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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:

Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
Rafik Tadros, Catherine Francis, Xiao Yun Xu, et al.
Nature Genetics (2021) Vol. 53, Iss. 2, pp. 128-134
Open Access | Times Cited: 229

Showing 1-25 of 229 citing articles:

Heart Disease and Stroke Statistics—2023 Update: A Report From the American Heart Association
Connie W. Tsao, Aaron W. Aday, Zaid Almarzooq, et al.
Circulation (2023) Vol. 147, Iss. 8
Open Access | Times Cited: 4138
2022 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death
Katja Zeppenfeld, Jacob Tfelt‐Hansen, Marta Riva, et al.
European Heart Journal (2022) Vol. 43, Iss. 40, pp. 3997-4126
Closed Access | Times Cited: 1677
2023 ESC Guidelines for the management of cardiomyopathies
Elena Arbelo, Alexandros Protonotarios, Juan R. Gimeno, et al.
European Heart Journal (2023) Vol. 44, Iss. 37, pp. 3503-3626
Open Access | Times Cited: 988
2024 Heart Disease and Stroke Statistics: A Report of US and Global Data From the American Heart Association
Seth S. Martin, Aaron W. Aday, Zaid Almarzooq, et al.
Circulation (2024) Vol. 149, Iss. 8
Open Access | Times Cited: 837
Plasma proteomic associations with genetics and health in the UK Biobank
Benjamin B. Sun, Joshua Chiou, Matthew Traylor, et al.
Nature (2023) Vol. 622, Iss. 7982, pp. 329-338
Open Access | Times Cited: 487
Evidence-Based Assessment of Genes in Dilated Cardiomyopathy
Elizabeth Jordan, Laiken Peterson, Tomohiko Ai, et al.
Circulation (2021) Vol. 144, Iss. 1, pp. 7-19
Open Access | Times Cited: 351
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases
Arthur A.M. Wilde, Christopher Semsarian, Manlio F. Márquez, et al.
EP Europace (2022) Vol. 24, Iss. 8, pp. 1307-1367
Open Access | Times Cited: 251
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity
Andrew R. Harper, Anuj Goel, Christopher Grace, et al.
Nature Genetics (2021) Vol. 53, Iss. 2, pp. 135-142
Open Access | Times Cited: 239
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases
Arthur A.M. Wilde, Christopher Semsarian, Manlio F. Márquez, et al.
Heart Rhythm (2022) Vol. 19, Iss. 7, pp. e1-e60
Open Access | Times Cited: 157
2024 AHA/ACC/AMSSM/HRS/PACES/SCMR Guideline for the Management of Hypertrophic Cardiomyopathy: A Report of the American Heart Association/American College of Cardiology Joint Committee on Clinical Practice Guidelines
Steve R. Ommen, Carolyn Y. Ho, Irfan M. Asif, et al.
Circulation (2024) Vol. 149, Iss. 23
Closed Access | Times Cited: 133
Genetic regulation of the human plasma proteome in 54,306 UK Biobank participants
Benjamin B. Sun, Joshua Chiou, Matthew Traylor, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 104
2024 AHA/ACC/AMSSM/HRS/PACES/SCMR Guideline for the Management of Hypertrophic Cardiomyopathy
Steve R. Ommen, Carolyn Y. Ho, Irfan M. Asif, et al.
Journal of the American College of Cardiology (2024) Vol. 83, Iss. 23, pp. 2324-2405
Closed Access | Times Cited: 85
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure
Michael G. Levin, Noah L. Tsao, Pankhuri Singhal, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 77
Dilated cardiomyopathy: causes, mechanisms, and current and future treatment approaches
Stéphane Heymans, Neal K. Lakdawala, Carsten Tschöpe, et al.
The Lancet (2023) Vol. 402, Iss. 10406, pp. 998-1011
Closed Access | Times Cited: 77
Genome-wide association studies of cardiovascular disease
Roddy Walsh, Sean J. Jurgens, Jeanette Erdmann, et al.
Physiological Reviews (2023) Vol. 103, Iss. 3, pp. 2039-2055
Closed Access | Times Cited: 44
Genetics of hypertrophic cardiomyopathy: established and emerging implications for clinical practice
Luís R. Lopes, Carolyn Y Ho, Perry Elliott
European Heart Journal (2024) Vol. 45, Iss. 30, pp. 2727-2734
Open Access | Times Cited: 15
Minor hypertrophic cardiomyopathy genes, major insights into the genetics of cardiomyopathies
Roddy Walsh, Joost A. Offerhaus, Rafik Tadros, et al.
Nature Reviews Cardiology (2021) Vol. 19, Iss. 3, pp. 151-167
Closed Access | Times Cited: 91
Phenotypic Expression and Outcomes in Individuals With Rare Genetic Variants of Hypertrophic Cardiomyopathy
Antonio de Marvao, Kathryn A. McGurk, Sean Zheng, et al.
Journal of the American College of Cardiology (2021) Vol. 78, Iss. 11, pp. 1097-1110
Open Access | Times Cited: 78
The Complex and Diverse Genetic Architecture of Dilated Cardiomyopathy
Ray E. Hershberger, Jason Cowan, Elizabeth Jordan, et al.
Circulation Research (2021) Vol. 128, Iss. 10, pp. 1514-1532
Open Access | Times Cited: 71
Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy
Luís R. Lopes, Soledad García-Hernández, Massimiliano Lorenzini, et al.
European Heart Journal (2021) Vol. 42, Iss. 32, pp. 3063-3073
Open Access | Times Cited: 68
Rare and Common Genetic Variation Underlying the Risk of Hypertrophic Cardiomyopathy in a National Biobank
Kiran J. Biddinger, Sean J. Jurgens, Dimitri J. Maamari, et al.
JAMA Cardiology (2022) Vol. 7, Iss. 7, pp. 715-715
Open Access | Times Cited: 42
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases
Arthur A.M. Wilde, Christopher Semsarian, Manlio F. Márquez, et al.
Journal of Arrhythmia (2022) Vol. 38, Iss. 4, pp. 491-553
Open Access | Times Cited: 40
Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death
Estefanía Martinez-Barrios, Simone Grassi, Marı́a Brión, et al.
Frontiers in Medicine (2023) Vol. 10
Open Access | Times Cited: 32
Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass
Shaan Khurshid, Julieta Lazarte, James P. Pirruccello, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 28
The penetrance of rare variants in cardiomyopathy-associated genes: A cross-sectional approach to estimating penetrance for secondary findings
Kathryn A. McGurk, Xiaolei Zhang, Pantazis Theotokis, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 9, pp. 1482-1495
Open Access | Times Cited: 25
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