Christophe Pécheux

2.4k total citations
26 papers, 1.0k citations indexed

About

Christophe Pécheux is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Surgery. According to data from OpenAlex, Christophe Pécheux has authored 26 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 3 papers in Surgery. Recurrent topics in Christophe Pécheux's work include Inflammasome and immune disorders (6 papers), Muscle Physiology and Disorders (5 papers) and Genetic Neurodegenerative Diseases (5 papers). Christophe Pécheux is often cited by papers focused on Inflammasome and immune disorders (6 papers), Muscle Physiology and Disorders (5 papers) and Genetic Neurodegenerative Diseases (5 papers). Christophe Pécheux collaborates with scholars based in France, Spain and Lebanon. Christophe Pécheux's co-authors include Catherine Dodé, Gilles Grateau, Marc Delpech, Serge Amselem, Philippe Reinert, M Dervichian, D Cattan, Cécile Cazeneuve, Rafaëlle Bernard and Jacques Bienvenu and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Christophe Pécheux

26 papers receiving 1000 citations

Peers

Countries citing papers authored by Christophe Pécheux

Since Specialization

Citations

This map shows the geographic impact of Christophe Pécheux'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 Pécheux with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christophe Pécheux more than expected).

Fields of papers citing papers by Christophe Pécheux

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christophe Pécheux. 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 Pécheux. The network helps show where Christophe Pécheux may publish in the future.

