La chirurgie prophylactique du sein : perspectives médicale, individuelle, familiale et sociale = The prophylactic mastectomy from a medical, individual and social angleEISINGER, Francois; JULIAN-REYNIER, Claire; SOBOL, Hagay et al.MS. Médecine sciences. 2001, Vol 17, Num 10, pp 1027-1030, issn 0767-0974Article

Tamoxifen and breast cancer risk in women harboring a BRCA1 germline mutation : computed efficacy, effectiveness and impactEISINGER, Francois; CHARAFE-JAUFFRET, Emmanuelle; JACQUEMIER, Jocelyne et al.International journal of oncology. 2001, Vol 18, Num 1, pp 5-10, issn 1019-6439Article

Pathology of ovarian cancers in BRCA1 and BRCA2 carriersLAKHANI, Sunil R; MANEK, Sanjiv; MEIJERS-HEIJBOER, Hanne et al.Clinical cancer research. 2004, Vol 10, Num 7, pp 2473-2481, issn 1078-0432, 9 p.Article

Identification et prise en charge des prédispositions héréditaires aux cancers du sein et de l'ovaire (mise à jour 2004) = Identification and management of hereditary breast/ovarian cancers (2004 update)EISINGER, Francois; BRESSAC, Brigitte; SOBOL, Hagay et al.Bulletin du cancer. 2004, Vol 91, Num 3, pp 219-237, issn 0007-4551, 19 p.Article

Variation in breast cancer risk with mutation position, smoking, alcohol, and chest X-ray history, in the French National BRCA1/2 carrier cohort (GENEPSO)LECARPENTIER, Julie; NOGUES, Catherine; GESTA, Paul et al.Breast cancer research and treatment. 2011, Vol 130, Num 3, pp 927-938, issn 0167-6806, 12 p.Article

Acquired resistance to imatinib and secondary KIT exon 13 mutation in gastrointestinal stromal tumourBERTUCCI, Francois; GONCALVES, Anthony; MONGES, Geneviève et al.Oncology reports. 2006, Vol 16, Num 1, pp 97-101, issn 1021-335X, 5 p.Article

PS2- expression in BRCA1-associated breast cancersCHARAFE-JAUFFRET, Emmanuelle; EISINGER, Francois; MATHOULIN-PORTIER, Marie-Pierre et al.Anticancer research. 2001, Vol 21, Num 4B, pp 2877-2881, issn 0250-7005Article

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

Phenotypic heterogeneity in multiple myeloma familiesLYNCH, Henry T; WATSON, Patrice; HOGG, David et al.Journal of clinical oncology. 2005, Vol 23, Num 4, pp 685-693, issn 0732-183X, 9 p.Article

Impact of gene patents on the cost-effective delivery of care: The case of BRCA1 genetic testingSEVILLA, Christine; JULIAN-REYNIER, Claire; EISINGER, Francois et al.International journal of technology assessment in health care. 2003, Vol 19, Num 2, pp 287-300, issn 0266-4623, 14 p.Article

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

Pediatric Mastocytosis Is a Clonal Disease Associated with D⁸¹⁶V and Other Activating c-KIT MutationsBODEMER, Christine; HERMINE, Olivier; LAUNAY, Jean-Marie et al.Journal of investigative dermatology. 2010, Vol 130, Num 3, pp 804-815, issn 0022-202X, 12 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

L'offre de tests de prédisposition génétique au cancer du sein ou de l'ovaire en France = The supply of breast/ovarian cancer genetic susceptibility tests in FranceSEVILLA, Christine; BOURRET, Pascale; NOGUES, Catherine et al.MS. Médecine sciences. 2004, Vol 20, Num 8-9, pp 788-792, issn 0767-0974, 5 p.Article

Effects of genetic consultation on perception of a family risk of breast/ovarian cancer and determinants of inaccurate perception after the consultationHUIART, Laetitia; EISINGER, Francois; STOPPA-LYONNET, Dominique et al.Journal of clinical epidemiology. 2002, Vol 55, Num 7, pp 665-675, issn 0895-4356Article

Diagnostic strategy for analytical scanning of BRCA1 gene by fluorescence-assisted mismatch analysis using large, bifluorescently labeled ampliconsRICEVUTO, Enrico; SOBOL, Hagay; STOPPA-LYONNET, Dominique et al.Clinical cancer research. 2001, Vol 7, Num 6, pp 1638-1646, issn 1078-0432Article

Les nouveaux consommateurs du génome : Les nouvelles frontières de la génomique = The new genome consumers : Surprising genomicsJULIAN-REYNIER, Claire; BOURRET, Pascale; SEVILLA, Christine et al.Biofutur (Puteaux). 2000, Num 206, pp 100-103, issn 0294-3506Article

Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAPLAGARDE, Arnaud; ROULEAU, Etienne; BIRNBAUM, Daniel et al.Journal of medical genetics. 2010, Vol 47, Num 10, pp 721-722, issn 0022-2593, 2 p.Article

High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorderPREUDHOMME, Claude; RENNEVILLE, Aline; MOZZICONACCI, Marie-Joelle et al.Blood. 2009, Vol 113, Num 22, pp 5583-5587, issn 0006-4971, 5 p.Article

Moesin expression is a marker of basal breast carcinomasCHARAFE -JAUFFRET, Emmanuelle; MONVILLE, Florence; SOBOL, Hagay et al.International journal of cancer. 2007, Vol 121, Num 8, pp 1779-1785, issn 0020-7136, 7 p.Article

Prediction of BRCA1 status in patients with breast cancer using estroqen receptor and basal phenotypeLAKHANI, Sunil R; REIS-FILHO, Jorge S; CHANG-CLAUDE, Jenny et al.Clinical cancer research. 2005, Vol 11, Num 14, pp 5175-5180, issn 1078-0432, 6 p.Article

Significant contribution of germline BRCA2 rearrangements in male breast cancer familiesTOURNIER, Isabelle; BRESSAC-DE PAILLERETS, Brigitte; LORTHOLARY, Alain et al.Cancer research (Baltimore). 2004, Vol 64, Num 22, pp 8143-8147, issn 0008-5472, 5 p.Article

Identification et prise en charge du syndrome HNPCC (hereditary non polyposis colon cancer), prédisposition héréditaire aux cancers du côlon, du rectum et de l'utérus = Identification and management of HNPCC syndrome (hereditary non polyposis colon cancer), hereditary predisposition to colorectal and endometrial adenocarcinomasOLSCHWANG, Sylviane; BONAÏTI, Catherine; THOMAS, Gilles et al.Bulletin du cancer. 2004, Vol 91, Num 4, pp 303-315, issn 0007-4551, 13 p.Article

Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21MCKAY, James D; LESUEUR, Fabienne; SOBOL, Hagay et al.American journal of human genetics. 2001, Vol 69, Num 2, pp 440-446, issn 0002-9297Article

Women's attitudes toward preventive strategies for hereditary breast or ovarian carcinoma differ from one country to another: Differences among English, French, and Canadian womenJULIAN-REYNIER, Claire M; BOUCHARD, Louise J; EVANS, D. Gareth et al.Cancer. 2001, Vol 92, Num 4, pp 959-968, issn 0008-543XArticle