Jocelyn Laporte

28.5k citations
300 papers · 22.4k · 3 hit papers · h-index 65

Impact in

  • Cell Biology top 0.05%
    • Cellular transport and secretion
    • Endoplasmic Reticulum Stress and Disease
  • Physiology top 0.1%

Papers in

  • Cell Biology 134
    • Cellular transport and secretion 114
  • Molecular Biology 198
    • Muscle Physiology and Disorders 76
    • Ubiquitin and proteasome pathways 57
    • Nuclear Structure and Function 24
    • Protein Tyrosine Phosphatases 20
Co-authors
Jean‐Louis Mandel (35 shared papers)Christine Kretz (31 shared papers)Belinda Simone Cowling (32 shared papers)Carina Wallgren‐Pettersson (10 shared papers)Johann Böhm (55 shared papers)Bernard Payrastre (17 shared papers)Karim Hnia (16 shared papers)Heinz Jungbluth (9 shared papers)
Journals
Neuromuscular Disorders (25 papers)Human Molecular Genetics (10 papers)Acta Neuropathologica (9 papers)Acta Neuropathologica Communications (9 papers)Proceedings of the National Academy of Sciences (8 papers)
Partner nations
FranceUnited StatesUnited Kingdom

In The Last Decade

Jocelyn Laporte

287 papers receiving 22.0k citations

Jocelyn Laporte's Hit Papers

Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 1 2021 · 2.0k citations
2.0k0+4+9Years since publication10002.0k3.0k4.0k
What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

  1. 2021 Autophagy
  2. 2016 Autophagy
  3. 2012 Autophagy

Peers

Jocelyn Laporte
Comparison fields: 5 of 174
  • Cell Biology 6.4k
  • Physiology 1.2k
  • Epidemiology 7.3k
  • Molecular Biology 12.1k
  • Aging 276
Replace Ichizo Nishino with:
Ichizo Nishino Japan
Heinz Jungbluth United Kingdom
Marek Michalak Canada
Geert Bultynck Belgium
Angelo Poletti Italy
Jonathan Backer United States
Markus A. Rüegg Switzerland
Matthias Gaestel Germany
Masato Koike Japan
Andrew P. Lieberman United States
Jocelyn Laporte relative to Ichizo Nishino Japan Ichizo Nishino's profile →
Citations per field
00.5×1.5×
Ichizo Nishino · 1×
Citations per year

