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Author/Creator Sobol, Hagay

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. Bayesian predictive model to assess BRCA2 mutational status according to clinical history: Early onset, metastatic phenotype or family history of breast/ovary cancer. Issue 6 (18th February 2021)

Authors:
Leon, Priscilla; Cancel‐Tassin, Geraldine; Bourdon, Violaine; Buecher, Bruno; Oudard, Stephane; Brureau, Laurent; Jouffe, Lionel; Blanchet, Pascal; Stoppa‐Lyonnet, Dominique; Coulet, Florence; Sobol, Hagay; Cussenot, Olivier
Journal:
Prostate
Issue:
Volume 81:Issue 6(2021)
Page Start:
318
Record Type:
Journal Article
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3. BRCA Share: A Collection of Clinical BRCA Gene Variants. Issue 12 (28th September 2016)

Authors:
Béroud, Christophe; Letovsky, Stanley I.; Braastad, Corey D.; Caputo, Sandrine M.; Beaudoux, Olivia; Bignon, Yves Jean; Bressac‐De Paillerets, Brigitte; Bronner, Myriam; Buell, Crystal M.; Collod‐Béroud, Gwenaëlle; Coulet, Florence; Derive, Nicolas; Divincenzo, Christina; Elzinga, Christopher D.;...
Journal:
Human mutation
Issue:
Volume 37:Issue 12(2016)
Page Start:
1318
Record Type:
Journal Article
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4. 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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5. Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAP. Issue 10 (3rd August 2010)

Authors:
Lagarde, Arnaud; Rouleau, Etienne; Ferrari, Anthony; Noguchi, Tetsuro; Qiu, Jinghua; Briaux, Adrien; Bourdon, Violaine; Rémy, Virginie; Gaildrat, Pascaline; Adélaïde, José; Birnbaum, Daniel; Lidereau, Rosette; Sobol, Hagay; Olschwang, Sylviane
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 10(2010)
Page Start:
721
Record Type:
Journal Article
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6. Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders. Issue 1 (December 2016)

Authors:
Latger-Cannard, Veronique; Philippe, Christophe; Bouquet, Alexandre; Baccini, Veronique; Alessi, Marie-Christine; Ankri, Annick; Bauters, Anne; Bayart, Sophie; Cornillet-Lefebvre, Pascale; Daliphard, Sylvie; Mozziconacci, Marie-Joelle; Renneville, Aline; Ballerini, Paola; Leverger, Guy; Sobol, Ha...
Journal:
Orphanet journal of rare diseases
Issue:
Volume 11:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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7. 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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