Jocelyn Laporte

27.7k citations

260 papers · 9.6k indexed · h-index 56

Impact in

Cell Biology top 0.1%
- Cellular transport and secretion
Molecular Biology top 0.5%
- Muscle Physiology and Disorders
- Ubiquitin and proteasome pathways
- Ion channel regulation and function
- Nuclear Structure and Function

Papers in

Cell Biology 124
- Cellular transport and secretion 106
Cellular and Molecular Neuroscience 51
- Genetic Neurodegenerative Diseases 35

Co-authors: Jean‐Louis Mandel Christine Kretz Belinda S. Cowling Johann Böhm Bernard Payrastre Carina Wallgren‐Pettersson Karim Hnia Anne‐Sophie Nicot
Journals: Neuromuscular Disorders (20 papers)Human Molecular Genetics (10 papers)Proceedings of the National Academy of Sciences (8 papers)Journal of Neuromuscular Diseases (8 papers)Human Mutation (7 papers)
Partner nations: France United States Germany

In The Last Decade

Jocelyn Laporte

251 papers receiving 9.5k citations

Peers

Countries citing papers authored by Jocelyn Laporte

Since Specialization

Citations

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

Fields of papers citing papers by Jocelyn Laporte

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Jocelyn Laporte, 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 Jocelyn Laporte Line = papers co-authored together Jocelyn Laporte links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	BIN1 gene replacement reverses BIN1-related centronuclear myopathy Molecular Therapy ·Barbro Tinner-Staines, Takashi Furukawa, Imran Ahmad, С Р Жакенова, Coralie Spiegelhalter, Jocelyn Laporte	2025	0
2	STIM1 in-frame deletion of eight amino acids in a patient with moderate tubular aggregate myopathy/Stormorken syndrome Journal of Medical Genetics ·Jualim Datiles Ovela, علی بهنام نیک, Jocelyn Laporte, Johann Böhm	2025	1
3	Potential compensatory mechanisms preserving cardiac function in myotubular myopathy Cellular and Molecular Life Sciences ·L. V. Kuprina, Imran Ahmad, David J. Reiss, Mu Wei-Xue, L. M. de Garcia, Jocelyn Laporte	2024	2
4	Uncovering the BIN1-SH3 interactome underpinning centronuclear myopathy eLife ·Gabriel Martin-Scruse, Evelina Edelweiss, Bastien Morlet, Luc Négroni, Mátyás Pajkos, Zsuzsanna Dosztányi, Søren Østergaard, Gilles Travé, Jocelyn Laporte, Gergő Gógl	2024	3
5	BIN1, Myotubularin, and Dynamin-2 Coordinate T-Tubule Growth in Cardiomyocytes Circulation Research ·Devi elfita Sari, 陈雨人, Michael Frisk, Sungjik Lim, Cathrine R. Carlson, Andreas Brech, Xin Shen, 中村緋奈美, Yufeng Hou, Tomi Tuomainen, Pasi Tavi, Peter P. Jones, Marianne Lunde, J. Andrew Wasserstrom, Jocelyn Laporte, Nina D. Ullrich, Geir Christensen, Jens Preben Morth, William E. Louch	2023	15
6	Inactivating the lipid kinase activity of PI3KC2β is sufficient to rescue myotubular myopathy in mice JCI Insight ·B.L. Broadhead, Mu Wei-Xue, T. Nishimoto, David J. Reiss, Christine Kretz, Gaëtan Chicanne, Bernard Payrastre, Bart Vanhaesebroeck, Jocelyn Laporte	2023	8
7	Mutation update for the ACTN2 gene Human Mutation ·彰諸橋, Montse Olivé, M. Sasidharan Pillai Indu, Erik Mondrow, Cristina Domínguez‐González, Mridul Johari, Annalaura Torella, Johann Böhm, D.L. Hinkamp, Vincenzo Nigro, Peter Hackman, Jocelyn Laporte, Bjarne Udd, Marco Savarese	2022	15
8	Mice with muscle-specific deletion of Bin1 recapitulate centronuclear myopathy and acute downregulation of dynamin 2 improves their phenotypes Molecular Therapy ·Dalila Maria Musa Belmiro, T. Nishimoto, P. M. Bodyako, R. Gómez, Joel Pel, David J. Reiss, Mu Wei-Xue, Nadia Messaddeq, Alireza Kahe, Christine Kretz, Belinda S. Cowling, Vincent Jacquemond, Jocelyn Laporte	2021	25
9	Multi-omics comparisons of different forms of centronuclear myopathies and the effects of several therapeutic strategies Molecular Therapy ·Lisa Gates, David J. Reiss, Joel Pel, Mesbah Namin S.A.R., 弘一高士, 白麟, B.L. Broadhead, G R Seward, Christine Kretz, Wolfgang Raffelsberger, Céline Keime, O.M. Dorchies, Julie Thompson, Jocelyn Laporte	2021	13
10	Functional analyses of STIM1 mutations reveal a common pathomechanism for tubular aggregate myopathy and Stormorken syndrome Neuropathology ·Purnima Mishra, Coralie Spiegelhalter, Dalila Maria Musa Belmiro, Jocelyn Laporte, Johann Böhm	2020	3
11	MISTIC: A prediction tool to reveal disease-relevant deleterious missense variants PLoS ONE ·Kirsley Chennen, Nur Hafizhah Binte Mohamad Rafi’ie, Xavière Lornage, Arnaud Kress, Johann Böhm, Julie Thompson, Jocelyn Laporte, Olivier Poch	2020	23
12	Differential physiological roles for BIN1 isoforms in skeletal muscle development, function and regeneration Disease Models & Mechanisms ·Ivana Prokic, Belinda S. Cowling, Fariba Sanaei, Christine Kretz, Hichem Tasfaout, Vincent Gache, کسری پورکرمانی, Olivia Wendling, Arnaud Ferry, Anne Toussaint, Christos Gavriilidis, T. Nishimoto, Catherine Koch, Jeanne Lainé, Roy Combe, Laurent Tiret, Vincent Jacquemond, Fanny Pilot‐Storck, Jocelyn Laporte	2020	25
13	Physiological impact and disease reversion for the severe form of centronuclear myopathy linked to dynamin JCI Insight ·B.L. Broadhead, Christine Kretz, Dalila Maria Musa Belmiro, Julien Ochala, Joel Pel, Norma B. Romero, Belinda S. Cowling, Jocelyn Laporte	2020	21
14	Tamoxifen prolongs survival and alleviates symptoms in mice with fatal X-linked myotubular myopathy Nature Communications ·Kristinn Einarsson, L. Neff, B.L. Broadhead, Hesham M. Ismail, Marta Sierra, Thomas Mercier, Laurent A. Décosterd, Jocelyn Laporte, Belinda S. Cowling, O.M. Dorchies, Léonardo Scapozza	2018	26
15	An Integrated Diagnosis Strategy for Congenital Myopathies PLoS ONE ·Johann Böhm, Nasim Vasli, Edoardo Malfatti, Stéphanie Le Gras, Claire Feger, Bernard Jost, Nicole Monnier, Julie Brocard, Hatice Karasoy, Marion Gérard, Maggie C. Walter, Peter Reilich, Valérie Biancalana, Christine Kretz, Nadia Messaddeq, Isabelle Marty, Joël Lunardi, Norma B. Romero, Jocelyn Laporte	2013	43
16	Correction: Altered Splicing of the BIN1 Muscle-Specific Exon in Humans and Dogs with Highly Progressive Centronuclear Myopathy PLoS Genetics ·Sani Abdullahi Aliero, Nasim Vasli, Marie Maurer, Belinda S. Cowling, G. Diane Shelton, Wolfram Kreß, Anne Toussaint, Ivana Nedeljković, Ulrike Schara, Thomas Anderson, Joachim Weis, Laurent Tiret, Jocelyn Laporte	2013	5
17	Defective Membrane Remodeling in Neuromuscular Diseases: Insights from Animal Models PLoS Genetics ·Belinda S. Cowling, Anne Toussaint, Jean Muller, Jocelyn Laporte	2012	43
18	Novel molecular diagnostic approaches for X-linked centronuclear (myotubular) myopathy reveal intronic mutations Neuromuscular Disorders ·Valérie Tosch, Nasim Vasli, Christine Kretz, Anne-Sophie Nicot, Lisa A. Krattiger, Nicolas Dondaine, Denis Oriot, Magalie Barth, Greene Holcomb, Norma B. Romero, Carsten G. Bönnemann, Андрій Павлович Панасюк, Craig Shifrin, Valérie Biancalana, Jocelyn Laporte	2010	26
19	T-tubule disorganization and defective excitation-contraction coupling in muscle fibers lacking myotubularin lipid phosphatase Proceedings of the National Academy of Sciences ·Lama Al‐Qusairi, Norbert Weiss, Anne Toussaint, Gasper Tabuni, Nadia Messaddeq, Christine Kretz, Despina Sanoudou, Alan H. Beggs, Bruno Allard, Jean‐Louis Mandel, Jocelyn Laporte, Vincent Jacquemond, Anna Buj‐Bello	2009	142
20	Subtle central and peripheral nervous system abnormalities in a family with centronuclear myopathy and a novel dynamin 2 gene mutation Neuromuscular Disorders ·Andoni Echaniz‐Laguna, Anne-Sophie Nicot, Sophie Carré, J. Franques, Christine Tranchant, Nicolas Dondaine, Valérie Biancalana, Jean‐Louis Mandel, Jocelyn Laporte	2007	39

