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Diabetes|October 1, 2015
American Diabetes Association and JDRF Research Symposium: Diabetes and the MicrobiomeClay F Semenkovich, Jayne Danska, Tamara Darsow, et al.Clinical Genetics|January 25, 2021
Two intronic cis-acting variants in both alleles of the POLR3A gene cause progressive spastic ataxia with hypodontiaAvi Fellner, Alexander Lossos, Elena Kogan, et al.Journal of Human Genetics|March 24, 2019
A novel TUFM homozygous variant in a child with mitochondrial cardiomyopathy expands the phenotype of combined oxidative phosphorylation deficiency 4Tova Hershkovitz, Alina Kurolap, Claudia Gonzaga-Jauregui, et al.The American Journal of Cardiology|August 8, 2009
Aspirin Resistance in healthy drug-naive men versus women (from the Heredity and Phenotype Intervention Heart Study)Haiqing Shen, William Herzog, MaryAnn Drolet, et al.Diabetes, Obesity & Metabolism|August 23, 2023
Pharmacogenetics of sodium-glucose co-transporter-2 inhibitors: Validation of a sex-agnostic pharmacodynamic biomarkerSimeon I Taylor, Hua-Ren Cherng, Zhinous Shahidzadeh Yazdi, et al.Human Heredity|June 15, 2007
Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order AmishWendy Post, Haiqing Shen, Coleen Damcott, et al.Medrxiv : the Preprint Server for Health Sciences|March 22, 2023
Pharmacogenetics of SGLT2 Inhibitors: Validation of a sex-agnostic pharmacodynamic biomarkerSimeon I Taylor, Hua-Ren Cherng, Zhinous Shahidzadeh Yazdi, et al.Circulation. Cardiovascular Genetics|October 28, 2016
Comprehensive Analysis of Established Dyslipidemia-Associated Loci in the Diabetes Prevention ProgramTibor V Varga, Alexandra H Winters, Kathleen A Jablonski, et al.Stroke|March 30, 2017
Pharmacogenetic Associations of β1-Adrenergic Receptor Polymorphisms With Cardiovascular Outcomes in the SPS3 Trial (Secondary Prevention of Small Subcortical Strokes)Oyunbileg Magvanjav, Caitrin W McDonough, Yan Gong, et al.The Journal of Clinical Endocrinology and Metabolism|June 8, 2004
Mutations in Gng3lg and AGPAT2 in Berardinelli-Seip congenital lipodystrophy and Brunzell syndrome: phenotype variability suggests important modifier effectsMao Fu, Rasa Kazlauskaite, Maria de Fátima Paiva Baracho, et al.Pageof 45