Christophe Verny

4.3k citations

51 papers · 1.9k indexed · 1 hit paper · h-index 20

Molecular Biology top 10%
Neurology top 2%
Cellular and Molecular Neuroscience top 5%
Physiology top 5%
Neurology top 5%

Co-authors: Franck Letournel Dominique Bonneau Pascal Reynier Patrizia Amati‐Bonneau Alexis Brice Vincent Procaccio Arnaud Chevrollier Laura Pieri
Topics: Mitochondrial Function and Pathology (17 papers)ATP Synthase and ATPases Research (13 papers)Hereditary Neurological Disorders (8 papers)
Cited by: Neurology Cellular and Molecular Neuroscience
Journals: SHILAP Revista de lepidopterologíaBrain Neurology
Partner nations: France Singapore United States

In The Last Decade

Christophe Verny

49 papers receiving 1.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

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

2013 531 citations Franck Letournel, Christophe Verny et al. Annals of Neurology profile →

Peers

Countries citing papers authored by Christophe Verny

Since Specialization

Citations

This map shows the geographic impact of Christophe Verny's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Christophe Verny with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christophe Verny more than expected).

Fields of papers citing papers by Christophe Verny

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christophe Verny. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Christophe Verny. The network helps show where Christophe Verny may publish in the future.

