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  • Rioux, John D. (author)

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

  • Article/chapterEnglish2001

Publisher, publication year, extent ...

  • Nature Publishing Group,2001
  • printrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:uu-487085
  • https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-487085URI
  • https://doi.org/10.1038/ng1001-223DOI

Supplementary language notes

  • Language:English
  • Summary in:English

Part of subdatabase

Classification

  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Linkage disequilibrium (LD) mapping provides a powerful method for fine-structure localization of rare disease genes, but has not yet been widely applied to common disease1. We sought to design a systematic approach for LD mapping and apply it to the localization of a gene (IBD5) conferring susceptibility to Crohn disease. The key issues are: (i) to detect a significant LD signal (ii) to rigorously bound the critical region and (iii) to identify the causal genetic variant within this region. We previously mapped the IBD5 locus to a large region spanning 18 cM of chromosome 5q31 (P<10−4). Using dense genetic maps of microsatellite markers and single-nucleotide polymorphisms (SNPs) across the entire region, we found strong evidence of LD. We bound the region to a common haplotype spanning 250 kb that shows strong association with the disease (P<2×10−7) and contains the cytokine gene cluster. This finding provides overwhelming evidence that a specific common haplotype of the cytokine region in 5q31 confers susceptibility to Crohn disease. However, genetic evidence alone is not sufficient to identify the causal mutation within this region, as strong LD across the region results in multiple SNPs having equivalent genetic evidence—each consistent with the expected properties of the IBD5 locus. These results have important implications for Crohn disease in particular and LD mapping in general.

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Daly, Mark J. (author)
  • Silverberg, Mark S. (author)
  • Lindblad, KerstinWhitehead Institute/Massachusetts Institute of Technology, Center for Genome Research, Cambridge, Massachusetts, USA(Swepub:uu)kerli865 (author)
  • Steinhart, Hillary (author)
  • Cohen, Zane (author)
  • Delmonte, Terrye (author)
  • Kocher, Kerry (author)
  • Miller, Katie (author)
  • Guschwan, Sheila (author)
  • Kulbokas, Edward J. (author)
  • O'Leary, Sinead (author)
  • Winchester, Ellen (author)
  • Dewar, Ken (author)
  • Green, Todd (author)
  • Stone, Valerie (author)
  • Chow, Christine (author)
  • Cohen, Albert (author)
  • Langelier, Diane (author)
  • Lapointe, Gilles (author)
  • Gaudet, Daniel (author)
  • Faith, Janet (author)
  • Branco, Nancy (author)
  • Bull, Shelley B. (author)
  • McLeod, Robin S. (author)
  • Griffiths, Anne M. (author)
  • Bitton, Alain (author)
  • Greenberg, Gordon R. (author)
  • Lander, Eric S. (author)
  • Siminovitch, Katherine A. (author)
  • Hudson, Thomas J. (author)
  • Whitehead Institute/Massachusetts Institute of Technology, Center for Genome Research, Cambridge, Massachusetts, USA (creator_code:org_t)

Related titles

  • In:Nature Genetics: Nature Publishing Group29:2, s. 223-2281061-40361546-1718

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