Marc FERRE MEng French Grande Ecole, PhD Bioinformatics

Présentation

Publications

Article dans une revue (36)

Genetic susceptibility to optic neuropathy in patients with alcohol use disorder Camille Delibes,Marc Ferré,Marine Rozet,Valérie Desquiret-Dumas,Alexis Descathaet al. Journal of Translational Medicine, 2024, 22 (1), pp.495. ⟨10.1186/s12967-024-05334-0⟩ Article dans une revue hal-04605126v1
The top 10 most frequently involved genes in hereditary optic neuropathies in 2186 probands Aude Rocatcher,Valérie Desquiret-Dumas,Majida Charif,Marc Ferré,Philippe Gohieret al. Brain - A Journal of Neurology , 2023, 146 (2), pp.455-460. ⟨10.1093/brain/awac395⟩ Article dans une revue hal-04320695v1
The top 10 most frequently involved genes in hereditary optic neuropathies in 2186 probands Aude Rocatcher,Valérie Desquiret-Dumas,Majida Charif,Marc Ferré,Philippe Gohieret al. Brain - A Journal of Neurology , 2023, 146 (2), pp.455-460. ⟨10.1093/brain/awac395⟩ Article dans une revue hal-04959530v1
NR2F1 database: 112 variants and 84 patients support refining the clinical synopsis of Bosch–Boonstra–Schaaf optic atrophy syndrome Benjamin Billiet,Patrizia Amati-Bonneau,Valérie Desquiret-Dumas,Khadidja Guehlouz,Dan Mileaet al. Human Mutation, 2022, 43 (2), pp.128-142. ⟨10.1002/humu.24305⟩ Article dans une revue hal-03861098v1
Deep learning shows no morphological abnormalities in neutrophils in Alzheimer's disease Floris Chabrun,Xavier Dieu,Nicolas Doudeau,Jennifer Gautier,Damien Luque-Pazet al. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring, 2021, 13 (1), ⟨10.1002/dad2.12146⟩ Article dans une revue hal-05432260v1
ACO2 clinicobiological dataset with extensive phenotype ontology annotation Khadidja Guehlouz,Thomas Foulonneau,Patrizia Amati-Bonneau,Majida Charif,Estelle Colinet al. Scientific Data , 2021, 8 (1), pp.205. ⟨10.1038/s41597-021-00984-x⟩ Article dans une revue hal-03861114v1
Achieving Expert-Level Interpretation of Serum Protein Electrophoresis through Deep Learning Driven by Human Reasoning Floris Chabrun,Xavier Dieu,Marc Ferre,Olivier Gaillard,Anthony Meryet al. Clinical Chemistry, 2021, 67 (10), pp.1406-1414. ⟨10.1093/clinchem/hvab133⟩ Article dans une revue hal-05432259v1
A Plasma Metabolomic Profiling of Exudative Age-Related Macular Degeneration Showing Carnosine and Mitochondrial Deficiencies Juan Manuel Chao de La Barca,Barnabé Rondet-Courbis,Marc Ferré,Jeanne Muller,Adrien Buissetet al. Journal of Clinical Medicine, 2020, 9 (3), pp.631. ⟨10.3390/jcm9030631⟩ Article dans une revue hal-02543202v1
Deciphering exome sequencing data: Bringing mitochondrial DNA variants to light Bastien Le Roux,Guy Lenaers,Xavier Zanlonghi,Patrizia Amati-Bonneau,Floris Chabrunet al. Human Mutation, 2019, 40 (12), pp.2430-2443. ⟨10.1002/humu.23885⟩ Article dans une revue hal-02975361v1
OPA1: 516 unique variants and 831 patients registered in an updated centralized Variome database Bastien Le Roux,Guy Lenaers,Xavier Zanlonghi,Patrizia Amati-Bonneau,Floris Chabrunet al. Orphanet Journal of Rare Diseases, 2019, 14 (1), ⟨10.1186/s13023-019-1187-1⟩ Article dans une revue hal-02388214v1
A Plasma Metabolomic Signature Involving Purine Metabolism in Human Optic Atrophy 1 (OPA1)-Related Disorders Cinzia Bocca,Judith Nzoughet,Stéphanie Leruez,Patrizia Amati-Bonneau,Marc Ferréet al. Investigative Ophthalmology & Visual Science, 2018, 59, pp.185-195. ⟨10.1167/iovs.17-23027⟩ Article dans une revue hal-01964499v1
