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Author/Creator Lasset, Christine

11. 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
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12. First estimates of diffuse gastric cancer risks for carriers of CTNNA1 germline pathogenic variants. Issue 12 (29th August 2022)

Authors:
Coudert, Marie; Drouet, Youenn; Delhomelle, Hélène; Svrcek, Magali; Benusiglio, Patrick R; Coulet, Florence; Clark, Dana Farengo; Katona, Bryson W; van Hest, Liselotte P; van der Kolk, Lizet E; Cats, Annemieke; van Dieren, Jolanda M; Nehoray, Bita; Slavin, Thomas; Spier, Isabel; Hüneburg, Robert;...
Journal:
Journal of medical genetics
Issue:
Volume 59:Issue 12(2022)
Page Start:
1189
Record Type:
Journal Article
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13. Four Years Analysis of Cancer Genetic Clinics Activity in France from 1994 to 1997: A Survey on 801 Patients. Issue 1 (17th June 2013)

Authors:
Sobol, Hagay; Bignon, Yves-Jean; Bonaiti, Catherine; Cuisenier, Jean; Lasset, Christine; Lortholary, Alain; Noguès, Catherine; Stoppa-Lyonnet, Dominique; Eisinger, François; The French Cooperative Network/Groupe Génétique et Cancer de la Fédération Nationale des Centres de Lutte Contre le Cancer,
Journal:
Disease markers
Issue:
Volume 15:Issue 1/3(1999)
Page Start:
15
Record Type:
Journal Article
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14. 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
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15. 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
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16. Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study. (12th October 2018)

Authors:
Qian, Frank; Wang, Shengfeng; Mitchell, Jonathan; McGuffog, Lesley; Barrowdale, Daniel; Leslie, Goska; Oosterwijk, Jan C; Chung, Wendy K; Evans, D Gareth; Engel, Christoph; Kast, Karin; Aalfs, Cora M; Adank, Muriel A; Adlard, Julian; Agnarsson, Bjarni A; Aittomäki, Kristiina; Alducci, Elisa; Andr...
Journal:
Journal of the National Cancer Institute
Issue:
Volume 111:Number 4(2019)
Page Start:
350
Record Type:
Journal Article
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17. 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
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18. Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2. Issue 1 (December 2016)

Authors:
Silvestri, Valentina; Barrowdale, Daniel; Mulligan, Anna; Neuhausen, Susan; Fox, Stephen; Karlan, Beth; Mitchell, Gillian; James, Paul; Thull, Darcy; Zorn, Kristin; Carter, Natalie; Nathanson, Katherine; Domchek, Susan; Rebbeck, Timothy; Ramus, Susan; Nussbaum, Robert; Olopade, Olufunmilayo; Rant...
Journal:
Breast cancer research
Issue:
Volume 18:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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19. Mutational spectrum in a worldwide study of 29, 700 families with BRCA1 or BRCA2 mutations. Issue 5 (12th March 2018)

Authors:
Rebbeck, Timothy R.; Friebel, Tara M.; Friedman, Eitan; Hamann, Ute; Huo, Dezheng; Kwong, Ava; Olah, Edith; Olopade, Olufunmilayo I.; Solano, Angela R.; Teo, Soo‐Hwang; Thomassen, Mads; Weitzel, Jeffrey N.; Chan, TL; Couch, Fergus J.; Goldgar, David E.; Kruse, Torben A.; Palmero, Edenir Inêz; Par...
Journal:
Human mutation
Issue:
Volume 39:Issue 5(2018)
Page Start:
593
Record Type:
Journal Article
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20. Parental disclosure of positive BRCA1/2 mutation status to children 10 years after genetic testing. Issue 6 (2nd July 2020)

Authors:
Troïan, Jaïs; Apostolidis, Thémis; Touzani, Rajae; Mouret-Fourme, Emmanuelle; Stoppa-Lyonnet, Dominique; Lasset, Christine; Berthet, Pascaline; Julian-Reynier, Claire; Mancini, Julien; Noguès, Catherine; Bouhnik, Anne-Déborah
Journal:
Psychology, health & medicine
Issue:
Volume 25:Issue 6(2020)
Page Start:
756
Record Type:
Journal Article
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