Pascale Guicheney
Inserm(FR)Sorbonne Université(FR)Fondation pour l’innovation en Cadiométabolisme et Nutrition(FR)
Publications by Year
Research Areas
Cardiac electrophysiology and arrhythmias, Muscle Physiology and Disorders, Ion channel regulation and function, Cardiomyopathy and Myosin Studies, Nuclear Structure and Function
Most-Cited Works
- → Genotype-Phenotype Correlation in the Long-QT Syndrome(2001)1,739 cited
- → A missense mutation in the αB-crystallin chaperone gene causes a desmin-related myopathy(1998)1,077 cited
- → A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome(1997)881 cited
- → An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing(2009)755 cited
- → Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy(1995)625 cited
- → Mutations in the Fukutin-Related Protein Gene (FKRP) Cause a Form of Congenital Muscular Dystrophy with Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan(2001)596 cited