Pascal and Francis Bibliographic Databases

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Impact of an information booklet on satisfaction and decision-making about BRCA genetic testingMANCINI, Julien; NOGUES, Catherine; LASSET, Christine et al.European journal of cancer (1990). 2006, Vol 42, Num 7, pp 871-881, issn 0959-8049, 11 p.Article

Cancer risk management strategies and perceptions of unaffected women 5 years after predictive genetic testing for B RCA1/2 mutationsJULIAN-REYNIER, Claire; MANCINI, Julien; MOURET-FOURME, Emmanuelle et al.European journal of human genetics. 2011, Vol 19, Num 5, pp 500-506, issn 1018-4813, 7 p.Article

Contribution of bioinformatics predictions and functional splicing assays to the interpretation of unclassified variants of the BRCA genesCHRISTOPHE THERY, Jean; KRIEGER, Sophie; BERTHET, Pascaline et al.European journal of human genetics. 2011, Vol 19, Num 10, pp 1052-1058, issn 1018-4813, 7 p.Article

Gliomes et mutations des gènes BRCA: association fortuite ou imputabilité ? = Gliomas and BRCA genes mutations: fortuitous association or imputability?GIRARDSTEIN-BOCCARA, Laura; MARI, Véronique; MET-DOMESTICI, Marie et al.Bulletin du cancer. 2014, Vol 101, Num 9, pp 795-802, issn 0007-4551, 8 p.Article

Breast and ovarian cancer screening of non-carriers from BRCA1/2 mutation-positive families: 2-year follow-up of cohorts from France and QuebecDORVAL, Michel; NOGUES, Catherine; BERTHET, Pascaline et al.European journal of human genetics. 2011, Vol 19, Num 5, pp 494-499, issn 1018-4813, 6 p.Article

Oral contraceptives and breast cancer risk in the international BRCA1/2 carrier cohort study : A report from EMBRACE, GENEPSO, GEO-HEBON, and the IBCCS collaborating groupBROHET, Richard M; GOLDGAR, David E; NOGUES, Catherine et al.Journal of clinical oncology. 2007, Vol 25, Num 25, pp 3831-3836, issn 0732-183X, 6 p.Article

Two novel variants in the 3'UTR of the BRCA1 gene in familial breast and/or ovarian cancerLHEUREUX, Stéphanie; LAMBERT, Bernard; KRIEGER, Sophie et al.Breast cancer research and treatment. 2011, Vol 125, Num 3, pp 885-891, issn 0167-6806, 7 p.Article

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor―negative breast cancer in the general populationANTONIOU, Antonis C; XIANSHU WANG; GHOUSSAINI, Maya et al.Nature genetics. 2010, Vol 42, Num 10, pp 885-892, issn 1061-4036, 8 p.Article

Common BRCA2 variants and modification of breast and ovarian cancer risk in BRCA1 mutation carriersHUGHES, David J; GINOLHAC, Sophie M; HARDOUIN, Agnès et al.Cancer epidemiology, biomarkers & prevention. 2005, Vol 14, Num 1, pp 265-267, issn 1055-9965, 3 p.Article

Le syndrome de Li-Fraumeni: mise au point, données nouvelles et recommandations pour la prise en charge = Li-Fraumeni syndrome : update, new data and guidelines for clinical managementFREBOURG, Thierry; ABEL, Anne; FEINGOLD, Josué et al.Bulletin du cancer. 2001, Vol 88, Num 6, pp 581-587, issn 0007-4551Article

Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch SyndromeBONADONA, Valérie; BONAITI, Bernard; COLAS, Chrystelle et al.JAMA, the journal of the American Medical Association. 2011, Vol 305, Num 22, pp 2304-2310, issn 0098-7484, 7 p.Article

The BRCA1 c.5434C→G (p.Pro1812Ala) variant induces a deleterious exon 23 skipping by affecting exonic splicing regulatory elementsGAILDRAT, Pascaline; KRIEGER, Sophie; THERY, Jean-Christophe et al.Journal of medical genetics. 2010, Vol 47, Num 6, pp 398-403, issn 0022-2593, 6 p.Article

AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers : A consortium of investigators of modifiers of BRCA1/2 studyCOUCH, Fergus J; SINILNIKOVA, Olga; PEOCK, Susan et al.Cancer epidemiology, biomarkers & prevention. 2007, Vol 16, Num 7, pp 1416-1421, issn 1055-9965, 6 p.Article

Breast cancer risk in BRCA1 and BRCA2 mutation carriers and polyglutamine repeat length in the AIB1 geneHUGHES, David J; GINOLHAC, Sophie M; GIRAUD, Sophie et al.International journal of cancer. 2005, Vol 117, Num 2, pp 230-233, issn 0020-7136, 4 p.Article

BRCA1 wild-type allele modifies risk of ovarian cancer in carriers of BRCA1 germ-line mutationsGINOLHAC, Sophie M; GAD, Sophie; MULLER, Danièle et al.Cancer epidemiology, biomarkers & prevention. 2003, Vol 12, Num 2, pp 90-95, issn 1055-9965, 6 p.Article

Le syndrome de Li-Fraumeni : mise au point, données nouvelles et recommandations pour la prise en charge = Li-Fraumeni's syndrome: up-to-date and management guidelinesFREBOURG, Thierry; ABEL, Anne; FEINGOLD, Josué et al.MTP. Médecine thérapeutique pédiatrie. 2001, Vol 4, Num 1, pp 35-40, issn 1286-5494Article

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