La maladie de Cowden et le gène PTEN : un exemple d'intégration réussie entre clinique et biologie = Cowden disease and the PTEN gene: a successfully clinical and biological combined approachLONGY, Michel.Bulletin du cancer. 2001, Vol 88, Num 12, pp 1153-1158, issn 0007-4551Article

Carcinome « molecular apocrine » et maladie de Cowden = Molecular apocrine carcinoma and disease of CowdenLONGY, Michel.Annales de pathologie (Print). 2012, Vol 32, issn 0242-6498, S42-S43, HS1Conference Paper

Bases moléculaires du diagnostic génétique = Molecular basis of diagnosis in geneticsLONGY, Michel.Gastroentérologie clinique et biologique. 2001, Vol 25, Num 4, pp B14-B17, issn 0399-8320, SUPConference Paper

Pharmacogenetics of human carboxylesterase 2, an enzyme involved in the activation of irinotecan into SN-38CHARASSON, Virginie; BELLOTT, Ricardo; MEYNARD, Delphine et al.Clinical pharmacology and therapeutics. 2004, Vol 76, Num 6, pp 528-535, issn 0009-9236, 8 p.Article

WNT pathway and mammary carcinogenesis: Loss of expression of candidate tumor suppressor gene SFRP1 in most invasive carcinomas except of the medullary typeUGOLINI, Francoise; CHARAFE-JAUFFRET, Emmanuelle; PEBUSQUE, Marie-Josèphe et al.Oncogene (Basingstoke). 2001, Vol 20, Num 41, pp 5810-5817, issn 0950-9232Article

Comprehensive analysis of PTEN status in breast carcinomasJONES, Natalie; BONNET, Françoise; MACGROGAN, Gaëtan et al.International journal of cancer (Print). 2013, Vol 133, Num 2, pp 323-334, issn 0020-7136, 12 p.Article

High-resolution integrated map encompassing the breast cancer loss of heterozygosity region on human chromosome 16q22.1FRENGEN, Eirik; ROCCA-SERRA, Philippe; JOHANSEN, Henning et al.Genomics (San Diego, Calif.). 2000, Vol 70, Num 3, pp 273-285, issn 0888-7543Article

Les formes héréditaires du cancer de l'ovaire: particularités clinico-biologiques et thérapeutiques = Hereditary ovarian carcinomas: clinico-biological features and treatmentFLOQUET, Anne; STOECKLE, Eberhard; CROCE, Sabrina et al.Bulletin du cancer. 2014, Vol 101, Num 2, pp 167-174, issn 0007-4551, 8 p.Article

Primary Cutaneous T-Cell Lymphomas Do not Show Specific NAV3 Gene Deletion or TranslocationMARTY, Marion; PROCHAZKOVA, Martina; LAHARANNE, Elodie et al.Journal of investigative dermatology. 2008, Vol 128, Num 10, pp 2458-2466, issn 0022-202X, 9 p.Article

Spectrum of CREBBP gene dosage anomalies in Rubinstein-Taybi Syndrome patientsSTEF, Marianne; SIMON, Delphine; LACOMBE, Didier et al.European journal of human genetics. 2007, Vol 15, Num 8, pp 843-847, issn 1018-4813, 5 p.Article

Spectrum of PTCH1 mutations in French patients with Gorlin syndromeBOUTET, Nathalie; BIGNON, Yves-Jean; DROUIN-GARRAUD, Valérie et al.Journal of investigative dermatology. 2003, Vol 121, Num 3, pp 478-481, issn 0022-202X, 4 p.Article

Ploidy and Large-Scale Genomic Instability Consistently Identify Basal-like Breast Carcinomas with BRCA1/2 InactivationPOPOVA, Tatiana; MANIE, Elodie; HOUDAYE, Claude et al.Cancer research (Chicago, Ill.). 2012, Vol 72, Num 21, pp 5454-5462, issn 0008-5472, 9 p.Article

Alterations of the p53 and PIK3CA/AKT/mTOR Pathways in Angiosarcomas: A Pattern Distinct From Other Sarcomas With Complex GenomicsITALIANO, Antoine; CHEN, Chun-Liang; THOMAS, Rachael et al.Cancer. 2012, Vol 118, Num 23, pp 5878-5887, issn 0008-543X, 10 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

Detection of a new mutation in KIT exon 9 in a gastrointestinal stromal tumorHOSTEIN, Isabelle; LONGY, Michel; GASTALDELLO, Bernadette et al.International journal of cancer. 2006, Vol 118, Num 8, pp 2089-2091, issn 0020-7136, 3 p.Article

Genetic polymorphisms of the XPG and XPD nucleotide excision repair genes in sarcoma patientsLE MORVAN, Valéric; LONGY, Michel; BONAÏTI-PELLIE, Catherine et al.International journal of cancer. 2006, Vol 119, Num 7, pp 1732-1735, issn 0020-7136, 4 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

Genome-Wide Analysis of Cutaneous T-Cell Lymphomas Identifies Three Clinically Relevant ClassesLAHARANNE, Elodie; OUMOUHOU, Naïma; MERLIO, Jean-Philippe et al.Journal of investigative dermatology. 2010, Vol 130, Num 6, pp 1707-1718, issn 0022-202X, 12 p.Article

No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a multi-center cohort studyREBBECK, Timothy R; ANTONIOU, Antonis C; GREENE, Mark H et al.Breast cancer research and treatment. 2009, Vol 115, Num 1, pp 185-192, issn 0167-6806, 8 p.Article

Segmental overgrowth, lipomatosis, arteriovenous malformation and epidermal nevus (SOLAMEN) syndrome is related to mosaic PTEN nullizygosityCAUX, Frédéric; PLAUCHU, Henri; LONGY, Michel et al.European journal of human genetics. 2007, Vol 15, Num 7, pp 767-773, issn 1018-4813, 7 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

Value of microsatellite instability typing in detecting hereditary non-polyposis colorectal cancer : A prospective multicentric study by the Association Aquitaine GastroBECOUARN, Yves; RULLIER, Anne; FREBOURG, Thierry et al.Gastroentérologie clinique et biologique. 2005, Vol 29, Num 6-7, pp 667-675, issn 0399-8320, 9 p.Article

Association between cowden syndrome and lhermitte-duclos disease: Report of two cases and review of the literature. CommentaryDERREY, Stéphane; PROUST, Francois; DEBONO, Bertrand et al.Surgical neurology. 2004, Vol 61, Num 5, pp 447-454, issn 0090-3019, 8 p.Article