Pascale Guicheney

Inserm — France

Medicine · Health Sciences

78h-index22.6kcitations407works0.52yr avg
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Research Topics

Cardiac electrophysiology and arrhythmias(117), Muscle Physiology and Disorders(104), Ion channel regulation and function(77), Cardiomyopathy and Myosin Studies(50), Nuclear Structure and Function(35)

Publications403 total

Endocardial I Overexpression and Fibrotic Remodeling Underlying Pause-Dependent Early Repolarization in Humans
JACC. Clinical electrophysiology·2026· 1 cited
BPS2026 – FAM189A2 deficiency promotes atrial fibrillation through ito current enhancement
Biophysical Journal·2026
Generation of a FAM189A2/ENTREP1 knockout human induced pluripotent stem cell line using CRISPR/Cas9 technology
Stem Cell Research·2025Open Access
Gene Therapy with the N-terminal Fragment of Na <sub>v</sub> 1.5 for Cardiac Channelopathies: A Novel Transcomplementation Mechanism Potentiating the Cardiac Sodium Current
2024· 1 citedOpen Access
Trafficking and Gating Cooperation Between Deficient Nav1.5-mutant Channels to Rescue INa
Frontiers in Bioscience-Landmark·2022· 6 citedOpen Access
The role of the M-band myomesin proteins in muscle integrity and cardiac disease
Journal of Biomedical Science·2022· 38 citedOpen Access
A Type 2 Ryanodine Receptor Variant in the Helical Domain 2 Associated with an Impairment of the Adrenergic Response
Journal of Personalized Medicine·2021· 6 citedOpen Access
In vivo Dominant-Negative Effect of an SCN5A Brugada Syndrome Variant
Frontiers in Physiology·2021· 19 citedOpen Access
A SPRY1 domain cardiac ryanodine receptor variant associated with short-coupled torsade de pointes
Scientific Reports·2021· 12 citedOpen Access
Inter-Regulation of Kv4.3 and Voltage-Gated Sodium Channels Underlies Predisposition to Cardiac and Neuronal Channelopathies
International Journal of Molecular Sciences·2020· 22 citedOpen Access
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
Circulation·2020· 134 citedOpen Access
Mitochondria and skeletal muscle deconditioning in a mouse model of autosomal dominant centronuclear myopathy
HAL (Le Centre pour la Communication Scientifique Directe)·2019
Correlative SICM‐FCM reveals changes in morphology and kinetics of endocytic pits induced by disease‐associated mutations in dynamin
The FASEB Journal·2019· 28 citedOpen Access
Clathrin plaques and associated actin anchor intermediate filaments in skeletal muscle
Molecular Biology of the Cell·2019· 49 citedOpen Access
An African loss-of-function CACNA1C variant p.T1787M associated with a risk of ventricular fibrillation
Scientific Reports·2018· 12 citedOpen Access
Characteristics of the rigid spine syndrome due to SEPN-1 myopathy. A long-term follow-up series of 21 patients
Annals of Physical and Rehabilitation Medicine·2018
Recovery of Scn5a-deficient mice cardiac conduction using AAVs.
HAL (Le Centre pour la Communication Scientifique Directe)·2018
Clathrin plaques form mechanotransducing platforms
2018· 2 cited
Mechanosensitive clathrin platforms anchor desmin intermediate filaments in skeletal muscle
2018· 4 citedOpen Access
P128Recovery of Scn5a-deficient mice cardiac conduction using AAVs
Cardiovascular Research·2018· 1 citedOpen Access
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Frequent Co-authors

Isabelle Denjoy(16), Michel Fardeau(11), Norma B. Romero(10), B. Estournet(9), Ana Ferreiro(9), Antoine Leenhardt(8), Jean‐Jacques Schott(7), Arthur A.M. Wilde(6), Myriam Berthet(6), Véronique Fressart(6), Marc Bitoun(6), Peter J. Schwartz(5), Eric Schulze‐Bahr(5), Ketty Schwartz(5), Vincent Probst(5), Sven Zumhagen(5), Wataru Shimizu(5), Haluk Topaloğlu(5), Svetlana Maugenre(5), Luciano Merlini(5)