Jocelyn Laporte - Concepedia

Author

Jocelyn Laporte

Also Known As

Cheung, Chun Hei Antonio, J LAPORTE, J Laporte, J P Laporte, J. LAPORTE, J. Laporte, J.F. Laporte, JOCELYN LAPORTE, Jocelyn F. Laporte, Jocelyn Franck Laporte

489

Publications

27.4K

Citations

H-Index

182

Concepts

All Affiliations

Inserm Institut de génétique et de biologie moléculaire et cellulaire Centre National de la Recherche Scientifique Université de Strasbourg Sorbonne Université

About

Jocelyn Laporte is an author at Inserm specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	44	96	10.7K
2	Natural Sciences	16	17	5.8K
3	Engineering	8	8	536
4	Health Sciences	8	8	402
5	Education	1	1	32

Jocelyn Laporte

183

Publications

22.5K

Citations

H-Index

Page 1

	Year	Citations
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) Daniel J. Klionsky, Kotb Abdelmohsen, Akihisa Abe, Autophagy	2016	5.9K
Guidelines for the use and interpretation of assays for monitoring autophagy Daniel J. Klionsky, Fábio Camargo Abdalla, Hagai Abeliovich, Autophagy MitophagyParticular Autophagy AssaysImmunologyCytoskeletonMultiple Assays	2012	4K
A gene mutated in X–linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast Jocelyn Laporte, Ling Hu, Christine Kretz, Nature Genetics Molecular PhysiologyGenetic DisorderNatural SciencesGeneticsMolecular Biology	1996	623
Mutations in dynamin 2 cause dominant centronuclear myopathy Marc Bitoun, Svetlana Maugenre, Pierre‐Yves Jeannet, Nature Genetics Mitochondrial MyopathyMendelian DisorderGenetic DisorderMedicineGenetics	2005	452
Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy Anne-Sophie Nicot, Anne Toussaint, Valérie Tosch, Nature Genetics ChromatinMendelian DisorderGenetic DisorderGeneticsMolecular Biology	2007	420
Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy Charlotte Fugier, Arnaud F. Klein, Caroline Hammer, Nature Medicine T Tubule AlterationsMedicineGeneticsPathologyMyotonic Dystrophy	2011	325
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 Hamid Azzedine, Alessandra Bolino, T. Taïeb, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyEarly-onset Glaucoma	2003	301
Control of autophagy initiation by phosphoinositide 3‐phosphatase jumpy Isabelle Vergne, Esteban Roberts, Rasha Elmaoued, The EMBO Journal	2009	264
Myotubularin, a phosphatase deficient in myotubular myopathy, acts on phosphatidylinositol 3-kinase and phosphatidylinositol 3-phosphate pathway F. Blondeau, Jocelyn Laporte, Stéphane Bodin, Human Molecular Genetics	2000	254
The lipid phosphatase myotubularin is essential for skeletal muscle maintenance but not for myogenesis in mice Anna Buj-Bello, Vincent Laugel, Nadia Messaddeq, Proceedings of the National Academy of Sciences	2002	220

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