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URL: http://fusion.sph.umich.edu/
Proper Citation: FUSION study (RRID:SCR_016580)
Description: Portal to map and identify genetic variants that predispose to type 2 diabetes mellitus (T2D) or are responsible for variability in diabetes-related quantitative traits. Used for analysis of affected-sibling-pair (ASP) families in Finland, and association fine mapping based on these family members and additional T2D cases and controls.
Abbreviations: FUSION
Synonyms: Finland United States Investigation of NIDDM genetics
Resource Type: data or information resource, disease-related portal, portal, topical portal
Keywords: map, identify, genetic, variant, predispose, type II diabetes, mellitus, T2D
Related Condition: type 2 diabetes
Availability: Registration required
Resource Name: FUSION study
Resource ID: SCR_016580
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Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400
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