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:
Assessment of the Diagnostic Yield of Combined Cardiomyopathy and Arrhythmia Genetic Testing
Lisa Dellefave‐Castillo, Allison L. Cirino, Thomas E. Callis, et al.
JAMA Cardiology (2022) Vol. 7, Iss. 9, pp. 966-966
Open Access | Times Cited: 54
Lisa Dellefave‐Castillo, Allison L. Cirino, Thomas E. Callis, et al.
JAMA Cardiology (2022) Vol. 7, Iss. 9, pp. 966-966
Open Access | Times Cited: 54
Showing 1-25 of 54 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: 1038
Elena Arbelo, Alexandros Protonotarios, Juan R. Gimeno, et al.
European Heart Journal (2023) Vol. 44, Iss. 37, pp. 3503-3626
Open Access | Times Cited: 1038
Genes Associated With Hypertrophic Cardiomyopathy
Sophie Hespe, Amber Waddell, Babken Asatryan, et al.
Journal of the American College of Cardiology (2025) Vol. 85, Iss. 7, pp. 727-740
Closed Access | Times Cited: 4
Sophie Hespe, Amber Waddell, Babken Asatryan, et al.
Journal of the American College of Cardiology (2025) Vol. 85, Iss. 7, pp. 727-740
Closed Access | Times Cited: 4
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
Estefanía Martinez-Barrios, Simone Grassi, Marı́a Brión, et al.
Frontiers in Medicine (2023) Vol. 10
Open Access | Times Cited: 32
Ethnicity, consanguinity, and genetic architecture of hypertrophic cardiomyopathy
Mona Allouba, Roddy Walsh, Alaa Afify, et al.
European Heart Journal (2023) Vol. 44, Iss. 48, pp. 5146-5158
Open Access | Times Cited: 23
Mona Allouba, Roddy Walsh, Alaa Afify, et al.
European Heart Journal (2023) Vol. 44, Iss. 48, pp. 5146-5158
Open Access | Times Cited: 23
Genetic Testing in Brugada Syndrome: A 30-Year Experience
Luigi Pannone, Antonio Bisignani, Randy Osei, et al.
Circulation Arrhythmia and Electrophysiology (2024) Vol. 17, Iss. 4
Closed Access | Times Cited: 10
Luigi Pannone, Antonio Bisignani, Randy Osei, et al.
Circulation Arrhythmia and Electrophysiology (2024) Vol. 17, Iss. 4
Closed Access | Times Cited: 10
Clinical Effect of Genetic Testing in Inherited Cardiovascular Diseases
Steffany Grondin, Benjamin Neveu, Iness Soltani, et al.
Journal of the American College of Cardiology (2025) Vol. 85, Iss. 10, pp. 988-999
Closed Access | Times Cited: 1
Steffany Grondin, Benjamin Neveu, Iness Soltani, et al.
Journal of the American College of Cardiology (2025) Vol. 85, Iss. 10, pp. 988-999
Closed Access | Times Cited: 1
ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel: Reappraisal of Genes associated with Hypertrophic Cardiomyopathy
Sophie Hespe, Amber Waddell, Babken Asatryan, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 6
Sophie Hespe, Amber Waddell, Babken Asatryan, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 6
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young
Megan J. Puckelwartz, Lorenzo L. Pesce, Edgar J. Hernández, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 5
Megan J. Puckelwartz, Lorenzo L. Pesce, Edgar J. Hernández, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 5
Diagnostic yield after next-generation sequencing in pediatric cardiovascular disease
Anne Slavotinek, Michelle L. Thompson, Lisa J. Martin, et al.
Human Genetics and Genomics Advances (2024) Vol. 5, Iss. 3, pp. 100286-100286
Open Access | Times Cited: 5
Anne Slavotinek, Michelle L. Thompson, Lisa J. Martin, et al.
Human Genetics and Genomics Advances (2024) Vol. 5, Iss. 3, pp. 100286-100286
Open Access | Times Cited: 5
Pathophysiology of dilated cardiomyopathy: from mechanisms to precision medicine
Marta Gigli, Davide Stolfo, Marco Merlo, et al.
Nature Reviews Cardiology (2024)
Closed Access | Times Cited: 5
Marta Gigli, Davide Stolfo, Marco Merlo, et al.
Nature Reviews Cardiology (2024)
Closed Access | Times Cited: 5
Hereditary Transthyretin Amyloidosis in Patients Referred to a Genetic Testing Program
Kunal Bhatt, Diego Delgado, Sami Khella, et al.
Journal of the American Heart Association (2024)
Closed Access | Times Cited: 4
Kunal Bhatt, Diego Delgado, Sami Khella, et al.
Journal of the American Heart Association (2024)
Closed Access | Times Cited: 4
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
Hernández Ma, Yun Wang, Yang Jia, et al.
Frontiers in Medicine (2025) Vol. 11
Open Access
Sudden Cardiac Death: The Role of Molecular Autopsy with Next-Generation Sequencing
Jennifer Fadoni, Agostinho Santos, António Amorim, et al.
