Scott J Hebbring

Nonparametric tests of association of multiple genes with human disease.

Daniel J Schaid, D. Schaid, S. Thibodeau, 2005, American journal of human genetics.

Identifying genetically driven clinical phenotypes using linear mixed models

Lisa Bastarache, Joshua C Denny, Dan M Roden, 2016, Nature Communications.

Mining Retrospective Data for Virtual Prospective Drug Repurposing: L-DOPA and Age-related Macular Degeneration

Darius M Moshfeghi, Stephen G Schwartz, Murray H Brilliant, 2015, The American journal of medicine.

Phenome-wide association study maps new diseases to the human major histocompatibility complex region

Katsushi Tokunaga, Zhan Ye, Murray H Brilliant, 2016, Journal of Medical Genetics.

Phenome-wide association studies (PheWASs) for functional variants

Zhan Ye, David Page, Murray H Brilliant, 2014, European Journal of Human Genetics.

Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants

Lisa Bastarache, Joshua C Denny, Dan M Roden, 2017, Science Translational Medicine.

SeqHBase: a big data toolset for family based sequencing data analysis

Peggy L Peissig, Zhan Ye, Gholson J Lyon, 2015, Journal of Medical Genetics.