Works matching AU Bonnet, Françoise

Results: 15

Spectrum of CREBBP gene dosage anomalies in Rubinstein–Taybi Syndrome patients.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 8, p. 843, doi. 10.1038/sj.ejhg.5201847

By:

Stef, Marianne;
Simon, Delphine;
Mardirossian, Béatrice;
Delrue, Marie-Ange;
Burgelin, Ingrid;
Hubert, Christophe;
Marche, Michèle;
Bonnet, Françoise;
Gorry, Philippe;
Longy, Michel;
Lacombe, Didier;
Coupry, Isabelle;
Arveiler, Benoît

Publication type:

Article

Segmental overgrowth, lipomatosis, arteriovenous malformation and epidermal nevus (SOLAMEN) syndrome is related to mosaic PTEN nullizygosity.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 7, p. 767, doi. 10.1038/sj.ejhg.5201823

By:

Caux, Frédéric;
Plauchu, Henri;
Chibon, Frédéric;
Faivre, Laurence;
Fain, Olivier;
Vabres, Pierre;
Bonnet, Françoise;
Selma, Zied Ben;
Laroche, Liliane;
Gérard, Marion;
Longy, Michel

Publication type:

Article

Genome-Wide Analysis of Cutaneous T-Cell Lymphomas Identifies Three Clinically Relevant Classes.

Published in:

Journal of Investigative Dermatology, 2010, v. 130, n. 6, p. 1707, doi. 10.1038/jid.2010.8

By:

Laharanne, Elodie;
Oumouhou, Naïma;
Bonnet, Françoise;
Carlotti, Martina;
Gentil, Catherine;
Chevret, Edith;
Jouary, Thomas;
Longy, Michel;
Vergier, Béatrice;
Beylot-Barry, Marie;
Merlio, Jean-Philippe

Publication type:

Article

Allelic imbalance, including deletion of PTEN/MMAC1, at the Cowden disease locus on 10q22-23, in hamartomas from patients with cowden syndrome and germline PTEN mutation.

Published in:

Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 61, doi. 10.1002/(SICI)1098-2264(199801)21:1<61::AID-GCC8>3.0.CO;2-6

By:

Marsh, Debbie J.;
Dahia, Patricia L. M.;
Coulon, Valérie;
Zheng, Zimu;
Dorion-Bonnet, Françoise;
Call, Katherine M.;
Little, Randall;
Lin, Albert Y.;
Eeles, Rosalind A.;
Goldstein, Alisa M.;
Hodgson, Shirley V.;
Richardson, Anne-Louise;
Robinson, Bruce G.;
Weber, H. Christian;
Longy, Michel;
Eng, Charis

Publication type:

Article

Loss of heterozygosity on chromosome arm 16q in breast cancer metastases.

Published in:

Genes, Chromosomes & Cancer, 1997, v. 19, n. 3, p. 185, doi. 10.1002/(SICI)1098-2264(199707)19:3<185::AID-GCC8>3.0.CO;2-U

By:

Driouch, Keltouma;
Dorion-Bonnet, Françoise;
Briffod, Marianne;
Champème, Marie-Hélène;
Longy, Michel;
Lidereau, Rosette

Publication type:

Article

FGFRI and PLAT genes and DNA amplification at 8p 12 in breast and ovarian cancers.

Published in:

Genes, Chromosomes & Cancer, 1993, v. 7, n. 4, p. 219, doi. 10.1002/gcc.2870070407

By:

Theillet, Charles;
Adelaide, José;
Louason, Geneviève;
Bonnet-Dorion, Françoise;
Jacquemier, Jocelyne;
Adnane, Jalila;
Longy, Michel;
Katsaros, Dionisi;
Sismondi, Piero;
Gaudray, Patrick;
Birnbaum, Daniel

Publication type:

Article

Comprehensive analysis of PTEN status in breast carcinomas.

Published in:

International Journal of Cancer, 2013, v. 133, n. 2, p. 323, doi. 10.1002/ijc.28021

By:

Jones, Natalie;
Bonnet, Françoise;
Sfar, Sana;
Lafitte, Marie;
Lafon, Delfine;
Sierankowski, Ghislaine;
Brouste, Véronique;
Banneau, Guillaume;
Tunon de Lara, Christine;
Debled, Marc;
MacGrogan, Gaëtan;
Longy, Michel;
Sevenet, Nicolas

Publication type:

Article

Alterations of the p53 and PIK3CA/AKT/mTOR pathways in angiosarcomas.

Published in:

Cancer (0008543X), 2012, v. 118, n. 23, p. 5878, doi. 10.1002/cncr.27614

By:

Italiano, Antoine;
Chen, Chun-Liang;
Thomas, Rachael;
Breen, Matthew;
Bonnet, Françoise;
Sevenet, Nicolas;
Longy, Michel;
Maki, Robert G.;
Coindre, Jean-Michel;
Antonescu, Cristina R.

Publication type:

Article

Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effort.

