Pitch-based carbon/nano-silicon composite, an efficient anode for Li-ion batteries

por Escamilla-Pérez, Angel Manuel, Roland, Aude, Giraud, Sophie, Guiraud, Céline, Virieux, Héloïse, Demoulin, Kévin, Oudart, Yohan, Louvain, Nicolas, Monconduit, Laure
Publicado 2019

Pheochromocytoma, paragangliomas, and pituitary adenoma: An unusual association in a patient with an SDHD mutation. Case report

por Lemelin, Annie, Lapoirie, Marion, Abeillon, Juliette, Lasolle, Hélène, Giraud, Sophie, Philouze, Pierre, Ceruse, Philippe, Raverot, Gérald, Vighetto, Alain, Borson-Chazot, Françoise
Publicado 2019

Sequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasia

por Giraud, Sophie, Bardel, Claire, Dupuis-Girod, Sophie, Carette, Marie-France, Gilbert-Dussardier, Brigitte, Riviere, Sophie, Saurin, Jean-Christophe, Eyries, Mélanie, Patri, Sylvie, Decullier, Evelyne, Calender, Alain, Lesca, Gaëtan
Publicado 2020

Renal cell tumour characteristics in patients with the Birt-Hogg-Dubé cancer susceptibility syndrome: a retrospective, multicentre study

por Benusiglio, Patrick R, Giraud, Sophie, Deveaux, Sophie, Méjean, Arnaud, Correas, Jean-Michel, Joly, Dominique, Timsit, Marc-Olivier, Ferlicot, Sophie, Verkarre, Virginie, Abadie, Caroline, Chauveau, Dominique, Leroux, Dominique, Avril, Marie-Françoise, Cordier, Jean-François, Richard, Stéphane
Publicado 2014

Overview of the Genetic Causes of Hereditary Breast and Ovarian Cancer Syndrome in a Large French Patient Cohort

por Bouras, Ahmed, Guidara, Souhir, Leone, Mélanie, Buisson, Adrien, Martin-Denavit, Tanguy, Dussart, Sophie, Lasset, Christine, Giraud, Sophie, Bonnet-Dupeyron, Marie-Noëlle, Kherraf, Zine-Eddine, Sanlaville, Damien, Fert-Ferrer, Sandra, Lebrun, Marine, Bonadona, Valerie, Calender, Alain, Boutry-Kryza, Nadia
Publicado 2023

Publisher Correction: Clinical outcome of breast cancer in carriers of BRCA1 and BRCA2 mutations according to molecular subtypes

por De Talhouet, Solene, Peron, Julien, Vuilleumier, Aurelie, Friedlaender, Alex, Viassolo, Valeria, Ayme, Aurélie, Bodmer, Alexandre, Treilleux, Isabelle, Lang, Noemie, Tille, Jean-Christophe, Chappuis, Pierre O., Buisson, Adrien, Giraud, Sophie, Lasset, Christine, Bonadona, Valerie, Trédan, Olivier, Labidi-Galy, S. Intidhar
Publicado 2020

Clinical outcome of breast cancer in carriers of BRCA1 and BRCA2 mutations according to molecular subtypes

por Talhouet, Solene De, Peron, Julien, Vuilleumier, Aurelie, Friedlaender, Alex, Viassolo, Valeria, Ayme, Aurélie, Bodmer, Alexandre, Treilleux, Isabelle, Lang, Noemie, Tille, Jean- Christophe, Chappuis, Pierre O., Buisson, Adrien, Giraud, Sophie, Lasset, Christine, Bonadona, Valerie, Trédan, Olivier, Labidi-Galy, S.Intidhar
Publicado 2020

