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Article: ENIGMA - evidence-based network for the interpretation of germline mutant alleles: an international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genes

TitleENIGMA - evidence-based network for the interpretation of germline mutant alleles: an international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genes
Authors
Issue Date2012
Citation
Human Mutation, 2012, v. 33 n. 1, p. 2-7 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/146428
ISI Accession Number ID
Funding AgencyGrant Number
NHMRC
NIHCA148112
CA116167
CA116167Z
CA116201
Breast Cancer Research Foundation
Italian Association for Cancer Research
German Cancer Aid107364
Centre of Molecular Medicine Cologne
Funding Information:

Contract grant sponsors: NHMRC (Senior Research Fellowship to A. B. S.); NIH (CA148112 and CA116167 to A.N.A.M.); Breast Cancer Research Foundation (to K.L.N.); Italian Association for Cancer Research (A. I. R. C. to P. R.); German Cancer Aid (grant 107364 to B. W.); Centre of Molecular Medicine Cologne (to B. W.); NIH (grant CA116167 to F.J.C. and D. E. G.); NIH Recovery Act supplement (CA116167Z to F.J.C.); NIH Specialized Program of Research Excellence (SPORE) in Breast Cancer (CA116201 to F.J.C.).

 

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dc.contributor.authorSpurdle, ABen_US
dc.contributor.authorHealey, Sen_US
dc.contributor.authorDevereau, Aen_US
dc.contributor.authorHogervorst, FBen_US
dc.contributor.authorMonteiro, ANen_US
dc.contributor.authorNathanson, KLen_US
dc.contributor.authorRadice, Pen_US
dc.contributor.authorStoppa-Lyonnet, Den_US
dc.contributor.authorTavtigian, Sen_US
dc.contributor.authorWappenschmidt, Ben_US
dc.contributor.authorCouch, FJen_US
dc.contributor.authorPertesi, Men_US
dc.contributor.authorCornell, Men_US
dc.contributor.authorRouleau, Een_US
dc.contributor.authorSharan, Sen_US
dc.contributor.authorRahman, Nen_US
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dc.contributor.authorWeitzel, Jen_US
dc.contributor.authorCampbell, Jen_US
dc.contributor.authorCummings,en_US
dc.contributor.authorMachakova, Een_US
dc.contributor.authorGoldgar, DEen_US
dc.contributor.authorOlopade, Fen_US
dc.contributor.authorGodwin, Aen_US
dc.contributor.authorOzcelik, Hen_US
dc.contributor.authorSeminara, Den_US
dc.contributor.authorGoldgar, Den_US
dc.contributor.authorCouch, Fen_US
dc.contributor.authorFackenthal, JDen_US
dc.contributor.authorThomassen, Men_US
dc.contributor.authorTeo, SHen_US
dc.contributor.authorHansen, TVen_US
dc.contributor.authorBorg, Aen_US
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dc.contributor.authorToland, Aen_US
dc.contributor.authorRogan, Pen_US
dc.contributor.authorHansen, TVen_US
dc.contributor.authorGuidugli, Len_US
dc.contributor.authorBrody, LCen_US
dc.contributor.authorHealey, Sen_US
dc.contributor.authorBrown, Men_US
dc.contributor.authorKwong, Aen_US
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dc.contributor.authorNederlof, Pen_US
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dc.contributor.authorPasini, Ben_US
dc.contributor.authorTommasi, Sen_US
dc.contributor.authorLafferty, Aen_US
dc.contributor.authorArisari, Aen_US
dc.contributor.authorKonstantopoulou, Ien_US
dc.contributor.authorPal, Ten_US
dc.contributor.authorSimard, Jen_US
dc.contributor.authorBonetti, Aen_US
dc.contributor.authorVoresco, Len_US
dc.contributor.authorPeissel, Ben_US
dc.contributor.authorEvans, DGen_US
dc.contributor.authorFoulkes, Wen_US
dc.contributor.authorSzabo, Cen_US
dc.contributor.authorvan Asperen, Cen_US
dc.contributor.authorJonkers, Jen_US
dc.contributor.authorWalker, Len_US
dc.contributor.authorMitchell, Gen_US
dc.contributor.authorGutierrez-Enriquez, Sen_US
dc.contributor.authorDiez, Oen_US
dc.contributor.authorMillot, Gen_US
dc.contributor.authorFostira, Fen_US
dc.contributor.authorSelkirk, Cen_US
dc.contributor.authorAntoniou, Aen_US
dc.contributor.authorMonteiro, Aen_US
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dc.contributor.authorRubinstein, WSen_US
dc.contributor.authorde la Hoya, Men_US
dc.contributor.authorDomchek, Sen_US
dc.contributor.authorCaputo, Sen_US
dc.contributor.authorHoudayer, Cen_US
dc.contributor.authorBlanco, Ien_US
dc.contributor.authorLazaro, Cen_US
dc.contributor.authorWhiley, Pen_US
dc.contributor.authorBecker, Aen_US
dc.contributor.authorAretini, Pen_US
dc.contributor.authorEccles, Den_US
dc.contributor.authorCaides, Ten_US
dc.contributor.authorViel, Aen_US
dc.contributor.authorIzatt, Len_US
dc.contributor.authorHogervorst, Fen_US
dc.contributor.authorRadice, Pen_US
dc.contributor.authorNathanson, Ken_US
dc.contributor.authorPedersen, ISen_US
dc.contributor.authorVreeswijk, Men_US
dc.contributor.authorNeuhausen, Sen_US
dc.contributor.authorYannoukakos, Ken_US
dc.contributor.authorTucker, Ken_US
dc.contributor.authorSouthey, Men_US
dc.contributor.authorLeary, Jen_US
dc.contributor.authorCaligo, MAen_US
dc.contributor.authorGarcia, EGen_US
dc.contributor.authorDevereau, Aen_US
dc.contributor.authorBrandao, Ren_US
dc.contributor.authorLidereau, Ren_US
dc.contributor.authorMontagna, Men_US
dc.date.accessioned2012-04-24T07:53:18Z-
dc.date.available2012-04-24T07:53:18Z-
dc.date.issued2012en_US
dc.identifier.citationHuman Mutation, 2012, v. 33 n. 1, p. 2-7en_US
dc.identifier.urihttp://hdl.handle.net/10722/146428-
dc.languageengen_US
dc.relation.ispartofHuman Mutationen_US
dc.titleENIGMA - evidence-based network for the interpretation of germline mutant alleles: an international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genesen_US
dc.typeArticleen_US
dc.identifier.emailKwong, A: avakwong@hkucc.hku.hken_US
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/humu.21628-
dc.identifier.pmid21990146-
dc.identifier.scopuseid_2-s2.0-84857691697-
dc.identifier.hkuros199324en_US
dc.identifier.volume33en_US
dc.identifier.issue1en_US
dc.identifier.spage2en_US
dc.identifier.epage7en_US
dc.identifier.isiWOS:000300705300002-

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