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An ancestry-enriched HNF4A variant and GP2 reveal distinct mechanisms of type 2 diabetes in exome-wide study of 13,674 cases and 41,024 controls.

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Title: An ancestry-enriched HNF4A variant and GP2 reveal distinct mechanisms of type 2 diabetes in exome-wide study of 13,674 cases and 41,024 controls.
Authors: Hodgson S, Bui V, Hu S, Maroteau C, Bigossi M, Huerta-Chagoya A, Nguyen T, Dawed AY, Koesterer R, Vora M, Stow D, Williamson A, Blee AM, Carrasco-Zanini Sanchez J, Baskar V, Jebarani S, Jacobs BM, Kalantzis G, Rison S, Walter K, Pennarun E, Taylor K, Hsu S, Manning A, Udler M, Martin HC, Barroso I, Flannick J, Fumagalli M, Radha V, Pradeepa R, Langenberg C, Mohan V, Anjana RM, van Heel DA, Mercader JM, Jamshidi Y, Finer S, Majithia AR, Siddiqui MK
Corporate Authors: Genes & Health Research Team, MDRF Research Team
Source: MedRxiv : the preprint server for health sciences [medRxiv] 2026 May 19. Date of Electronic Publication: 2026 May 19.
Publication Type: Journal Article; Preprint
Journal Info: Country of Publication: United States NLM ID: 101767986 Publication Model: Electronic Cited Medium: Internet NLM ISO Abbreviation: medRxiv Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
FullText Text:
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An: 42238389
AccessLevel: 2
PubType: Academic Journal
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  Data: <i>Country of Publication: </i>United States <i>NLM ID: </i>101767986 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>NLM ISO Abbreviation: </i>medRxiv <i>Subsets: </i>PubMed not MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=42238389
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        Value: 10.1101/2025.09.24.25336527
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