Penetrance, Journal of Clinical Oncology, vol.25, issue.11, pp.1329-1362, 2007. ,
DOI : 10.1200/JCO.2006.09.1066
Cancer Risks Associated With Germline Mutations in <emph type="ital">MLH1</emph>, <emph type="ital">MSH2</emph>, and <emph type="ital">MSH6</emph> Genes in Lynch Syndrome, JAMA, vol.305, issue.22, pp.2304-2314, 2011. ,
DOI : 10.1001/jama.2011.743
Identification et prise en charge des prédispositions héréditaires aux cancers du sein et de l'ovaire (mise à jour, Bull Cancer, vol.91, pp.219-256, 2004. ,
Management of an Inherited Predisposition to Breast Cancer, New England Journal of Medicine, vol.357, issue.2, pp.154-62, 2007. ,
DOI : 10.1056/NEJMcp071286
Identification et prise en charge du syndrome HNPCC (Hereditary NonPolyposis Colon Cancer), prédisposition héréditaire aux cancers du côlon, du rectum et de l'utérus, Bull Cancer, vol.91, pp.303-318, 2004. ,
Recommendations for the Care of Individuals With an Inherited Predisposition to Lynch Syndrome, JAMA, vol.296, issue.12, pp.1507-1524, 2006. ,
DOI : 10.1001/jama.296.12.1507
Risk prediction models for familial breast cancer, Future Oncology, vol.2, issue.2, pp.257-74, 2006. ,
DOI : 10.2217/14796694.2.2.257
Determining Carrier Probabilities for Breast Cancer???Susceptibility Genes BRCA1 and BRCA2, The American Journal of Human Genetics, vol.62, issue.1, pp.145-58, 1998. ,
DOI : 10.1086/301670
The BOADICEA model of genetic susceptibility to breast and ovarian cancer, British Journal of Cancer, vol.88, pp.1580-90, 2004. ,
DOI : 10.1038/sj.bjc.6602175
A breast cancer prediction model incorporating familial and personal risk factors, Statistics in Medicine, vol.6, issue.7, pp.111-1130, 2004. ,
DOI : 10.1002/sim.1668
A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO, Journal of Medical Genetics, vol.41, issue.6, pp.474-80, 2004. ,
DOI : 10.1136/jmg.2003.017996
Update on the Manchester Scoring System for BRCA1 and BRCA2 testing, Journal of Medical Genetics, vol.42, issue.7, p.39, 2005. ,
DOI : 10.1136/jmg.2005.031989
Consultations de génétique et prédisposition aux cancers du sein, Risques héréditaires de cancers du sein et de l'ovaire: Quelle prise en charge? Paris: Inserm, 1998. ,
Nouveau système de score pour le diagnostic des prédispositions aux cancers du sein et de l'ovaire associées à BRCA1, Bull Cancer, vol.98, issue.2, pp.779-95, 2011. ,
Addition of pathology and biomarker information significantly improves the performance of the Manchester scoring system for BRCA1 and BRCA2 testing, Journal of Medical Genetics, vol.46, issue.12, pp.811-828, 2009. ,
DOI : 10.1136/jmg.2009.067850
URL : https://hal.archives-ouvertes.fr/hal-00552701
Germline mutation and genome instability, European Journal of Cancer Prevention, vol.8, issue.1, pp.33-40, 1999. ,
DOI : 10.1097/00008469-199912001-00006
Population BRCA1 and BRCA2 Mutation Frequencies and Cancer Penetrances: A Kin-Cohort Study in Ontario, Canada, JNCI Journal of the National Cancer Institute, vol.98, issue.23, pp.1694-706, 2006. ,
DOI : 10.1093/jnci/djj465
Cancer risks in BRCA2 families: estimates for sites other than breast and ovary, Journal of Medical Genetics, vol.42, issue.9, pp.711-730, 2005. ,
DOI : 10.1136/jmg.2004.028829
