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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:

Genetic Insights into Primary Restrictive Cardiomyopathy
Andreas Brodehl, Brenda Gerull
Journal of Clinical Medicine (2022) Vol. 11, Iss. 8, pp. 2094-2094
Open Access | Times Cited: 27

Showing 1-25 of 27 citing articles:

Epigenetics in LMNA-Related Cardiomyopathy
Yinuo Wang, Gergana Dobreva
Cells (2023) Vol. 12, Iss. 5, pp. 783-783
Open Access | Times Cited: 24
Sudden Cardiac Death in the Young: State-of-the-Art Review in Molecular Autopsy
Cecilia Salzillo, Vincenza Sansone, Francesco Napolitano
Current Issues in Molecular Biology (2024) Vol. 46, Iss. 4, pp. 3313-3327
Open Access | Times Cited: 9
Genetic testing for inherited cardiovascular diseases. A position statement of the Polish Cardiac Society endorsed by Polish Society of Human Genetics and Cardiovascular Patient Communities
Elżbieta Katarzyna Biernacka, Tadeusz Osadnik, Zofia T. Bilińska, et al.
Kardiologia Polska (2024) Vol. 82, Iss. 5, pp. 569-593
Open Access | Times Cited: 4
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
Structural and functional insights into α-actinin isoforms and their implications in cardiovascular disease
Maya Noureddine, Halina Mikolajek, Neil V. Morgan, et al.
The Journal of General Physiology (2025) Vol. 157, Iss. 2
Closed Access
Activation of the cGAS-STING pathway mediated by Irgm1 contributes to the development of restrictive cardiomyopathy induced by cTnIR193H mutation
Bo Pan, Xiaoli Yan, Jiajin Li, et al.
Research Square (Research Square) (2025)
Closed Access
Gene diagnostics for cardiovascular diseases
Eric Schulze‐Bahr, Sabine Klaassen, Brenda Gerull, et al.
Deleted Journal (2023) Vol. 17, Iss. 5, pp. 300-349
Closed Access | Times Cited: 10
Application of next generation sequencing in cardiology: current and future precision medicine implications
Eirini Papadopoulou, Dimitra Bouzarelou, George S. Tsaousis, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 8
The N-Terminal Part of the 1A Domain of Desmin Is a Hot Spot Region for Putative Pathogenic DES Mutations Affecting Filament Assembly
Andreas Brodehl, Stephanie Holler, Jan Gummert, et al.
Cells (2022) Vol. 11, Iss. 23, pp. 3906-3906
Open Access | Times Cited: 12
Prevalence and Impact of Arrhythmia on Outcomes in Restrictive Cardiomyopathy—A Report from the Beijing Municipal Health Commission Information Center (BMHCIC) Database
Haiyan Wang, Sitong Liu, Xilin Zhang, et al.
Journal of Clinical Medicine (2023) Vol. 12, Iss. 3, pp. 1236-1236
Open Access | Times Cited: 5
The role of noncoding genetic variants in cardiomyopathy
Myo Htet, Shunyao Lei, Sheetal Bajpayi, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 4
Clinical features, etiology and survival in patients with restrictive cardiomyopathy: A single center experience
Justyna Szczygieł, Piotr Michałek, Grażyna Truszkowska, et al.
Kardiologia Polska (2023)
Open Access | Times Cited: 4
Genetics of congenital heart disease
Amy E. Roberts, Ronald V. Lacro
Elsevier eBooks (2024), pp. 55-63
Closed Access | Times Cited: 1
Exploring the role of exosomes in the pathogenesis and treatment of cardiomyopathies: A comprehensive literature review
Shadiya FawzuAmeer, Manar Elsaka, Summaiya Kahtoon, et al.
Life Sciences (2024) Vol. 357, pp. 123063-123063
Open Access | Times Cited: 1
Identification of a Missense Mutation in the FLNC Gene from a Chinese Family with Restrictive Cardiomyopathy
Jin‐Tang Dong, Wenjuan Zhang, Qianwen Chen, et al.
Journal of Multidisciplinary Healthcare (2024) Vol. Volume 17, pp. 5363-5373
Open Access | Times Cited: 1
Cardiac Amyloidosis Versus Other Restrictive Cardiomyopathies: A Retrospective Analysis of Cardiovascular Outcomes and Arrhythmic Burden
Andrew Sagalov, Waqas Ullah, Yevgeniy Brailovsky, et al.
Clinical Medicine Insights Cardiology (2024) Vol. 18
Open Access | Times Cited: 1
Phosphorylation Mimetic of Myosin Regulatory Light Chain Mitigates Cardiomyopathy-Induced Myofilament Impairment in Mouse Models of RCM and DCM
Katarzyna Kaźmierczak, Jingsheng Liang, Luis Guillermo Maura, et al.
Life (2023) Vol. 13, Iss. 7, pp. 1463-1463
Open Access | Times Cited: 2
The N-terminal Part of the 1A Domain of Desmin Is a Hot Spot Region for Putative Pathogenic DES Mutations Affecting the Filament Assembly
Andreas Brodehl, Stephanie Holler, Jan Gummert, et al.
(2022)
Open Access | Times Cited: 3
Generation of human induced pluripotent stem cell line from a patient with restrictive cardiomyopathy
Jingxian Li, Jinxiu Jiang, Lingqun Ye, et al.
Stem Cell Research (2024) Vol. 76, pp. 103370-103370
Open Access
Genetics in the diagnosis and treatment of cardiovascular diseases
Kevin P. Bliden, Sahib Singh, Roni Shanoada, et al.
Journal of Translational Genetics and Genomics (2024) Vol. 8, Iss. 2, pp. 186-206
Open Access
Cardiomyopathies – Inherited subtypes and phenocopies
Athanasios Bakalakos, Perry Elliott
Elsevier eBooks (2024), pp. 191-221
Closed Access
Biallelic potential disease-causing missense variants in TAF1A in two siblings with infantile restrictive cardiomyopathy
Nan Jiang, Wenyuan Xu, Aliaa H. Abdelhakim, et al.
European Journal of Medical Genetics (2024) Vol. 71, pp. 104968-104968
Open Access
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
An ABCC9 Missense Variant Is Associated with Sudden Cardiac Death and Dilated Cardiomyopathy in Juvenile Dogs
Eva Furrow, Nicole M. Tate, Katie M. Minor, et al.
Genes (2023) Vol. 14, Iss. 5, pp. 988-988
Open Access | Times Cited: 1
Heart transplant outcomes in restrictive cardiomyopathy: UNOS registry analysis of the last three decades
Daniel Miklin, E.C. DePasquale
JHLT Open (2023) Vol. 3, pp. 100031-100031
Open Access | Times Cited: 1
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