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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:

Genotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals
Elham Kayvanpour, Farbod Sedaghat‐Hamedani, Ali Amr, et al.
Clinical Research in Cardiology (2016) Vol. 106, Iss. 2, pp. 127-139
Closed Access | Times Cited: 197

Showing 26-50 of 197 citing articles:

Integrative Omics Approach to Identifying Genes Associated With Atrial Fibrillation
Biqi Wang, Kathryn L. Lunetta, Josée Dupuis, et al.
Circulation Research (2019) Vol. 126, Iss. 3, pp. 350-360
Open Access | Times Cited: 49
New Insights in RBM20 Cardiomyopathy
David C. Lennermann, Johannes Backs, Maarten M. G. van den Hoogenhof
Current Heart Failure Reports (2020) Vol. 17, Iss. 5, pp. 234-246
Open Access | Times Cited: 48
A missense mutation in the RSRSP stretch of Rbm20 causes dilated cardiomyopathy and atrial fibrillation in mice
Kensuke Ihara, Tetsuo Sasano, Yuichi Hiraoka, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 41
Genotype and Cardiac Outcomes in Pediatric Dilated Cardiomyopathy
Rabia Khan, Elfriede Pahl, Lisa Dellefave‐Castillo, et al.
Journal of the American Heart Association (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 34
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
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
The Genetic Landscape of Cardiomyopathies
Brenda Gerull, Sabine Klaassen, Andreas Brodehl
Cardiac and vascular biology (2019), pp. 45-91
Closed Access | Times Cited: 37
Meta-Analysis of Dilated Cardiomyopathy Using Cardiac RNA-Seq Transcriptomic Datasets
Ahmad Alimadadi, Patricia B. Munroe, Bina Joe, et al.
Genes (2020) Vol. 11, Iss. 1, pp. 60-60
Open Access | Times Cited: 36
Predicting sustained ventricular arrhythmias in dilated cardiomyopathy: a meta‐analysis and systematic review
Arjan Sammani, Elham Kayvanpour, Laurens P. Bosman, et al.
ESC Heart Failure (2020) Vol. 7, Iss. 4, pp. 1430-1441
Open Access | Times Cited: 36
Retrospective Analysis of Clinical Genetic Testing in Pediatric Primary Dilated Cardiomyopathy: Testing Outcomes and the Effects of Variant Reclassification
Daniel Quiat, Leora Witkowski, Hana Zouk, et al.
Journal of the American Heart Association (2020) Vol. 9, Iss. 11
Open Access | Times Cited: 36
Dilated cardiomyopathies and non-compaction cardiomyopathy
Anja Hänselmann, Christian Veltmann, Johann Bauersachs, et al.
Herz (2020) Vol. 45, Iss. 3, pp. 212-220
Open Access | Times Cited: 35
Genetics of Cardiomyopathy: Clinical and Mechanistic Implications for Heart Failure
Kyung‐Hee Kim, Naveen L. Pereira
Korean Circulation Journal (2021) Vol. 51, Iss. 10, pp. 797-797
Open Access | Times Cited: 30
Cardiomyopathies in Children and Systemic Disorders When Is It Useful to Look beyond the Heart?
Valentina Lodato, Giovanni Parlapiano, Federica Calì, et al.
Journal of Cardiovascular Development and Disease (2022) Vol. 9, Iss. 2, pp. 47-47
Open Access | Times Cited: 19
NHC/ SHA 2023 Focused update of the 2019 guidelines for the management of heart failure
Waleed Al Habeeb, Adel Tash, Abdelfatah Elasfar, et al.
Journal of the Saudi Heart Association (2023) Vol. 35, Iss. 1
Open Access | Times Cited: 11
Alternative splicing factors and cardiac disease: more than just mis-splicing?
Zachery R. Gregorich, Wei Guo
RNA (2025), pp. rna.080332.124-rna.080332.124
Closed Access
Contemporary Insights into LMNA Cardiomyopathy
Iswaree Devi Balakrishnan, Neal K. Lakdawala
Current Cardiology Reports (2025) Vol. 27, Iss. 1
Closed Access
Systematic Review, Meta-Analysis, and Population Study to Determine the Biologic Sex Ratio in Dilated Cardiomyopathy
Natalie Bergan, Ishika Prachee, Lara Curran, et al.
Circulation (2025)
Closed Access
Cardiac phenotypes in LMNA mutations
Leila Rouhi
Current Opinion in Cardiology (2025)
Closed Access
Association of the TTN, PDK4, and RNF207 mutations with dilated cardiomyopathy in Dobermanns from the United Kingdom
Luke C. Dutton, Andrew Crosland, Joanna Dukes‐McEwan, et al.
PLoS ONE (2025) Vol. 20, Iss. 3, pp. e0319932-e0319932
Open Access
Genetic testing of cardiomyopathies: position statement of the Cardiological Society of India
Ajay Bahl, Sandeep Seth, Perundurai S. Dhandapany, et al.
Indian Heart Journal (2025)
Open Access
Dilated cardiomyopathy: from genes and molecules to potential treatments
Xiumei Wang, Zekun Lang, Ze‐Yi Yan, et al.
Molecular and Cellular Biochemistry (2025)
Closed Access
Characteristics and pharmacological responsiveness in hiPSC models of inherited cardiomyopathy
Merel Gerritse, Willem B. van Ham, Chris Denning, et al.
Pharmacology & Therapeutics (2025), pp. 108845-108845
Open Access
Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3
Jirko Kühnisch, Christopher Herbst, Nadya Al‐Wakeel‐Marquard, et al.
Clinical Genetics (2019) Vol. 96, Iss. 6, pp. 549-559
Open Access | Times Cited: 35
Exploring the Crosstalk Between LMNA and Splicing Machinery Gene Mutations in Dilated Cardiomyopathy
Hind C. Zahr, Diana E. Jaalouk
Frontiers in Genetics (2018) Vol. 9
Open Access | Times Cited: 34
Atrial fibrillation in patients with inherited cardiomyopathies
Cynthia Yeung, Andrés Enríquez, Laiden Suarez‐Fuster, et al.
EP Europace (2018) Vol. 21, Iss. 1, pp. 22-32
Closed Access | Times Cited: 33

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