Integrative analysis of dysregulated microRNAs and mRNAs in multiple recurrent synchronized renal tumors from patients with von Hippel-Lindau disease

por Gattolliat, Charles-Henry, Couvé, Sophie, Meurice, Guillaume, Oréar, Cédric, Droin, Nathalie, Chiquet, Mathieu, Ferlicot, Sophie, Verkarre, Virginie, Vasiliu, Viorel, Molinié, Vincent, Méjean, Arnaud, Dessen, Philippe, Giraud, Sophie, Bressac-De-Paillerets, Brigitte, Gardie, Betty, Teh, Bin Tean, Richard, Stéphane, Gad, Sophie
Publicado 2018

Genetic variation in the functional ENG allele inherited from the non-affected parent associates with presence of pulmonary arteriovenous malformation in hereditary hemorrhagic tel...

por Letteboer, Tom G. W., Benzinou, Michael, Merrick, Christopher B., Quigley, David A., Zhau, Kechen, Kim, Il-Jin, To, Minh D., Jablons, David M., van Amstel, Johannes K. P., Westermann, Cornelius J. J., Giraud, Sophie, Dupuis-Girod, Sophie, Lesca, Gaetan, Berg, Jonathan H., Balmain, Allan, Akhurst, Rosemary J.
Publicado 2015

International initiative for a curated SDHB variant database improving the diagnosis of hereditary paraganglioma and pheochromocytoma

por Ben Aim, Laurene, Maher, Eamonn R, Cascon, Alberto, Barlier, Anne, Giraud, Sophie, Ercolino, Tonino, Pigny, Pascal, Clifton-Bligh, Roderick J, Mirebeau-Prunier, Delphine, Mohamed, Amira, Favier, Judith, Gimenez-Roqueplo, Anne-Paule, Schiavi, Francesca, Toledo, Rodrigo A, Dahia, Patricia L, Robledo, Mercedes, Bayley, Jean Pierre, Burnichon, Nelly
Publicado 2022

Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated with up-regulation of mitochondrial gene expression

por Klomp, Jeff A, Petillo, David, Niemi, Natalie M, Dykema, Karl J, Chen, Jindong, Yang, Ximing J, Sääf, Annika, Zickert, Peter, Aly, Markus, Bergerheim, Ulf, Nordenskjöld, Magnus, Gad, Sophie, Giraud, Sophie, Denoux, Yves, Yonneau, Laurent, Méjean, Arnaud, Vasiliu, Viorel, Richard, Stéphane, MacKeigan, Jeffrey P, Teh, Bin T, Furge, Kyle A
Publicado 2010

Genomic expression and single-nucleotide polymorphism profiling discriminates chromophobe renal cell carcinoma and oncocytoma

por Tan, Min-Han, Wong, Chin Fong, Tan, Hwei Ling, Yang, Ximing J, Ditlev, Jonathon, Matsuda, Daisuke, Khoo, Sok Kean, Sugimura, Jun, Fujioka, Tomoaki, Furge, Kyle A, Kort, Eric, Giraud, Sophie, Ferlicot, Sophie, Vielh, Philippe, Amsellem-Ouazana, Delphine, Debré, Bernard, Flam, Thierry, Thiounn, Nicolas, Zerbib, Marc, Benoît, Gérard, Droupy, Stéphane, Molinié, Vincent, Vieillefond, Annick, Tan, Puay Hoon, Richard, Stéphane, Teh, Bin Tean
Publicado 2010

Germline mutations in the new E1’ cryptic exon of the VHL gene in patients with tumours of von Hippel-Lindau disease spectrum or with paraganglioma

por Buffet, Alexandre, Calsina, Bruna, Flores, Shahida, Giraud, Sophie, Lenglet, Marion, Romanet, Pauline, Deflorenne, Elisa, Aller, Javier, Bourdeau, Isabelle, Bressac-de Paillerets, Brigitte, Calatayud, María, Dehais, Caroline, De Mones Del Pujol, Erwan, Elenkova, Atanaska, Herman, Philippe, Kamenický, Peter, Lejeune, Sophie, Sadoul, Jean Louis, Barlier, Anne, Richard, Stephane, Favier, Judith, Burnichon, Nelly, Gardie, Betty, Dahia, Patricia L, Robledo, Mercedes, Gimenez-Roqueplo, Anne-Paule
Publicado 2020

GEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Pathogenic Variant Carriers

por Lesueur, Fabienne, Mebirouk, Noura, Jiao, Yue, Barjhoux, Laure, Belotti, Muriel, Laurent, Maïté, Léone, Mélanie, Houdayer, Claude, Bressac-de Paillerets, Brigitte, Vaur, Dominique, Sobol, Hagay, Noguès, Catherine, Longy, Michel, Mortemousque, Isabelle, Fert-Ferrer, Sandra, Mouret-Fourme, Emmanuelle, Pujol, Pascal, Venat-Bouvet, Laurence, Bignon, Yves-Jean, Leroux, Dominique, Coupier, Isabelle, Berthet, Pascaline, Mari, Véronique, Delnatte, Capucine, Gesta, Paul, Collonge-Rame, Marie-Agnès, Giraud, Sophie, Bonadona, Valérie, Baurand, Amandine, Faivre, Laurence, Buecher, Bruno, Lasset, Christine, Gauthier-Villars, Marion, Damiola, Francesca, Mazoyer, Sylvie, Caputo, Sandrine M., Andrieu, Nadine, Stoppa-Lyonnet, Dominique
Publicado 2018

Gene‐ and pathway‐level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility

por Lonjou, Christine, Eon‐Marchais, Séverine, Truong, Thérèse, Dondon, Marie‐Gabrielle, Karimi, Mojgan, Jiao, Yue, Damiola, Francesca, Barjhoux, Laure, Le Gal, Dorothée, Beauvallet, Juana, Mebirouk, Noura, Cavaciuti, Eve, Chiesa, Jean, Floquet, Anne, Audebert‐Bellanger, Séverine, Giraud, Sophie, Frebourg, Thierry, Limacher, Jean‐Marc, Gladieff, Laurence, Mortemousque, Isabelle, Dreyfus, Hélène, Lejeune‐Dumoulin, Sophie, Lasset, Christine, Venat‐Bouvet, Laurence, Bignon, Yves‐Jean, Pujol, Pascal, Maugard, Christine M., Luporsi, Elisabeth, Bonadona, Valérie, Noguès, Catherine, Berthet, Pascaline, Delnatte, Capucine, Gesta, Paul, Lortholary, Alain, Faivre, Laurence, Buecher, Bruno, Caron, Olivier, Gauthier‐Villars, Marion, Coupier, Isabelle, Mazoyer, Sylvie, Monraz, Luis‐Cristobal, Kondratova, Maria, Kuperstein, Inna, Guénel, Pascal, Barillot, Emmanuel, Stoppa‐Lyonnet, Dominique, Andrieu, Nadine, Lesueur, Fabienne
Publicado 2021

Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation

por Ribeiro Guerra, Maximiliano, Coignard, Juliette, Eon-Marchais, Séverine, Dondon, Marie-Gabrielle, Le Gal, Dorothée, Beauvallet, Juana, Mebirouk, Noura, Belotti, Muriel, Caron, Olivier, Gauthier-Villars, Marion, Coupier, Isabelle, Buecher, Bruno, Lortholary, Alain, Fricker, Jean-Pierre, Gesta, Paul, Noguès, Catherine, Faivre, Laurence, Berthet, Pascaline, Luporsi, Elisabeth, Delnatte, Capucine, Bonadona, Valérie, Maugard, Christine M., Pujol, Pascal, Lasset, Christine, Longy, Michel, Bignon, Yves-Jean, Adenis-Lavignasse, Claude, Venat-Bouvet, Laurence, Dreyfus, Hélène, Gladieff, Laurence, Mortemousque, Isabelle, Audebert-Bellanger, Séverine, Soubrier, Florent, Giraud, Sophie, Lejeune-Dumoulin, Sophie, Limacher, Jean-Marc, Chiesa, Jean, Fajac, Anne, Floquet, Anne, Eisinger, François, Tinat, Julie, Fert-Ferrer, Sandra, Colas, Chrystelle, Frebourg, Thierry, Damiola, Francesca, Barjhoux, Laure, Cavaciuti, Eve, Mazoyer, Sylvie, Tardivon, Anne, Lesueur, Fabienne, Stoppa-Lyonnet, Dominique, Andrieu, Nadine
Publicado 2021

