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List of works by Christophe Verny

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

scientific article published in January 2018

Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot-Marie-Tooth type 2A disease.

scientific article

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases

article

Adult-onset cerebral X-linked adrenoleukodystrophy with major contrast-enhancement mimicking acquired disease.

scientific article

Adult-onset genetic leukoencephalopathies: a MRI pattern-based approach in a comprehensive study of 154 patients.

scientific article published on 19 December 2014

Assembly defects induce oxidative stress in inherited mitochondrial complex I deficiency.

scientific article

COMT Val158Met Polymorphism Modulates Huntington's Disease Progression

scientific article

Clinical and genetic characteristics of late-onset Huntington's disease

scientific article

Dissociation between decision-making under risk and decision-making under ambiguity in premanifest and manifest Huntington's disease

scientific article

Effectiveness of anti-psychotics and related drugs in the Huntington French-speaking group cohort

scientific article (publication date: 2014)

Episodic memory decline in Huntington's disease, a binding deficit?

scientific article

Estimation of the inbreeding coefficient through use of genomic data

scientific article

Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity.

scientific article published on 10 November 2009

G51D α‐synuclein mutation causes a novel Parkinsonian–pyramidal syndrome ⬇️

scientific article published on April 1, 2013

GJA1 Variants Cause Spastic Paraplegia Associated with Cerebral Hypomyelination

scientific article published on 25 April 2019

Hereditary optic neuropathies share a common mitochondrial coupling defect.

scientific article published in June 2008

Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respiration.

scientific article

Improved locus-specific database for OPA1 mutations allows inclusion of advanced clinical data.

scientific article

In vivo evidence for the selective subcortical degeneration in Huntington's disease.

scientific article

Language processing within the striatum: evidence from a PET correlation study in Huntington's disease

scientific article published on 11 March 2008

Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutations.

scientific article published on 21 September 2010

New practical definitions for the diagnosis of autosomal recessive spastic ataxia of Charlevoix-Saguenay

scientific article published on 20 August 2015

OPA1 R445H mutation in optic atrophy associated with sensorineural deafness.

scientific article published in December 2005

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes

scientific article

OPA1-associated disorders: phenotypes and pathophysiology.

scientific article published on 21 April 2009

Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathy

scientific article published on May 2010

Sensorineural hearing loss in OPA1-linked disorders.

scientific article

Targeted Metabolomics Reveals Early Dominant Optic Atrophy Signature in Optic Nerves of Opa1delTTAG/+ Mice.

scientific article published in February 2017

The metabolomic signature of Leber's hereditary optic neuropathy reveals endoplasmic reticulum stress

scientific article published on 15 September 2016

Validation of the first quality-of-life measurement for patients with Huntington's disease: the Huntington Quality of Life Instrument

scientific article published in July 2012

pH as a biomarker of neurodegeneration in Huntington's disease: a translational rodent-human MRS study.

scientific article

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