Bernard Prudhon

1.0k citations

15 papers · 618 · h-index 12

Impact in

Cell Biology top 5%
- Cellular transport and secretion
- Microtubule and mitosis dynamics
Cellular and Molecular Neuroscience top 10%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders

Papers in

Molecular Biology 11
- Nuclear Structure and Function 6
- Muscle Physiology and Disorders 4
- RNA regulation and disease 2
- Metabolism, Diabetes, and Cancer 1
Cell Biology 11
- Cellular transport and secretion 11
- Microtubule and mitosis dynamics 4

Co-authors: Marc Bitoun (14 shared papers)Pascale Guicheney (8 shared papers)Anne‐Cécile Durieux (4 shared papers)Stéphane Vassilopoulos (4 shared papers)Jorge A. Bevilacqua (3 shared papers)Norma B. Romero (4 shared papers)Jeanne Lainé (3 shared papers)Maud Beuvin (4 shared papers)
Journals: Molecular Therapy — Nucleic Acids (4 papers)Human Mutation (1 paper)Scientific Reports (1 paper)Current Gene Therapy (1 paper)Traffic (1 paper)
Partner nations: France Chile Argentina

In The Last Decade

Bernard Prudhon

15 papers receiving 612 citations

Peers

Countries citing papers authored by Bernard Prudhon

Since Specialization

Citations

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

Fields of papers citing papers by Bernard Prudhon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Bernard Prudhon, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Bernard Prudhon Line = papers co-authored together Bernard Prudhon links everyone, so they are left out of the graph.

