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...

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

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

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

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

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

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

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

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

por 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
Publicado 2014

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

por 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
Publicado en Medicine (Baltimore) (2020)

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

por 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
Publicado en J Pathol Clin Res (2016)

Telomere status in chronic lymphocytic leukemia with TP53 disruption

por 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
Publicado en Oncotarget (2016)

Is BRCA2 involved in early onset colorectal cancer risk?

por 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
Publicado en Clin Genet (2019)

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

por 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
Publicado en Hered Cancer Clin Pract (2019)

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

por 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
Publicado en 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

por 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
Publicado en BMC Med Genet (2015)