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  • amundsen, siljaUniversitetet i Oslo,University of Oslo (author)

A comprehensive screen for SNP associations on chromosome region 5q31-33 in Swedish/Norwegian celiac disease families.

  • Article/chapterEnglish2007

Publisher, publication year, extent ...

  • 2007-06-06
  • Springer Science and Business Media LLC,2007

Numbers

  • LIBRIS-ID:oai:gup.ub.gu.se/42674
  • https://gup.ub.gu.se/publication/42674URI
  • https://doi.org/10.1038/sj.ejhg.5201870DOI
  • https://research.chalmers.se/publication/42674URI
  • https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-11888URI

Supplementary language notes

  • Language:English

Part of subdatabase

Classification

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

Notes

  • Celiac disease (CD) is a gluten-induced enteropathy, which results from the interplay between environmental and genetic factors. There is a strong human leukocyte antigen (HLA) association with the disease, and HLA-DQ alleles represent a major genetic risk factor. In addition to HLA-DQ, non-HLA genes appear to be crucial for CD development. Chromosomal region 5q31–33 has demonstrated linkage with CD in several genome-wide studies, including in our Swedish/Norwegian cohort. In a European meta-analysis 5q31–33 was the only region that reached a genome-wide level of significance except for the HLA region. To identify the genetic variant(s) responsible for this linkage signal, we performed a comprehensive single nucleotide polymorphism (SNP) association screen in 97 Swedish/Norwegian multiplex families who demonstrate linkage to the region. We selected tag SNPs from a 16 Mb region representing the 95% confidence interval of the linkage peak. A total of 1404 SNPs were used for the association analysis. We identified several regions with SNPs demonstrating moderate single- or multipoint associations. However, the isolated association signals appeared insufficient to account for the linkage signal seen in our cohort. Collective effects of multiple risk genes within the region, incomplete genetic coverage or effects related to copy number variation are possible explanations for our findings.

Subject headings and genre

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

  • Adamovic, Svetlana,1965Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik,Institute of Biomedicine, Department of Medical and Clinical Genetics,University of Gothenburg(Swepub:gu)xadasv (author)
  • Hellqvist, ÅsaGothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik,Institute of Biomedicine, Department of Medical and Clinical Genetics,University of Gothenburg(Swepub:gu)xhelas (author)
  • Nilsson, Staffan,1956Gothenburg University,Göteborgs universitet,Institutionen för matematiska vetenskaper, matematisk statistik,Department of Mathematical Sciences, Mathematical Statistics,Chalmers tekniska högskola,Chalmers University of Technology,University of Gothenburg(Swepub:cth)staffan (author)
  • Gudjonsdottir, Audur,1959Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences,University of Gothenburg(Swepub:gu)xgudau (author)
  • Ascher, Henry,1953Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences,University of Gothenburg(Swepub:gu)xasche (author)
  • Ek, Johan (author)
  • Larsson, KristinaUppsala universitet,Institutionen för medicinska vetenskaper (author)
  • Wahlström, Jan,1939Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik,Institute of Biomedicine, Department of Medical and Clinical Genetics,University of Gothenburg(Swepub:gu)xwahja (author)
  • Lie, Benedicte (author)
  • Sollid, Ludvig MUniversitetet i Oslo,University of Oslo (author)
  • Torinsson Naluai, Åsa,1968Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik,Institute of Biomedicine, Department of Medical and Clinical Genetics,University of Gothenburg(Swepub:gu)xnalas (author)
  • Universitetet i OsloInstitutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik (creator_code:org_t)

Related titles

  • In:European Journal of Human genetics: Springer Science and Business Media LLC15:9, s. 980-9871018-48131476-5438

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