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Diabetologia|June 26, 2024
Associations between diabetes-related genetic risk scores and residual beta cell function in type 1 diabetes: the GUTDM1 studyCoco M Fuhri Snethlage, Manon Balvers, Bart Ferwerda, et al.
Medrxiv : the Preprint Server for Health Sciences|December 25, 2025
Genetic risk in extremely early onset type 1 diabetesAmber M Luckett, Georgia Bonfield, Gareth Hawkes, et al.
American Journal of Human Genetics|March 21, 2026
Bi-allelic variants in the non-protein-coding minor spliceosome components RNU6ATAC and RNU4ATAC cause syndromic monogenic autoimmune diabetesMatthew B Johnson, James Russ-Silsby, Paul A Blair, et al.
Diabetes, Obesity & Metabolism|July 14, 2025
Persisting plasma proinsulin levels in a cohort of 482 individuals with long-standing type 1 diabetes mellitusDouwe Frank de Wit, Coco Marjolein Fuhri Snethlage, Rana Minab, et al.
Journal of Medical Genetics|November 29, 2013
The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotypeAlexander J Hamilton, Coralie Bingham, Timothy J McDonald, et al.
Alimentary Pharmacology & Therapeutics|August 14, 2020
A single nucleotide polymorphism genetic risk score to aid diagnosis of coeliac disease: a pilot study in clinical careSeth A Sharp, Samuel E Jones, Robert A Kimmitt, et al.
Diabetes Care|July 22, 2025
Contrasting Adult and Pediatric Populations in a Cohort of At-Risk Relatives in The T1D TrialNet Pathway to Prevention StudyErin L Templeman, Lauric A Ferrat, Nicholas Thomas, et al.
Research Square|February 20, 2025
A type 1 diabetes prediction model has utility across multiple screening settings with recalibrationErin L Templeman, Lauric A Ferrat, Hemang M Parikh, et al.
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