SwePub
Sök i LIBRIS databas

  Extended search

WFRF:(Martinsson Arne)
 

Search: WFRF:(Martinsson Arne) > Genome-wide linkage...

  • Bergman, AnnikaGothenburg 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,Department of Clinical Genetics, Sahlgrenska Academy, Göteborg University, Göteborg, Sweden (author)

Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families : Suggestive linkage to 10q23.32-q25.3

  • Article/chapterEnglish2007

Publisher, publication year, extent ...

  • 2006
  • John Wiley & Sons,2007
  • printrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:hj-39623
  • https://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-39623URI
  • https://doi.org/10.1002/gcc.20405DOI
  • https://gup.ub.gu.se/publication/52223URI
  • https://research.chalmers.se/publication/52223URI

Supplementary language notes

  • Language:English
  • Summary in:English

Part of subdatabase

Classification

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

Notes

  • The two breast cancer genes BRCA1 and BRCA2 were identified more than 10 years ago and, depending on population, mutations in these genes are responsible for a varying percentage of familial breast cancer. In more than half the families, the increased risk of breast cancer cannot be explained by mutations in these genes, and the goal of this study was to locate novel susceptibility genes. One of the main difficulties in identifying the cause of hereditary non-BRCA1/BRCA2 breast cancer is genetic heterogeneity, possibly due to multiple, incompletely penetrant susceptibility genes, along with ethnic and geographic differences. In this study, one large family and 13 small to medium-sized families with multiple cases of breast cancer were analyzed by genome-wide linkage analysis. The genome scan was performed by genotype analysis of 10,000 SNP markers on microarrays. The strongest evidence of linkage (HLOD 2.34) was obtained on chromosome region 10q23.32-q25.3. A further two regions were identified, with LOD scores above 2.10 on 12q14-q21 and 19p13.3-q12. In a subset of families of western Swedish origin, two regions generated LOD scores exceeding 1.8: 10q23.32-q25.3 and 19q13.12-q13.32. The large family in the study exceeded LOD 1.5 in three regions: 10q23.32-q25.3, 19q13.12-q13.32, and 17p13. Our results indicate that one or more of the suggested regions may harbor genes that are involved in the development of breast cancer. 

Subject headings and genre

  • MEDICIN OCH HÄLSOVETENSKAP Klinisk medicin Cancer och onkologi hsv//swe
  • MEDICAL AND HEALTH SCIENCES Clinical Medicine Cancer and Oncology hsv//eng
  • BRCA1 protein
  • BRCA2 protein
  • article
  • breast cancer
  • cancer genetics
  • cancer research
  • cancer susceptibility
  • chromosome 10q
  • chromosome 12q
  • chromosome 17p
  • chromosome 19p
  • chromosome 19q
  • clinical article
  • ethnicity
  • female
  • gene identification
  • gene mutation
  • genetic heterogeneity
  • genetic linkage
  • genetic susceptibility
  • genome analysis
  • genotype
  • geographic distribution
  • heredity
  • human
  • marker gene
  • microarray analysis
  • oncogene
  • population genetics
  • priority journal
  • single nucleotide polymorphism
  • Sweden
  • tumor suppressor gene
  • Breast Neoplasms
  • Chromosomes
  • Human
  • Pair 10
  • European Continental Ancestry Group
  • Genes
  • BRCA1
  • Genes
  • BRCA2
  • Genome
  • Human
  • Humans
  • Linkage (Genetics)
  • Polymorphism
  • Single Nucleotide
  • Breast Neoplasms
  • genetics
  • Chromosomes
  • Human
  • Pair 10
  • European Continental Ancestry Group
  • Female
  • Genes
  • BRCA1
  • BRCA2
  • Genome
  • Humans
  • Linkage (Genetics)
  • Polymorphism
  • Single Nucleotide

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

  • Karlsson, Per,1963Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences,University of Gothenburg,Department of Oncology, Sahlgrenska Academy, Göteborg University, Göteborg, Sweden(Swepub:gu)xkperd (author)
  • Berggren, Jonna,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,Department of Clinical Genetics, Sahlgrenska Academy, Göteborg University, Göteborg, Sweden(Swepub:gu)xbejon (author)
  • Martinsson, Tommy,1956Gothenburg 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,Department of Clinical Genetics, Sahlgrenska Academy, Göteborg University, Göteborg, Sweden(Swepub:gu)xmarto (author)
  • Björck, KarinSwegene Bioinformatics, Sahlgrenska Academy, Göteborg University, Göteborg, Sweden(Swepub:gu)xbjork (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,Swegene Bioinformatics, Sahlgrenska Academy, Göteborg University, Göteborg, Sweden(Swepub:cth)staffan (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,Department of Clinical Genetics, Sahlgrenska Academy, Göteborg University, Göteborg, Sweden(Swepub:gu)xwahja (author)
  • Wallgren, Arne,1940Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences,University of Gothenburg,Department of Oncology, Sahlgrenska Academy, Göteborg University, Göteborg, Sweden(Swepub:gu)xwalar (author)
  • Nordling, Margareta,1962Gothenburg 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,Department of Clinical Genetics, Sahlgrenska Academy, Göteborg University, Göteborg, Sweden(Swepub:gu)xnmarx (author)
  • Göteborgs universitetInstitutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik (creator_code:org_t)

Related titles

  • In:Genes, Chromosomes and Cancer: John Wiley & Sons46:3, s. 302-3091045-22571098-2264

Internet link

Find in a library

To the university's database

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view