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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:

Frequency, Penetrance, and Variable Expressivity of Dilated Cardiomyopathy–Associated Putative Pathogenic Gene Variants in UK Biobank Participants
Ravi A. Shah, Babken Asatryan, Ghaith Sharaf Dabbagh, et al.
Circulation (2022) Vol. 146, Iss. 2, pp. 110-124
Open Access | Times Cited: 61

Showing 1-25 of 61 citing articles:

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
Prospective study design and data analysis in UK Biobank
Naomi E. Allen, Ben Lacey, Debbie A. Lawlor, et al.
Science Translational Medicine (2024) Vol. 16, Iss. 729
Open Access | Times Cited: 40
Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project
Robert C. Green, Nidhi Shah, Casie A. Genetti, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 7, pp. 1034-1045
Open Access | Times Cited: 26
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
Prevalence, Cardiac Phenotype, and Outcomes of Transthyretin Variants in the UK Biobank Population
Nay Aung, Hannah Nicholls, C. Anwar A. Chahal, et al.
JAMA Cardiology (2024) Vol. 9, Iss. 11, pp. 964-964
Closed Access | Times Cited: 8
Genetically transitional disease: a new concept in genomic medicine
Qingping Yao, Peter D. Gorevic, Bo Shen, et al.
Trends in Genetics (2022) Vol. 39, Iss. 2, pp. 98-108
Closed Access | Times Cited: 28
Genetic testing in early-onset atrial fibrillation
Shinwan Kany, Sean J. Jurgens, Joel Rämö, et al.
European Heart Journal (2024) Vol. 45, Iss. 34, pp. 3111-3123
Closed Access | Times Cited: 7
Penetrance of Dilated Cardiomyopathy in Genotype-Positive Relatives
Eva Cabrera-Romero, Juan Pablo Ochoa, Roberto Barriales‐Villa, et al.
Journal of the American College of Cardiology (2024) Vol. 83, Iss. 17, pp. 1640-1651
Open Access | Times Cited: 5
Association Between Clonal Hematopoiesis and Left Ventricular Reverse Remodeling in Nonischemic Dilated Cardiomyopathy
Shunsuke Inoue, Toshiyuki Ko, Akito Shindo, et al.
JACC Basic to Translational Science (2024) Vol. 9, Iss. 8, pp. 956-967
Open Access | Times Cited: 5
Vinculin haploinsufficiency impairs integrin-mediated costamere remodeling on stiffer microenvironments
Aileena C Nelson, Thomas G. Molley, Gisselle Gonzalez, et al.
Journal of Molecular and Cellular Cardiology (2025)
Closed Access
Advances in genetic diagnosis and therapy of hereditary heart disease: a bibliometric review from 2004 to 2024
Hernández Ma, Yun Wang, Yang Jia, et al.
Frontiers in Medicine (2025) Vol. 11
Open Access
Contemporary Insights into LMNA Cardiomyopathy
Iswaree Devi Balakrishnan, Neal K. Lakdawala
Current Cardiology Reports (2025) Vol. 27, Iss. 1
Closed Access
The association between systemic inflammation markers and the risk of incident dilated cardiomyopathy: a prospective study of 351,148 participants
Xihang Fu, Xiaodie Li, Xinxin Gao, et al.
Biomarkers (2025), pp. 1-8
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
Natural History, Phenotype Spectrum, and Clinical Outcomes of Desmin ( DES )-Associated Cardiomyopathy
Babken Asatryan, Marina Rieder, Brittney Murray, et al.
Circulation Genomic and Precision Medicine (2025)
Closed Access
Evaluation of Women with Peripartum or Dilated Cardiomyopathy and Their First-Degree Relatives: The DCM Precision Medicine Study
E. Kransdorf, Rashmi Jain, Jonathan O. Mead, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Actionable genetic variants in 4,198 Scottish participants from the Orkney and Shetland founder populations and implementation of return of results
Shona M. Kerr, Lucija Klarić, Marisa D. Muckian, et al.
The American Journal of Human Genetics (2025)
Open Access
Predicted Deleterious Variants in Cardiomyopathy Genes Prognosticate Mortality and Composite Outcomes in the UK Biobank
Babken Asatryan, Ravi A. Shah, Ghaith Sharaf Dabbagh, et al.
JACC Heart Failure (2023) Vol. 12, Iss. 5, pp. 918-932
Open Access | Times Cited: 10
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
Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy
Sean L. Zheng, Albert Henry, Douglas Cannie, et al.
Nature Genetics (2024) Vol. 56, Iss. 12, pp. 2646-2658
Open Access | Times Cited: 3
Dilated cardiomyopathy due to a novel combination of TTN and BAG3 genetic variants: From acute heart failure to subclinical phenotypes
Irene Bottillo, Carla Giordano, Maria Pia Ciccone, et al.
Cardiovascular Pathology (2024) Vol. 73, pp. 107675-107675
Open Access | Times Cited: 2
The Genetic Evaluation of Dilated Cardiomyopathy
Quan M. Bui, Jeffrey Ding, Kimberly N. Hong, et al.
Structural Heart (2023) Vol. 7, Iss. 5, pp. 100200-100200
Open Access | Times Cited: 5
Genome-wide association analysis reveals insights into the molecular etiology underlying dilated cardiomyopathy
Sean Zheng, Albert Henry, Douglas Cannie, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 5
Actionable Genotypes and Life Span in Iceland
Brynjar Ö. Jensson, Kári Stéfansson, Patrick Sulem
New England Journal of Medicine (2024) Vol. 390, Iss. 10, pp. 957-960
Closed Access | Times Cited: 1
Genetics and Molecular Mechanisms of Idiopathic Dilated Cardiomyopathy, a Possible Guide to Individualized Management
Diana-Aurora Arnăutu, Octavian-Marius Cretu, Daniel Lighezan, et al.
(2024)
Open Access | Times Cited: 1
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