High mitochondrial DNA copy number is associated with longer survival in young patients with glioblastoma

द्वारा Dardaud, Laure-Marie, Bris, Céline, Desquiret-Dumas, Valérie, Boisselier, Blandine, Tabouret, Emeline, Mokhtari, Karima, Figarella-Branger, Dominique, Rousseau, Audrey, Procaccio, Vincent
में प्रकाशित Neuro Oncol (2019)

CBMT-11. HIGH MITOCHONDRIAL DNA COPY NUMBER IS ASSOCIATED WITH LONGER SURVIVAL IN YOUNG PATIENTS WITH GLIOBLASTOMA

द्वारा Rousseau, Audrey, Dardaud, Laure-Marie, Bris, Céline, Desquiret-Dumas, Valérie, Boisselier, Blandine, Tabouret, Emeline, Mokhtari, Karima, Figarella-Branger, Dominique, Procaccio, Vincent
में प्रकाशित Neuro Oncol (2019)

Bioinformatics Tools and Databases to Assess the Pathogenicity of Mitochondrial DNA Variants in the Field of Next Generation Sequencing

द्वारा Bris, Céline, Goudenege, David, Desquiret-Dumas, Valérie, Charif, Majida, Colin, Estelle, Bonneau, Dominique, Amati-Bonneau, Patrizia, Lenaers, Guy, Reynier, Pascal, Procaccio, Vincent
में प्रकाशित Front Genet (2018)

Use of Next-Generation Sequencing for the Molecular Diagnosis of 1,102 Patients With a Autosomal Optic Neuropathy

द्वारा Charif, Majida, Bris, Céline, Goudenège, David, Desquiret-Dumas, Valérie, Colin, Estelle, Ziegler, Alban, Procaccio, Vincent, Reynier, Pascal, Bonneau, Dominique, Lenaers, Guy, Amati-Bonneau, Patrizia
में प्रकाशित Front Neurol (2021)

Stable and Local Reservoirs of Mycobacterium ulcerans Inferred from the Nonrandom Distribution of Bacterial Genotypes, Benin

द्वारा Coudereau, Clément, Besnard, Alban, Robbe-Saule, Marie, Bris, Céline, Kempf, Marie, Johnson, Roch Christian, Brou, Télésphore Yao, Gnimavo, Ronald, Eyangoh, Sara, Khater, Fida, Marion, Estelle
में प्रकाशित Emerg Infect Dis (2020)

Novel NDUFS4 gene mutation in an atypical late-onset mitochondrial form of multifocal dystonia

द्वारा Bris, Celine, Rouaud, Tiphaine, Desquiret-Dumas, Valerie, Gueguen, Naig, Goudenege, David, Barth, Magalie, Bonneau, Dominique, Amati-Bonneau, Patrizia, Lenaers, Guy, Reynier, Pascal, Lebre, Anne-Sophie, Procaccio, Vincent
में प्रकाशित Neurol Genet (2017)

Mitochondrial DNA Instability Is Common in HIV-Exposed Uninfected Newborns

द्वारा Monnin, Audrey, Desquiret-Dumas, Valérie, Méda, Nicolas, Goudenège, David, Bris, Céline, Kankasa, Chipepo, Singata-Madliki, Mandisa, Tylleskar, Thorkild, Procaccio, Vincent, Nagot, Nicolas, Van de Perre, Philippe, Reynier, Pascal, Molès, Jean-Pierre
में प्रकाशित J Clin Med (2021)

First characterization of LHON pedigrees in North Africa

द्वारा Bouzidi, Aymane, Aboussair, Nisrine, Charif, Majida, Amalou, Ghita, Goudenège, David, Desquiret-Dumas, Valérie, Bris, Céline, Sifeddine, Najat, Nahili, Halima, Elqabli, Meriem, Dafir, Kenza, Kandil, Mostafa, Amati-Bonneau, Patrizia, Procaccio, Vincent, Barakat, Abdelhamid, Lenaers, Guy
में प्रकाशित Eye (Lond) (2020)

Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy

द्वारा Charif, Majida, Chevrollier, Arnaud, Gueguen, Naïg, Bris, Céline, Goudenège, David, Desquiret-Dumas, Valérie, Leruez, Stéphanie, Colin, Estelle, Meunier, Audrey, Vignal, Catherine, Smirnov, Vasily, Defoort-Dhellemmes, Sabine, Drumare Bouvet, Isabelle, Goizet, Cyril, Votruba, Marcela, Jurkute, Neringa, Yu-Wai-Man, Patrick, Tagliavini, Francesca, Caporali, Leonardo, La Morgia, Chiara, Carelli, Valerio, Procaccio, Vincent, Zanlonghi, Xavier, Meunier, Isabelle, Reynier, Pascal, Bonneau, Dominique, Amati-Bonneau, Patrizia, Lenaers, Guy
में प्रकाशित Neurol Genet (2020)

Dominant ACO2 mutations are a frequent cause of isolated optic atrophy

द्वारा Charif, Majida, Gueguen, Naïg, Ferré, Marc, Elkarhat, Zouhair, Khiati, Salim, LeMao, Morgane, Chevrollier, Arnaud, Desquiret-Dumas, Valerie, Goudenège, David, Bris, Céline, Kane, Selma, Alban, Jennifer, Chupin, Stéphanie, Wetterwald, Céline, Caporali, Leonardo, Tagliavini, Francesca, LaMorgia, Chiara, Carbonelli, Michele, Jurkute, Neringa, Barakat, Abdelhamid, Gohier, Philippe, Verny, Christophe, Barth, Magalie, Procaccio, Vincent, Bonneau, Dominique, Zanlonghi, Xavier, Meunier, Isabelle, Weisschuh, Nicole, Schimpf-Linzenbold, Simone, Tonagel, Felix, Kellner, Ulrich, Yu-Wai-Man, Patrick, Carelli, Valerio, Wissinger, Bernd, Amati-Bonneau, Patrizia, Reynier, Pascal, Lenaers, Guy
में प्रकाशित Brain Commun (2021)

Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children and Young Adults

द्वारा Charif, Majida, Nasca, Alessia, Thompson, Kyle, Gerber, Sylvie, Makowski, Christine, Mazaheri, Neda, Bris, Céline, Goudenège, David, Legati, Andrea, Maroofian, Reza, Shariati, Gholamreza, Lamantea, Eleonora, Hopton, Sila, Ardissone, Anna, Moroni, Isabella, Giannotta, Melania, Siegel, Corinna, Strom, Tim M., Prokisch, Holger, Vignal-Clermont, Catherine, Derrien, Sabine, Zanlonghi, Xavier, Kaplan, Josseline, Hamel, Christian P., Leruez, Stephanie, Procaccio, Vincent, Bonneau, Dominique, Reynier, Pascal, White, Frances E., Hardy, Steven A., Barbosa, Inês A., Simpson, Michael A., Vara, Roshni, Perdomo Trujillo, Yaumara, Galehdari, Hamind, Deshpande, Charu, Haack, Tobias B., Rozet, Jean-Michel, Taylor, Robert W., Ghezzi, Daniele, Amati-Bonneau, Patrizia, Lenaers, Guy
में प्रकाशित JAMA Neurol (2017)