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-authors

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

20 of 20 papers shown

Showing the 20 most-cited of 300 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Autophagy ·Daniel J. Klionsky, Kotb Abdelmohsen, Akihisa Abe, Md. Joynal Abedin, Hagai Abeliovich, Abraham Acevedo‐Arozena, Hiroaki Adachi, Christopher M. Adams
Hit paper breakdown →		20164660
2
Guidelines for the use and interpretation of assays for monitoring autophagy
Autophagy ·Daniel J. Klionsky, Fábio Camargo Abdalla, Hagai Abeliovich, Robert T. Abraham, Abraham Acevedo‐Arozena, Khosrow Adeli, Lotta Agholme, Maria Carmen Agnello
Hit paper breakdown →		20123543
3
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 1
Autophagy ·Daniel J. Klionsky, Amal Kamal Abdel‐Aziz, Sara Abdelfatah, Mahmoud Abdellatif, Asghar Abdoli, Steffen Abel, Hagai Abeliovich, Marie H. Abildgaard
Hit paper breakdown →		20212038
4
A gene mutated in X–linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast
Nature Genetics ·Jocelyn Laporte, Ling Hu, Christine Kretz, Jean‐Louis Mandel, Petra Kioschis, Johannes F. Coy, Sabine M. Klauck, Annemarie Poustka
1996527
5
Mutations in dynamin 2 cause dominant centronuclear myopathy
Nature Genetics ·Marc Bitoun, Svetlana Maugenre, Pierre‐Yves Jeannet, Emmanuelle Lacène, Xavier Cano Ferrer, Pascal Laforêt, Jean‐Jacques Martin, Jocelyn Laporte
2005361
6
Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy
Nature Genetics ·Anne-Sophie Nicot, Anne-Christin Toussaint, Valérie Tosch, Christine Kretz, Carina Wallgren‐Pettersson, Erik Iwarsson, Helen Kingston, Jean‐Marie Garnier
2007320
7
Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy
Nature Medicine ·Charlotte Fugier, Arnaud F. Klein, Caroline Hammer, Stéphane Vassilopoulos, Ylva Ivarsson, Anne-Christin Toussaint, Valérie Tosch, Alban Vignaud
2011276
8
Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated with Early-Onset Glaucoma
The American Journal of Human Genetics ·Hamid Azzedine, Alessandra Bolino, T. Taïeb, Nazha Birouk, Marco Di Duca, Ahmed Bouhouche, Soufiène Benamou, Amel Mrabet
2003246
9
Centronuclear (myotubular) myopathy
Orphanet Journal of Rare Diseases ·Heinz Jungbluth, Carina Wallgren‐Pettersson, Jocelyn Laporte
2008239
10
Control of autophagy initiation by phosphoinositide 3‐phosphatase jumpy
The EMBO Journal ·Isabelle Vergne, Esteban Roberts, Rasha Elmaoued, Valérie Tosch, Mónica A. Delgado, Tassula Proikas‐Cezanne, Jocelyn Laporte, Vojo P. Deretic
2009232
11
Myotubularin, a phosphatase deficient in myotubular myopathy, acts on phosphatidylinositol 3-kinase and phosphatidylinositol 3-phosphate pathway
Human Molecular Genetics ·F. Blondeau, Jocelyn Laporte, Stéphane Bodin, Giulio Superti‐Furga, Bernard Payrastre, Jean‐Louis Mandel
2000227
12
The lipid phosphatase myotubularin is essential for skeletal muscle maintenance but not for myogenesis in mice
Proceedings of the National Academy of Sciences ·Anna Buj-Bello, Vincent Laugel, Nadia Messaddeq, Jocelyn Laporte, Jean‐François Pellissier, Jean‐Louis Mandel +1 other
2002197
13
MTM1 mutations in X-linked myotubular myopathy
Human Mutation ·Jocelyn Laporte, Val�rie Biancalana, Stephan M. Tanner, Wolfram Kreß, Vreni Schneider, Carina Wallgren‐Pettersson, Franziska Herger, Anna Buj‐Bello
2000186
14
Recessive truncating titin gene, TTN , mutations presenting as centronuclear myopathy
Neurology ·Ozge Ceyhan‐Birsoy, Pankaj B. Agrawal, Carlos Hidalgo, Klaus Schmitz‐Abe, Elizabeth T. DeChene, Lindsay C. Swanson, Rachel Soemedi, Nasim Vasli
2013174
15
Constitutive Activation of the Calcium Sensor STIM1 Causes Tubular-Aggregate Myopathy
The American Journal of Human Genetics ·Johann Böhm, Frédéric Chevessier, Catherine E. Koch, Shahram Attarian, Claire Feger, Daniel Hantaı̈, Pascal Laforêt, Karima Ghorab
2013173
16
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-Christin Toussaint, Céline Berbey, Nadia Messaddeq, Christine Kretz, Despina Sanoudou, Alan H. Beggs
2009156
17
A phosphoinositide conversion mechanism for exit from endosomes
Nature ·Katharina Ketel, Michael I. Krauss, Anne‐Sophie Nicot, Dmytro Puchkov, Marnix Wieffer, Rainer Mueller, Devaraj Subramanian, Carsten Schultz
2016155
18
Myotubularins, a large disease-associated family of cooperating catalytically active and inactive phosphoinositides phosphatases
Human Molecular Genetics ·Jocelyn Laporte, Florence Bedez, Alessandra Bolino, Jean‐Louis Mandel
2003153
19
Myotubularin Regulates the Function of the Late Endosome through the GRAM Domain-Phosphatidylinositol 3,5-Bisphosphate Interaction
Journal of Biological Chemistry ·Kazuya Tsujita, Toshiki Itoh, Takeshi Ijuin, Akitsugu Yamamoto, Assia Shisheva, Jocelyn Laporte, Tadaomi Takenawa
2004135
20
T-tubule biogenesis and triad formation in skeletal muscle and implication in human diseases
Skeletal Muscle ·Lama Al‐Qusairi, Jocelyn Laporte
2011132

About Jocelyn Laporte

Jocelyn Laporte is a scholar working on Cell Biology, Molecular Biology, Cardiology and Cardiovascular Medicine, Cellular and Molecular Neuroscience and Genetics, having authored 300 papers that have together received 22.4k indexed citations. Recurring topics across this work include Cellular transport and secretion (114 papers), Muscle Physiology and Disorders (76 papers), Ubiquitin and proteasome pathways (57 papers), Cardiomyopathy and Myosin Studies (55 papers), Genetic Neurodegenerative Diseases (41 papers), Nuclear Structure and Function (24 papers), Neurogenetic and Muscular Disorders Research (24 papers) and Protein Tyrosine Phosphatases (20 papers). The work is most often cited by research in Cell Biology (6.4k citations), Physiology (1.2k citations), Epidemiology (7.3k citations), Molecular Biology (12.1k citations) and Aging (276 citations). Jocelyn Laporte has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Jean‐Louis Mandel, Christine Kretz, Belinda Simone Cowling, Carina Wallgren‐Pettersson, Johann Böhm, Bernard Payrastre, Karim Hnia, Heinz Jungbluth, Anne‐Sophie Nicot and Norma Beatriz Romero. Their work appears in journals such as Neuromuscular Disorders, Human Molecular Genetics, Acta Neuropathologica, Acta Neuropathologica Communications and Proceedings of the National Academy of Sciences.

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Ichizo NishinoBreakdown of academic impact, for papers by Heinz JungbluthBreakdown of academic impact, for papers by Marek MichalakBreakdown of academic impact, for papers by Geert BultynckBreakdown of academic impact, for papers by Angelo PolettiBreakdown of academic impact, for papers by Jonathan BackerBreakdown of academic impact, for papers by Markus A. RüeggBreakdown of academic impact, for papers by Matthias GaestelBreakdown of academic impact, for papers by Masato KoikeBreakdown of academic impact, for papers by Andrew P. Lieberman