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:
The p.Ala2430Val mutation in filamin C causes a "hypertrophic myofibrillar cardiomyopathy"
Anne Schänzer, Elisabeth Schumann, Diana Zengeler, et al.
Journal of Muscle Research and Cell Motility (2021) Vol. 42, Iss. 2, pp. 381-397
Closed Access | Times Cited: 6
Anne Schänzer, Elisabeth Schumann, Diana Zengeler, et al.
Journal of Muscle Research and Cell Motility (2021) Vol. 42, Iss. 2, pp. 381-397
Closed Access | Times Cited: 6
Showing 6 citing articles:
The Role of Signalling Pathways in Myocardial Fibrosis in Hypertrophic Cardiomyopathy
Patryk Skórka, Jakub Piotrowski, Estera Bakinowska, et al.
Reviews in Cardiovascular Medicine (2025) Vol. 26, Iss. 2
Open Access
Patryk Skórka, Jakub Piotrowski, Estera Bakinowska, et al.
Reviews in Cardiovascular Medicine (2025) Vol. 26, Iss. 2
Open Access
Understanding the molecular basis of cardiomyopathy
Marie‐Louise Bang, Julius Bogomolovas, Ju Chen
AJP Heart and Circulatory Physiology (2021) Vol. 322, Iss. 2, pp. H181-H233
Open Access | Times Cited: 25
Marie‐Louise Bang, Julius Bogomolovas, Ju Chen
AJP Heart and Circulatory Physiology (2021) Vol. 322, Iss. 2, pp. H181-H233
Open Access | Times Cited: 25
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
Aleksey Muravyev, Т. Л. Вершинина, Pavel Tesner, et al.
Orphanet Journal of Rare Diseases (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 12
Drosophila CRISPR/Cas9 mutants as tools to analyse cardiac filamin function and pathogenicity of human FLNC variants
Flavie Ader, Maria Russi, L. Tixier-Cardoso, et al.
Biology Open (2022)
Open Access | Times Cited: 4
Flavie Ader, Maria Russi, L. Tixier-Cardoso, et al.
Biology Open (2022)
Open Access | Times Cited: 4
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
Daria V. Goliusova, Margarita Y Sharikova, Kristina A Lavrenteva, et al.
Biochemistry (Moscow) (2024) Vol. 89, Iss. 9, pp. 1546-1557
Closed Access
Neuropathologie I: Muskuläre Erkrankungen
Anne Schänzer, Carsten Dittmayer, Štefan Porubský, et al.
Deleted Journal (2022) Vol. 44, Iss. 2, pp. 104-112
Open Access
Anne Schänzer, Carsten Dittmayer, Štefan Porubský, et al.
Deleted Journal (2022) Vol. 44, Iss. 2, pp. 104-112
Open Access