About Jocelyn Laporte

Jocelyn Laporte is a scholar working on Cell Biology, Cellular and Molecular Neuroscience, Molecular Biology, Sensory Systems and Cardiology and Cardiovascular Medicine, having authored 260 papers that have together received 9.6k indexed citations. Recurring topics across this work include Cellular transport and secretion (106 papers), Muscle Physiology and Disorders (66 papers), Ubiquitin and proteasome pathways (54 papers), Cardiomyopathy and Myosin Studies (46 papers), Genetic Neurodegenerative Diseases (35 papers), Neurogenetic and Muscular Disorders Research (21 papers), Protein Tyrosine Phosphatases (20 papers) and Nuclear Structure and Function (19 papers). The work is most often cited by research in Cell Biology (4.5k citations), Molecular Biology (7.0k citations), Genetics (1.0k citations), Cellular and Molecular Neuroscience (1.8k citations) and Physiology (403 citations). Jocelyn Laporte has collaborated with scholars based in France, United States and Germany. Frequent co-authors include Jean‐Louis Mandel, Christine Kretz, Belinda S. Cowling, Johann Böhm, Bernard Payrastre, Carina Wallgren‐Pettersson, Karim Hnia, Anne‐Sophie Nicot, Valérie Tosch and Heinz Jungbluth. Their work appears in journals such as Neuromuscular Disorders, Human Molecular Genetics, Proceedings of the National Academy of Sciences, Journal of Neuromuscular Diseases and Human Mutation.

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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