D. Goudenège

发表

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

C. Bris, D. Goudenège, V. Desquiret-Dumas, 2018, Front. Genet..

CoBaltDB: Complete bacterial and archaeal orfeomes subcellular localization database and associated resources

Stéphane Avner, Céline Lucchetti-Miganeh, Frédérique Barloy-Hubler, 2010, BMC Microbiology.

SORGOdb: Superoxide Reductase Gene Ontology curated DataBase

D. Goudenège, David Thybert, F. Barloy-Hubler, 2011, BMC Microbiology.

Cancer/Testis Antigens into mitochondria: a hub between spermatogenesis, tumorigenesis and mitochondrial physiology adaptation.

D. Goudenège, G. Lenaers, S. Khiati, 2020, Mitochondrion.

Outer membrane vesicles are vehicles for the delivery of Vibrio tasmaniensis virulence factors to oyster immune cells.

D. Goudenège, S. Wai, Y. Couté, 2015, Environmental microbiology.

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

Robert W. Taylor, T. Strom, H. Prokisch, 2018, JAMA neurology.

eKLIPse: a sensitive tool for the detection and quantification of mitochondrial DNA deletions from next-generation sequencing data

C. Bris, D. Goudenège, V. Desquiret-Dumas, 2018, Genetics in Medicine.

Divergence in bacterial ecology is reflected by difference in population genetic structure, phage-predator load and host range

D. Goudenège, K. M. Wegner, M. Monot, 2022, bioRxiv.

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

C. Bris, D. Goudenège, V. Desquiret-Dumas, 2021, Frontiers in Neurology.

Warburg-like effect is a hallmark of complex I assembly defects.

D. Goudenège, V. Desquiret-Dumas, D. Bonneau, 2019, Biochimica et biophysica acta. Molecular basis of disease.

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

M. Votruba, C. La Morgia, P. Yu-Wai-Man, 2020, Neurology: Genetics.

Next-Generation Sequencing Identifies Novel PMPCA Variants in Patients with Late-Onset Dominant Optic Atrophy

C. Bris, D. Goudenège, V. Desquiret-Dumas, 2022, Genes.

Mitochondrial DNA Instability Is Common in HIV-Exposed Uninfected Newborns

J. Molès, C. Bris, D. Goudenège, 2021, Journal of clinical medicine.

Glutamate-Induced Deregulation of Krebs Cycle in Mitochondrial Encephalopathy Lactic Acidosis Syndrome Stroke-Like Episodes (MELAS) Syndrome Is Alleviated by Ketone Body Exposure

C. Bris, D. Goudenège, V. Desquiret-Dumas, 2022, Biomedicines.

Erratum to: Genome sequence of Vibrio diabolicus and identification of the exopolysaccharide HE800 biosynthesis locus

G. LaPointe, D. Goudenège, F. Le Roux, 2014, Applied Microbiology and Biotechnology.

Populations, not clones, are the unit of vibrio pathogenesis in naturally infected oysters

D. Goudenège, Alexandra Calteau, B. Petton, 2014, The ISME Journal.

Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment

C. Drissi, C. Bris, D. Goudenège, 2022, Bioscience reports.

A single regulatory gene is sufficient to alter Vibrio aestuarianus pathogenicity in oysters.

S. Mangenot, D. Goudenège, D. Mazel, 2015, Environmental microbiology.

Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy

H. Wilhelm, D. Goudenège, Majida Charif, 2019, The Journal of clinical investigation.

Next generation sequencing in family with MNGIE syndrome associated to optic atrophy: Novel homozygous POLG mutation in the C-terminal sub-domain leading to mtDNA depletion.

C. Bris, D. Goudenège, V. Desquiret-Dumas, 2019, Clinica chimica acta; international journal of clinical chemistry.

High‐throughput sequencing revealed a novel SETX mutation in a Hungarian patient with amyotrophic lateral sclerosis

P. Klivényi, D. Goudenège, V. Procaccio, 2017, Brain and behavior.

Improved detection of mitochondrial DNA instability in mitochondrial genome maintenance disorders

M. Martin-Négrier, C. Bris, D. Goudenège, 2021, Genetics in Medicine.

CLUH couples mitochondrial distribution to the energetic and metabolic status

D. Logan, D. Goudenège, V. Desquiret-Dumas, 2017, Journal of Cell Science.

Phage–host coevolution in natural populations

Kathryn M. Kauffman, E. Rocha, S. Chenivesse, 2022, Nature Microbiology.

Long-Term Persistence of Mitochondrial DNA Instability in HIV-Exposed Uninfected Children during and after Exposure to Antiretroviral Drugs and HIV

J. Molès, C. Bris, D. Goudenège, 2022, Biomedicines.

Cancer/Testis Antigen 55 is required for cancer cell proliferation and mitochondrial DNA maintenance.

Y. Pommier, D. Goudenège, V. Desquiret-Dumas, 2022, Mitochondrion.

Mutations in aARS genes revealed by targeted next-generation sequencing in patients with mitochondrial diseases

C. Bris, D. Goudenège, V. Desquiret-Dumas, 2020, Molecular Biology Reports.

Genome sequence of Vibrio diabolicus and identification of the exopolysaccharide HE800 biosynthesis locus

G. LaPointe, D. Goudenège, F. L. Roux, 2014, Applied Microbiology and Biotechnology.

Co-Exposure of Cardiomyocytes to IFN-γ and TNF-α Induces Mitochondrial Dysfunction and Nitro-Oxidative Stress: Implications for the Pathogenesis of Chronic Chagas Disease Cardiomyopathy

H. Nakaya, M. Mano, D. Goudenège, 2021, Frontiers in Immunology.

A snapshot of some pLI score pitfalls

D. Goudenège, E. Colin, D. Bonneau, 2019, Human mutation.

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

C. Bris, D. Goudenège, V. Desquiret-Dumas, 2017, Neurology: Genetics.

NOVEL NDUFS 4 GENE MUTATION IN AN ATYPICAL LATE-ONSET MITOCHONDRIAL FORM OF MULTIFOCAL DYSTONIA Mitochondrial

D. Goudenège, V. Desquiret-Dumas, D. Bonneau, 2022 .

Comparative genomics of pathogenic lineages of Vibrio nigripulchritudo identifies virulence-associated traits

C. Médigue, E. Krin, S. Mangenot, 2013, The ISME Journal.

Dominant ACO2 mutations are a frequent cause of isolated optic atrophy

M. Carbonelli, P. Gohier, P. Yu-Wai-Man, 2021, Brain communications.

Deep sequencing shows that oocytes are not prone to accumulate mtDNA heteroplasmic mutations during ovarian ageing

C. Bris, D. Goudenège, V. Desquiret-Dumas, 2017, Human reproduction.

First characterization of LHON pedigrees in North Africa

C. Bris, D. Goudenège, V. Desquiret-Dumas, 2020, Eye.

Phage inducible chromosomal minimalist island (PICMI), a family of satellites of marine virulent phages

E. Rocha, D. Goudenège, M. Marbouty, 2023, bioRxiv.

CoBaltDB: Complete bacterial and archaeal orfeomes subcellular localization database and associated resources

D. Goudenège, F. Barloy-Hubler, S. Avner, 2010, BMC Microbiology.