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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:

Lamin and the heart
Gabriella Captur, Eloisa Arbustini, Gisèle Bonne, et al.
Heart (2017) Vol. 104, Iss. 6, pp. 468-479
Open Access | Times Cited: 121

Showing 1-25 of 121 citing articles:

Advances in the Genetic Basis and Pathogenesis of Sarcomere Cardiomyopathies
Raquel Yotti, Christine E. Seidman, Jonathan G. Seidman
Annual Review of Genomics and Human Genetics (2019) Vol. 20, Iss. 1, pp. 129-153
Open Access | Times Cited: 153
Complex roads from genotype to phenotype in dilated cardiomyopathy: scientific update from the Working Group of Myocardial Function of the European Society of Cardiology
Antoine Bondue, Eloisa Arbustini, Anna Monica Bianco, et al.
Cardiovascular Research (2018) Vol. 114, Iss. 10, pp. 1287-1303
Open Access | Times Cited: 95
Cardiac Phenotypes in Hereditary Muscle Disorders
Eloisa Arbustini, Alessandro Di Toro, Lorenzo Giuliani, et al.
Journal of the American College of Cardiology (2018) Vol. 72, Iss. 20, pp. 2485-2506
Open Access | Times Cited: 88
Phenotypic and Genetic Characteristics of Lipodystrophy: Pathophysiology, Metabolic Abnormalities, and Comorbidities
Barış Akıncı, Rasimcan Meral, Elif A Oral
Current Diabetes Reports (2018) Vol. 18, Iss. 12
Closed Access | Times Cited: 86
Intermediate filaments in cardiomyopathy
Mary Tsikitis, Zoi Galata, Manolis Mavroidis, et al.
Biophysical Reviews (2018) Vol. 10, Iss. 4, pp. 1007-1031
Open Access | Times Cited: 84
Disrupting the LINC complex by AAV mediated gene transduction prevents progression of Lamin induced cardiomyopathy
Ruth Jinfen Chai, Hendrikje Werner, Peter Yiqing Li, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 64
Natural History of MYH7-Related Dilated Cardiomyopathy
Fernando de Frutos, Juan Pablo Ochoa, Marina Navarro Peñalver, et al.
Journal of the American College of Cardiology (2022) Vol. 80, Iss. 15, pp. 1447-1461
Open Access | Times Cited: 53
REALM-DCM: A Phase 3, Multinational, Randomized, Placebo-Controlled Trial of ARRY-371797 in Patients With Symptomatic LMNA -Related Dilated Cardiomyopathy
Pablo García‐Pavía, José F. Rodríguez‐Palomares, Gianfranco Sinagra, et al.
Circulation Heart Failure (2024) Vol. 17, Iss. 7
Open Access | Times Cited: 10
Chromatin compartment dynamics in a haploinsufficient model of cardiac laminopathy
Alessandro Bertero, Paul Fields, Alec S.T. Smith, et al.
The Journal of Cell Biology (2019) Vol. 218, Iss. 9, pp. 2919-2944
Open Access | Times Cited: 59
Scaffold, mechanics and functions of nuclear lamins
Amnon Buxboim, Rafael Kronenberg‐Tenga, Sarka Salajkova, et al.
FEBS Letters (2023) Vol. 597, Iss. 22, pp. 2791-2805
Open Access | Times Cited: 18
Primate Model Carrying LMNA Mutation Develops Dilated Cardiomyopathy
Xiang Luo, Hao Jia, Fang Wang, et al.
JACC Basic to Translational Science (2024) Vol. 9, Iss. 3, pp. 380-395
Open Access | Times Cited: 6
Modeling Skeletal Muscle Laminopathies Using Human Induced Pluripotent Stem Cells Carrying Pathogenic LMNA Mutations
Heather Steele-Stallard, Luca Pinton, Shilpita Sarcar, et al.
Frontiers in Physiology (2018) Vol. 9
Open Access | Times Cited: 55
Linker of nucleoskeleton and cytoskeleton complex proteins in cardiomyopathy
Matthew J. Stroud
Biophysical Reviews (2018) Vol. 10, Iss. 4, pp. 1033-1051
Open Access | Times Cited: 54
Sirtuin 6: A potential therapeutic target for cardiovascular diseases
Saiyang Xie, Wei Deng, Qizhu Tang
Pharmacological Research (2020) Vol. 163, pp. 105214-105214
Closed Access | Times Cited: 40
Genetics and Pharmacogenetics of Atrial Fibrillation
Asia Owais, Miles Barney, Olivia T Ly, et al.
JACC Basic to Translational Science (2024) Vol. 9, Iss. 7, pp. 918-934
Open Access | Times Cited: 5
The role of genetic testing in management and prognosis of individuals with inherited cardiomyopathies
Sophie Hespe, Belinda Gray, Rajesh Puranik, et al.
Trends in Cardiovascular Medicine (2024)
Closed Access | Times Cited: 5
Increasing autophagy and blocking Nrf2 suppress laminopathy-induced age-dependent cardiac dysfunction and shortened lifespan
Shruti Bhide, Adriana S. Trujillo, Maureen T. O'Connor, et al.
Aging Cell (2018) Vol. 17, Iss. 3
Open Access | Times Cited: 46
Amelioration of desmin network defects by αB-crystallin overexpression confers cardioprotection in a mouse model of dilated cardiomyopathy caused by LMNA gene mutation
Zoi Galata, Ismini Kloukina, Ioanna Kostavasili, et al.
Journal of Molecular and Cellular Cardiology (2018) Vol. 125, pp. 73-86
Open Access | Times Cited: 44
Sinus node dysfunction: current understanding and future directions
Pavan Manoj, Jitae A. Kim, Stephanie Kim, et al.
AJP Heart and Circulatory Physiology (2022) Vol. 324, Iss. 3, pp. H259-H278
Open Access | Times Cited: 22
Atomic Force Microscopy (AFM) Applications in Arrhythmogenic Cardiomyopathy
Brisa Peña, Mostafa Adbel-Hafiz, Maria A. Cavasin, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 7, pp. 3700-3700
Open Access | Times Cited: 20
Genotype-phenotype insights of pediatric dilated cardiomyopathy
Ying Dai, Yan Wang, Youfei Fan, et al.
Frontiers in Pediatrics (2025) Vol. 13
Open Access
The Cutting Edge: The Role of mTOR Signaling in Laminopathies
Francesca Chiarini, Camilla Evangelisti, Vittoria Cenni, et al.
International Journal of Molecular Sciences (2019) Vol. 20, Iss. 4, pp. 847-847
Open Access | Times Cited: 34
Cardiac conduction diseases: understanding the molecular mechanisms to uncover targets for future treatments
Tingting Li, Qussay Marashly, Jitae A. Kim, et al.
Expert Opinion on Therapeutic Targets (2024) Vol. 28, Iss. 5, pp. 385-400
Closed Access | Times Cited: 3
Missense and Non-Missense Lamin A/C Gene Mutations Are Similarly Associated with Major Arrhythmic Cardiac Events: A 20-Year Single-Centre Experience
Cinzia Forleo, Maria Cristina Carella, Paolo Basile, et al.
Biomedicines (2024) Vol. 12, Iss. 6, pp. 1293-1293
Open Access | Times Cited: 3
Elevated TGF β2 serum levels in Emery-Dreifuss Muscular Dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processes
Pia Bernasconi, Nicola Carboni, Giulia Ricci, et al.
Nucleus (2018) Vol. 9, Iss. 1, pp. 337-349
Open Access | Times Cited: 30
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