Publications by authors named "Anna Shestak"

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Case Report: Loss-of-function TRPM4 mutation p.L91Δ implicated in progressive cardiac conduction defect.
Anne-Flore Hämmerli, Daniela Ross-Kaschitza, Prakash Arullampalam, Anna Shestak, Jimmy Jyh-Ming Juang

Front Physiol· November 2025

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Allelic dropout in the endoglin () gene caused by common duplication beyond the primer binding site.
Anna G Shestak, Victoria A Rumyantseva, Elena V Zaklyazminskaya

Front Genet· June 2025

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Novel Gain-of-Function Mutation in the Kv11.1 Channel Found in the Patient with Brugada Syndrome and Mild QTc Shortening.
Denis Abramochkin, Bowen Li, Han Zhang, Ekaterina Kravchuk, Tatiana Nesterova, Anna Shestak

Biochemistry (Mosc)· March 2024

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Novel Mutation Glu98Lys in Cardiac Tropomyosin Alters Its Structure and Impairs Myocardial Relaxation.
Alexander M Matyushenko, Victoria V Nefedova, Anastasia M Kochurova, Galina V Kopylova, Natalia A Koubassova, Anna G Shestak

Int J Mol Sci· August 2023

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Diagnostic yield and variant reassessment in the genes encoding Nav1.5 channel in Russian patients with Brugada syndrome.
Elena Zaklyazminskaya, Anna Shestak, Dmitry Podolyak, Vera Komoliatova, Leonid Makarov

Front Pharmacol· August 2022

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Variable Clinical Appearance of the Kir2.1 Rare Variants in Russian Patients with Long QT Syndrome.
Elena Zaklyazminskaya, Margarita Polyak, Anna Shestak, Mariam Sadekova, Vera Komoliatova

Genes (Basel)· March 2022

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Coexistence of Two Rare Genetic Variants in Canonical and Non-canonical Exons of : A Potential Source of Misinterpretation.
Anna G Shestak, Leonid M Makarov, Vera N Komoliatova, Irina V Kolesnikova, Liubov O Skorodumova

Front Genet· September 2021

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Allelic Dropout Is a Common Phenomenon That Reduces the Diagnostic Yield of PCR-Based Sequencing of Targeted Gene Panels.
Anna G Shestak, Anna A Bukaeva, Siamak Saber, Elena V Zaklyazminskaya

Front Genet· February 2021

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Calmodulin binds to the N-terminal domain of the cardiac sodium channel Na1.5.
Zizun Wang, Sarah H Vermij, Valentin Sottas, Anna Shestak, Daniela Ross-Kaschitza

Channels (Austin)· December 2020

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Lack of association between mitochondrial DNA haplogroups J and T and clinical manifestation in Russian patients with Brugada syndrome.
Maria Golubenko, Vadim Mikhailov, Valeria Rusinova, Anna Shestak, Elena Zaklyazminskaya

Biomed Rep· September 2020

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Compound heterozygous mutations in and in a patient with severe Andersen-Tawil syndrome.
Margarita E Polyak, Anna Shestak, Dmitriy Podolyak, Elena Zaklyazminskaya

BMJ Case Rep· August 2020

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Clinical Classification of Arrhythmogenic Right Ventricular Cardiomyopathy.
Yulia Lutokhina, Olga Blagova, Alexander Nedostup, Svetlana Alexandrova, Anna Shestak

Pulse (Basel)· August 2020

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Dilated cardiomyopathy with severe arrhythmias in Emery-Dreifuss muscular dystrophy: from ablation to heart transplantation.
Olga Blagova, Alexander Nedostup, Dmitry Shumakov, Vitaly Poptsov, Anna Shestak

J Atr Fibrillation· December 2016

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Simultaneous Non-Invasive Epicardial and Endocardial Mapping in Patients With Brugada Syndrome: New Insights Into Arrhythmia Mechanisms.
Boris Rudic, Maria Chaykovskaya, Alexey Tsyganov, Vitaly Kalinin, Erol Tülümen, Anna Shestak

J Am Heart Assoc· November 2016

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Characterization of 2 genetic variants of Na(v) 1.5-arginine 689 found in patients with cardiac arrhythmias.
Valentin Sottas, Jean-Sébastien Rougier, Florian Jousset, Jan P Kucera, Anna Shestak

J Cardiovasc Electrophysiol· September 2013

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