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Plos One|February 28, 2017
Medico-economic impact of MSKCC non-sentinel node prediction nomogram for ER-positive HER2-negative breast cancersHélène Bonsang-Kitzis, Delphine Mouttet-Boizat, Eugénie Guillot, et al.
Human Mutation|June 9, 2012
CFTR mutation combinations producing frequent complex alleles with different clinical and functional outcomesAyman El-Seedy, Emmanuelle Girodon, Caroline Norez, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|November 20, 2010
In vitro antibacterial activity of doripenem against clinical isolates from French teaching hospitals: proposition of zone diameter breakpointsC Lascols, P Legrand, A Mérens, et al.
Cancers|May 14, 2022
Surgical Implications of Advanced Low-Grade Serous Ovarian Cancer: Analysis of the Database of the Tumeurs Malignes Rares Gynécologiques NetworkHélène Bonsang-Kitzis, Nabilah Panchbhaya, Anne-Sophie Bats, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 14, 2019
Interaction between Molecular Subtypes and Stromal Immune Infiltration before and after Treatment in Breast Cancer Patients Treated with Neoadjuvant ChemotherapyAnne-Sophie Hamy, Hélène Bonsang-Kitzis, Diane De Croze, et al.
Oncogene|May 20, 2021
Metastasis-suppressor NME1 controls the invasive switch of breast cancer by regulating MT1-MMP surface clearanceCatalina Lodillinsky, Laetitia Fuhrmann, Marie Irondelle, et al.
Breast Cancer Research and Treatment|January 29, 2018
Lymphovascular invasion after neoadjuvant chemotherapy is strongly associated with poor prognosis in breast carcinomaAnne-Sophie Hamy, Giang-Thanh Lam, Enora Laas, et al.
Gynecologic Oncology|April 4, 2020
Fertility and prognosis of borderline ovarian tumor after conservative management: Results of the multicentric OPTIBOT study by the GINECO & TMRG groupAudrey Chevrot, Nicolas Pouget, Anne-Sophie Bats, et al.
Human Mutation|June 13, 2017
CFTR-France, a national relational patient database for sharing genetic and phenotypic data associated with rare CFTR variantsMireille Claustres, Corinne Thèze, Marie des Georges, et al.
European Journal of Human Genetics : EJHG|December 20, 2017
CHARGE syndrome: a recurrent hotspot of mutations in CHD7 IVS25 analyzed by bioinformatic tools and minigene assaysMarine Legendre, Montserrat Rodriguez-Ballesteros, Massimiliano Rossi, et al.
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