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Christophe Verny | Researchclopedia

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Christophe Verny

118

Works

4,301

Citations

30

h-index

45

i10-index

Research Topics

Mitochondrial Function and Pathology ATP Synthase and ATPases Research Genetic Neurodegenerative Diseases

Affiliations

Centre National de la Recherche Scientifique2013–2024

Inserm2004–2025

Université Nantes Angers Le Mans2013–2015

Sorbonne Université1992–2006

Instituto de Investigaciones Biomédicas Sols-Morreale2007–2007

Top Works

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

Suzanne Lesage,Mathieu Anheim,et al.

2013713 citations

Metabolism and Genetic Disorders

Hereditary Neurological Disorders

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

Patrizia Amati‐Bonneau,Maria Lucia Valentino,et al.

2007513 citations

Phenotype associated with APP duplication in five families

L. Cabrejo,Lucie Guyant‐Maréchal,et al.

2006331 citations

Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification

Gaël Nicolas,Cyril Pottier,et al.

2013232 citations

OPA1 R445H mutation in optic atrophy associated with sensorineural deafness

Patrizia Amati‐Bonneau,Agnès Guichet,et al.

2005167 citations

Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel <i>OPA1</i> mutations

Marc FerrÃ©,Dominique Bonneau,et al.

2009164 citations

OPA1-associated disorders: Phenotypes and pathophysiology

Patrizia Amati‐Bonneau,Dan Miléa,et al.

2009139 citations

Spine deformities in Charcot-Marie-Tooth 4C caused by <i>SH3TC2</i> gene mutations

Hamid Azzedine,N. Ravisé,et al.

2006105 citations

Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease

O. Dubourg,Hamid Azzedine,et al.

200689 citations