Published in:

Nucleic Acids Research, 2020, v. 48, n. 3, p. 1600, doi. 10.1093/nar/gkz1212

By:

Leman, Raphaël;
Gaildrat, Pascaline;
Le Gac, Gérald;
Ka, Chandran;
Fichou, Yann;
Audrezet, Marie-Pierre;
Caux-Moncoutier, Virginie;
Caputo, Sandrine M;
Boutry-Kryza, Nadia;
Léone, Mélanie;
Mazoyer, Sylvie;
Bonnet-Dorion, Françoise;
Sevenet, Nicolas;
Guillaud-Bataille, Marine;
Rouleau, Etienne;
Bressac-de Paillerets, Brigitte;
Wappenschmidt, Barbara;
Rossing, Maria;
Muller, Danielle;
Bourdon, Violaine

Publication type:

Article

5′ Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints.

Published in:

Cancers, 2021, v. 13, n. 13, p. 3171, doi. 10.3390/cancers13133171

By:

Caputo, Sandrine M.;
Telly, Dominique;
Briaux, Adrien;
Sesen, Julie;
Ceppi, Maurizio;
Bonnet, Françoise;
Bourdon, Violaine;
Coulet, Florence;
Castera, Laurent;
Delnatte, Capucine;
Hardouin, Agnès;
Mazoyer, Sylvie;
Schultz, Inès;
Sevenet, Nicolas;
Uhrhammer, Nancy;
Bonnet, Céline;
Tilkin-Mariamé, Anne-Françoise;
Houdayer, Claude;
Moncoutier, Virginie;
Andrieu, Catherine

Publication type:

Article

A homozygous balanced reciprocal translocation suggests LINC00237 as a candidate gene for MOMO (macrosomia, obesity, macrocephaly, and ocular abnormalities) syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 11, p. 2849, doi. 10.1002/ajmg.a.35694

By:

Vu, Phi Yen;
Toutain, Jérôme;
Cappellen, David;
Delrue, Marie-Ange;
Daoud, Hussein;
Moneim, Azza Abd El;
Barat, Pascal;
Montaubin, Orianne;
Bonnet, Françoise;
Dai, Zong Qi;
Philippe, Christophe;
Tran, Cong Toai;
Rooryck, Caroline;
Arveiler, Benoît;
Saura, Robert;
Briault, Sylvain;
Lacombe, Didier;
Taine, Laurence

Publication type:

Article

Combined tumor genomic profiling and exome sequencing in a breast cancer family implicates ATM in tumorigenesis: A proof of principle study.

Published in:

Genes, Chromosomes & Cancer, 2017, v. 56, n. 11, p. 788, doi. 10.1002/gcc.22482

By:

Bubien, Virginie;
Bonnet, Françoise;
Dupiot‐Chiron, Jennifer;
Barouk‐Simonet, Emmanuelle;
Jones, Natalie;
de Reynies, Aurélien;
MacGrogan, Gaëtan;
Sevenet, Nicolas;
Letouzé, Eric;
Longy, Michel

Publication type:

Article

Deletion of Chromosomes 13q and 14q Is a Common Feature of Tumors with BRCA2 Mutations.

Published in:

PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0052079

By:

Rouault, Audrey;
Banneau, Guillaume;
MacGrogan, Gaëtan;
Jones, Natalie;
Elarouci, Nabila;
Barouk-Simonet, Emmanuelle;
Venat, Laurence;
Coupier, Isabelle;
Letouzé, Eric;
Aurélien de Reyniés;
Bonnet, Françoise;
Iggo, Richard;
Sévenet, Nicolas;
Longy, Michel

Publication type:

Article

In vivo patterns of Bcl-2 family protein expression in breast carcinomas in relation to apoptosis.

Published in:

Journal of Pathology, 1999, v. 187, n. 4, p. 410, doi. 10.1002/(SICI)1096-9896(199903)187:4<410::AID-PATH266>3.0.CO;2-F

By:

Rochaix, Philippe;
Krajewski, Stanislaw;
Reed, John C.;
Bonnet, Françoise;
Voigt, Jean-Jacques;
Brousset, Pierre

Publication type:

Article

Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/ in vitro studies on BRCA1 and BRCA2 variants.

Published in:

Human Mutation, 2012, v. 33, n. 8, p. 1228, doi. 10.1002/humu.22101

By:

Houdayer, Claude;
Caux-Moncoutier, Virginie;
Krieger, Sophie;
Barrois, Michel;
Bonnet, Françoise;
Bourdon, Violaine;
Bronner, Myriam;
Buisson, Monique;
Coulet, Florence;
Gaildrat, Pascaline;
Lefol, Cédrick;
Léone, Mélanie;
Mazoyer, Sylvie;
Muller, Danielle;
Remenieras, Audrey;
Révillion, Françoise;
Rouleau, Etienne;
Sokolowska, Joanna;
Vert, Jean-Philippe;
Lidereau, Rosette

Publication type:

Article