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Genetic Epidemiology|June 18, 2016
Family-Based Rare Variant Association Analysis: A Fast and Efficient Method of Multivariate Phenotype Association AnalysisLongfei Wang, Sungyoung Lee, Jungsoo Gim, et al.
Genetic Epidemiology|January 1, 1989
Remarks on ascertainmentW J Ewens, N C Shute
Genetic Epidemiology|May 16, 2019
Integrative analysis of Dupuytren's disease identifies novel risk locus and reveals a shared genetic etiology with BMIMegan Major, Malika K Freund, Kathryn S Burch, et al.
Genetic Epidemiology|January 1, 1987
Coagulation factor XIII: genetic linkage studies with F13BK Bender, S Bissbort, A Klein, et al.
Genetic Epidemiology|October 19, 2021
Penalized mediation models for multivariate dataDaniel J Schaid, Ozan Dikilitas, Jason P Sinnwell, et al.
Genetic Epidemiology|April 28, 2022
Gene-environment interaction in type 2 diabetes in Korean cohorts: Interaction of a type 2 diabetes polygenic risk score with triglyceride and cholesterol on fasting glucose levelsJi Eun Lim, Ji-One Kang, Tae-Woong Ha, et al.
Genetic Epidemiology|February 16, 2022
Integrating external controls in case-control studies improves power for rare-variant testsYatong Li, Seunggeun Lee
Genetic Epidemiology|February 16, 2022
Interaction between genetics and smoking in determining risk of coronary artery diseasesYunfeng Huang, Qin Hui, Marta Gwinn, et al.
Genetic Epidemiology|September 22, 2018
Adjustment for covariates using summary statistics of genome-wide association studiesTao Wang, Xiaonan Xue, Xianhong Xie, et al.
Genetic Epidemiology|October 10, 2018
The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotypeIan B Stanaway, Taryn O Hall, Elisabeth A Rosenthal, et al.
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