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Natalia Sonicheva‐Paterson

Observed names: N Sonicheva, N. A. Sonicheva, N. Sonicheva, Natalia A. Sonicheva, Natalia A. Sonicheva-Paterson, Natalia Sonicheva-Paterson, Natasha Sonicheva-Paterson, Н. А. Соничева-Патерсон
ORCID: 0000-0001-7766-1251
Observed ORCID: 0000-0001-7766-1251
OpenAlex ID: A5040371883
First-in-human study of TN-201, an AAV9 gene replacement therapy in MYBPC3 -associated hypertrophic cardiomyopathy: initial safety, pharmacodynamic, and imaging results from MyPEAK-1
2025 · Milind Y Desai, Sherif F Nagueh, et al. · Cardiovascular Research · 25
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Deletions of specific exons of FHOD3 detected by next‐generation sequencing are associated with hypertrophic cardiomyopathy
2020 · Juan P. Ochoa, Luis R. Lopes, et al. · Clinical Genetics · 21
Clinical features of pediatric Danon disease and the importance of early diagnosis
2023 · Leila Gandaeva, Natalia Sonicheva-Paterson, et al. · International Journal of Cardiology · 11
A cryptic splice-altering KCNQ1 variant in trans with R259L leading to Jervell and Lange-Nielsen syndrome
2021 · Mario Torrado, Germán Fernández, et al. · npj Genomic Medicine · 11
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A More Accurate Diagnosis of Hypertrophic Cardiomyopathy
2025 · William J. McKenna, Federico M. Asch, et al. · Journal of the American College of Cardiology · 6
Cardiology: genetics’ time
2020 · Health in Code, La Coruña, Spain, Natalia A. Sonicheva, et al. · Consilium Medicum · 4
Cardiac phenotype of Fabry Disease
2018 · M. S. Kharlap, R. P. Myasnikov, et al. · Russian Journal of Cardiology · 4
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High rate of seroeligibility among MYBPC3-associated hypertrophic cardiomyopathy patients for TN-201, an adeno-associated virus serotype 9 MYBPC3 gene therapy
2025 · Milind Y. Desai, Daniele Massera, et al. · Frontiers in Medicine · 3
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Возможности генетической диагностики для определения тактики лечения у пациентов с семейной гиперхолестеринемией
2023 · В. Сергиенко И., А. Н. Мешков, et al. · Атеросклероз и дислипидемии · 1
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Pulse Reduction in Management of Hypertrophic Cardiomyopathy (two Clinical Cases)
2017 · N. S. Krylova, E. A. Kovalevskaya, et al. · Russian Journal of Cardiology · 1
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Spanish founder variant in MYBPC3: implications of diagnostic criteria, clinical phenotype, and prognosis
2026 · Angel Júdez-Serrano, Jesús Wagih-Gómez, et al. · Revista Española de Cardiología (English Edition)
Comprehensive Genetic Study of Russian Hypertrophic Cardiomyopathy Identifies MYBPC3 c.3697C>T as the Predominant Variant in Pediatric and Adult Cohorts
2025 · Leila A. Gandaeva, Olga S. Chumakova, et al. · medRxiv
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Reciprocated tachycardias in cardiac laminopathy: a clinical case report
2025 · Evgeny Zhelyakov, Natalia Sonicheva-Paterson, et al. · European Heart Journal - Case Reports
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Frequency of genetic mutations or polymorphisms in patients with different probability of familial hypercholesterolemia and established ischemic heart disease
2020 · Y. Prus, I. Sergienko, et al. · Atherosclerosis
P4633The frequency of mutations in patients with familial hypercholesterolemia who underwent acute coronary syndrome and patients with stable ischemic heart disease
2019 · Y Prus, I Sergienko, et al. · European Heart Journal
Familial Hypercholesterolaemia In The North-West Region Of Russia
2019 · V. Konstantinov, T. Kuznetsova, et al. · Atherosclerosis
Complete Regression Of Xanthomata In 2 Years Old Girl With Homozygous Beta-Sitosterolemia Treated With Ezetimibe 5 Mg/Day
2019 · A. Susekov, V. Solovyev, et al. · Atherosclerosis
Works count: 17
Citation count: 87
H-index: 5
I10-index: 4
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