1. Association and performance of polygenic risk scores for breast cancer among French women presenting or not a familial predisposition to the disease. (January 2023) Authors: Jiao, Yue; Truong, Thérèse; Eon-Marchais, Séverine; Mebirouk, Noura; Caputo, Sandrine M.; Dondon, Marie-Gabrielle; Karimi, Mojgan; Le Gal, Dorothée; Beauvallet, Juana; Le Floch, Édith; Dandine-Roulland, Claire; Bacq-Daian, Delphine; Olaso, Robert; Albuisson, Juliette; Audebert-Bellanger, Séverine... Journal: European journal of cancer Issue: Volume 179(2023) Page Start: 76 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores. (28th July 2021) Authors: Barnes, Daniel R; Silvestri, Valentina; Leslie, Goska; McGuffog, Lesley; Dennis, Joe; Yang, Xin; Adlard, Julian; Agnarsson, Bjarni A; Ahmed, Munaza; Aittomäki, Kristiina; Andrulis, Irene L; Arason, Adalgeir; Arnold, Norbert; Auber, Bernd; Azzollini, Jacopo; Balmaña, Judith; Barkardottir, Rosa B; ... Journal: Journal of the National Cancer Institute Issue: Volume 114:Number 1(2022) Page Start: 109 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Comparison of the Screening Practices of Unaffected Noncarriers under 40 and between 40 and 49 in BRCA1/2 Families. Issue 4 (25th January 2013) Authors: Duprez, Christelle; Christophe, Véronique; Milhabet, Isabelle; Krzeminski, Aurélie; Adenis, Claude; Berthet, Pascaline; Peyrat, Jean‐Philippe; Vennin, Philippe Journal: Journal of genetic counseling Issue: Volume 22:Issue 4(2013) Page Start: 469 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Contribution of germline deleterious variants in the RAD51 paralogs to breast and ovarian cancers. (December 2017) Authors: Golmard, Lisa; Castéra, Laurent; Krieger, Sophie; Moncoutier, Virginie; Abidallah, Khadija; Tenreiro, Henrique; Laugé, Anthony; Tarabeux, Julien; Millot, Gael; Nicolas, André; Laé, Marick; Abadie, Caroline; Berthet, Pascaline; Polycarpe, Florence; Frébourg, Thierry; Elan, Camille; Pauw, Antoine; ... Journal: European journal of human genetics Issue: Volume 25:Number 12(2017) Page Start: 1345 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing. Issue 8 (13th November 2018) Authors: Girard, Elodie; Eon‐Marchais, Séverine; Olaso, Robert; Renault, Anne‐Laure; Damiola, Francesca; Dondon, Marie‐Gabrielle; Barjhoux, Laure; Goidin, Didier; Meyer, Vincent; Le Gal, Dorothée; Beauvallet, Juana; Mebirouk, Noura; Lonjou, Christine; Coignard, Juliette; Marcou, Morgane; Cavaciuti, Eve; B... Journal: International journal of cancer Issue: Volume 144:Issue 8(2019) Page Start: 1962 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. GENESIS: a French national resource to study the missing heritability of breast cancer. Issue 1 (December 2016) Authors: Sinilnikova, Olga; Dondon, Marie-Gabrielle; Eon-Marchais, Séverine; Damiola, Francesca; Barjhoux, Laure; Marcou, Morgane; Verny-Pierre, Carole; Sornin, Valérie; Toulemonde, Lucie; Beauvallet, Juana; Le Gal, Dorothée; Mebirouk, Noura; Belotti, Muriel; Caron, Olivier; Gauthier-Villars, Marion; Coup... Journal: BMC cancer Issue: Volume 16:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Gene‐ and pathway‐level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility. Issue 8 (9th January 2021) Authors: Lonjou, Christine; Eon‐Marchais, Séverine; Truong, Thérèse; Dondon, Marie‐Gabrielle; Karimi, Mojgan; Jiao, Yue; Damiola, Francesca; Barjhoux, Laure; Le Gal, Dorothée; Beauvallet, Juana; Mebirouk, Noura; Cavaciuti, Eve; Chiesa, Jean; Floquet, Anne; Audebert‐Bellanger, Séverine; Giraud, Sophie; Fre... Journal: International journal of cancer Issue: Volume 148:Issue 8(2021) Page Start: 1895 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. How and when to refer patients for oncogenetic counseling in the era of PARP inhibitors. (February 2020) Authors: Neviere, Zoé; De La Motte Rouge, Thibault; Floquet, Anne; Johnson, Alison; Berthet, Pascaline; Joly, Florence Journal: Therapeutic advances in medical oncology Issue: Volume 12(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32, 295 women. Issue 1 (December 2016) Authors: Rebbeck, Timothy; Friebel, Tara; Mitra, Nandita; Wan, Fei; Chen, Stephanie; Andrulis, Irene; Apostolou, Paraskevi; Arnold, Norbert; Arun, Banu; Barrowdale, Daniel; Benitez, Javier; Berger, Raanan; Berthet, Pascaline; Borg, Ake; Buys, Saundra; Caldes, Trinidad; Carter, Jonathan; Chiquette, Jocelyn... Journal: Breast cancer research Issue: Volume 18:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Landscape of pathogenic variations in a panel of 34 genes and cancer risk estimation from 5131 HBOC families. (December 2018) Authors: Castéra, Laurent; Harter, Valentin; Muller, Etienne; Krieger, Sophie; Goardon, Nicolas; Ricou, Agathe; Rousselin, Antoine; Paimparay, Germain; Legros, Angelina; Bruet, Olivia; Quesnelle, Céline; Domin, Florian; San, Chankannira; Brault, Baptiste; Fouillet, Robin; Abadie, Caroline; Béra, Odile; Be... Journal: Genetics in medicine Issue: Volume 20:Number 12(2018) Page Start: 1677 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