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Gene|September 20, 2022
Role of 19 SNPs in 10 genes with type 2 diabetes in the Pakistani populationNetasha Khan, Andrew D Paterson, Delnaz Roshandel, et al.The Journal of Clinical Endocrinology and Metabolism|September 16, 2020
Genome-Wide Association for HbA1c in Malay Identified Deletion on SLC4A1 that Influences HbA1c Independent of GlycemiaJin-Fang Chai, Shih-Ling Kao, Chaolong Wang, et al.Arthritis Research & Therapy|September 12, 2008
Reduced proportions of natural killer T cells are present in the relatives of lupus patients and are associated with autoimmunityJoan Wither, Yong-chun Cai, Sooyeol Lim, et al.Journal of Medical Genetics|October 26, 2010
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disabilityAlistair T Pagnamenta, Hameed Khan, Susan Walker, et al.BMJ Open Diabetes Research & Care|January 16, 2026
Association of genetic variation with age at diagnosis in type 1 diabetesCharlotte E Vollenbrock, Delnaz Roshandel, Kristine E Lee, et al.American Journal of Medical Genetics|December 20, 2000
Long repeat tracts at SCA8 in major psychosisJ B Vincent, Q P Yuan, M Schalling, et al.Diabetologia|February 7, 2018
Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetesDelnaz Roshandel, Rose Gubitosi-Klug, Shelley B Bull, et al.BMC Medical Genetics|October 16, 2020
Associations of NOD2 polymorphisms with Erysipelotrichaceae in stool of in healthy first degree relatives of Crohn's disease subjectsWilliams Turpin, Larbi Bedrani, Osvaldo Espin-Garcia, et al.Diabetes|September 12, 2019
Evaluation of the Genetic Association Between Adult Obesity and Neuropsychiatric DiseasePriska Stahel, Avital Nahmias, Shawn K Sud, et al.Diabetes|January 25, 2019
Genetic Determinants of Glycated Hemoglobin in Type 1 DiabetesAnna Syreeni, Niina Sandholm, Jingjing Cao, et al.Pageof 44