Christophe Verny

4.3k total citations · 1 hit paper
51 papers, 1.9k citations indexed

About

Christophe Verny is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Christophe Verny has authored 51 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 11 papers in Neurology and 10 papers in Cellular and Molecular Neuroscience. Recurrent topics in Christophe Verny's work include Mitochondrial Function and Pathology (17 papers), ATP Synthase and ATPases Research (13 papers) and Hereditary Neurological Disorders (8 papers). Christophe Verny is often cited by papers focused on Mitochondrial Function and Pathology (17 papers), ATP Synthase and ATPases Research (13 papers) and Hereditary Neurological Disorders (8 papers). Christophe Verny collaborates with scholars based in France, Singapore and United States. Christophe Verny's co-authors include Franck Letournel, Dominique Bonneau, Pascal Reynier, Patrizia Amati‐Bonneau, Vincent Procaccio, Alexis Brice, Arnaud Chevrollier, Aurélie Honoré, Luc Bousset and Karine Madiona and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

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 — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Christophe Verny France	20	853	701	578	421	285	51	1.9k
Serena Giannelli Italy	24	1.3k 1.5×	216 0.3×	516 0.9×	234 0.6×	290 1.0×	33	1.9k
Jesse D. Sengillo United States	21	1.1k 1.2×	456 0.7×	284 0.5×	624 1.5×	842 3.0×	74	2.4k
Francesco Saccà Italy	28	843 1.0×	807 1.2×	753 1.3×	155 0.4×	244 0.9×	125	2.2k
Ali Benomar Morocco	21	1.5k 1.7×	709 1.0×	1.7k 2.9×	99 0.2×	346 1.2×	69	2.3k
Anh H. Pham United States	7	1.1k 1.3×	310 0.4×	295 0.5×	290 0.7×	79 0.3×	12	1.5k
Wendy Hobbs United States	11	924 1.1×	749 1.1×	850 1.5×	187 0.4×	337 1.2×	17	1.9k
Michael Klinkenberg Germany	17	737 0.9×	634 0.9×	333 0.6×	313 0.7×	134 0.5×	19	1.4k
Stephan Züchner United States	23	854 1.0×	381 0.5×	853 1.5×	129 0.3×	397 1.4×	68	2.0k
Giovanna Zorzi Italy	30	898 1.1×	1.1k 1.5×	891 1.5×	206 0.5×	706 2.5×	101	2.5k
Aleksandar Raković Germany	20	1.0k 1.2×	866 1.2×	502 0.9×	317 0.8×	187 0.7×	40	1.9k

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

Letournel, Franck, Silvia Pozzi, Jean‐Pierre Julien, et al.. (2023). Transactive response DNA-binding protein 43 is enriched at the centrosome in human cells. Brain. 146(9). 3624–3633. 3 indexed citations

Codron, Philippe, Franck Letournel, Serge Marty, et al.. (2020). STochastic Optical Reconstruction Microscopy (STORM) reveals the nanoscale organization of pathological aggregates in human brain. Neuropathology and Applied Neurobiology. 47(1). 127–142. 28 indexed citations

Veillard, D., Karine Baumstarck, Gilles Edan, et al.. (2020). Assessing the experience of the quality of care of patients living with multiple sclerosis and their caregivers: The MusiCare questionnaire. European Journal of Neurology. 28(3). 910–920. 3 indexed citations

Leruez, Stéphanie, Christophe Verny, Dominique Bonneau, et al.. (2018). Cyclosporine A does not prevent second-eye involvement in Leber’s hereditary optic neuropathy. Orphanet Journal of Rare Diseases. 13(1). 33–33. 13 indexed citations

Codron, Philippe, Arnaud Chevrollier, Mariame Selma Kane, et al.. (2016). Increased mitochondrial fusion in a autosomal recessive CMT2A family with mitochondrial GTPase mitofusin 2 mutations. Journal of the Peripheral Nervous System. 21(4). 365–369. 8 indexed citations

Leruez, Stéphanie, Patrizia Amati‐Bonneau, Christophe Verny, et al.. (2014). Mitochondrial dysfunction affecting visual pathways. Revue Neurologique. 170(5). 344–354. 11 indexed citations

Tanguy, J.Y., et al.. (2013). Complications vasculaires de la bromocriptine dans la période du post-partum. Revue Neurologique. 169. A83–A83.

Miléa, Dan & Christophe Verny. (2012). Neuropathies optiques héréditaires. Revue Neurologique. 168(10). 706–709. 7 indexed citations

Cassereau, Julien, I. Cochereau, Catherine Vignal, et al.. (2010). Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathy. Journal of Neurology Neurosurgery & Psychiatry. 81(5). 578–580. 15 indexed citations

10.

Lenaers, Guy, Patrizia Amati‐Bonneau, Cécile Delettre, et al.. (2010). De la levure aux maladies neurodégénératives. médecine/sciences. 26(10). 836–841. 7 indexed citations

11.

Verny, Christophe, Valérie Desquiret‐Dumas, Arnaud Chevrollier, et al.. (2010). Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation. Mitochondrion. 11(1). 70–75. 62 indexed citations

12.

Guillet, Virginie, Arnaud Chevrollier, Julien Cassereau, et al.. (2009). Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity. Mitochondrion. 10(2). 115–124. 38 indexed citations

13.

Guillet, Virginie, Naïg Guéguen, Christophe Verny, et al.. (2009). Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot–Marie–Tooth type 2A disease. Neurogenetics. 11(1). 127–133. 29 indexed citations

14.

Verny, Christophe, Patrizia Amati‐Bonneau, Franck Letournel, et al.. (2008). Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitis. Diabetes & Metabolism. 34(6). 620–626. 22 indexed citations

15.

Cassereau, Julien, Arnaud Chevrollier, Naïg Guéguen, et al.. (2008). Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K). Neurogenetics. 10(2). 145–150. 65 indexed citations

16.

Dubourg, O., Hamid Azzedine, Christophe Verny, et al.. (2006). Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease. NeuroMolecular Medicine. 8(1-2). 75–85. 66 indexed citations

17.

Amati‐Bonneau, Patrizia, Agnès Guichet, Aurélien Olichon, et al.. (2005). OPA1 R445H mutation in optic atrophy associated with sensorineural deafness. Annals of Neurology. 58(6). 958–963. 120 indexed citations

18.

Baumgartner, Ralf W., B. Guillon, Vivien Pautot, et al.. (2005). Isolated Horner’s Syndrome May Herald Stroke. Cerebrovascular Diseases. 19(4). 274–275. 9 indexed citations

19.

Verny, Christophe, Patrizia Amati‐Bonneau, Frédéric Dubas, et al.. (2005). Atrophie optique, cataracte et signes extra-pyramidaux par mutation du gène OPA3. Revue Neurologique. 161(4). 451–454. 13 indexed citations

20.

Bonneau, Dominique, et al.. (2004). Les facteurs génétiques dans les troubles spécifiques du langage oral. Archives de Pédiatrie. 11(10). 1213–1216. 7 indexed citations

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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