# | Title | Journal | Year | Citations |
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1 | Consistent Estimation in Mendelian Randomization with Some Invalid Instruments Using a Weighted Median Estimator | Genetic Epidemiology | 2016 | 4,142 |
2 | Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized Data | Genetic Epidemiology | 2013 | 2,705 |
3 | MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes | Genetic Epidemiology | 2010 | 1,718 |
4 | Pedigree disequilibrium tests for multilocus haplotypes | Genetic Epidemiology | 2003 | 1,094 |
5 | Bias due to participant overlap in two‐sample Mendelian randomization | Genetic Epidemiology | 2016 | 961 |
6 | Implementing a unified approach to family-based tests of association | Genetic Epidemiology | 2000 | 777 |
7 | Estimation of the multiple testing burden for genomewide association studies of nearly all common variants | Genetic Epidemiology | 2008 | 699 |
8 | Heterogeneity testing in meta-analysis of genome searches | Genetic Epidemiology | 2005 | 657 |
9 | A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms | Genetic Epidemiology | 2008 | 646 |
10 | Estimation of significance thresholds for genomewide association scans | Genetic Epidemiology | 2008 | 618 |
11 | Estimation of individual admixture: Analytical and study design considerations | Genetic Epidemiology | 2005 | 571 |
12 | Empirical bayes methods and false discovery rates for microarrays | Genetic Epidemiology | 2002 | 569 |
13 | Programs for pedigree analysis: Mendel, Fisher, and dGene | Genetic Epidemiology | 1988 | 562 |
14 | Power of multifactor dimensionality reduction for detecting gene-gene interactions in the presence of genotyping error, missing data, phenocopy, and genetic heterogeneity | Genetic Epidemiology | 2003 | 515 |
15 | Truncated product method for combiningP-values | Genetic Epidemiology | 2002 | 457 |
16 | An evaluation of statistical approaches to rare variant analysis in genetic association studies | Genetic Epidemiology | 2010 | 452 |
17 | Family-based tests for associating haplotypes with general phenotype data: Application to asthma genetics | Genetic Epidemiology | 2004 | 395 |
18 | Quality control and quality assurance in genotypic data for genome‐wide association studies | Genetic Epidemiology | 2010 | 389 |
19 | Bayes factors for genome‐wide association studies: comparison with P‐values | Genetic Epidemiology | 2009 | 369 |
20 | A comparison of sib-pair linkage tests for disease susceptibility loci | Genetic Epidemiology | 1985 | 365 |
21 | On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles | Genetic Epidemiology | 2002 | 363 |
22 | The role of haplotypes in candidate gene studies | Genetic Epidemiology | 2004 | 349 |
23 | Detecting association in a case-control study while correcting for population stratification | Genetic Epidemiology | 2001 | 341 |
24 | A balanced accuracy function for epistasis modeling in imbalanced datasets using multifactor dimensionality reduction | Genetic Epidemiology | 2007 | 337 |
25 | Bivariate quantitative trait linkage analysis: Pleiotropy versus co-incident linkages | Genetic Epidemiology | 1997 | 335 |
26 | Robust Inference of Population Structure for Ancestry Prediction and Correction of Stratification in the Presence of Relatedness | Genetic Epidemiology | 2015 | 330 |
27 | Genetic covariation between neuroticism and the symptoms of anxiety and depression | Genetic Epidemiology | 1984 | 326 |
28 | Haseman and Elston revisited | Genetic Epidemiology | 2000 | 324 |
29 | Identifying SNPs predictive of phenotype using random forests | Genetic Epidemiology | 2005 | 321 |
30 | Polygenic scores via penalized regression on summary statistics | Genetic Epidemiology | 2017 | 297 |
31 | Avoiding the high Bonferroni penalty in genome‐wide association studies | Genetic Epidemiology | 2010 | 296 |
32 | Evaluating associations of haplotypes with traits | Genetic Epidemiology | 2004 | 293 |
33 | A comparison of robust Mendelian randomization methods using summary data | Genetic Epidemiology | 2020 | 290 |
34 | Apolipoprotein E polymorphism in a Danish population compared to findings in 45 other study populations around the world | Genetic Epidemiology | 1992 | 285 |
35 | Transethnic meta‐analysis of genomewide association studies | Genetic Epidemiology | 2011 | 282 |
36 | A Better Coefficient of Determination for Genetic Profile Analysis | Genetic Epidemiology | 2012 | 274 |
37 | Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases | Genetic Epidemiology | 2011 | 265 |
38 | Evidence for further breast cancer susceptibility genes in addition toBRCA1 andBRCA2 in a population-based study | Genetic Epidemiology | 2001 | 263 |
39 | Genetic linkage and complex diseases, with special reference to psychiatric disorders | Genetic Epidemiology | 1990 | 251 |
40 | Pathway analysis by adaptive combination of P‐values | Genetic Epidemiology | 2009 | 248 |
41 | Multiethnic polygenic risk scores improve risk prediction in diverse populations | Genetic Epidemiology | 2017 | 248 |
42 | Heritability of body size and muscle strength in young adulthood: a study of one million Swedish men | Genetic Epidemiology | 2008 | 237 |
43 | Sibling correlations and segregation analysis of age-related maculopathy: The beaver dam eye study | Genetic Epidemiology | 1994 | 229 |
44 | Genetic model testing and statistical power in population-based association studies of quantitative traits | Genetic Epidemiology | 2007 | 224 |
45 | On multiple‐testing correction in genome‐wide association studies | Genetic Epidemiology | 2008 | 216 |
46 | Case/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 effects | Genetic Epidemiology | 2004 | 214 |
47 | Polygenic inheritance of breast cancer: Implications for design of association studies | Genetic Epidemiology | 2003 | 213 |
48 | STrengthening the REporting of Genetic Association Studies (STREGA)—an extension of the STROBE statement | Genetic Epidemiology | 2009 | 211 |
49 | Asymptotic tests of association with multiple SNPs in linkage disequilibrium | Genetic Epidemiology | 2009 | 208 |
50 | Accounting for Population Stratification in DNA Methylation Studies | Genetic Epidemiology | 2014 | 207 |