Nicole Monnier
Inserm(FR)Université de Strasbourg(FR)
Publications by Year
Research Areas
Muscle Physiology and Disorders, Ion channel regulation and function, Cardiomyopathy and Myosin Studies, Neurogenetic and Muscular Disorders Research, Coagulation, Bradykinin, Polyphosphates, and Angioedema
Most-Cited Works
- → Malignant-Hyperthermia Susceptibility Is Associated with a Mutation of the a1-Subunit of the Human Dihydropyridine-Sensitive L-Type Voltage-Dependent Calcium-Channel Receptor in Skeletal Muscle(1997)416 cited
- → Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase(2009)365 cited
- → Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human(2012)258 cited
- → Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France(2000)250 cited
- → Mutations and polymorphisms of the skeletal muscle α-actin gene (ACTA1)(2009)242 cited
- → An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptor