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...

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

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

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

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

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

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

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

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

Autor 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
Vydáno 2014

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

Autor 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
Vydáno v Medicine (Baltimore) (2020)

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

Autor 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
Vydáno v J Pathol Clin Res (2016)

Telomere status in chronic lymphocytic leukemia with TP53 disruption

Autor 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
Vydáno v Oncotarget (2016)

Is BRCA2 involved in early onset colorectal cancer risk?

Autor 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
Vydáno v Clin Genet (2019)

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

Autor 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
Vydáno v Hered Cancer Clin Pract (2019)

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

Autor 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
Vydáno v 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

Autor 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
Vydáno v BMC Med Genet (2015)