<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>REGENTS OF THE UNIVERSITY OF MICHIGAN - ANN ARBOR</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA275030</full_dataset_link><scientific_name>Homo sapiens</scientific_name><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.)</long_description><repository>ENA</repository><description_synonyms>study.</description_synonyms><name_synonyms>Human, Modern., human being, Man (Taxonomy), Homo sapiens, man, Man, human, Modern Man</name_synonyms></additional><is_claimable>false</is_claimable><name>Homo sapiens</name><description>FUSION Cohort Study</description><dates><last_updated>2025-09-24</last_updated><first_public>2015-02-12</first_public></dates><accession>PRJNA275030</accession><cross_references><taxon>9606</taxon></cross_references></HashMap>