Daniel Hantaı̈ - Concepedia

Author

Daniel Hantaı̈

Also Known As

D HANTAI, D Hantai, D Hantaï, D. Hantai, D. Hantaï, D. Hantaï, Daniel Hantai, Daniel Hantaï, Daniel Hantaï, Daniel Hantaı̈

111

Publications

3.5K

Citations

H-Index

Concepts

All Affiliations

Inserm Institut de Myologie Sorbonne Université Centre National de la Recherche Scientifique Assistance Publique – Hôpitaux de Paris

About

Daniel Hantaı̈ is an author at Inserm specializing in medicine, cell biology, and physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	20	1.1K
2	Health Sciences	7	7	603
3	Natural Sciences	2	2	58
4	Social Sciences	2	2	52
5	Engineering	1	1	208

Daniel Hantaı̈

Publications

2.3K

Citations

H-Index

Page 1

	Year	Citations
Muscle inactivation of mTOR causes metabolic and dystrophin defects leading to severe myopathy Valérie Risson, Laetitia Mazelin, Mila Roceri, The Journal of Cell Biology Muscle FunctionMetabolic RemodelingCellular PhysiologyOrthopaedic SurgeryDystrophin Defects	2009	368
Constitutive Activation of the Calcium Sensor STIM1 Causes Tubular-Aggregate Myopathy Johann Böhm, Frédéric Chevessier, A. Maues de Paula, The American Journal of Human Genetics MechanobiologyEngineeringConstitutive ActivationPhysiologyCytoskeleton	2013	208
MUSK, a new target for mutations causing congenital myasthenic syndrome Frédéric Chevessier, Brice Faraut, Aymeric Ravel‐Chapuis, Human Molecular Genetics	2004	185
Identification of an Agrin Mutation that Causes Congenital Myasthenia and Affects Synapse Function Caroline Huzé, Stéphanie Bauché, Pascale Richard, The American Journal of Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsCauses Congenital Myasthenia	2009	166
Muscle histone deacetylase 4 upregulation in amyotrophic lateral sclerosis: potential role in reinnervation ability and disease progression Gaëlle Bruneteau, Thomas Simonet, Stéphanie Bauché, Brain	2013	132
Lamin A/C–mediated neuromuscular junction defects in Emery-Dreifuss muscular dystrophy Alexandre Méjat, V. Decostre, Juan Li, The Journal of Cell Biology	2009	116
Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophy Sophie Nicole, Amina Chaouch, T. Torbergsen, Brain Distal Muscle WeaknessMuscle FunctionAgrin MutationsOrthopaedic SurgeryKinesiology	2014	100
The origin of tubular aggregates in human myopathies Frédéric Chevessier, Stéphanie Bauché, Jean‐Paul Leroy, The Journal of Pathology	2005	92
Endplate denervation correlates with Nogo-A muscle expression in amyotrophic lateral sclerosis patients Gaëlle Bruneteau, Stéphanie Bauché, José‐Luis González de Aguilar, Annals of Clinical and Translational Neurology	2015	89
126th International Workshop: Congenital Myasthenic Syndromes, 24–26 September 2004, Naarden, The Netherlands David Beeson, Daniel Hantaı̈, Hanns Lochmüller, Neuromuscular Disorders Developmental AnomalySeptember 2004Congenital Myasthenic SyndromesInternational WorkshopPediatrics	2005	87

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