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Journal of Immunology (Baltimore, Md. : 1950)|August 22, 2007
Association of TLR4 polymorphisms with symptomatic respiratory syncytial virus infection in high-risk infants and young childrenAgnes A Awomoyi, Prasad Rallabhandi, Toni I Pollin, et al.
Diabetes Care|July 4, 2012
The C allele of ATM rs11212617 does not associate with metformin response in the Diabetes Prevention ProgramJose C Florez, Kathleen A Jablonski, Andrew Taylor, et al.
Menopause (New York, N.Y.)|May 9, 2023
Association of parity with body mass index and cardiometabolic risk in high-parous womenShisi He, Patrick F McArdle, Kathleen A Ryan, et al.
American Journal of Medical Genetics. Part A|September 1, 2021
The burden of pathogenic variants in clinically actionable genes in a founder populationMegan T Lynch, Kristin A Maloney, Toni I Pollin, et al.
The New England Journal of Medicine|July 21, 2006
TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention ProgramJose C Florez, Kathleen A Jablonski, Nick Bayley, et al.
Clinical Pediatrics|March 15, 2023
Gastrointestinal and Sleep Issues in Toddlers With Autism Versus Other Neurodevelopmental DisordersKatrine Zlatnik, Anna Milliken, Meredith Weaver, et al.
Diabetes|November 25, 2004
Polymorphism in the calsequestrin 1 (CASQ1) gene on chromosome 1q21 is associated with type 2 diabetes in the old order AmishMao Fu, Coleen M Damcott, Mona Sabra, et al.
Nicotine & Tobacco Research : Official Journal of the Society for Research on Nicotine and Tobacco|March 4, 2014
Familial aggregation of tobacco use behaviors among Amish menKatie L Nugent, Amber Million-Mrkva, Joshua Backman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 15, 2018
Monogenic diabetes in overweight and obese youth diagnosed with type 2 diabetes: the TODAY clinical trialJeffrey W Kleinberger, Kenneth C Copeland, Rachelle G Gandica, et al.
Circulation. Cardiovascular Genetics|December 15, 2017
Identity-by-Descent Mapping Identifies Major Locus for Serum Triglycerides in Amerindians Largely Explained by an <i>APOC3</i> Founder MutationWen-Chi Hsueh, Anup K Nair, Sayuko Kobes, et al.
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