All Works

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15 of 15 papers shown

#	Work
1	Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onset Annals of Neurology ·Marc Bitoun, Jorge A. Bevilacqua, Bernard Prudhon, Svetlana Maugenre, Ana Lía Taratuto, Soledad Monges, Fabiana Lubieniecki, Claude Cancès, Emmanuelle Uro‐Coste, M. Mayer, Michel Fardeau, Norma B. Romero, Pascale Guicheney	2007	104
2	Dynamin 2 and human diseases Journal of Molecular Medicine ·Anne‐Cécile Durieux, Bernard Prudhon, Pascale Guicheney, Marc Bitoun	2010	98
3	A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice Human Molecular Genetics ·Anne‐Cécile Durieux, Alban Vignaud, Bernard Prudhon, Mai Thao Viou, Maud Beuvin, Stéphane Vassilopoulos, B. Fraysse, Arnaud Ferry, Jeanne Lainé, Norma B. Romero, Pascale Guicheney, Marc Bitoun	2010	91
4	Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis Human Mutation ·Marc Bitoun, Anne‐Cécile Durieux, Bernard Prudhon, Jorge A. Bevilacqua, Adrien Herlédan, Vehary Sakanyan, Andoni Urtizberea, Luis Cartier, Norma B. Romero, Pascale Guicheney	2009	67
5	A Centronuclear Myopathy – Dynamin 2 Mutation Impairs Autophagy in Mice Traffic ·Anne‐Cécile Durieux, Stéphane Vassilopoulos, Jeanne Lainé, B. Fraysse, Laura Briñas, Bernard Prudhon, Josiane Castells, Damien Freyssenet, Gisèle Bonne, Pascale Guicheney, Marc Bitoun	2012	44
6	Allele‐specific silencing therapy for Dynamin 2‐related dominant centronuclear myopathy EMBO Molecular Medicine ·Delphine Trochet, Bernard Prudhon, Maud Beuvin, Cécile Peccate, Stéphanie Lorain, Laura Julien, Sofia Benkhelifa‐Ziyyat, Aymen Rabai, Kamel Mamchaoui, Arnaud Ferry, Jocelyn Laporte, Pascale Guicheney, Stéphane Vassilopoulos, Marc Bitoun	2017	43
7	A novel mutation in the dynamin 2 gene in a Charcot-Marie-Tooth type 2 patient: Clinical and pathological findings Neuromuscular Disorders ·Marc Bitoun, Tanya Stojkovic, Bernard Prudhon, Claude‐Alain Maurage, Philippe Latour, Patrick Vermersch, Pascale Guicheney	2008	37
8	Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy Molecular Therapy — Nucleic Acids ·Fériel Azibani, Astrid Brull, Ludovic Arandel, Maud Beuvin, Isabelle Nelson, Arnaud Jollet, Esma Ziat, Bernard Prudhon, Sofia Benkhelifa‐Ziyyat, Marc Bitoun, Stéphanie Lorain, Gisèle Bonne, A. Bertrand	2017	32
9	A NEW CENTRONUCLEAR MYOPATHY PHENOTYPE DUE TO A NOVEL DYNAMIN 2 MUTATION Neurology ·Marc Bitoun, Jorge A. Bevilacqua, B. Eymard, Bernard Prudhon, M Fardeau, Pascale Guicheney, Norma B. Romero	2009	28
10	Therapy for Dominant Inherited Diseases by Allele-Specific RNA Interference: Successes and Pitfalls Current Gene Therapy ·Delphine Trochet, Bernard Prudhon, Stéphane Vassilopoulos, Marc Bitoun	2015	23
11	Administration of insulin?like growth factor?1 (IGF?1) improves both structure and function of delta?sarcoglycan deficient cardiac muscle in the hamster Basic Research in Cardiology ·Armelle Serose, Bernard Prudhon, André Salmon, Marie Agnes Doyennette, Marc Fiszman, Yves Fromes	2004	18
12	Nuclear defects in skeletal muscle from a Dynamin 2-linked centronuclear myopathy mouse model Scientific Reports ·Anaïs Fongy, Sestina Falcone, Jeanne Lainé, Bernard Prudhon, Aurea B. Martins-Bach, Marc Bitoun	2019	15
13	Reprogramming the Dynamin 2 mRNA by Spliceosome-mediated RNA Trans-splicing Molecular Therapy — Nucleic Acids ·Delphine Trochet, Bernard Prudhon, Arnaud Jollet, Stéphanie Lorain, Marc Bitoun	2016	10
14	Development of versatile allele-specific siRNAs able to silence all the dominant dynamin 2 mutations Molecular Therapy — Nucleic Acids ·Swati Dudhal, Lylia Mekzine, Bernard Prudhon, Karishma Soocheta, Bruno Cadot, Kamel Mamchaoui, Delphine Trochet, Marc Bitoun	2022	6
15	Benefits of therapy by dynamin-2-mutant-specific silencing are maintained with time in a mouse model of dominant centronuclear myopathy Molecular Therapy — Nucleic Acids ·Delphine Trochet, Bernard Prudhon, Lylia Mekzine, Mégane Lemaître, Maud Beuvin, Laura Julien, Sofia Benkhelifa‐Ziyyat, Mai Thao Bui, Norma B. Romero, Marc Bitoun	2022	2

About Bernard Prudhon

Bernard Prudhon is a scholar working on Molecular Biology, Cell Biology, Cellular and Molecular Neuroscience, Surgery and Epidemiology, having authored 15 papers that have together received 618 indexed citations. Recurring topics across this work include Cellular transport and secretion (11 papers), Nuclear Structure and Function (6 papers), Microtubule and mitosis dynamics (4 papers), Genetic Neurodegenerative Diseases (4 papers), Muscle Physiology and Disorders (4 papers), Hereditary Neurological Disorders (2 papers), RNA regulation and disease (2 papers) and Metabolism, Diabetes, and Cancer (1 paper). The work is most often cited by research in Cell Biology (334 citations), Cellular and Molecular Neuroscience (207 citations), Molecular Biology (421 citations), Genetics (60 citations) and Cardiology and Cardiovascular Medicine (126 citations). Bernard Prudhon has collaborated with scholars based in France, Chile and Argentina. Frequent co-authors include Marc Bitoun, Pascale Guicheney, Anne‐Cécile Durieux, Stéphane Vassilopoulos, Jorge A. Bevilacqua, Norma B. Romero, Jeanne Lainé, Maud Beuvin, B. Fraysse and Delphine Trochet. Their work appears in journals such as Molecular Therapy — Nucleic Acids, Human Mutation, Scientific Reports, Current Gene Therapy and Traffic.

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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