Co-authorship network of co-authors of Christophe Verny

This figure shows the co-authorship network connecting the top 25 collaborators of Christophe Verny. A scholar is included among the top collaborators of Christophe Verny based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Christophe Verny. Christophe Verny is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Upstream open reading frame-introducing variants in patients with primary familial brain calcification 2024 ·European Journal of Human Genetics ·Anne Rovelet‐Lecrux,(unknown),Olivier Quenez,(unknown),Kévin Cassinari,Anne‐Claire Richard,Anne Boland,Jean‐François Deleuze,Cyril Goizet,(unknown),Christophe Verny,Karine Nguyen,Magalie Lecourtois,Gaël Nicolas	2
2	Transactive response DNA-binding protein 43 is enriched at the centrosome in human cells 2023 ·Brain ·(unknown),(unknown),(unknown),Franck Letournel,Silvia Pozzi,Jean‐Pierre Julien,(unknown),Delphine Bohl,Stéphanie Millecamps,Christophe Verny,Julien Cassereau,Guy Lenaers,Arnaud Chevrollier,Anne‐Marie Tassin,Philippe Codron	3
3	STochastic Optical Reconstruction Microscopy (STORM) reveals the nanoscale organization of pathological aggregates in human brain 2020 ·Neuropathology and Applied Neurobiology ·Philippe Codron,Franck Letournel,Serge Marty,(unknown),(unknown),Mathilde Duchesne,Christophe Verny,Guy Lenaers,Charles Duyckaerts,Jean‐Pierre Julien,Julien Cassereau,Arnaud Chevrollier	28
4	Cyclosporine A does not prevent second-eye involvement in Leber’s hereditary optic neuropathy 2018 ·Orphanet Journal of Rare Diseases ·Stéphanie Leruez,Christophe Verny,Dominique Bonneau,Vincent Procaccio,Guy Lenaers,Patrizia Amati‐Bonneau,Pascal Reynier,(unknown),Adriana Prundean,Christophe Orssaud,Xavier Zanlonghi,Marie‐Bénédicte Rougier,Caroline Tilikete,Dan Miléa	13
5	OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology 2015 ·Neurobiology of Disease ·Juan Manuel Chao de la Barca,Delphine Mirebeau‐Prunier,Patrizia Amati‐Bonneau,Marc Ferré,Emmanuelle Sarzi,Céline Bris,Stéphanie Leruez,Arnaud Chevrollier,Valérie Desquiret‐Dumas,Naïg Guéguen,Christophe Verny,Christian Hamel,Dan Miléa,Vincent Procaccio,Dominique Bonneau,Guy Lenaers,Pascal Reynier	43
6	Mitochondrial dysfunction affecting visual pathways 2014 ·Revue Neurologique ·Stéphanie Leruez,Patrizia Amati‐Bonneau,Christophe Verny,Pascal Reynier,Vincent Procaccio,Dominique Bonneau,Dan Milea	11
7	Neuropathies optiques héréditaires 2012 ·Revue Neurologique ·Dan Miléa,Christophe Verny	7
8	Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathy 2010 ·Journal of Neurology Neurosurgery & Psychiatry ·(unknown),Julien Cassereau,I. Cochereau,Catherine Vignal,Olivier Pajot,J.Y. Tanguy,Xavier Zanlonghi,Pascal Reynier,(unknown),(unknown),Dominique Bonneau,Christophe Verny	15
9	De la levure aux maladies neurodégénératives 2010 ·médecine/sciences ·Guy Lenaers,Patrizia Amati‐Bonneau,Cécile Delettre,Arnaud Chevrollier,Christophe Verny,Dan Miléa,Vincent Procaccio,Dominique Bonneau,Christian Hamel,Pascal Reynier	7
10	Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity 2009 ·Mitochondrion ·Virginie Guillet,Arnaud Chevrollier,Julien Cassereau,Franck Letournel,Naïg Guéguen,Laurence Richard,Valérie Desquiret‐Dumas,Christophe Verny,Vincent Procaccio,Patrizia Amati‐Bonneau,Pascal Reynier,Dominique Bonneau	38
11	Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot–Marie–Tooth type 2A disease 2009 ·Neurogenetics ·Virginie Guillet,Naïg Guéguen,Christophe Verny,Marc Ferré,(unknown),Dominique Loiseau,Vincent Procaccio,Patrizia Amati‐Bonneau,Dominique Bonneau,Pascal Reynier,Arnaud Chevrollier	29
12	Middle Cerebral Artery Dissection Gives Rise to Giant Serpentine Aneurysm 2008 ·Cerebrovascular Diseases ·Christophe Verny,Marc Gotkine,A. Pasco,Frédéric Dubas	10
13	Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitis 2008 ·Diabetes & Metabolism ·Christophe Verny,Patrizia Amati‐Bonneau,Franck Letournel,Benjamin Person,Nina Dib,Marie‐Claire Malinge,Abdelhamid Slama,Cédric Le Maréchal,Claude Férec,Vincent Procaccio,Pascal Reynier,Dominique Bonneau	22
14	Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K) 2008 ·Neurogenetics ·Julien Cassereau,Arnaud Chevrollier,Naïg Guéguen,Marie‐Claire Malinge,Franck Letournel,Guillaume Nicolas,Laurence Richard,Marc Ferré,Christophe Verny,Frédéric Dubas,Vincent Procaccio,Patrizia Amati‐Bonneau,Dominique Bonneau,Pascal Reynier	65
15	Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease 2006 ·NeuroMolecular Medicine ·O. Dubourg,Hamid Azzedine,Christophe Verny,(unknown),Nazha Birouk,Riadh Gouider,Mustafa A. Salih,Ahmed Bouhouche,(unknown),(unknown),M Mayer,Merle Ruberg,Mériem Tazir,Alexis Brice,Éric Leguern	66
16	Phenotype associated with APP duplication in five families 2006 ·Brain ·L. Cabrejo,Lucie Guyant‐Maréchal,A. Laquérrière,Martine Vercelletto,(unknown),C. Thomas-Antérion,Christophe Verny,Franck Letournel,Florence Pasquier,Anne Vital,Frédéric Checler,Thierry Frébourg,Dominique Campion,Didier Hannequin	218
17	OPA1 R445H mutation in optic atrophy associated with sensorineural deafness 2005 ·Annals of Neurology ·Patrizia Amati‐Bonneau,Agnès Guichet,Aurélien Olichon,Arnaud Chevrollier,(unknown),Stéphanie Miot,Carmen Ayuso,Sylvie Odent,(unknown),Christophe Verny,M. Calmels,Gilles Simard,Pascale Belenguer,Jing Wang,Jean‐Luc Puel,Christian Hamel,Yves Malthièry,Dominique Bonneau,Guy Lenaers,Pascal Reynier	120
18	Isolated Horner’s Syndrome May Herald Stroke 2005 ·Cerebrovascular Diseases ·(unknown),Ralf W. Baumgartner,B. Guillon,Vivien Pautot,Rainer Dziewas,(unknown),Matthias Sturzenegger,Pierre Garnier,Xavier Ducrocq,D. Saudeau,Jean‐Philippe Neau,Vincent Larrue,Fabrice Vuillier,J Boulliat,(unknown),Christophe Verny,Frédéric Dubas	9
19	Atrophie optique, cataracte et signes extra-pyramidaux par mutation du gène OPA3 2005 ·Revue Neurologique ·Christophe Verny,Patrizia Amati‐Bonneau,Frédéric Dubas,Yves Malthièry,Pascal Reynier,Dominique Bonneau	13
20	Les facteurs génétiques dans les troubles spécifiques du langage oral 2004 ·Archives de Pédiatrie ·Dominique Bonneau,Christophe Verny,(unknown)	7

About Christophe Verny

Christophe Verny is a scholar working on Neurology, Neurology and Ophthalmology, having authored 51 papers that have together received 1.9k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (17 papers), ATP Synthase and ATPases Research (13 papers) and Hereditary Neurological Disorders (8 papers). The work is most often cited by research in Neurology (701 citations), Neurology (285 citations) and Cellular and Molecular Neuroscience (578 citations). Christophe Verny has collaborated with scholars based in France, Singapore and United States. Frequent co-authors include Franck Letournel, Dominique Bonneau, Pascal Reynier, Patrizia Amati‐Bonneau, Alexis Brice, Vincent Procaccio, Arnaud Chevrollier, Laura Pieri, Suzanne Lesage and Ronald Melki. Their work appears in journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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