Porta, Massimo; Toppila, Iiro; Sandholm, Niina et al. (2016) Variation in SLC19A3 and Protection From Microvascular Damage in Type 1 Diabetes. Diabetes 65:1022-30
|
Eny, Karen M; Orchard, Trevor J; Miller, Rachel Grace et al. (2015) Caffeine Consumption Contributes to Skin Intrinsic Fluorescence in Type 1 Diabetes. Diabetes Technol Ther 17:726-34
|
DCCT/EDIC Research Group; Aiello, Lloyd Paul; Sun, Wanjie et al. (2015) Intensive diabetes therapy and ocular surgery in type 1 diabetes. N Engl J Med 372:1722-33
|
Poirier, Julia G; Faye, Laura L; Dimitromanolakis, Apostolos et al. (2015) Resampling to Address the Winner's Curse in Genetic Association Analysis of Time to Event. Genet Epidemiol 39:518-28
|
McGee, P; Steffes, M; Nowicki, M et al. (2014) Insulin secretion measured by stimulated C-peptide in long-established Type 1 diabetes in the Diabetes Control and Complications Trial (DCCT)/ Epidemiology of Diabetes Interventions and Complications (EDIC) cohort: a pilot study. Diabet Med 31:1264-8
|
Simpson, Claire L; Wojciechowski, Robert; Oexle, Konrad et al. (2014) Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. PLoS One 9:e107110
|
Eny, Karen M; Lutgers, Helen L; Maynard, John et al. (2014) GWAS identifies an NAT2 acetylator status tag single nucleotide polymorphism to be a major locus for skin fluorescence. Diabetologia 57:1623-34
|
Pop-Busui, Rodica; Cleary, Patricia A; Braffett, Barbara H et al. (2013) Association between cardiovascular autonomic neuropathy and left ventricular dysfunction: DCCT/EDIC study (Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications). J Am Coll Cardiol 61:447-454
|
Verhoeven, Virginie J M; Hysi, Pirro G; Wojciechowski, Robert et al. (2013) Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nat Genet 45:314-8
|
Stambolian, Dwight; Wojciechowski, Robert; Oexle, Konrad et al. (2013) Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error. Hum Mol Genet 22:2754-64
|
Showing the most recent 10 out of 60 publications