Publications
149
Citations
3,503
Est. group size
~16
Recurring co-author estimate
Active years
30
Publishing since 1997
Isabelle Deschênes studies how heart cells generate electrical signals, focusing on cardiac ion channels—proteins that control the flow of charged particles (like sodium and chloride) across cell membranes to produce heartbeats. Her work examines how mutations and regulatory proteins affect these channels, using techniques such as patient-derived stem cell models, structural biology, and electrophysiology (measurement of electrical activity in cells) to understand and potentially treat heart rhythm disorders like long QT syndrome and Brugada syndrome.
Publication output has fluctuated over the past decade, with a peak around 2017-2018, a dip in 2019-2020, and a partial recovery to a moderate, steady pace of roughly 6-12 papers per year in recent years.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Structural basis of human Na <sub>v</sub> 1.5 gating mechanisms
Proceedings of the National Academy of Sciences · 2025
- Structural and Functional Mechanisms Underlying Activation Gate Dynamics and IFM Motif Accessibility in Human Na <sub>v</sub> 1.5
bioRxiv (Cold Spring Harbor Laboratory) · 2025
- Chloride intracellular channel (CLIC) 6 forms a redox-sensitive anion channel
Biophysical Journal · 2024
- Persistent PKA activation redistributes NaV1.5 to the cell surface of adult rat ventricular myocytes
The Journal of General Physiology · 2024
- Precision medicine for long QT syndrome: patient-specific iPSCs take the lead
Expert Reviews in Molecular Medicine · 2023
- Biophysical characterization of chloride intracellular channel 6 (CLIC6)
Journal of Biological Chemistry · 2023
- Protein 14-3-3 Influences the Response of the Cardiac Sodium Channel Nav1.5 to Antiarrhythmic Drugs
Journal of Pharmacology and Experimental Therapeutics · 2022
- Trafficking and Gating Cooperation Between Deficient Nav1.5-mutant Channels to Rescue INa
Frontiers in Bioscience-Landmark · 2022
- iPSC-derived cardiomyocytes from patients with myotonic dystrophy type 1 have abnormal ion channel functions and slower conduction velocities
Scientific Reports · 2021
- Long QT syndrome – Bench to bedside
Heart Rhythm O2 · 2021
- Generation and Expansion of Human Cardiomyocytes from Patient Peripheral Blood Mononuclear Cells
Journal of Visualized Experiments · 2021
- Expression defect of the rare variant/Brugada mutation R1512W depends upon the SCN5A splice variant background and can be rescued by mexiletine and the common polymorphism H558R
Channels · 2021
- Generation and Expansion of Human Cardiomyocytes from Patient Peripheral Blood Mononuclear Cells
Journal of Visualized Experiments · 2021
- Statin-induced anti-HMGCR myopathy: successful therapeutic strategies for corticosteroid-free remission in 55 patients
Arthritis Research & Therapy · 2020
- Intercellular Sodium Regulates Repolarization in Cardiac Tissue with Sodium Channel Gain of Function
Biophysical Journal · 2020
- Biophysical Journal×11
- Circulation×9
- DRYAD×7
- Circulation Research×6
- Heart Rhythm×6
- Sándor Györke
Medicine · The Ohio State University
- Xiaoping Wan
Medicine · The Ohio State University
- Vladimir Bogdanov
Medicine · The Ohio State University
- Radmila Terentyeva
Medicine · The Ohio State University
- Seth H. Weinberg
Medicine · The Ohio State University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
Claim or correct this profile