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Frontiers in Physiology|February 14, 2022
Use of hiPSC-Derived Cardiomyocytes to Rule Out Proarrhythmic Effects of Drugs: The Case of Hydroxychloroquine in COVID-19Luca Sala, Vladislav Leonov, Manuela Mura, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 28, 2020
Desmin mutations result in mitochondrial dysfunction regardless of their aggregation propertiesNatalia Smolina, Aleksandr Khudiakov, Anastasiya Knyazeva, et al.
Stem Cell Research|February 15, 2020
Generation of two iPSC lines (FAMRCi006-A and FAMRCi006-B) from patient with dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy associated with genetic variant LMNAp.Arg527ProKseniya Perepelina, Polina Klauzen, Aleksandr Khudiakov, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|August 10, 2020
Sodium current abnormalities and deregulation of Wnt/β-catenin signaling in iPSC-derived cardiomyocytes generated from patient with arrhythmogenic cardiomyopathy harboring compound genetic variants in plakophilin 2 geneAleksandr Khudiakov, Anastasia Zaytseva, Kseniya Perepelina, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|February 12, 2026
Beyond Transconductance: Cell-Polymer Coupling Determines Fidelity in Action Potential Recording via Electrolyte-Gated Polymer TransistorsGiulia Zoe Zemignani, Elena Mancinelli, Gabriele Tullii, et al.
Stem Cell Research|July 14, 2020
Generation of two iPSC lines (FAMRCi007-A and FAMRCi007-B) from patient with Emery-Dreifuss muscular dystrophy and heart rhythm abnormalities carrying genetic variant LMNA p.Arg249GlnKseniya Perepelina, Aleksandra Kostina, Polina Klauzen, et al.
Cardiovascular Research|May 14, 2026
Machine learning-guided risk stratification for Long QT Syndrome genetic variants with hiPSC-derived cardiomyocytesAleksandr Khudiakov, Manuela Mura, Federica Giannetti, et al.
Nature Communications|August 30, 2025
Non-invasive action potential recordings using printed electrolyte-gated polymer field-effect transistorsAdrica Kyndiah, Giulia Zoe Zemignani, Carlotta Ronchi, et al.
Frontiers in Genetics|July 13, 2019
Truncating Variant in Myof Gene Is Associated With Limb-Girdle Type Muscular Dystrophy and CardiomyopathyArtem Kiselev, Raquel Vaz, Anastasia Knyazeva, et al.
Human Mutation|June 3, 2018
De novo mutations in FLNC leading to early-onset restrictive cardiomyopathy and congenital myopathyArtem Kiselev, Raquel Vaz, Anastasia Knyazeva, et al.
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