{"database":"ENA","file_versions":[],"scores":null,"additional":{"omics_type":["Genomics"],"center_name":["REGENTS OF THE UNIVERSITY OF MICHIGAN - ANN ARBOR"],"full_dataset_link":["https://www.ebi.ac.uk/ena/browser/view/PRJNA275030"],"scientific_name":["Homo sapiens"],"long_description":["The Finland-United States Investigation of NIDDM Genetics (FUSION) study is a long-term effort to identify genetic variants that predispose to type 2 diabetes (T2D) or that impact the variability of T2D-related quantitative traits. The initial effort involved linkage analysis of affected-sibling-pair (ASP) families based on over 5,000 individuals living in Finland, and association fine mapping based on these family members and additional T2D cases and controls. We completed a genome-wide association scan on 1161 T2D cases and 1174 normal glucose tolerant (NGT) controls. Individual-level data is available for the 919 T2D cases and 787 NGT controls who reconsented to the use of their data or are deceased ( http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000100). In addition, we selected these 919 T2D cases and a matched set of 919 NGT controls (774 overlapping with GWAS) for targeted sequencing of 78 genes associated with glucose... (for more see dbGaP study page.)"],"repository":["ENA"],"description_synonyms":["study."],"name_synonyms":["Human, Modern., human being, Man (Taxonomy), Homo sapiens, man, Man, human, Modern Man"],"additional_accession":[]},"is_claimable":false,"name":"Homo sapiens","description":"FUSION Cohort Study","dates":{"last_updated":"2025-09-24","first_public":"2015-02-12"},"accession":"PRJNA275030","cross_references":{"taxon":["9606"]}}