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Nature Metabolism|January 27, 2026
Unravelling the molecular mechanisms causal to type 2 diabetes across global populations and disease-relevant tissuesOzvan Bocher, Ana Luiza Arruda, Satoshi Yoshiji, et al.JAMA Ophthalmology|December 20, 2019
Association of Genetic Variation With KeratoconusBennet J McComish, Srujana Sahebjada, Yelena Bykhovskaya, et al.Science (New York, N.Y.)|October 28, 2006
A genome-wide association study identifies IL23R as an inflammatory bowel disease geneRichard H Duerr, Kent D Taylor, Steven R Brant, et al.Nature|September 3, 2013
A statin-dependent QTL for GATM expression is associated with statin-induced myopathyLara M Mangravite, Barbara E Engelhardt, Marisa W Medina, et al.Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
Unravelling the molecular mechanisms causal to type 2 diabetes across global populations and disease-relevant tissuesOzvan Bocher, Ana Luiza Arruda, Satoshi Yoshiji, et al.Genes and Immunity|February 5, 2008
An SNP linkage scan identifies significant Crohn's disease loci on chromosomes 13q13.3 and, in Jewish families, on 1p35.2 and 3q29Y Y Shugart, M S Silverberg, R H Duerr, et al.European Journal of Human Genetics : EJHG|February 11, 2016
Association of the IGF1 gene with fasting insulin levelsSara M Willems, Belinda K Cornes, Jennifer A Brody, et al.Human Genetics|December 3, 2014
Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levelsJacklyn N Hellwege, Nicholette D Palmer, W Mark Brown, et al.Scientific Reports|January 28, 2022
Upregulated heme biosynthesis increases obstructive sleep apnea severity: a pathway-based Mendelian randomization studyHeming Wang, Nuzulul Kurniansyah, Brian E Cade, et al.Human Molecular Genetics|August 1, 1997
Insulin-dependent diabetes mellitus (IDDM) is associated with CTLA4 polymorphisms in multiple ethnic groupsM P Marron, L J Raffel, H J Garchon, et al.Pageof 126