lymphoma |
| Q38379199 | Genetics and brain morphology |
| Q34762509 | Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East Asians |
| Q30252068 | Genome-wide association studies in pediatric chronic kidney disease |
| Q46904091 | Genome-wide association study identifies the GLDC/IL33 locus associated with survival of osteosarcoma patients |
| Q94521621 | Genome-wide association study of emotional empathy in children |
| Q24288766 | How to make more published research true |
| Q37716328 | Identification of IDUA and WNT16 Phosphorylation-Related Non-Synonymous Polymorphisms for Bone Mineral Density in Meta-Analyses of Genome-Wide Association Studies |
| Q35882550 | Identification of a novel FGFRL1 MicroRNA target site polymorphism for bone mineral density in meta-analyses of genome-wide association studies |
| Q64113992 | Identifying Multi-Omics Causers and Causal Pathways for Complex Traits |
| Q49787376 | Impact of LMP7 (rs2071543) gene polymorphism in increasing cancer risk: evidence from a meta-analysis and trial sequential analysis |
| Q92745284 | Meta-MultiSKAT: Multiple phenotype meta-analysis for region-based association test |
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| Q64077315 | Meta-analysis of genome-wide association studies provides insights into genetic control of tomato flavor |
| Q35626453 | Molecular basis and genetic predisposition to intracranial aneurysm |
| Q28390801 | Multivariate Analysis of Anthropometric Traits Using Summary Statistics of Genome-Wide Association Studies from GIANT Consortium |
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| Q24289398 | Publication and other reporting biases in cognitive sciences: detection, prevalence, and prevention |
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| Q53099181 | Research: increasing value, reducing waste - Authors' reply |
| Q47654883 | Runs of homozygosity: windows into population history and trait architecture. |
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