Louis Viollet
Publications by Year
Research Areas
Neurogenetic and Muscular Disorders Research, RNA modifications and cancer, Muscle Physiology and Disorders, RNA Research and Splicing, Cardiomyopathy and Myosin Studies
Most-Cited Works
- → Identification and characterization of a spinal muscular atrophy-determining gene(1995)3,939 cited
- → De novo mutations in ATP1A3 cause alternating hemiplegia of childhood(2012)418 cited
- → Structure and Organization of the Human Survival Motor Neurone (SMN) Gene(1996)251 cited
- → Early onset collagen VI myopathies: Genetic and clinical correlations(2010)132 cited
- → Resistance strength training exercise in children with spinal muscular atrophy(2015)103 cited
- → Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association.(1996)92 cited
- → Study of LPIN1, LPIN2 and LPIN3 in rhabdomyolysis and exercise‐induced myalgia(2012)90 cited
- → The Nuclear Factor κB–Activator Gene PLEKHG5 Is Mutated in a Form of Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset(2007)88 cited
- → Large scale deletions of the 5q13 region are specific to Werdnig-Hoffmann disease.(1996)87 cited
- → Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7(2009)79 cited