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The Journal of Infectious Diseases|February 1, 2011
Host genetic determinants of T cell responses to the MRKAd5 HIV-1 gag/pol/nef vaccine in the step trialJacques Fellay, Nicole Frahm, Kevin V Shianna, et al.Cold Spring Harbor Molecular Case Studies|July 21, 2018
Exome sequencing of an adolescent with nonalcoholic fatty liver disease identifies a clinically actionable case of Wilson diseaseJulia Wattacheril, Patrick R Shea, Saeed Mohammad, et al.Nature Genetics|December 8, 2009
Geographical genomics of human leukocyte gene expression variation in southern MoroccoYoussef Idaghdour, Wendy Czika, Kevin V Shianna, et al.Genome Biology|March 9, 2007
Alternative ion channel splicing in mesial temporal lobe epilepsy and Alzheimer's diseaseErin L Heinzen, Woohyun Yoon, Michael E Weale, et al.Nature Communications|August 11, 2017
Annotating pathogenic non-coding variants in genic regionsSahar Gelfman, Quanli Wang, K Melodi McSweeney, et al.Pharmacogenetics and Genomics|December 14, 2007
Promoter polymorphisms and allelic imbalance in ABCB1 expressionCorinne Loeuillet, Michael Weale, Samuel Deutsch, et al.American Journal of Medical Genetics. Part A|June 10, 2003
Haplotype analysis of the growth hormone releasing hormone receptor locus in three apparently unrelated kindreds from the indian subcontinent with the identical mutation in the GHRH receptorMichael P Wajnrajch, Joseph M Gertner, Alisa S Sokoloff, et al.JAMA Network Open|October 28, 2022
Risk Variants in the Exomes of Children With Critical IllnessJoshua E Motelow, Natalie C Lippa, Joseph Hostyk, et al.Medrxiv : the Preprint Server for Health Sciences|October 24, 2023
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.JAMA Cardiology|December 16, 2020
Assessing the Role of Rare Genetic Variation in Patients With Heart FailureGundula Povysil, Olympe Chazara, Keren J Carss, et al.Pageof 34