Diagnostics (2025) Vol. 15, Iss. 4, pp. 460-460
Open Access
Jennifer Fadoni, Agostinho Santos, António Amorim, et al.
Diagnostics (2025) Vol. 15, Iss. 4, pp. 460-460
Open Access
Sudden cardiac death: the role of molecular autopsy with next-generation sequencing
Jennifer Fadoni, Agostinho Santos, Laura Cainé, et al.
Journal of Forensic and Legal Medicine (2025), pp. 102837-102837
Closed Access
Jennifer Fadoni, Agostinho Santos, Laura Cainé, et al.
Journal of Forensic and Legal Medicine (2025), pp. 102837-102837
Closed Access
Genetik der Kardiomyopathien und Arrhythmien – Risikobeurteilung und Therapieperspektive
Michael J. Wisdom, Benjamin Meder
Deleted Journal (2025)
Closed Access
Michael J. Wisdom, Benjamin Meder
Deleted Journal (2025)
Closed Access
Genetic Testing for Cardiovascular Disease
James L. Laws, Giovanni Davogustto, Quinn S. Wells
Journal of the American College of Cardiology (2025) Vol. 85, Iss. 10, pp. 1000-1002
Closed Access
James L. Laws, Giovanni Davogustto, Quinn S. Wells
Journal of the American College of Cardiology (2025) Vol. 85, Iss. 10, pp. 1000-1002
Closed Access
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum
David S.M. Lee, Kathleen M. Cardone, David Zhang, et al.
Nature Genetics (2025)
Closed Access
David S.M. Lee, Kathleen M. Cardone, David Zhang, et al.
Nature Genetics (2025)
Closed Access
The Prenatal Diagnosis and Perinatal Management of Congenital Long QT Syndrome: A Comprehensive Literature Review and Recent Updates
Stefani Samples, Sara Cherny, Nitin Madan, et al.
Journal of Cardiovascular Development and Disease (2025) Vol. 12, Iss. 4, pp. 156-156
Open Access
Stefani Samples, Sara Cherny, Nitin Madan, et al.
Journal of Cardiovascular Development and Disease (2025) Vol. 12, Iss. 4, pp. 156-156
Open Access
Emerging risk factors for heart failure in younger populations: A growing public health concern
Razieh Parizad, Akash Batta, Juniali Hatwal, et al.
World Journal of Cardiology (2025) Vol. 17, Iss. 4
Closed Access
Razieh Parizad, Akash Batta, Juniali Hatwal, et al.
World Journal of Cardiology (2025) Vol. 17, Iss. 4
Closed Access
Genetic Testing in Early-Onset Atrial Fibrillation
Olivia S. Anderson, Thomas P. Cappola, Sharlene Day
JAMA Cardiology (2025)
Closed Access
Olivia S. Anderson, Thomas P. Cappola, Sharlene Day
JAMA Cardiology (2025)
Closed Access
Mechanisms of Sarcomere Protein Mutation-Induced Cardiomyopathies
David Y. Barefield, Alejandro Álvarez-Arce, Kelly Araujo
Current Cardiology Reports (2023) Vol. 25, Iss. 6, pp. 473-484
Open Access | Times Cited: 10
David Y. Barefield, Alejandro Álvarez-Arce, Kelly Araujo
Current Cardiology Reports (2023) Vol. 25, Iss. 6, pp. 473-484
Open Access | Times Cited: 10
Application of next generation sequencing in cardiology: current and future precision medicine implications
Eirini Papadopoulou, Dimitra Bouzarelou, George S. Tsaousis, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 8
Eirini Papadopoulou, Dimitra Bouzarelou, George S. Tsaousis, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 8
Evolving cardiovascular genetic counseling needs in the era of precision medicine
Ana Morales, Jessica Goehringer, Despina Sanoudou
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 8
Ana Morales, Jessica Goehringer, Despina Sanoudou
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 8
Genetic Evaluation and Screening in Cardiomyopathies: Opportunities and Challenges for Personalized Medicine
Sahana Aiyer, Emilia Kalutskaya, Arianne Clare Agdamag, et al.
Journal of Personalized Medicine (2023) Vol. 13, Iss. 6, pp. 887-887
Open Access | Times Cited: 7
Sahana Aiyer, Emilia Kalutskaya, Arianne Clare Agdamag, et al.
Journal of Personalized Medicine (2023) Vol. 13, Iss. 6, pp. 887-887
Open Access | Times Cited: 7
Advances in the diagnosis and treatment of transthyretin amyloid cardiomyopathy
Joban Vaishnav, Emily Brown, Kavita Sharma
Progress in Cardiovascular Diseases (2024) Vol. 82, pp. 113-124
Closed Access | Times Cited: 2
Joban Vaishnav, Emily Brown, Kavita Sharma
Progress in Cardiovascular Diseases (2024) Vol. 82, pp. 113-124
Closed Access | Times Cited: 2
