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Author/Creator Mortemousque, Isabelle

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
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2. 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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3. 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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4. 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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5. Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma. Issue 4 (12th March 2011)

Authors:
Gardie, Betty; Remenieras, Audrey; Kattygnarath, Darouna; Bombled, Johny; Lefèvre, Sandrine; Perrier-Trudova, Victoria; Rustin, Pierre; Barrois, Michel; Slama, Abdelhamid; Avril, Marie-Françoise; Bessis, Didier; Caron, Olivier; Caux, Frédéric; Collignon, Patrick; Coupier, Isabelle; Cremin, Carol;...
Journal:
Journal of medical genetics
Issue:
Volume 48:Issue 4(2011)
Page Start:
226
Record Type:
Journal Article
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6. SMARCA4‐Mutated Atypical Teratoid/Rhabdoid Tumor with Retained BRG1 Expression. Issue 3 (15th October 2015)

Authors:
Masliah‐Planchon, Julien; Machet, Marie‐Christine; Fréneaux, Paul; Jourdain, Anne; Mortemousque, Isabelle; Raïs, Khadija Aït; Ballet, Stelly; Jouvet, Anne; Figarella‐Branger, Dominique; Delattre, Olivier; Bourdeaut, Franck
Journal:
Pediatric blood & cancer
Issue:
Volume 63:Issue 3(2016)
Page Start:
568
Record Type:
Journal Article
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