Co-authorship network of co-authors of Christophe Pécheux

This figure shows the co-authorship network connecting the top 25 collaborators of Christophe Pécheux. A scholar is included among the top collaborators of Christophe Pécheux 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 Pécheux. Christophe Pécheux 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	Retrospective analysis and reclassification of DYSF variants in a large French series of dysferlinopathy patients 2021 ·Genetics in Medicine ·(unknown), (unknown), (unknown), Marc Bartoli, (unknown), Nathalie Bonello‐Palot, Christophe Pécheux, Karine Nguyen, Nicolas Lévy, Svetlana Gorokhova, Martin Krahn	14
2	Le séquençage d’ADN à haut débit en pratique clinique 2017 ·Archives de Pédiatrie ·Caroline Lacoste, Alexandre Fabre, Christophe Pécheux, Nicolas Lévy, Martin Krahn, (unknown), Nathalie Bonello‐Palot, Catherine Badens, Patrice Bourgeois	3
3	Coverage analysis of lists of genes involved in heterogeneous genetic diseases following benchtop exome sequencing using the ion proton 2016 ·Journal of Genetics ·Caroline Lacoste, Jean‐Pierre Desvignes, David Salgado, Christophe Pécheux, Laurent Villard, Marc Bartoli, Christophe Béroud, Nicolas Lévy, Catherine Badens, Martin Krahn	2
4	Rhinal hypometabolism on FDG PET in healthy APO-E4 carriers: impact on memory function and metabolic networks 2015 ·European Journal of Nuclear Medicine and Molecular Imaging ·Mira Didic, Olivier Félician, (unknown), Rafaëlle Bernard, Christophe Pécheux, O. Mundler, Mathieu Ceccaldi, Éric Guedj	12
5	Clinical heterogeneity and a high proportion of novel mutations in a Chinese cohort of patients with dysferlinopathy 2014 ·Neurology India ·Jianying Xi, Gaëlle Blandin, Jiahong Lu, Sushan Luo, Wenhua Zhu, Christophe Béroud, Christophe Pécheux, Véronique Labelle, Nicolas Lévy, (unknown), Chongbo Zhao, (unknown)	24
6	A novel CRYAB mutation resulting in multisystemic disease 2011 ·Neuromuscular Disorders ·Sabrina Sacconi, Léonard Feasson, Jean Christophe Antoine, Christophe Pécheux, Rafaëlle Bernard, Ana María Cobo, Alberto Casarin, Leonardo Salviati, Claude Desnuelle, Andoni Urtizberea	72
7	A Naturally Occurring Human Minidysferlin Protein Repairs Sarcolemmal Lesions in a Mouse Model of Dysferlinopathy 2010 ·Science Translational Medicine ·Martin Krahn, Nicolas Wein, Marc Bartoli, William Lostal, Sébastien Courrier, (unknown), Karine Nguyen, Christophe Vial, Nathalie Streichenberger, Véronique Labelle, D. Depétris, Christophe Pécheux, France Leturcq, Pierre Cau, Isabelle Richard, Nicolas Lévy	59
8	Myopathies distales avec mutations du gène GNE : à propos de quatre cas 2008 ·Revue Neurologique ·Anthony Béhin, O. Dubourg, (unknown), Christophe Pécheux, Rafaëlle Bernard, Nicolas Lévy, B. Eymard	12
9	G.P.4.15 CAPN3 mutations in patients with idiopathic eosinophilic myositis: A predystrophic stage of LGMD2A? 2007 ·Neuromuscular Disorders ·Martin Krahn, F. Hanisch, María Goicoechea, Ewout J. N. Groen, Christophe Pécheux, F. García-Bragado, Robert B. Layzer, France Leturcq, (unknown), J. Andoni Urtizberea, Amets Sáenz, Kate Bushby, Nicolas Lévy, Adolfo López de Munaín	3
10	Transcriptional explorations of CAPN3 identify novel splicing mutations, a large‐sized genomic deletion and evidence for messenger RNA decay 2007 ·Clinical Genetics ·Martin Krahn, Christophe Pécheux, Françoise Chapon, Christophe Béroud, Valérie Drouin‐Garraud, Pascal Laforêt, (unknown), I. Pénisson-Besnier, Rafaëlle Bernard, J. Andoni Urtizberea, France Leturcq, Nicolas Lévy	18
11	CAPN3 mutations in patients with idiopathic eosinophilic myositis 2006 ·Annals of Neurology ·Martin Krahn, Adolfo López de Munaín, Nathalie Streichenberger, Rafaëlle Bernard, Christophe Pécheux, Hervé Testard, José Luis Peña Segura, (unknown), Ana Cabello, Norma B. Romero, Juan José Poza, (unknown), Xavier Ferrer, María Goicoechea, F. García-Bragado, France Leturcq, J. Andoni Urtizberea, Nicolas Lévy	75
12	X Chromosome-Linked Kallmann Syndrome: Clinical Heterogeneity in Three Siblings Carrying an Intragenic Deletion of theKAL-1Gene 2003 ·The Journal of Clinical Endocrinology & Metabolism ·Nathalie Massin, Christophe Pécheux, Corinne Eloit, (unknown), (unknown), Frédérique Kuttenn, Jean‐Pierre Hardelin, Catherine Dodé, Philippe Touraine	64
13	The enlarging clinical, genetic, and population spectrum of tumor necrosis factor receptor–associated periodic syndrome 2002 ·Arthritis & Rheumatism ·Catherine Dodé, Marc André, Thierry Bienvenu, Pierre Hausfater, Christophe Pécheux, Jacques Bienvenu, Jean‐Claude Lecron, Philippe Reinert, D Cattan, Jean‐Charles Piette, Marie‐France Szajnert, Marc Delpech, Gilles Grateau, (unknown)	151
14	Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutations 2001 ·European Journal of Human Genetics ·Issam Mansour, Valérie Delague, Cécile Cazeneuve, Catherine Dodé, Éliane Chouery, Christophe Pécheux, Myrna Medlej‐Hashim, Nabiha Salem, (unknown), (unknown), Marie‐Paule Lefranc, M. Goossens, Marc Delpech, Serge Amselem, Jacques Loiselet, Gilles Grateau, André Mégarbané, Roger Naman	57
15	A novel missense mutation (C30S) in the gene encoding tumor necrosis factor receptor 1 linked to autosomal-dominant recurrent fever with localized myositis in a French family 2000 ·Arthritis & Rheumatism ·Catherine Dodé, T. Papo, Claire Fieschi, Christophe Pécheux, Élisabeth Dion, Françoise Picard, P Godeau, Jacques Bienvenu, Jean‐Charles Piette, Marc Delpech, Gilles Grateau	52
16	MEFV-Gene Analysis in Armenian Patients with Familial Mediterranean Fever: Diagnostic Value and Unfavorable Renal Prognosis of the M694V Homozygous Genotype—Genetic and Therapeutic Implications 1999 ·The American Journal of Human Genetics ·Cécile Cazeneuve, Tamara Sarkisian, Christophe Pécheux, M Dervichian, Brigitte Nédelec, Philippe Reinert, (unknown), Jean‐Claude Kouyoumdjian, (unknown), Marc Delpech, Michel Goossens, Catherine Dodé, Gilles Grateau, Serge Amselem	203
17	Fibrinogen Act chain mutation (Arg554 Leu) associated with hereditary renal amyloidosis in a French family 1998 ·Amyloid ·(unknown), Véronique Fournier, C Billerey, E Justrabo, D Chevet, D Droz, Christophe Pécheux, Marc Delpech, Gilles Grateau	11
18	Sequence analysis of the CAG triplet repeats region in the Huntington disease gene (IT15) in several mammalian species. 1996 ·PubMed ·Christophe Pécheux, (unknown), Kaplan Jc, Catherine Dodé	5
19	Diagnosis of “sporadic” Huntington's disease 1995 ·Journal of the Neurological Sciences ·Alexandra Dürr, Catherine Dodé, (unknown), Christophe Pécheux, B. Pillon, J Feingold, J.‐C. Kaplan, Yves Agid, Alexis Brice	23
20	Sequence analysis of the CCG polymorphic region adjacent to the CAG triplet repeat of the HD gene in normal and HD chromosomes. 1995 ·Journal of Medical Genetics ·Christophe Pécheux, (unknown), Alexandra Dürr, Yves Agid, J Feingold, Alexis Brice, (unknown), Josseline Kaplan	20

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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