Estimating penetrance from family data using a retrospective likelihood when ascertainment depends on genotype and age of onsetCARAYOL, Jérome; BONAÏTI-PELLIE, Catherine.Genetic epidemiology. 2004, Vol 27, Num 2, pp 109-117, issn 0741-0395, 9 p.Article

Où en est l'épidémiologie des cancers en l'an 2001 ? = What is going on in cancer epidemiology in 2001 ?BONAÏTI-PELLIE, Catherine; DOYON, Francoise; LE, Monique G et al.MS. Médecine sciences. 2001, Vol 17, Num 5, pp 586-595, issn 0767-0974Article

On the use of sibling recurrence risks to select environmental factors liable to interact with genetic risk factorsKAZMA, Rémi; BONAÏTI-PELLIE, Catherine; NORRIS, Jill M et al.European journal of human genetics. 2010, Vol 18, Num 1, pp 88-94, issn 1018-4813, 7 p.Article

Génétique et santé = Genetic and healthBOIS, Etienne; BONAITI-PELLIE, Catherine; FEINGOLD, Josué et al.Enfant en milieu tropical. 1989, Num 179, pp 5-50, issn 0013-7561Serial Issue

TTR familial amyloid polyneuropathy: does a mitochondrial polymorphism entirely explain the parent-of-origin difference in penetrance?BONAITI, Bernard; OLSSON, Malin; HELLMAN, Urban et al.European journal of human genetics. 2010, Vol 18, Num 8, pp 948-952, issn 1018-4813, 5 p.Article

Ethics and observational studies in medical research: various rules in a common frameworkCLAUDOT, Frédérique; ALLA, François; FRESSON, Jeanne et al.International journal of epidemiology. 2009, Vol 38, Num 4, pp 1104-1108, issn 0300-5771, 5 p.Article

Estimating penetrance from multiple case families with predisposing mutations: extension of the 'genotype-restricted likelihood' (GRL) methodBONAÏTI, Bernard; BONADONA, Valérie; PERDRY, Hervé et al.European journal of human genetics. 2011, Vol 19, Num 2, pp 173-179, issn 1018-4813, 7 p.Article

Genetics of nonsyndromic cleft lip with or without cleft palate: is there a Mendelian sub-entity?GAJDOS, Vincent; BAHUAU, Michel; ROBERT-GNANSIA, Elisabeth et al.Annales de génétique (Paris). 2004, Vol 47, Num 1, pp 29-39, issn 0003-3995, 11 p.Article

Thyroid developmental anomalies in first degree relatives of children with congenital hypothyroidismLEGER, Juliane; MARINOVIC, Daniella; GAREL, Catherine et al.The Journal of clinical endocrinology and metabolism. 2002, Vol 87, Num 2, pp 575-580, issn 0021-972XArticle

Nineteen years of national screening for congenital hypothyroidism : Familial cases with thyroid dysgenesis suggest the involvement of genetic factorsCASTANET, Mireille; POLAK, Michel; BONAÏTI-PELLIE, Catherine et al.The Journal of clinical endocrinology and metabolism. 2001, Vol 86, Num 5, pp 2009-2014, issn 0021-972XArticle

Estimating cancer risk in HNPCC by the GRL methodALARCONL, Flora; LASSET, Christine; CARAYOL, Jérome et al.European journal of human genetics. 2007, Vol 15, Num 8, pp 831-836, issn 1018-4813, 6 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

Nouveau système de score pour le diagnostic des prédispositions aux cancers du sein et de l'ovaire associées à BRCA1/2 = A new scoring system for the diagnosis of BRCA1/2 associated breast-ovarian cancer predispositionBONAÏTI, Bernard; ALARCON, Flora; BONADONA, Valérie et al.Bulletin du cancer. 2011, Vol 98, Num 7, pp 779-795, issn 0007-4551, 17 p.Article

Sensitivity and predictive value of criteria for p53 germline mutation screeningCHOMPRET, Agnès; ABEL, Anne; STOPPA-LYONNET, Dominique et al.Journal of medical genetics. 2001, Vol 38, Num 1, pp 43-47, issn 0022-2593Article

Genetic polymorphisms of matrix metalloproteinase 12 and 13 genes are implicated in endometriosis progressionBORGHESE, Bruno; CHICHE, Jean-Daniel; VERNEREY, Déwi et al.Human reproduction (Oxford. Print). 2008, Vol 23, Num 5, pp 1207-1213, issn 0268-1161, 7 p.Article

Absence of association between a functional polymorphism of ALOX15 gene and infertility in endometriosisBORGHESE, Bruno; GAYET, Vanessa; CHICHE, Jean-Daniel et al.Fertility and sterility. 2009, Vol 91, Num 4, pp 1414-1416, issn 0015-0282, 3 p., SUPArticle

Traitement de l'information en matière de recherche dans le domaine de la santé : Nul n'est censé ignorer la loi ! = Treatment of information on personal health data for research purposes: nobody should ignore the lawBONAÏTI-PELLIE, Catherine; ARVEUX, Patrick; SIMON, Dominique et al.MS. Médecine sciences. 2009, Vol 25, Num 1, pp 93-97, issn 0767-0974, 5 p.Article

The International Testicular Cancer Linkage Consortium: A clinicopathologic descriptive analysis of 461 familial malignant testicular germ cell tumor kindredMAI, Phuong L; FRIEDLANDER, Michael; HEIDENREICH, Axel et al.Urologic oncology. 2010, Vol 28, Num 5, pp 492-499, issn 1078-1439, 8 p.Article

Genetic epidemiology of neuroblastoma: A study of 426 cases at the Institut Gustave-Roussy in FranceSHOJAEI-BROSSEAU, Taraneh; CHOMPRET, Agnès; ABEL, Anne et al.Pediatric blood & cancer. 2004, Vol 42, Num 1, pp 99-105, issn 1545-5009, 7 p.Article

Possible relationship between the van der Woude syndrome (vWS) locus and nonsyndromic cleft lip with or without cleft palate (NSCL/P)HOUDAYER, Claude; BONAÏTI-PELLIE, Catherine; ERGUY, Caroline et al.American journal of medical genetics. 2001, Vol 104, Num 1, pp 86-92, issn 0148-7299Article

Mitochondrial D310 mutations in colorectal adenomas : An early but not causative genetic event during colorectal carcinogenesisLEGRAS, Antoine; LIEVRE, Astrid; PENNA, Christophe et al.International journal of cancer. 2008, Vol 122, Num 10, pp 2242-2248, issn 0020-7136, 7 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

The Y deletion gr/gr and susceptibility to testicular germ cell tumorNATHANSON, Katherine L; KANETSKY, Peter A; LOHYNSKA, Radka et al.American journal of human genetics. 2005, Vol 77, Num 6, pp 1034-1043, issn 0002-9297, 10 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

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