Subretinal fibrosis is associated with fundus pulverulentus in pseudoxanthoma elasticum. J Ebran,Ludovic Martin,Nastassia Navasiolava,Marc Ferré,Dan Mileaet al. Graefe's Archive for Clinical and Experimental Ophthalmology, 2018, 256, pp.699-707 Article dans une revue hal-02104309v1
Multiethnic involvement in autosomal-dominant optic atrophy in Singapore J Loo,S Singhal,A Rukmini,S Tow,Patrizia Amati-Bonneauet al. Eye, 2017, 31, pp.475-480. ⟨10.1038/eye.2016.255⟩ Article dans une revue hal-02104157v1
Targeted Metabolomics Reveals Early Dominant Optic Atrophy Signature in Optic Nerves of Opa1 delTTAG/+ Mice Juan Manuel Chao de la Barca,Gilles Simard,Emmanuelle Sarzi,Tanguy Chaumette,Guillaume Rousseauet al. Investigative Ophthalmology & Visual Science, 2017, 58 (2), pp.812-820. ⟨10.1167/iovs.16-21116⟩ Article dans une revue hal-01784466v1
The metabolomic signature of Leber's hereditary optic neuropathy reveals endoplasmic reticulum stress Juan Manuel Chao de La Barca,Gilles Simard,Patrizia Amati-Bonneau,Zainab Safiedeen,Delphine Mirebeau-Prunieret al. Brain - A Journal of Neurology , 2016, 139 (11), pp.2864-2876. ⟨10.1093/brain/aww222⟩ Article dans une revue hal-02103390v1
OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology Juan Manuel Chao de La Barca,Delphine Mirebeau-Prunier,Patrizia Amati-Bonneau,Marc Ferré,Emmanuelle Sarziet al. Neurobiology of Disease, 2015, pp.20-26. ⟨10.1016/j.nbd.2015.08.015⟩ Article dans une revue istex hal-01392230v1
Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome Estelle Colin,Huynh Cong,G. Mollet,Agnés Guichet,O. Gribouvalet al. American Journal of Human Genetics, 2014, 95 (6), pp.637 - 48. ⟨10.1016/j.ajhg.2014.10.011⟩ Article dans une revue hal-03404021v1
Are zona pellucida genes involved in recurrent oocyte lysis observed during in vitro fertilization? Marc Ferré,Patrizia Amati-Bonneau,C. Moriniere,Véronique Ferré-L’hotellier,S. Lemerleet al. Journal of Assisted Reproduction and Genetics, 2014, 31 (2), pp.221 - 7. ⟨10.1007/s10815-013-0141-8⟩ Article dans une revue hal-03403940v1
Early-onset Behr syndrome due to compound heterozygous mutations in OPA1 Dominique Bonneau,Estelle Colin,Florine Oca,Marc Ferré,Arnaud Chevrollieret al. Brain - A Journal of Neurology , 2014, Non spécifié. ⟨10.1093/brain/awu184⟩ Article dans une revue hal-03403967v1
Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders Sylvie Bannwarth,Vincent Procaccio,Anne-Sophie Lebre,Claude Jardel,A. Chaussenotet al. Journal of Medical Genetics, 2013, 50 (10), pp.704 - 14. ⟨10.1136/jmedgenet-2013-101604⟩ Article dans une revue hal-03404064v1
Resveratrol induces a mitochondrial complex I-dependent increase in NADH oxidation responsible for sirtuin activation in liver cells Valérie Desquiret-Dumas,Naïg Gueguen,Géraldine Leman,Stephanie Baron,Valerie Nivet-Antoineet al. Journal of Biological Chemistry, 2013, 288 (51), pp.36662 - 75. ⟨10.1074/jbc.M113.466490⟩ Article dans une revue hal-03404098v1
Is ABCC6 a genuine mitochondrial protein? Marc Ferré,Pascal Reynier,Arnaud Chevrollier,Delphine Prunier-Mirebeau,Georges Lefthériotiset al. BMC Research Notes, 2013, 6 (1), pp.427. ⟨10.1186/1756-0500-6-427⟩ Article dans une revue inserm-00877607v1
Sensorineural hearing loss in OPA1-linked disorders Stéphanie Leruez,Dan Milea,Sabine Defoort-Dhellemmes,Estelle Colin,M. Crochetet al. Brain - A Journal of Neurology , 2013, 136 (Pt 7), Non spécifié. ⟨10.1093/brain/aws340⟩ Article dans une revue hal-03404095v1
