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Human Heredity|February 20, 2017
Human Birth Weight and Reproductive Immunology: Testing for Interactions between Maternal and Offspring KIR and HLA-C GenesMichelle M Clark, Olympe Chazara, Eric M Sobel, et al.
Molecular Phylogenetics and Evolution|June 17, 2015
Genome-wide ultraconserved elements exhibit higher phylogenetic informativeness than traditional gene markers in percomorph fishesPrincess S Gilbert, Jonathan Chang, Calvin Pan, et al.
Cancer Prevention Research (Philadelphia, Pa.)|September 15, 2020
Genome-wide Association Analysis of Proinflammatory Cytokines and Gene-lifestyle Interaction for Invasive Breast Cancer Risk: The WHI dbGaP StudySu Yon Jung, Peter A Scott, Jeanette C Papp, et al.
Gigascience|June 4, 2020
Iterative hard thresholding in genome-wide association studies: Generalized linear models, prior weights, and double sparsityBenjamin B Chu, Kevin L Keys, Christopher A German, et al.
BMC Systems Biology|November 7, 2008
Integrated weighted gene co-expression network analysis with an application to chronic fatigue syndromeAngela P Presson, Eric M Sobel, Jeanette C Papp, et al.
American Journal of Human Genetics|January 7, 2023
Unsupervised discovery of ancestry-informative markers and genetic admixture proportions in biobank-scale datasetsSeyoon Ko, Benjamin B Chu, Daniel Peterson, et al.
Frontiers in Genetics|June 5, 2013
The systems genetics resource: a web application to mine global data for complex disease traitsAtila van Nas, Calvin Pan, Leslie A Ingram-Drake, et al.
Circulation. Cardiovascular Genetics|November 6, 2014
Shared molecular pathways and gene networks for cardiovascular disease and type 2 diabetes mellitus in women across diverse ethnicitiesKei Hang K Chan, Yen-Tsung Huang, Qingying Meng, et al.
The Journal of Clinical Endocrinology and Metabolism|February 7, 2013
Common genetic variants in peroxisome proliferator-activated receptor-γ (PPARG) and type 2 diabetes risk among Women's Health Initiative postmenopausal womenKei Hang K Chan, Tianhua Niu, Yunsheng Ma, et al.
Investigative Ophthalmology & Visual Science|April 2, 2010
Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYCAnthony J Aldave, George O D Rosenwasser, Vivek S Yellore, et al.
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