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{"family": "Saleheen", "given": "Danish", "initials": "D"}, {"family": "Hansen", "given": "Torben", "initials": "T"}, {"family": "Pedersen", "given": "Oluf", "initials": "O"}, {"family": "M\u00e4gi", "given": "Reedik", "initials": "R"}, {"family": "Langenberg", "given": "Claudia", "initials": "C"}, {"family": "Wareham", "given": "Nicholas J", "initials": "NJ"}, {"family": "Maeda", "given": "Shiro", "initials": "S"}, {"family": "Kadowaki", "given": "Takashi", "initials": "T"}, {"family": "Lee", "given": "Juyoung", "initials": "J"}, {"family": "Millwood", "given": "Iona Y", "initials": "IY"}, {"family": "Walters", "given": "Robin G", "initials": "RG"}, {"family": "Stefansson", "given": "Kari", "initials": "K"}, {"family": "Myers", "given": "Simon R", "initials": "SR"}, {"family": "Ferrer", "given": "Jorge", "initials": "J"}, {"family": "Gaulton", "given": "Kyle J", "initials": "KJ"}, {"family": "Meigs", "given": "James B", "initials": "JB"}, {"family": "Mohlke", "given": "Karen L", "initials": "KL"}, {"family": "Gloyn", "given": "Anna L", "initials": "AL"}, {"family": "Bowden", "given": "Donald W", "initials": "DW"}, {"family": "Below", "given": "Jennifer E", "initials": "JE"}, {"family": "Chambers", "given": "John C", "initials": "JC"}, {"family": "Sim", "given": "Xueling", "initials": "X"}, {"family": "Boehnke", "given": "Michael", "initials": "M"}, {"family": "Rotter", "given": "Jerome I", "initials": "JI"}, {"family": "McCarthy", "given": "Mark I", "initials": "MI"}, {"family": "Morris", "given": "Andrew P", "initials": "AP", "orcid": "0000-0002-6805-6014", "researcher": {"href": "https://publications-affiliated.scilifelab.se/researcher/aaff6a0afcdf464a8de49c2ece7399e2.json"}}], "type": "journal article", "published": "2022-05-00", "journal": {"title": "Nat. Genet.", "issn": "1546-1718", "volume": "54", "issue": "5", "pages": "560-572", "issn-l": "1061-4036"}, "abstract": "We assembled an ancestrally diverse collection of genome-wide association studies (GWAS) of type 2 diabetes (T2D) in 180,834 affected individuals and 1,159,055 controls (48.9% non-European descent) through the Diabetes Meta-Analysis of Trans-Ethnic association studies (DIAMANTE) Consortium. Multi-ancestry GWAS meta-analysis identified 237 loci attaining stringent genome-wide significance (P < 5 \u00d7 10-9), which were delineated to 338 distinct association signals. Fine-mapping of these signals was enhanced by the increased sample size and expanded population diversity of the multi-ancestry meta-analysis, which localized 54.4% of T2D associations to a single variant with >50% posterior probability. This improved fine-mapping enabled systematic assessment of candidate causal genes and molecular mechanisms through which T2D associations are mediated, laying the foundations for functional investigations. Multi-ancestry genetic risk scores enhanced transferability of T2D prediction across diverse populations. Our study provides a step toward more effective clinical translation of T2D GWAS to improve global health for all, irrespective of genetic background.", "doi": "10.1038/s41588-022-01058-3", "pmid": "35551307", "labels": [], "xrefs": [{"db": "mid", "key": "NIHMS1792335"}, {"db": "pmc", "key": "PMC9179018"}, {"db": "pii", "key": "10.1038/s41588-022-01058-3"}], "notes": [], "created": "2026-08-21T11:51:43.657Z", "modified": "2026-08-21T11:51:44.129Z"}]}