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(WFRF:(Ahlbom Anders)) srt2:(2005-2009) pers:(Swerdlow Anthony)
 

Search: (WFRF:(Ahlbom Anders)) srt2:(2005-2009) pers:(Swerdlow Anthony) > Comprehensive analy...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004406naa a2200709 4500
001oai:DiVA.org:umu-9063
003SwePub
008080228s2008 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:116733740
024a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-90632 URI
024a https://doi.org/10.1093/jnci/djn0042 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1167337402 URI
040 a (SwePub)umud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Bethke, Lara4 aut
2451 0a Comprehensive analysis of DNA repair gene variants and risk of meningioma
264 c 2008-02-20
264 1b Oxford University Press,c 2008
338 a print2 rdacarrier
520 a Background: Meningiomas account for up to 37% of all primary brain tumors. Genetic susceptibility to meningioma is well established, with the risk among relatives of meningioma patients being approximately threefold higher than that in the general population. A relationship between risk of meningioma and exposure to ionizing radiation is also well known and led us to examine whether variants in DNA repair genes contribute to disease susceptibility.Methods: We analyzed 1127 tagging single-nucleotide polymorphisms (SNPs) that were selected to capture most of the common variation in 136 DNA repair genes in five case–control series (631 case patients and 637 control subjects) from four countries in Europe. We also analyzed 388 putative functional SNPs in these genes for their association with meningioma. All statistical tests were two-sided.Results: The SNP rs4968451, which maps to intron 4 of the gene that encodes breast cancer susceptibility gene 1–interacting protein 1, was consistently associated with an increased risk of developing meningioma. Across the five studies, the association was highly statistically significant (trend odds ratio = 1.57, 95% confidence interval = 1.28 to 1.93; Ptrend = 8.95 × 10−6; P = .009 after adjusting for multiple testing).Conclusions: We have identified a novel association between rs4968451 and meningioma risk. Because approximately 28% of the European population are carriers of at-risk genotypes for rs4968451, the variant is likely to make a substantial contribution to the development of meningioma.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Cancer och onkologi0 (SwePub)302032 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Cancer and Oncology0 (SwePub)302032 hsv//eng
653 a genes
653 a genetic predisposition to disease
653 a genotype
653 a introns
653 a meningioma
653 a single nucleotide polymorphism radiation
653 a ionizing
653 a breast cancer
653 a primary brain tumors
653 a dna repair gene
700a Murray, Anne4 aut
700a Webb, Emily4 aut
700a Schoemaker, Minouk4 aut
700a Muir, Kenneth4 aut
700a McKinney, Patricia4 aut
700a Hepworth, Sarah4 aut
700a Dimitropoulou, Polyxeni4 aut
700a Lophatananon, Artitaya4 aut
700a Feychting, Mariau Karolinska Institutet4 aut
700a Lönn, Stefanu Karolinska Institutet4 aut
700a Ahlbom, Andersu Karolinska Institutet4 aut
700a Malmer, Beatriceu Umeå universitet,Onkologi4 aut0 (Swepub:umu)bema0010
700a Henriksson, Rogeru Umeå universitet,Onkologi4 aut0 (Swepub:umu)rohe0003
700a Auvinen, Anssi4 aut
700a Kiuru, Anne4 aut
700a Salminen, Tiina4 aut
700a Johansen, Christoffer4 aut
700a Collatz Christensen, Helle4 aut
700a Kosteljanetz, Michael4 aut
700a Swerdlow, Anthony4 aut
700a Houlston, Richard4 aut
710a Karolinska Institutetb Onkologi4 org
773t Journal of the National Cancer Instituted : Oxford University Pressg 100:4, s. 270-276q 100:4<270-276x 0027-8874x 1460-2105
856u https://academic.oup.com/jnci/article-pdf/100/4/270/17309949/djn004.pdf
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-9063
8564 8u https://doi.org/10.1093/jnci/djn004
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:116733740

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