Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/147117
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dc.contributor.authorTomlinson, Ian P.-
dc.contributor.authorDunlop, Malcolm-
dc.contributor.authorCampbell, Harry-
dc.contributor.authorZanke, Brent W.-
dc.contributor.authorGallinger, Steven-
dc.contributor.authorHudson, Thomas J.-
dc.contributor.authorKoessler, Thibaud-
dc.contributor.authorPharoah, Paul D. P.-
dc.contributor.authorNiittymäki, Iina-
dc.contributor.authorTuupanen, Sari-
dc.contributor.authorAaltonen, Lauri A.-
dc.contributor.authorHemminki, Kari-
dc.contributor.authorLindblom, Annika-
dc.contributor.authorFörsti, Asta-
dc.contributor.authorSieber, Oliver-
dc.contributor.authorLipton, Lara-
dc.contributor.authorVan Wezel, Tom-
dc.contributor.authorMorreau, Hans-
dc.contributor.authorWijnen, Juul-
dc.contributor.authorDevilee, Peter-
dc.contributor.authorMatsuda, Kenji-
dc.contributor.authorNakamura, Yusuke-
dc.contributor.authorCastellví Bel, Sergi-
dc.contributor.authorRuiz-Ponte, Clara-
dc.contributor.authorCastells Garangou, Antoni-
dc.contributor.authorCarracedo Álvarez, Ángel-
dc.contributor.authorHo, J.W.-
dc.contributor.authorSham, Pak Chung-
dc.contributor.authorHofstra, Robert-
dc.contributor.authorVodicka, Pavel-
dc.contributor.authorBrenner, Hermann-
dc.contributor.authorHampe, Jochen-
dc.contributor.authorSchafmayer, Clemens-
dc.contributor.authorTepel, Juergen-
dc.contributor.authorSchreiber, Stefan-
dc.contributor.authorVölzke, Henry-
dc.contributor.authorLerch, Markus M.-
dc.contributor.authorSchmidt, Christian A.-
dc.contributor.authorBuch, Stephan-
dc.contributor.authorMoreno Aguado, Víctor-
dc.date.accessioned2020-01-07T16:03:55Z-
dc.date.available2020-01-07T16:03:55Z-
dc.date.issued2010-07-15-
dc.identifier.issn0007-0920-
dc.identifier.urihttp://hdl.handle.net/2445/147117-
dc.description.abstractIt is now recognised that a part of the inherited risk of colorectal cancer (CRC) can be explained by the co-inheritance of low-penetrance genetic variants. The accumulated experience to date in identifying these variants has served to highlight difficulties in conducting statistically and methodologically rigorous studies and follow-up analyses. The COGENT (COlorectal cancer GENeTics) consortium includes 20 research groups in Europe, Australia, the Americas, China and Japan. The overarching goal of COGENT is to identify and characterise low-penetrance susceptibility variants for CRC through association-based analyses. In this study, we review the rationale for identifying low-penetrance variants for CRC and our proposed strategy for establishing COGENT.-
dc.format.extent8 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherCancer Research UK-
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1038/sj.bjc.6605338-
dc.relation.ispartofBritish Journal of Cancer, 2010, vol. 102, num. 2, p. 447-454-
dc.relation.urihttps://doi.org/10.1038/sj.bjc.6605338-
dc.rights(c) Tomlinson, Ian P. et al., 2010-
dc.sourceArticles publicats en revistes (Ciències Clíniques)-
dc.subject.classificationCàncer colorectal-
dc.subject.classificationGenètica-
dc.subject.classificationPolimorfisme genètic-
dc.subject.otherColorectal cancer-
dc.subject.otherGenetics-
dc.subject.otherGenetic polymorphisms-
dc.titleCOGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec593140-
dc.date.updated2020-01-07T16:03:55Z-
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/223678/EU//CHIBCHA-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid19920828-
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
Articles publicats en revistes (Medicina)
Articles publicats en revistes (Ciències Clíniques)

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