Standardized mitochondrial analysis gives new insights into mitochondrial dynamics and OPA1 function Arnaud Chevrollier,Julien Cassereau,Marc Ferré,Jennifer Alban,Valérie Desquiret-Dumaset al. International journal of biochemistry & cell biology, 2012, 44 (6), pp.980 - 8. ⟨10.1016/j.biocel.2012.03.006⟩ Article dans une revue istex hal-03404105v1
Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respiration. Claire Angebault,Naïg Gueguen,Valérie Desquiret-Dumas,Arnaud Chevrollier,Virginie Guilletet al. BMC Research Notes, 2011, 4 (1), pp.557. ⟨10.1186/1756-0500-4-557⟩ Article dans une revue inserm-00673659v1
A locus-specific database for mutations in GDAP1 allows analysis of genotype-phenotype correlations in Charcot-Marie-Tooth diseases type 4A and 2K. Julien Cassereau,Arnaud Chevrollier,Dominique Bonneau,Christophe Verny,Vincent Procaccioet al. Orphanet Journal of Rare Diseases, 2011, 6 (1), pp.87. ⟨10.1186/1750-1172-6-87⟩ Article dans une revue inserm-00683147v1
Les atrophies optiques héréditaires Clarisse Scherer,Vincent Procaccio,Marc Ferré,Virginie Guillet,Pascal Reynieret al. Revue Neurologique, 2010, 166 (12), pp.959 - 65. ⟨10.1016/j.neurol.2010.07.033⟩ Article dans une revue hal-03408477v1
Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot–Marie–Tooth type 2A disease Virginie Guillet,Naïg Gueguen,Christophe Verny,Marc Ferré,Chadi Homedanet al. neurogenetics, 2010, 11 (1), pp.127 - 133. ⟨10.1007/s10048-009-0207-z⟩ Article dans une revue istex hal-03406912v1
Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation Christophe Verny,Naïg Gueguen,Valérie Desquiret-Dumas,Arnaud Chevrollier,Adriana Prundeanet al. Mitochondrion, 2010, 11 (1), pp.70 - 75. ⟨10.1016/j.mito.2010.07.006⟩ Article dans une revue istex hal-03408492v1
Acute and late-onset optic atrophy due to a novel OPA1 mutation leading to a mitochondrial coupling defect Yannick Nochez,Sophie Arsene,Naïg Gueguen,Arnaud Chevrollier,Marc Ferréet al. Molecular Vision, 2009, 15, pp.598 - 608 Article dans une revue hal-03406919v1
OPA1-associated disorders: Phenotypes and pathophysiology Patrizia Amati-Bonneau,Dan Milea,Dominique Bonneau,Arnaud Chevrollier,Marc Ferréet al. International Journal of Biochemistry and Cell Biology, 2009, 41 (10), pp.1855 - 1865. ⟨10.1016/j.biocel.2009.04.012⟩ Article dans une revue istex hal-03406909v1
Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K) Julien Cassereau,Arnaud Chevrollier,Naïg Gueguen,Marie-Claire Malinge,Franck Letournelet al. neurogenetics, 2009, 10 (2), pp.145 - 150. ⟨10.1007/s10048-008-0166-9⟩ Article dans une revue istex hal-03403277v1
OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background. Denis Pierron,Marc Ferré,Christophe Rocher,Arnaud Chevrollier,Pascal Murailet al. BMC Medical Genetics, 2009, 10 (1), pp.70. ⟨10.1186/1471-2350-10-70⟩ Article dans une revue inserm-00663623v1
Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations. Marc Ferré,Dominique Bonneau,Dan Milea,Arnaud Chevrollier,Christophe Vernyet al. Human Mutation, 2009, 30 (7), pp.E692-705. ⟨10.1002/humu.21025⟩ Article dans une revue inserm-00372261v1
Reversible optic neuropathy with OPA1 exon 5b mutation. Karen Cornille,Dan Milea,Patrizia Amati-Bonneau,Vincent Procaccio,Lydie Zazounet al. Annals of Neurology, 2008, 63 (5), pp.667-71. ⟨10.1002/ana.21376⟩ Article dans une revue istex inserm-00287509v1
Hereditary optic neuropathies share a common mitochondrial coupling defect. Arnaud Chevrollier,Virginie Guillet,Dominique Loiseau,Naïg Gueguen,Marie-Anne Pou de Crescenzoet al. Annals of Neurology, 2008, 63 (6), pp.794-8. ⟨10.1002/ana.21385⟩ Article dans une revue istex hal-00282865v1