Publication & Citation Trends
Most Cited Works
Publications
184 total
N‐ <scp>WASP</scp> is required for Amphiphysin‐2/ <scp>BIN</scp> 1‐dependent nuclear positioning and triad organization in skeletal muscle and is involved in the pathophysiology of centronuclear myopathy PDF
Cited by 115
OpenAlex
Single Delivery of an Adeno-Associated Viral Construct to Transfer the <i>CASQ2</i> Gene to Knock-In Mice Affected by Catecholaminergic Polymorphic Ventricular Tachycardia Is Able to Cure the Disease From Birth to Advanced Age PDF
Cited by 113
OpenAlex
Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human PDF
Cited by 259
OpenAlex
Oxidative stress and successful antioxidant treatment in models of RYR1-related myopathy PDF
Cited by 119
OpenAlex
Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion PDF
Cited by 172
OpenAlex
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization PDF
Cited by 116
OpenAlex
Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores
Cited by 105
OpenAlex
Physiological relationships among physical, sensory, and morphological attributes of texture in tomato fruits
Cited by 134
OpenAlex
Research Topics
Ion channel regulation and function
(57)
Muscle Physiology and Disorders
(37)
Cardiomyopathy and Myosin Studies
(25)
Cardiac electrophysiology and arrhythmias
(19)
Genetic Neurodegenerative Diseases
(19)
Frequent Co-Authors
Affiliations
Université Paris-Sud
Centre National de la Recherche Scientifique
Defence Research and Development Canada
Bern University of Applied Sciences
Institut National de la Recherche Agronomique