Overview of the Type I Diabetes Genetics Consortium

被引:0
作者
S S Rich
B Akolkar
P Concannon
H Erlich
J E Hilner
C Julier
G Morahan
J Nerup
C Nierras
F Pociot
J A Todd
机构
[1] Center for Public Health Genomics,Department of Public Health Sciences
[2] University of Virginia,Division of Diabetes
[3] University of Virginia,Department of Biochemistry and Molecular Genetics
[4] Endocrinology,Department of Biostatistics
[5] and Metabolic Diseases,Department of Medical Genetics
[6] The National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK),undefined
[7] National Institutes of Health,undefined
[8] University of Virginia,undefined
[9] Roche Molecular Systems,undefined
[10] School of Public Health,undefined
[11] University of Alabama at Birmingham,undefined
[12] Inserm U730,undefined
[13] Centre National de Génotypage,undefined
[14] Centre for Diabetes Research,undefined
[15] The Western Australian Institute for Medical Research,undefined
[16] and Centre for Medical Research,undefined
[17] University of Western Australia,undefined
[18] Steno Diabetes Center,undefined
[19] Juvenile Diabetes Research Foundation International,undefined
[20] Cambridge Institute for Medical Research,undefined
[21] Juvenile Diabetes Research Foundation/Wellcome Trust Diabetes and Inflammation Laboratory,undefined
[22] University of Cambridge,undefined
[23] Addenbrooke's Hospital,undefined
来源
Genes & Immunity | 2009年 / 10卷
关键词
type I diabetes; autoantibodies; HLA; families; linkage; association;
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摘要
The Type I Diabetes Genetics Consortium (T1DGC) is an international, multicenter research program with two primary goals. The first goal is to identify genomic regions and candidate genes whose variants modify an individual's risk of type I diabetes (T1D) and help explain the clustering of the disease in families. The second goal is to make research data available to the research community and to establish resources that can be used by, and that are fully accessible to, the research community. To facilitate the access to these resources, the T1DGC has developed a Consortium Agreement (http://www.t1dgc.org) that specifies the rights and responsibilities of investigators who participate in Consortium activities. The T1DGC has assembled a resource of affected sib-pair families, parent–child trios, and case–control collections with banks of DNA, serum, plasma, and EBV-transformed cell lines. In addition, both candidate gene and genome-wide (linkage and association) studies have been performed and displayed in T1DBase (http://www.t1dbase.org) for all researchers to use in their own investigations. In this supplement, a subset of the T1DGC collection has been used to investigate earlier published candidate genes for T1D, to confirm the results from a genome-wide association scan for T1D, and to determine associations with candidate genes for other autoimmune diseases or with type II diabetes that may be involved with β-cell function.
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页码:S1 / S4
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