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Plos One|January 24, 2013
Rare variant analysis for family-based designGourab De, Wai-Ki Yip, Iuliana Ionita-Laza, et al.
BMC Proceedings|March 1, 2012
Identifying causal rare variants of disease through family-based analysis of Genetics Analysis Workshop 17 data setWai-Ki Yip, Gourab De, Benjamin A Raby, et al.
BMC Genetics|March 2, 2013
A general semi-parametric approach to the analysis of genetic association studies in population-based designsSharon Lutz, Wai-Ki Yip, John Hokanson, et al.
BMC Genetics|December 22, 2007
EFBAT: exact family-based association testsKady Schneiter, James H Degnan, Christopher Corcoran, et al.
American Journal of Human Genetics|April 28, 2006
Polymorphism in maternal LRP8 gene is associated with fetal growthLin Wang, Xiaobin Wang, Nan Laird, et al.
Genetic Epidemiology|May 3, 2012
Is it rare or common?Kaustubh Adhikari, Taofik AlChawa, Kerstin Ludwig, et al.
Blood|January 6, 2012
Selective expansion of polyfunctional pathogen-specific CD4(+) T cells in HIV-1-infected patients with immune reconstitution inflammatory syndromeYolanda D Mahnke, Jamieson H Greenwald, Rebecca DerSimonian, et al.
Plos One|August 7, 2010
The effect of leflunomide on cycling and activation of T-cells in HIV-1-infected participantsSarah W Read, Mary DeGrezia, Emily J Ciccone, et al.
Statistical Applications in Genetics and Molecular Biology|December 4, 2009
Statistical screening method for genetic factors influencing susceptibility to common diseases in a two-stage genome-wide association studyYasunori Sato, Nan Laird, Hideki Suganami, et al.
Genetic Epidemiology|September 25, 2014
A novel method for detecting association between DNA methylation and diseases using spatial informationWai-Ki Yip, Heide Fier, Dawn L DeMeo, et al.
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