Clinical relevance of 8q23, 15q13 and 18q21 SNP genotyping to evaluate colorectal cancer risk

por Baert-Desurmont, Stéphanie, Charbonnier, Françoise, Houivet, Estelle, Ippolito, Lorena, Mauillon, Jacques, Bougeard, Marion, Abadie, Caroline, Malka, David, Duffour, Jacqueline, Desseigne, Françoise, Colas, Chrystelle, Pujol, Pascal, Lejeune, Sophie, Dugast, Catherine, Buecher, Bruno, Faivre, Laurence, Leroux, Dominique, Gesta, Paul, Coupier, Isabelle, Guimbaud, Rosine, Berthet, Pascaline, Manouvrier, Sylvie, Cauchin, Estelle, Prieur, Fabienne, Laurent-Puig, Pierre, Lebrun, Marine, Jonveaux, Philippe, Chiesa, Jean, Caron, Olivier, Morin-Meschin, Marie-Emmanuelle, Polycarpe-Osaer, Florence, Giraud, Sophie, Zaanan, Aziz, Bonnet, Delphine, Mansuy, Ludovic, Bonadona, Valérie, El Chehadeh, Salima, Duhoux, François, Gauthier-Villars, Marion, Saurin, Jean-Christophe, Collonge-Rame, Marie- Agnès, Brugières, Laurence, Wang, Qing, Bressac-de Paillerets, Brigitte, Rey, Jean-Marc, Toulas, Christine, Buisine, Marie-Pierre, Bronner, Myriam, Sokolowska, Joanna, Hardouin, Agnès, Cailleux, Anne-Françoise, Sebaoui, Hakim, Blot, Julien, Tinat, Julie, Benichou, Jacques, Frebourg, Thierry
Publicado 2016

TUMOSPEC: A Nation-Wide Study of Hereditary Breast and Ovarian Cancer Families with a Predicted Pathogenic Variant Identified through Multigene Panel Testing

por Lesueur, Fabienne, Eon-Marchais, Séverine, Bonnet-Boissinot, Sarah, Beauvallet, Juana, Dondon, Marie-Gabrielle, Golmard, Lisa, Rouleau, Etienne, Garrec, Céline, Martinez, Mathilde, Toulas, Christine, Nguyen, Tan Dat, Brayotel, Fanny, Crivelli, Louise, Maugard, Christine M., Bubien, Virginie, Sevenet, Nicolas, Gesta, Paul, Chieze-Valero, Stéphanie, Nambot, Sophie, Goussot, Vincent, Mari, Véronique, Popovici, Cornel, Prieur, Fabienne, Morin-Meschin, Marie-Emmanuelle, Tinat, Julie, Lortholary, Alain, Dreyfus, Hélène, Bidart, Marie, Collonge-Rame, Marie-Agnès, Mozelle-Nivoix, Monique, Gladieff, Laurence, Giraud, Sophie, Boutry-Kryza, Nadia, Chiesa, Jean, Denizeau, Philippe, Bignon, Yves-Jean, Uhrhammer, Nancy, Cohen-Haguenauer, Odile, Vilquin, Paul, Mailliez, Audrey, Coupier, Isabelle, Rey, Jean-Marc, Lacaze, Elodie, Béra, Odile, Colas, Chrystelle, Coulet, Florence, Delnatte, Capucine, Houdayer, Claude, Lasset, Christine, Lemonnier, Jérôme, Longy, Michel, Noguès, Catherine, Stoppa-Lyonnet, Dominique, Vaur, Dominique, Andrieu, Nadine, Caron, Olivier
Publicado 2021

Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing

por Girard, Elodie, Eon‐Marchais, Séverine, Olaso, Robert, Renault, Anne‐Laure, Damiola, Francesca, Dondon, Marie‐Gabrielle, Barjhoux, Laure, Goidin, Didier, Meyer, Vincent, Le Gal, Dorothée, Beauvallet, Juana, Mebirouk, Noura, Lonjou, Christine, Coignard, Juliette, Marcou, Morgane, Cavaciuti, Eve, Baulard, Céline, Bihoreau, Marie‐Thérèse, Cohen‐Haguenauer, Odile, Leroux, Dominique, Penet, Clotilde, Fert‐Ferrer, Sandra, Colas, Chrystelle, Frebourg, Thierry, Eisinger, François, Adenis, Claude, Fajac, Anne, Gladieff, Laurence, Tinat, Julie, Floquet, Anne, Chiesa, Jean, Giraud, Sophie, Mortemousque, Isabelle, Soubrier, Florent, Audebert‐Bellanger, Séverine, Limacher, Jean‐Marc, Lasset, Christine, Lejeune‐Dumoulin, Sophie, Dreyfus, Hélène, Bignon, Yves‐Jean, Longy, Michel, Pujol, Pascal, Venat‐Bouvet, Laurence, Bonadona, Valérie, Berthet, Pascaline, Luporsi, Elisabeth, Maugard, Christine M., Noguès, Catherine, Delnatte, Capucine, Fricker, Jean‐Pierre, Gesta, Paul, Faivre, Laurence, Lortholary, Alain, Buecher, Bruno, Caron, Olivier, Gauthier‐Villars, Marion, Coupier, Isabelle, Servant, Nicolas, Boland, Anne, Mazoyer, Sylvie, Deleuze, Jean‐François, Stoppa‐Lyonnet, Dominique, Andrieu, Nadine, Lesueur, Fabienne
Publicado 2018

GENESIS: a French national resource to study the missing heritability of breast cancer

por Sinilnikova, Olga M., Dondon, Marie-Gabrielle, Eon-Marchais, Séverine, Damiola, Francesca, Barjhoux, Laure, Marcou, Morgane, Verny-Pierre, Carole, Sornin, Valérie, Toulemonde, Lucie, Beauvallet, Juana, Le Gal, Dorothée, Mebirouk, Noura, Belotti, Muriel, Caron, Olivier, Gauthier-Villars, Marion, Coupier, Isabelle, Buecher, Bruno, Lortholary, Alain, Dugast, Catherine, Gesta, Paul, Fricker, Jean-Pierre, Noguès, Catherine, Faivre, Laurence, Luporsi, Elisabeth, Berthet, Pascaline, Delnatte, Capucine, Bonadona, Valérie, Maugard, Christine M., Pujol, Pascal, Lasset, Christine, Longy, Michel, Bignon, Yves-Jean, Adenis, Claude, Venat-Bouvet, Laurence, Demange, Liliane, Dreyfus, Hélène, Frenay, Marc, Gladieff, Laurence, Mortemousque, Isabelle, Audebert-Bellanger, Séverine, Soubrier, Florent, Giraud, Sophie, Lejeune-Dumoulin, Sophie, Chevrier, Annie, Limacher, Jean-Marc, Chiesa, Jean, Fajac, Anne, Floquet, Anne, Eisinger, François, Tinat, Julie, Colas, Chrystelle, Fert-Ferrer, Sandra, Penet, Clotilde, Frebourg, Thierry, Collonge-Rame, Marie-Agnès, Barouk-Simonet, Emmanuelle, Layet, Valérie, Leroux, Dominique, Cohen-Haguenauer, Odile, Prieur, Fabienne, Mouret-Fourme, Emmanuelle, Cornélis, François, Jonveaux, Philippe, Bera, Odile, Cavaciuti, Eve, Tardivon, Anne, Lesueur, Fabienne, Mazoyer, Sylvie, Stoppa-Lyonnet, Dominique, Andrieu, Nadine
Publicado 2016