Guy Lenaers

1962 -

educated at: University of Toulouse

occupation: researcher

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Articles 131

Date

Title

Authors

2022-09-15

Syndromic Hearing Loss in Moroccan families is associated to homozygous missense variants in COL4A3 and MASP1

Majida Charif, Abdelhamid Barakat, Guy Lenaers
2020-01-28

A Data Mining Metabolomics Exploration of Glaucoma

Pascal Reynier, Guy Lenaers
2020-02-27

A Plasma Metabolomic Profiling of Exudative Age-Related Macular Degeneration Showing Carnosine and Mitochondrial Deficiencies

Marc Ferre, Pascal Reynier, Guy Lenaers
2020-01-01

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

Emmanuelle Sarzi, Maria Solà, Cécile Delettre, Majida Charif, Guy Lenaers
2020-03-23

Metabolomics hallmarks OPA1 variants correlating with their in-vitro phenotype and predicting clinical severity

Guy Lenaers
2020-03-25

Isopropyl-phloroglucinol-DHA protects outer retinal cells against lethal dose of all-trans-retinal

Philippe Brabet, Guy Lenaers
2020-04-21

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

Faiza Fakhfakh, Mongia Hachicha, Majida Charif, Guy Lenaers, Céline Bris, David Goudenège, Patrizia Amati-Bonneau
2020-01-02

First characterization of LHON pedigrees in North Africa

Ghita Amalou, Majida Charif, Abdelhamid Barakat, Guy Lenaers, Céline Bris, David Goudenège, Patrizia Amati-Bonneau
2020-01-10

Lactic Acidosis Together with GM-CSF and M-CSF Induces Human Macrophages toward an Inflammatory Protumor Phenotype

Mario Campone, Guy Lenaers, Cinzia Bocca
2020-05-20

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

Majida Charif, Arnaud Chevrollier, Neringa Jurkute, Leonardo Caporali, Chiara La Morgia, Guy Lenaers
2020-11-02

A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family

Majida Charif, Abdelhamid Barakat, Guy Lenaers
2020-12-07

A rod-cone dystrophy is systematically associated to the RTN4IP1 recessive optic atrophy

Majida Charif, Guy Lenaers
2019-09-10

OPA1: 516 unique variants and 831 patients registered in an updated centralized Variome database

Pascal Reynier, Marc Ferre, Guy Lenaers
2019-09-23

Metabolomics reveals highly regional specificity of cerebral sexual dimorphism in mice

Pascal Reynier, Guy Lenaers
2019-07-27

Hereditary spastic paraplegia and prominent sensorial involvement: think MAG mutations!

Agathe Roubertie, Guillaume Taieb, Cécile Delettre, Emmanuelle Sarzi, Majida Charif, Guy Lenaers
2019-04-15

The Metabolomic Signature of Opa1 Deficiency in Rat Primary Cortical Neurons Shows Aspartate/Glutamate Depletion and Phospholipids Remodeling

Guillaume Tcherkez, Guy Lenaers
2018-04-01

Reply: The expanding neurological phenotype of DNM1L-related disorders

Arnaud Chevrollier, Vincent Procaccio, Pascal Reynier, Benoit Funalot, Josseline Kaplan, Majida Charif, Guy Lenaers, Patrizia Amati-Bonneau
2018-06-29

Glycosylation as new pharmacological strategies for diseases associated with excessive angiogenesis

Guy Lenaers
2018-05-17

Study of mitochondrial function in placental insufficiency

Naïg Gueguen, Pascal Reynier, Guillaume Legendre, Vincent Procaccio, Guy Lenaers
2018-03-06

Alteration of Extracellular Nucleotide Metabolism in Pseudoxanthoma Elasticum

Gennady Yegutkin, Daniel Henrion, Guy Lenaers
2018-11-05

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

Benoit Rucheton, Pascal Reynier, Vincent Procaccio, Guy Lenaers, Patrizia Amati-Bonneau
2018-11-03

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

Leila Ammar-Keskes, Vincent Procaccio, Pascal Reynier, Faiza Fakhfakh, Mongia Hachicha, Majida Charif, Guy Lenaers, Patrizia Amati-Bonneau
2018

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

Pascal Reynier, Vincent Procaccio, Majida Charif, Guy Lenaers
2018-01-01

A Plasma Metabolomic Signature Involving Purine Metabolism in Human Optic Atrophy 1 (OPA1)-Related Disorders

Cinzia Bocca, Marc Ferre, Arnaud Chevrollier, Vincent Procaccio, Pascal Reynier, Guy Lenaers, Patrizia Amati-Bonneau, Christophe Verny
2018-02-06

OPA1 gene therapy prevents retinal ganglion cell loss in a Dominant Optic Atrophy mouse model

Emmanuelle Sarzi, Cécile Delettre, Guy Lenaers
2018-02-19

Light action spectrum on oxidative stress and mitochondrial damage in A2E-loaded retinal pigment epithelium cells

Mélanie Marie, Guy Lenaers
2018-02-15

OPA1: How much do we know to approach therapy?

Valentina Del Dotto, Guy Lenaers
2018-02-17

Cyclosporine A does not prevent second-eye involvement in Leber's hereditary optic neuropathy

Vincent Procaccio, Pascal Reynier, Guy Lenaers, Patrizia Amati-Bonneau
2018-02-14

The accumulation of assembly intermediates of the mitochondrial complex I matrix arm is reduced by limiting glucose uptake in a neuronal-like model of MELAS syndrome

Naïg Gueguen, Arnaud Chevrollier, Daniel Henrion, Pascal Reynier, Vincent Procaccio, Guy Lenaers
2018-02-01

A Plasma Metabolomic Signature of the Exfoliation Syndrome Involves Amino Acids, Acylcarnitines, and Polyamines

Vincent Procaccio, Pascal Reynier, Guy Lenaers, Patrizia Amati-Bonneau
2018-01-24

AP4 deficiency: A novel form of neurodegeneration with brain iron accumulation?

Rita Horvath, Majida Charif, Guy Lenaers
2017-03-01

Blocking mitochondrial calcium release in Schwann cells prevents demyelinating neuropathies

Guy Lenaers

Human - wd:Q56488643

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