Multiple type 2 diabetes susceptibility genes following genome-wide association scan in UK samples

By Eleftheria Zeggini, M. Weedon, C. Lindgren, T. Frayling, K. Elliott, H. Lango, Nicholas J. Timpson, J. Perry, N. W. Rayner, R. Freathy and 16 more. Science, 2007

2,209 citations recorded by the source corpus.

The molecular mechanisms involved in the development of type 2 diabetes are poorly understood. Starting from genome-wide genotype data for 1924 diabetic cases and 2938 population controls generated by the Wellcome Trust Case Control Consortium, we set out to detect replicated diabetes association signals through analysis of 3757 additional cases and 5346 controls and by integration of our findings with equivalent data from other international consortia. We detected diabetes susceptibility loci in and around the genes CDKAL1, CDKN2A/CDKN2B, and IGF2BP2 and confirmed the recently described associations at HHEX/IDE and SLC30A8. Our findings provide insight into the genetic architecture of type 2 diabetes, emphasizing the contribution of multiple variants of modest effect. The regions identified underscore the importance of pathways influencing pancreatic beta cell development and function in the etiology of type 2 diabetes.

Subfields: Genetics, Molecular Biology, Surgery

View Paper: https://www.semanticscholar.org/paper/3acd41eeafe82b68094fdf0a487d8781b01fb790

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In Genetics

  1. Naomi R. Wray
  2. Peter M. Visscher
  3. John P. A. Ioannidis
  4. Bogdan Pasaniuc
  5. Michael E. Goddard
  6. Gonçalo R. Abecasis
  7. Alkes L Price
  8. Mark J. Daly

In Molecular Biology

  1. Manuel Serrano
  2. M. Blasco
  3. M. Collado
  4. Cristen J. Willer
  5. Yurii S. Aulchenko
  6. Peter M. Visscher
  7. Gonçalo R. Abecasis
  8. Y. Ding

In Surgery

  1. Manuel Serrano
  2. Peter Kraft
  3. Mark J. Daly
  4. Nick Wareham
  5. John P. A. Ioannidis
  6. David Altshuler
  7. Eleftheria Zeggini
  8. James B. Meigs

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