BRACAVENIR - impact of a psychoeducational intervention on expectations and coping in young women (aged 18–30 years) exposed to a high familial breast/ovarian cancer risk: study pr...

অনুযায়ী Kwiatkowski, Fabrice, Dessenne, Pascal, Laquet, Claire, Daures, Jean-Pierre, Gay-Bellile, Mathilde, Bignon, Yves-Jean
প্রকাশিত Trials (2016)

Early Onset Multiple Primary Tumors in Atypical Presentation of Cowden Syndrome Identified by Whole-Exome-Sequencing

অনুযায়ী Cavaillé, Mathias, Ponelle-Chachuat, Flora, Uhrhammer, Nancy, Viala, Sandrine, Gay-Bellile, Mathilde, Privat, Maud, Bidet, Yannick, Bignon, Yves-Jean
প্রকাশিত Front Genet (2018)

Feedback of extended panel sequencing in 1530 patients referred for suspicion of hereditary predisposition to adult cancers

অনুযায়ী Cavaillé, Mathias, Uhrhammer, Nancy, Privat, Maud, Ponelle‐Chachuat, Flora, Gay‐Bellile, Mathilde, Lepage, Mathis, Viala, Sandrine, Bidet, Yannick, Bignon, Yves‐Jean
প্রকাশিত Clin Genet (2020)

Analysis of 11 candidate genes in 849 adult patients with suspected hereditary cancer predisposition

অনুযায়ী Cavaillé, Mathias, Uhrhammer, Nancy, Privat, Maud, Ponelle‐Chachuat, Flora, Gay‐Bellile, Mathilde, Lepage, Mathis, Molnar, Ioana, Viala, Sandrine, Bidet, Yannick, Bignon, Yves‐Jean
প্রকাশিত Genes Chromosomes Cancer (2020)

An unusual clinical severity of 16p11.2 deletion syndrome caused by unmasked recessive mutation of CLN3

অনুযায়ী Pebrel-Richard, Céline, Debost-Legrand, Anne, Eymard-Pierre, Eléonore, Greze, Victoria, Kemeny, Stéphan, Gay-Bellile, Mathilde, Gouas, Laetitia, Tchirkov, Andreï, Vago, Philippe, Goumy, Carole, Francannet, Christine
প্রকাশিত 2014

PERCEPTION Trial protocol: Comparison of predictive and prognostic capacities of neutrophil, lymphocyte, and platelet counts and tumor-infiltrating lymphocytes in triple negative b...

অনুযায়ী Lusho, Sejdi, Durando, Xavier, Bidet, Yannick, Molnar, Ioana, Kossai, Myriam, Bernadach, Maureen, Lacrampe, Nathalie, Veyssiere, Hugo, Cavaille, Mathias, Gay-Bellile, Mathilde, Radosevic-Robin, Nina, Abrial, Catherine
প্রকাশিত Medicine (Baltimore) (2020)

ERCC1 and telomere status in breast tumours treated with neoadjuvant chemotherapy and their association with patient prognosis

অনুযায়ী Gay‐Bellile, Mathilde, Romero, Pierre, Cayre, Anne, Véronèse, Lauren, Privat, Maud, Singh, Shalini, Combes, Patricia, Kwiatkowski, Fabrice, Abrial, Catherine, Bignon, Yves‐Jean, Vago, Philippe, Penault‐Llorca, Frédérique, Tchirkov, Andreï
প্রকাশিত J Pathol Clin Res (2016)

Telomere status in chronic lymphocytic leukemia with TP53 disruption

অনুযায়ী Guièze, Romain, Pages, Mélanie, Véronèse, Lauren, Combes, Patricia, Lemal, Richard, Gay-bellile, Mathilde, Chauvet, Martine, Callanan, Mary, Kwiatkowski, Fabrice, Pereira, Bruno, Vago, Philippe, Bay, Jacques-Olivier, Tournilhac, Olivier, Tchirkov, Andreï
প্রকাশিত Oncotarget (2016)

Is BRCA2 involved in early onset colorectal cancer risk?

অনুযায়ী Gay‐Bellile, Mathilde, Privat, Maud, Martins, Alexandra, Caputo, Sandrine M., Pebrel‐Richard, Céline, Cavaillé, Mathias, Viala, Sandrine, Corsini, Carole, Rodrigues, Michael, Barnich, Nicolas, Bidet, Yannick, Uhrhammer, Nancy, Bignon, Yves‐Jean
প্রকাশিত Clin Genet (2019)

BRACAVENIR: an observational study of expectations and coping in young women with high hereditary risk of breast and ovarian cancer

অনুযায়ী Kwiatkowski, Fabrice, Gay-Bellile, Mathilde, Dessenne, Pascal, Laquet, Claire, Boussion, Véronique, Béguinot, Marie, Petit, Marie-Françoise, Grémeau, Anne-Sophie, Verlet, Céline, Chaptal, Charlotte, Broult, Marilyn, Jouvency, Sylvie, Duclos, Martine, Bignon, Yves-Jean
প্রকাশিত Hered Cancer Clin Pract (2019)

TERT promoter status and gene copy number gains: effect on TERT expression and association with prognosis in breast cancer

অনুযায়ী Gay-Bellile, Mathilde, Véronèse, Lauren, Combes, Patricia, Eymard-Pierre, Eleonore, Kwiatkowski, Fabrice, Dauplat, Marie-Mélanie, Cayre, Anne, Privat, Maud, Abrial, Catherine, Bignon, Yves-Jean, Mouret-Reynier, Marie-Ange, Vago, Philippe, Penault-Llorca, Frédérique, Tchirkov, Andrei
প্রকাশিত Oncotarget (2017)

Insertion of an extra copy of Xq22.2 into 1p36 results in functional duplication of the PLP1 gene in a girl with classical Pelizaeus-Merzbacher disease

অনুযায়ী Masliah-Planchon, Julien, Dupont, Céline, Vartzelis, George, Trimouille, Aurélien, Eymard-Pierre, Eléonore, Gay-Bellile, Mathilde, Renaldo, Florence, Dorboz, Imen, Pagan, Cécile, Quentin, Samuel, Elmaleh, Monique, Kotsogianni, Christina, Konstantelou, Elissavet, Drunat, Séverine, Tabet, Anne-Claude, Boespflug-Tanguy, Odile
প্রকাশিত BMC Med Genet (2015)