Publications de Catherine NOGUES
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                                  Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.
                              
            
            
                              
                  American Journal of Human Genetics
                
                                             2021
                                  ;
                                                            108
                                            (10)
                                                                :
                                1907-1923.
                          
                                                                        
                                                      
            
          
        
            
            
              
                                  Oral Contraceptive Use and Breast Cancer Risk: Retrospective and Prospective Analyses From a BRCA1 and BRCA2 Mutation Carrier Cohort Study.
                              
            
            
                              
                  JNCI Cancer Spectrum
                
                                             2021
                                  ;
                                                            2
                                            (2)
                                                                :
                                pky023.
                          
                                                                        
                                                      
            
          
        
            
            
              
                                  A new hybrid record linkage process to make epidemiological databases interoperable: application to the GEMO and GENEPSO studies involving BRCA1 and BRCA2 mutation carriers.
                              
            
            
                              
                  BMC Medical Research Methodology
                
                                             2021
                                  ;
                                                            21
                                            (1)
                                                                :
                                155.
                          
                                                      
                  
                
                                      
            
          
        
            
            
              
                                  Gene‐ and pathway‐level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility.
                              
            
            
                              
                  International Journal of Cancer
                
                                             2021
                                  ;
                                                            148
                                            (8)
                                                                :
                                1895-1909.
                          
                                                                        
                                                      
            
          
        
            
            
              
                                  Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study.
                              
            
            
                              
                  American Journal of Obstetrics and Gynecology
                
                                             2021
                                  ;
                                                            225
                                            (1)
                                                                :
                                51.e1-51.e17.
                          
                                                                        
                                                      
            
          
        
            
            
              
                                  National recommendations of the French Genetics and Cancer Group - Unicancer on the modalities of multi-genes panel analyses in hereditary predispositions to tumors of the digestive tract.
                              
            
            
                              
                  European Journal of Medical Genetics
                
                                             2020
                                  ;
                                                            63
                                            (12)
                                                                :
                                104080.
                          
                                                                        
                                                      
            
          
        
            
            
              
                                  Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants.
                              
            
            
                              
                  Genetics in Medicine
                
                                             2020
                                  ;
                                                            22
                                            (10)
                                                                :
                                1653-1666.
                          
                                                                        
                                                      
            
          
        
            
            
              
                                  Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers.
                              
            
            
                              
                  Breast Cancer Research
                
                                             2020
                                  ;
                                                            22
                                            (1)
                                                                :
                                8.
                          
                                                      
                  
                
                                      
            
          
        
            
            
              
                                  Alcohol consumption, cigarette smoking, and risk of breast cancer for BRCA1 and BRCA2 mutation carriers: results from The BRCA1 and BRCA2 Cohort Consortium.
                              
            
            
                              
                  Cancer Epidemiology, Biomarkers and Prevention
                
                                             2019
                                  ;
                                                            27
                                                                              :
                                cebp.0546.2019.
                          
                                                                        
                                                      
            
          
        
            
            
              
                                  Les femmes à haut risque de cancer du sein : quelle attitude ?
                              
            
            
                              
                  La Presse Médicale
                
                                             2019
                                  ;
                                                            48
                                            (10)
                                                                :
                                1092-1100.
                          
                                    
            
          
        
            
            
              
                                  Uptake of genetic counseling among adult children of BRCA1/2 mutation carriers in France.
                              
            
            
                              
                  Psycho-Oncology
                
                                             2019
                                  ;
                                                            28
                                            (9)
                                                                :
                                1894-1900.
                          
                                    
            
          
        
            
            
              
                                  Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing.
                              
            
            
                              
                  International Journal of Cancer
                
                                             2019
                                  ;
                                                            144
                                            (8)
                                                                :
                                1962-1974.
                          
                                                                        
                                                      
            
          
        
            
            
              
                                  The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations.
                              
            
            
                              
                  JNCI Cancer Spectrum
                
                                             2018
                                  ;
                                                            2
                                            (4)
                                                                :
                                pky078.
                          
                                                                        
                                                      
            
          
        
            
            
              
                                  The French Genetic and Cancer Consortium guidelines for multigene panel analysis in hereditary breast and ovarian cancer predisposition.
                              
            
            
                              
                  Bulletin du Cancer
                
                                             2018
                                  ;
                                                            105
                                            (10)
                                                                :
                                907-917.
                          
                                    
            
          
        
            
            
              
                                  How Can Contingent Valuation Inform the Bioethics Debate? Evidence from a Survey on Hereditary Cancers in France.
                              
            
            
                              
                  Revue Economique
                
                                             2017
                                  ;
                                                            68
                                            (3)
                                                                :
                                379--404.
                          
                                    
            
          
        
            
            
              
                                  Mutation screening of MIR146A/B and BRCA1/2 3′-UTRs in the GENESIS study.
                              
            
            
                              
                  European Journal of Human Genetics
                
                                             2016
                                  ;
                                                            24
                                            (9)
                                                                :
                                1324-1329.
                          
