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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood
Aleksey Muravyev, Т. Л. Вершинина, Pavel Tesner, et al.
Orphanet Journal of Rare Diseases (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 12

Showing 12 citing articles:

Accurate Classification of Non-ischemic Cardiomyopathy
Yifan Wang, Hao Jia, Jiangping Song
Current Cardiology Reports (2023) Vol. 25, Iss. 10, pp. 1299-1317
Open Access | Times Cited: 14
Familial restrictive cardiomyopathy with novel missense variant of uncertain significance in the FLNC gene
Ryo Nakayama, Toshikazu Tanaka, Shunsuke Inoue, et al.
ESC Heart Failure (2025)
Open Access
The clinical and genetic spectrum of pediatric hypertrophic cardiomyopathy manifesting before one year of age
S. G. Fetisova, Olesya Melnik, Е. С. Васичкина, et al.
Pediatric Research (2025)
Closed Access
The FLNC Ala1186Val Variant Linked to Cytoplasmic Body Myopathy and Cardiomyopathy Causes Protein Instability
Marion Onnée, A. Bénézit, Sultan Bastu, et al.
Biomedicines (2024) Vol. 12, Iss. 2, pp. 322-322
Open Access | Times Cited: 3
Novel Filamin C Myofibrillar Myopathy Variants Cause Different Pathomechanisms and Alterations in Protein Quality Systems
Dominik Sellung, Lorena Heil, Nassam Daya, et al.
Cells (2023) Vol. 12, Iss. 9, pp. 1321-1321
Open Access | Times Cited: 6
Distinct molecular features of FLNC mutations, associated with different clinical phenotypes
Klimenko E.S, Zaytseva A.K, Sorokina M.Yu, et al.
Cytoskeleton (2024)
Open Access | Times Cited: 1
Analysis of Slow Inactivation of Nav1.5 Channels in the Development of Hereditary Heart Pathology
А. К. Зайцева, Kseniya Perepelina, Anna Kostareva
Cell and Tissue Biology (2024) Vol. 18, Iss. 3, pp. 324-333
Closed Access
Analysis of the role of Na<sub>v</sub>1.5 slow inactivation in the development of inherited cardiac pathology
Anastasia K. Zaytseva, Kseniya Perepelina, Anna Kostareva
Tsitologiya (2024) Vol. 66, Iss. 1, pp. 54-63
Closed Access
Rare filamin C variants among patients with hypertrophic cardiomyopathy referred for septal myectomy
S. E. Andreeva, А. В. Гурщенков, V. V. Zaĭtsev, et al.
Russian Journal of Cardiology (2024) Vol. 29, Iss. 10, pp. 5942-5942
Open Access
The phenotypic and genetic features of arrhythmogenic cardiomyopathy in the pediatric population
O. А. Kofeynikova, D. Yu. Alekseeva, Т. Л. Вершинина, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 1
Role of Filamin C in Muscle Cells
Daria V. Goliusova, Margarita Y Sharikova, Kristina A Lavrenteva, et al.
Biochemistry (Moscow) (2024) Vol. 89, Iss. 9, pp. 1546-1557
Closed Access
Myopathies with Myofibrillar Pathology
Pitcha Chompoopong, Margherita Milone
Current clinical neurology (2023), pp. 193-211
Closed Access
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