Inhibition of the Proprotein Convertases Represses the Invasiveness of Human Primary Melanoma Cells with Altered p53, CDKN2A and N-Ras Genes

Por Lalou, Claude, Scamuffa, Nathalie, Mourah, Samia, Plassa, Francois, Podgorniak, Marie-Pierre, Soufir, Nadem, Dumaz, Nicolas, Calvo, Fabien, Basset-Seguin, Nicole, Khatib, Abdel-Majid
Publicado em 2010

A Large French Case-Control Study Emphasizes the Role of Rare Mc1R Variants in Melanoma Risk

Por Hu, Hui-Han, Benfodda, Mériem, Dumaz, Nicolas, Gazal, Steven, Descamps, Vincent, Bourillon, Agnès, Basset-Seguin, Nicole, Riffault, Angélique, Ezzedine, Khaled, Bagot, Martine, Bensussan, Armand, Saiag, Philippe, Grandchamp, Bernard, Soufir, Nadem
Publicado em 2014

Genotype/Phenotype Analyses for 53 Crohn’s Disease Associated Genetic Polymorphisms

Por Jung, Camille, Colombel, Jean-Frédéric, Lemann, Marc, Beaugerie, Laurent, Allez, Matthieu, Cosnes, Jacques, Vernier-Massouille, Gwenola, Gornet, Jean-Marc, Gendre, Jean-Pierre, Cezard, Jean-Pierre, Ruemmele, Frank M., Turck, Dominique, Merlin, Françoise, Zouali, Habib, Libersa, Christian, Dieudé, Philippe, Soufir, Nadem, Thomas, Gilles, Hugot, Jean-Pierre
Publicado em 2012

Inherited variants in the MC1R gene and survival from cutaneous melanoma: a BioGenoMEL study

Por Davies, John R, Randerson-Moor, Juliette, Kukalizch, Kairen, Harland, Mark, Kumar, Rajiv, Madhusudan, Srinivasan, Nagore, Eduardo, Hansson, Johan, Höiom, Veronica, Ghiorzo, Paola, Gruis, Nelleke A, Kanetsky, Peter A, Wendt, Judith, Pjanova, Dace, Puig, Susana, Saiag, Philippe, Schadendorf, Dirk, Soufir, Nadem, Okamoto, Ichiro, Affleck, Paul, García-Casado, Zaida, Ogbah, Zighereda, Ozola, Aija, Queirolo, Paola, Sucker, Antje, Barrett, Jennifer H, van Doorn, Remco, Bishop, D Timothy, Newton-Bishop, Julia
Publicado em 2012

Germline BAP1 Mutations Predispose to Renal Cell Carcinomas

Por Popova, Tatiana, Hebert, Lucie, Jacquemin, Virginie, Gad, Sophie, Caux-Moncoutier, Virginie, Dubois-d’Enghien, Catherine, Richaudeau, Bénédicte, Renaudin, Xavier, Sellers, Jason, Nicolas, André, Sastre-Garau, Xavier, Desjardins, Laurence, Gyapay, Gabor, Raynal, Virginie, Sinilnikova, Olga M., Andrieu, Nadine, Manié, Elodie, de Pauw, Antoine, Gesta, Paul, Bonadona, Valérie, Maugard, Christine M., Penet, Clotilde, Avril, Marie-Françoise, Barillot, Emmanuel, Cabaret, Odile, Delattre, Olivier, Richard, Stéphane, Caron, Olivier, Benfodda, Meriem, Hu, Hui-Han, Soufir, Nadem, Bressac-de Paillerets, Brigitte, Stoppa-Lyonnet, Dominique, Stern, Marc-Henri
Publicado em 2013

Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants

Por Puntervoll, Hanne Eknes, Yang, Xiaohong R, Vetti, Hildegunn Høberg, Bachmann, Ingeborg M, Avril, Marie Françoise, Benfodda, Meriem, Catricalà, Caterina, Dalle, Stéphane, Duval-Modeste, Anne B, Ghiorzo, Paola, Grammatico, Paola, Harland, Mark, Hayward, Nicholas K, Hu, Hui-Han, Jouary, Thomas, Martin-Denavit, Tanguy, Ozola, Aija, Palmer, Jane M, Pastorino, Lorenza, Pjanova, Dace, Soufir, Nadem, Steine, Solrun J, Stratigos, Alexander J, Thomas, Luc, Tinat, Julie, Tsao, Hensin, Veinalde, Rūta, Tucker, Margaret A, Bressac-de Paillerets, Brigitte, Newton-Bishop, Julia A, Goldstein, Alisa M, Akslen, Lars A, Molven, Anders
Publicado em 2013

Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations

Por Mercier, Sandra, Küry, Sébastien, Salort-Campana, Emmanuelle, Magot, Armelle, Agbim, Uchenna, Besnard, Thomas, Bodak, Nathalie, Bou-Hanna, Chantal, Bréhéret, Flora, Brunelle, Perrine, Caillon, Florence, Chabrol, Brigitte, Cormier-Daire, Valérie, David, Albert, Eymard, Bruno, Faivre, Laurence, Figarella-Branger, Dominique, Fleurence, Emmanuelle, Ganapathi, Mythily, Gherardi, Romain, Goldenberg, Alice, Hamel, Antoine, Igual, Jeanine, Irvine, Alan D., Israël-Biet, Dominique, Kannengiesser, Caroline, Laboisse, Christian, Le Caignec, Cédric, Mahé, Jean-Yves, Mallet, Stéphanie, MacGowan, Stuart, McAleer, Maeve A., McLean, Irwin, Méni, Cécile, Munnich, Arnold, Mussini, Jean-Marie, Nagy, Peter L., Odel, Jeffrey, O’Regan, Grainne M., Péréon, Yann, Perrier, Julie, Piard, Juliette, Puzenat, Eve, Sampson, Jacinda B., Smith, Frances, Soufir, Nadem, Tanji, Kurenai, Thauvin, Christel, Ulane, Christina, Watson, Rosemarie M., Khumalo, Nonhlanhla P., Mayosi, Bongani M., Barbarot, Sébastien, Bézieau, Stéphane
Publicado no Orphanet J Rare Dis (2015)