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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 51-75 of 197 citing articles:

Bromocriptine treatment in patients with peripartum cardiomyopathy and right ventricular dysfunction
Aiden Haghikia, Johannes Schwab, Jens Vogel‐Claussen, et al.
Clinical Research in Cardiology (2018) Vol. 108, Iss. 3, pp. 290-297
Open Access | Times Cited: 33
The Emerging Role of the RBM20 and PTBP1 Ribonucleoproteins in Heart Development and Cardiovascular Diseases
Stefania Fochi, Pamela Lorenzi, Marilisa Galasso, et al.
Genes (2020) Vol. 11, Iss. 4, pp. 402-402
Open Access | Times Cited: 32
Epigenetic-sensitive liquid biomarkers and personalised therapy in advanced heart failure: a focus on cell-free DNA and microRNAs
Gelsomina Mansueto, Giuditta Benincasa, Nunzia Della Mura, et al.
Journal of Clinical Pathology (2020) Vol. 73, Iss. 9, pp. 535-543
Open Access | Times Cited: 29
Diagnosis and Risk Prediction of Dilated Cardiomyopathy in the Era of Big Data and Genomics
Arjan Sammani, Annette F. Baas, Folkert W. Asselbergs, et al.
Journal of Clinical Medicine (2021) Vol. 10, Iss. 5, pp. 921-921
Open Access | Times Cited: 25
Homozygous TNNI3 Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the Literature
Ugo Sorrentino, Ilaria Gabbiato, Chiara Canciani, et al.
Genes (2023) Vol. 14, Iss. 3, pp. 748-748
Open Access | Times Cited: 10
Role of non‐coding variants in cardiovascular disease
Katayoun Heshmatzad, Niloofar Naderi, Majid Maleki, et al.
Journal of Cellular and Molecular Medicine (2023) Vol. 27, Iss. 12, pp. 1621-1636
Open Access | Times Cited: 10
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
Genetic Characterization of Dilated Cardiomyopathy in Romanian Adult Patients
Oana Raluca Voinescu, Bogdana Ioana Ionescu, Sebastian Militaru, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 5, pp. 2562-2562
Open Access | Times Cited: 3
Navigating the penetrance and phenotypic spectrum of inherited cardiomyopathies
Frans Serpa, Caitlin M. Finn, Usman A. Tahir
Heart Failure Reviews (2024) Vol. 29, Iss. 5, pp. 873-881
Closed Access | Times Cited: 3
Personalized care in dilated cardiomyopathy: Rationale and study design of the activeDCM trial
Farbod Sedaghat‐Hamedani, Ali Amr, Theresa Betz, et al.
ESC Heart Failure (2024) Vol. 11, Iss. 6, pp. 4400-4406
Open Access | Times Cited: 3
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy
Claire Horvat, Renée Johnson, Lien Lam, et al.
Genetics in Medicine (2018) Vol. 21, Iss. 1, pp. 133-143
Open Access | Times Cited: 29
Differences between familial and sporadic dilated cardiomyopathy: ESC EORP Cardiomyopathy & Myocarditis registry
Folkert W. Asselbergs, Arjan Sammani, Perry Elliott, et al.
ESC Heart Failure (2020) Vol. 8, Iss. 1, pp. 95-105
Open Access | Times Cited: 27
Genetic Basis and Genotype–Phenotype Correlations in Han Chinese Patients with Idiopathic Dilated Cardiomyopathy
Xinlin Zhang, Jun Xie, Rongfang Lan, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 24
Cardiac Organoids to Model and Heal Heart Failure and Cardiomyopathies
Magali Seguret, Eva Vermersch, Charlène Jouve, et al.
Biomedicines (2021) Vol. 9, Iss. 5, pp. 563-563
Open Access | Times Cited: 23
The titin N2B and N2A regions: biomechanical and metabolic signaling hubs in cross-striated muscles
Robbert van der Pijl, Andrea A. Domenighetti, Farah Sheikh, et al.
Biophysical Reviews (2021) Vol. 13, Iss. 5, pp. 653-677
Open Access | Times Cited: 22
Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort: The Use of Genetic Testing in Risk Stratification
Marijke H. van der Meulen, Johanna C. Herkert, Susanna L. den Boer, et al.
Circulation Genomic and Precision Medicine (2022)
Open Access | Times Cited: 15
Clustering of Cardiac Transcriptome Profiles Reveals Unique
Job A.J. Verdonschot, Ping Wang, Kasper Derks, et al.
JACC Basic to Translational Science (2023) Vol. 8, Iss. 4, pp. 406-418
Open Access | Times Cited: 9
Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies
M. Jansen, Remco de Brouwer, Fahima Hassanzada, et al.
JACC Heart Failure (2023) Vol. 12, Iss. 1, pp. 134-147
Closed Access | Times Cited: 8
Comprehensive review on gene mutations contributing to dilated cardiomyopathy
Shipeng Wang, Zhiyu Zhang, Jiahuan He, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 8
Genetic determinants of responsiveness to mesenchymal stem cell injections in non-ischemic dilated cardiomyopathy
Angela C. Rieger, Robert J. Myerburg, Victoria Florea, et al.
EBioMedicine (2019) Vol. 48, pp. 377-385
Open Access | Times Cited: 25
Dilated cardiomyopathy: a new insight into the rare but common cause of heart failure
Prerna Giri, Amrita Mukhopadhyay, Mohini Gupta, et al.
Heart Failure Reviews (2021) Vol. 27, Iss. 2, pp. 431-454
Closed Access | Times Cited: 20
Identification of SCN5a p.C335R Variant in a Large Family with Dilated Cardiomyopathy and Conduction Disease
Farbod Sedaghat‐Hamedani, Sabine Rebs, Ibrahim El‐Battrawy, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 23, pp. 12990-12990
Open Access | Times Cited: 20
A novel risk model for predicting potentially life-threatening arrhythmias in non-ischemic dilated cardiomyopathy (DCM-SVA risk)
Elham Kayvanpour, Arjan Sammani, Farbod Sedaghat‐Hamedani, et al.
International Journal of Cardiology (2021) Vol. 339, pp. 75-82
Open Access | Times Cited: 19
Molecular genetics in 4408 cardiomyopathy probands and 3008 relatives in Norway: 17 years of genetic testing in a national laboratory
Tonje Talsnes Stava, Trond P. Leren, Martin P. Bogsrud
European Journal of Preventive Cardiology (2022) Vol. 29, Iss. 13, pp. 1789-1799
Open Access | Times Cited: 12
Pharmacogenetics of chemotherapy treatment response and -toxicities in patients with osteosarcoma: a systematic review
Evelien G. E. Hurkmans, Annouk C. A. M. Brand, Job A.J. Verdonschot, et al.
BMC Cancer (2022) Vol. 22, Iss. 1
Open Access | Times Cited: 12

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