Breast Cancer Risk Among Male BRCA1 and BRCA2 Mutation Carriers, JNCI Journal of the National Cancer Institute, vol.99, issue.23, pp.1811-1825, 2007. ,
DOI : 10.1093/jnci/djm203
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267289
Mixture models for cancer survival analysis: application to population-based data with covariates, Statistics in Medicine, vol.101, issue.4, pp.441-54, 1999. ,
DOI : 10.1002/(SICI)1097-0258(19990228)18:4<441::AID-SIM23>3.0.CO;2-M
Estimating penetrance from multiple case families with predisposing mutations: extension of the ???genotype-restricted likelihood??? (GRL) method, European Journal of Human Genetics, vol.33, issue.2, pp.173-182, 2011. ,
DOI : 10.1038/ejhg.2010.158
URL : https://hal.archives-ouvertes.fr/hal-00583530
Cancer incidence and mortality in France over the period 1980???2005, Revue d'??pid??miologie et de Sant?? Publique, vol.56, issue.3, pp.159-75, 1980. ,
DOI : 10.1016/j.respe.2008.03.117
URL : https://hal.archives-ouvertes.fr/hal-00538673
-Negative Breast Cancer, Journal of Clinical Oncology, vol.26, issue.26, pp.4282-4290, 2008. ,
DOI : 10.1200/JCO.2008.16.6231
URL : https://hal.archives-ouvertes.fr/hal-00894139
Locoregional Relapse and Distant Metastasis in Conservatively Managed Triple Negative Early-Stage Breast Cancer, Journal of Clinical Oncology, vol.24, issue.36, pp.5652-5659, 2006. ,
DOI : 10.1200/JCO.2006.06.5664
A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes, British Journal of Cancer, vol.60, issue.1, pp.76-83, 2002. ,
DOI : 10.1086/318181
High frequency of BRCA1/2 germline mutations in consecutive ovarian cancer patients in Poland, Gynecologic Oncology, vol.108, issue.2, pp.433-440, 2008. ,
DOI : 10.1016/j.ygyno.2007.09.035
Prediction of BRCA1/2 mutation status in patients with ovarian cancer from a hospital-based cohort, Genetics in Medicine, vol.351, issue.3, pp.173-182, 2007. ,
DOI : 10.1097/GIM.0b013e318032e4ab
Prevalence and Penetrance of Germline BRCA1 and BRCA2 Mutations in a Population Series of 649 Women with Ovarian Cancer, The American Journal of Human Genetics, vol.68, issue.3, pp.700-710, 2001. ,
DOI : 10.1086/318787
PEL: an unbiased method for estimating age-dependent genetic disease risk from pedigree data unselected for family history, Genetic Epidemiology, vol.9, issue.5, pp.379-85, 2009. ,
DOI : 10.1002/gepi.20390
URL : https://hal.archives-ouvertes.fr/inserm-00358140
Four-Generation families in France, Popul Eng Sel, vol.9, pp.75-101, 1997. ,
How many children and how many siblings in France in the last century?, Popul Societies, vol.373, pp.1-4, 2001. ,
A General Model for the Genetic Analysis of Pedigree Data, Human Heredity, vol.21, issue.6, pp.523-565, 1971. ,
DOI : 10.1159/000152448
Oncogénétique: estimation des besoins de la populations en France pour les 10 ans à venir, Bull Cancer, vol.96, pp.875-900, 2009. ,
Predicting the likelihood of carrying a BRCA1 or BRCA2 mutation: validation of BOADICEA, BRCAPRO, IBIS, Myriad and the Manchester scoring system using data from UK genetics clinics, Journal of Medical Genetics, vol.45, issue.7, pp.425-456, 2008. ,
DOI : 10.1136/jmg.2007.056556
Why are the majority of hereditary cases of early-onset breast cancer sporadic? A simulation study, Cancer Epidemiol Biomarkers Prev, vol.9, pp.805-817, 2000. ,