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Genetic Epidemiology|December 27, 2016
Evidence for SNP-SNP interaction identified through targeted sequencing of cleft case-parent triosYanzi Xiao, Margaret A Taub, Ingo Ruczinski, et al.
Genetic Epidemiology|December 27, 2016
Impact of genotyping errors on statistical power of association tests in genomic analyses: A case studyLin Hou, Ning Sun, Shrikant Mane, et al.
Genetic Epidemiology|December 3, 2016
Whole exome association of rare deletions in multiplex oral cleft familiesJack Fu, Terri H Beaty, Alan F Scott, et al.
Genetic Epidemiology|January 30, 2008
On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association testIuliana Ionita-Laza, George H Perry, Benjamin A Raby, et al.
Genetic Epidemiology|February 14, 2008
A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphismsXiaoyi Gao, Joshua Starmer, Eden R Martin
Genetic Epidemiology|March 12, 2014
The association between global DNA methylation and telomere length in a longitudinal study of boilermakersJason Y Y Wong, Immaculata De Vivo, Xihong Lin, et al.
Genetic Epidemiology|February 14, 2017
Gene-based segregation method for identifying rare variants in family-based sequencing studiesDandi Qiao, Christoph Lange, Nan M Laird, et al.
Genetic Epidemiology|February 9, 2017
Detecting association of rare and common variants based on cross-validation prediction errorXinlan Yang, Shuaichen Wang, Shuanglin Zhang, et al.
Genetic Epidemiology|March 20, 2019
A simple approximation to bias in the genetic effect estimates when multiple disease states share a clinical diagnosisIryna Lobach, Inyoung Kim, Alexander Alekseyenko, et al.
Genetic Epidemiology|April 6, 2017
A genome-wide linkage and association analysis of imputed insertions and deletions with cardiometabolic phenotypes in Mexican Americans: The Insulin Resistance Atherosclerosis Family StudyChuan Gao, Fang-Chi Hsu, Latchezar M Dimitrov, et al.
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