                                                                        
                                                      
            
          
        
            
            
              
                                  “Maybe they have found something new” participants’ views on returning cohort psychosocial survey results.
                              
            
            
                              
                  Health Expectations
                
                                             2015
                                  ;
                                                            18
                                            (6)
                                                                :
                                2425-2436.
                          
                                                      
                  
                
                                      
            
          
        
            
            
              
                                  Targeted Sequencing of the Mitochondrial Genome of Women at High Risk of Breast Cancer without Detectable Mutations in BRCA1/2.
                              
            
            
                              
                  PLoS ONE
                
                                             2015
                                  ;
                                                            10
                                            (9)
                                                                :
                                e0136192.
                          
                                                      
                  
                
                                      
            
          
        
            
            
              
                                  Impact of BRCA1/2 mutation on young women’s 5-year parenthood rates: a prospective comparative study (GENEPSO-PS cohort).
                              
            
            
                              
                  Familial Cancer
                
                                             2015
                                  ;
                                                            14
                                            (2)
                                                                :
                                273-279.
                          
                                    
            
          
        
            
            
              
                                  Breast Cancer Risk Associated with Estrogen Exposure and Truncating Mutation Location in BRCA1/2 Carriers.
                              
            
            
                              
                  Cancer Epidemiology, Biomarkers and Prevention
                
                                             2015
                                  ;
                                                            24
                                            (4)
                                                                :
                                698-707.
                          
                                                                        
                                                      
            
          
        
            
            
              
                                  [Having a child and PND/PGD access in women with a BRCA1/2 mutation? Different approach whether ill or healthy].
                              
            
            
                              
                  Bulletin du Cancer
                
                                             2014
                                  ;
                                                            101
                                            (11)
                                                                :
                                1001-1008.
                          
                                                                        
                                                      
            
          
        
            
            
              
                                  Which factors predict proposal and uptake of psychological counselling after BRCA1/2 test result disclosure?
                              
            
            
                              
                  Psycho-Oncology
                
                                             2014
                                  ;
                                                            23
                                            (4)
                                                                :
                                420-427.
                          
                                                                        
                                                      
            
          
        
            
            
              
                                  Psychometric properties of a French version of a Dutch scale for assessing breast and body image (BBIS) in healthy women.
                              
            
            
                              
                  BMC Women's Health
                
                                             2013
                                  ;
                                                            13
                                            (1)
                                                                :
                                24.
                          
                                                      
                  
                
                                      
            
          
        
            
            
              
                                  Cancer risk management strategies and perceptions of unaffected women five years after predictive genetic testing for BRCA1/2 mutations.
                              
            
            
                              
                  European Journal of Human Genetics
                
                                             2011
                                  .
                                                                                    
                                                                        
                                                      
            
          
        
            
            
              
                                  Variation in breast cancer risk with mutation position smoking alcohol and chest X-ray history in the French National BRCA1/2 carrier cohort (GENEPSO).
                              
            
            
                              
                  Breast Cancer Research and Treatment
                
                                             2011
                                  ;
                                                            130
                                            (3)
                                                                :
                                927-938.
                          
                                                                        
                                                      
            
          
        
            
            
              
                                  Variation of Breast Cancer Risk in the French National BRCA1/2 Carrier Cohort (GENEPSO).
                              
            
            
                                             2009
                                  ;
                                                            33
                                            (8)
                                                                :
                                page 819, 229.
                          
                                    
            
          
        
            
            
              
                                  [Cancer genetics: estimation of the needs of the population in France for the next ten years].
                              
            
            
                              
                  Bulletin du Cancer
                
                                             2009
                                  ;
                                                            96
                                            (9)
                                                                :
                                875-900.
                          
                                                                        
                                                      
            
          
        
            
            
              
                                  BRCA penetrance for breast and ovarian cancers: a heterogeneity study.
                              
            
            
                                             2006
                                  ;
                                                            31
                                            (5)
                                                                :
                                page 474, 86.
                          
                                    
            
          
        
            
            
              
                                  Effect of chest X-rays on the risk of breast cancer among BRCA1/2 mutation carriers in the international BRCA1/2 carrier cohort study: a report from the EMBRACE, GENEPSO, GEO-HEBON, and IBCCS Collaborators' Group.
                              
            
            
                              
                  Journal of Clinical Oncology
                
                                             2006
                                  ;
                                                            24
                                            (21)
                                                                :
                                3361-6.
                          
                                                                        
                                                      
            
          
        
            
            
              
                                  Pregnancies, breast-feeding, and breast cancer risk in the International BRCA1/2 Carrier Cohort Study (IBCCS).
                              
            
            
                              
                  J Natl Cancer Inst
                
                                             2006
                                  ;
                                                            98
                                            (8)
                                                                :
                                535-44.
                          
                                                                        
                                                      
            
          
        
            
            
              
                                  Estimation du risque de cancer associé aux gènes BRCA : étude GENECAN.
                              
            
            
                                             2006
                                  ;
                                                            22
                                            (HS2)
                                                                :
                                page 19, CO43/203.
                          
                                    
            
          
         
         
         
         
         
         
        