2.0(top 20%)
impact factor
2.7K(top 10%)
papers
80.9K(top 5%)
citations
112(top 5%)
h-index
2.0(top 20%)
impact factor
3.5K
all documents
89.8K
doc citations
201(top 5%)
g-index

Top Articles

#TitleJournalYearCitations
1Consistent Estimation in Mendelian Randomization with Some Invalid Instruments Using a Weighted Median EstimatorGenetic Epidemiology20164,142
2Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized DataGenetic Epidemiology20132,705
3MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypesGenetic Epidemiology20101,718
4Pedigree disequilibrium tests for multilocus haplotypesGenetic Epidemiology20031,094
5Bias due to participant overlap in two‐sample Mendelian randomizationGenetic Epidemiology2016961
6Implementing a unified approach to family-based tests of associationGenetic Epidemiology2000777
7Estimation of the multiple testing burden for genomewide association studies of nearly all common variantsGenetic Epidemiology2008699
8Heterogeneity testing in meta-analysis of genome searchesGenetic Epidemiology2005657
9A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphismsGenetic Epidemiology2008646
10Estimation of significance thresholds for genomewide association scansGenetic Epidemiology2008618
11Estimation of individual admixture: Analytical and study design considerationsGenetic Epidemiology2005571
12Empirical bayes methods and false discovery rates for microarraysGenetic Epidemiology2002569
13Programs for pedigree analysis: Mendel, Fisher, and dGeneGenetic Epidemiology1988562
14Power of multifactor dimensionality reduction for detecting gene-gene interactions in the presence of genotyping error, missing data, phenocopy, and genetic heterogeneityGenetic Epidemiology2003515
15Truncated product method for combiningP-valuesGenetic Epidemiology2002457
16An evaluation of statistical approaches to rare variant analysis in genetic association studiesGenetic Epidemiology2010452
17Family-based tests for associating haplotypes with general phenotype data: Application to asthma geneticsGenetic Epidemiology2004395
18Quality control and quality assurance in genotypic data for genome‐wide association studiesGenetic Epidemiology2010389
19Bayes factors for genome‐wide association studies: comparison with P‐valuesGenetic Epidemiology2009369
20A comparison of sib-pair linkage tests for disease susceptibility lociGenetic Epidemiology1985365
21On the advantage of haplotype analysis in the presence of multiple disease susceptibility allelesGenetic Epidemiology2002363
22The role of haplotypes in candidate gene studiesGenetic Epidemiology2004349
23Detecting association in a case-control study while correcting for population stratificationGenetic Epidemiology2001341
24A balanced accuracy function for epistasis modeling in imbalanced datasets using multifactor dimensionality reductionGenetic Epidemiology2007337
25Bivariate quantitative trait linkage analysis: Pleiotropy versus co-incident linkagesGenetic Epidemiology1997335
26Robust Inference of Population Structure for Ancestry Prediction and Correction of Stratification in the Presence of RelatednessGenetic Epidemiology2015330
27Genetic covariation between neuroticism and the symptoms of anxiety and depressionGenetic Epidemiology1984326
28Haseman and Elston revisitedGenetic Epidemiology2000324
29Identifying SNPs predictive of phenotype using random forestsGenetic Epidemiology2005321
30Polygenic scores via penalized regression on summary statisticsGenetic Epidemiology2017297
31Avoiding the high Bonferroni penalty in genome‐wide association studiesGenetic Epidemiology2010296
32Evaluating associations of haplotypes with traitsGenetic Epidemiology2004293
33A comparison of robust Mendelian randomization methods using summary dataGenetic Epidemiology2020290
34Apolipoprotein E polymorphism in a Danish population compared to findings in 45 other study populations around the worldGenetic Epidemiology1992285
35Transethnic meta‐analysis of genomewide association studiesGenetic Epidemiology2011282
36A Better Coefficient of Determination for Genetic Profile AnalysisGenetic Epidemiology2012274
37Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseasesGenetic Epidemiology2011265
38Evidence for further breast cancer susceptibility genes in addition toBRCA1 andBRCA2 in a population-based studyGenetic Epidemiology2001263
39Genetic linkage and complex diseases, with special reference to psychiatric disordersGenetic Epidemiology1990251
40Pathway analysis by adaptive combination of P‐valuesGenetic Epidemiology2009248
41Multiethnic polygenic risk scores improve risk prediction in diverse populationsGenetic Epidemiology2017248
42Heritability of body size and muscle strength in young adulthood: a study of one million Swedish menGenetic Epidemiology2008237
43Sibling correlations and segregation analysis of age-related maculopathy: The beaver dam eye studyGenetic Epidemiology1994229
44Genetic model testing and statistical power in population-based association studies of quantitative traitsGenetic Epidemiology2007224
45On multiple‐testing correction in genome‐wide association studiesGenetic Epidemiology2008216
46Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effectsGenetic Epidemiology2004214
47Polygenic inheritance of breast cancer: Implications for design of association studiesGenetic Epidemiology2003213
48STrengthening the REporting of Genetic Association Studies (STREGA)—an extension of the STROBE statementGenetic Epidemiology2009211
49Asymptotic tests of association with multiple SNPs in linkage disequilibriumGenetic Epidemiology2009208
50Accounting for Population Stratification in DNA Methylation StudiesGenetic Epidemiology2014207