Publication Detail
The publication detail shows the title, authors (with indicators showing other profiled authors), information on the publishing organization, abstract and a link to the article in PubMed. This abstract is what is used to create the fingerprint of the publication. If any grants are referenced by the publication, they will be listed here as well.
Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations.
Evadnie Rampersaud; Coleen M Damcott; Mao Fu; Haiqing Shen; Patrick McArdle; Xiaolian Shi; John Shelton; Jing Yin; Yen-Pei C Chang; Sandra H Ott; et al. (Profiled Authors: Coleen M Damcott; Mao Fu; Patrick McArdle; Braxton D Mitchell Jr.; Jeffrey R O'Connell; Alan R Shuldiner; Yen-Pei Chang)
Division of Endocrinology, Diabetes and Nutrition, University of Maryland School of Medicine, 660 West Redwood St., Room 494, Baltimore, MD 21201, USA.
Diabetes 2007;56(12):3053-62.
OBJECTIVE: We sought to identify type 2 diabetes susceptibility genes through a genome-wide association scan (GWAS) in the Amish. RESEARCH DESIGN AND METHODS: DNA from 124 type 2 diabetic case subjects and 295 control subjects with normal glucose tolerance were genotyped on the Affymetrix 100K single nucleotide polymorphism (SNP) array. A total of 82,485 SNPs were tested for association with type 2 diabetes. Type 2 diabetes-associated SNPs were further prioritized by the following: 1) associations with 5 oral glucose tolerance test (OGTT) traits in 427 nondiabetic Amish subjects, and 2) in silico replication from three independent 100L SNP GWASs (Framingham Heart Study Caucasians, Pima Indians, and Mexican Americans) and a 500K GWAS in Scandinavians. RESULTS: The strongest association (P = 1.07 x 10(-5)) was for rs2237457, which is located in growth factor receptor-bound protein 10 (Grb10), an adaptor protein that regulate insulin receptor signaling. rs2237457 was also strongly associated with OGTT glucose area under the curve in nondiabetic subjects (P = 0.001). Of the 1,093 SNPs associated with type 2 diabetes at P < 0.01, 67 SNPs demonstrated associations with at least one OGTT trait in nondiabetic individuals; 80 SNPs were nominally associated with type 2 diabetes in one of the three independent 100K GWASs, 3 SNPs (rs2540317 in MFSD9, rs10515353 on chromosome 5, and rs2242400 in BCAT1 were associated with type 2 diabetes in more than one population), and 11 SNPs were nominally associated with type 2 diabetes in Scandinavians. One type 2 diabetes-associated SNP (rs3845971, located in FHIT) showed replication with OGTT traits and also in another population. CONCLUSIONS: Our GWAS of type 2 diabetes identified several gene variants associated with type 2 diabetes, some of which are worthy of further study.
5 Originating Grant
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1.
SHULDINER, ALAN R.
Mid-Atlantic Nutrition Obesity Research Center
15 September 2005 - 31 August 2015
NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
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2.
STANLEY, WILLIAM C
Training Grant in Cardiac and Vascular Cell Biology
1 April 2003 - 31 July 2014
NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
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3.
Pallone, Thomas L
Training Grant in Cardiac and Vascular Cell Biology
1 April 2003 - 31 March 2008
NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
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4.
Reece, E Albert
General Clinical Research Center
1 March 2002 - 30 June 2010
NATIONAL CENTER FOR RESEARCH RESOURCES
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5.
Shuldiner, Alan R
Genetics of Diabetes in the Amish
1 July 2000 - 31 March 2009
NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
Scientific Context
This section shows information related to the publication - computed using the fingerprint of the publication - including related publications, related experts and related grants with fingerprints representing significant amounts of overlap between their fingerprint and this publication. The red dots indicate whether those experts or terms appear within the publication, thereby showing potential and actual connections.
Related Publications
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1.
2003Wen-Chi Hsueh; Pamela L St Jean; Braxton D Mitchell; Toni I Pollin; William C Knowler; Margaret G Ehm; Callum J Bell; Hakan Sakul; Michael J Wagner; Daniel K Burns; et al.
Diabetes 2003;52(2):550-7. -
2.
2010Cristopher V Van Hout; Albert M Levin; Evadnie Rampersaud; Haiqing Shen; Jeffrey R O'Connell; Braxton D Mitchell; Alan R Shuldiner; Julie A Douglas
Extent and distribution of linkage disequilibrium in the Old Order Amish.
Genetic epidemiology 2010;34(2):146-50. -
3.
2007Wendy Post; Haiqing Shen; Coleen Damcott; Dan E Arking; W H Linda Kao; Paul A Sack; Kathleen A Ryan; Aravinda Chakravarti; Braxton D Mitchell; Alan R Shuldiner
Human heredity 2007;64(4):214-9.
Related Topics
Appears in this Publication
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Genome Wide Association Stud...
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Single Nucleotide Polymorphi...
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European Continental Ancestr...
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Genetic Predisposition to Di...
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Related Experts
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