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The Journal of Clinical Investigation|February 2, 2021
Residual β cell function in long-term type 1 diabetes associates with reduced incidence of hypoglycemiaRose A Gubitosi-Klug, Barbara H Braffett, Susan Hitt, et al.Kidney International Reports|July 19, 2019
Intrafamilial Variability of ADPKDMatthew B Lanktree, Elsa Guiard, Weili Li, et al.Gastroenterology|June 19, 2014
Germline mutation of RPS20, encoding a ribosomal protein, causes predisposition to hereditary nonpolyposis colorectal carcinoma without DNA mismatch repair deficiencyTaina T Nieminen, Marie-Françoise O'Donohue, Yunpeng Wu, et al.Nature Metabolism|July 23, 2020
DNA methylation mediates development of HbA1c-associated complications in type 1 diabetesZhuo Chen, Feng Miao, Barbara H Braffett, et al.Nature Genetics|October 4, 2016
Association of host genome with intestinal microbial composition in a large healthy cohortWilliams Turpin, Osvaldo Espin-Garcia, Wei Xu, et al.Diabetes|February 2, 2020
Rare Genetic Variants of Large Effect Influence Risk of Type 1 DiabetesVincenzo Forgetta, Despoina Manousaki, Roman Istomine, et al.Journal of Medical Genetics|December 1, 2020
Linkage analysis identifies an isolated strabismus locus at 14q12 overlapping with FOXG1 syndrome regionXin Cynthia Ye, Nicole M Roslin, Andrew D Paterson, et al.BMJ Open|March 11, 2022
Cohort profile: genomic data for 26 622 individuals from the Canadian Longitudinal Study on Aging (CLSA)Vincenzo Forgetta, Rui Li, Corinne Darmond-Zwaig, et al.Investigative Ophthalmology & Visual Science|March 22, 2017
Novel 25 kb Deletion of MERTK Causes Retinitis Pigmentosa With Severe ProgressionDaniel R Evans, Jane S Green, Gordon J Johnson, et al.Blood|July 15, 2020
Enhancer-gene rewiring in the pathogenesis of Quebec platelet disorderMinggao Liang, Asim Soomro, Subia Tasneem, et al.Pageof 44