Spectrum of mutations in monogenic diabetes genes identified from high-throughput DNA sequencing of 6888 individuals-Reference-Cited by-同舟云学术

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Spectrum of mutations in monogenic diabetes genes identified from high-throughput DNA sequencing of 6888 individuals

Published:2017-12 Issue:1 Volume:15 Page:
ISSN:1741-7015
Container-title:BMC Medicine
language:en
Short-container-title:BMC Med

Author:

Bansal Vikas,Gassenhuber Johann,Phillips Tierney,Oliveira Glenn,Harbaugh Rebecca,Villarasa Nikki,Topol Eric J.,Seufferlein Thomas,Boehm Bernhard O.

Publisher

Springer Science and Business Media LLC

Subject

General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s12916-017-0977-3.pdf

Reference83 articles.

1. McCarthy MI. Genetics of T2DM in 2016: Biological and translational insights from T2DM genetics. Nat Rev Endocrinol. 2017;13(2):71–2.

2. Bonnefond A, Froguel P. Rare and common genetic events in type 2 diabetes: what should biologists know? Cell Metab. 2015;21(3):357–68.

3. Scott LJ, Mohlke KL, Bonnycastle LL, et al. A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science. 2007;316:1341–5.

4. Voight BF, Scott LJ, Steinthorsdottir V, et al. Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat Genet. 2010;42:579–89.

5. Bonnefond A, Froguel P, Vaxillaire M. The emerging genetics of type 2 diabetes. Trends Mol Med. 2010;16:407–16.

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