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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.

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Showing 1-25 of 55 citing articles:

2020 ESC Guidelines for the management of adult congenital heart disease
Helmut Baumgartner, Julie De Backer, Sonya V. Babu‐Narayan, et al.
European Heart Journal (2020) Vol. 42, Iss. 6, pp. 563-645
Open Access | Times Cited: 1552
2024 ESC Guidelines for the management of peripheral arterial and aortic diseases
Lucia Mazzolai, Gisela Teixidó‐Turà, Stefano Lanzi, et al.
European Heart Journal (2024)
Open Access | Times Cited: 132
Clinical relevance of genotype–phenotype correlations beyond vascular events in a cohort study of 1500 Marfan syndrome patients with FBN1 pathogenic variants
Pauline Arnaud, Olivier Milleron, Nadine Hanna, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 7, pp. 1296-1304
Open Access | Times Cited: 98
Pregnancy in congenital heart disease: risk prediction and counselling
Iris M. van Hagen, Jolien W. Roos‐Hesselink
Heart (2020) Vol. 106, Iss. 23, pp. 1853-1861
Open Access | Times Cited: 76
The Cardiac Genome Clinic: implementing genome sequencing in pediatric heart disease
Miriam S. Reuter, Rajiv Chaturvedi, Eriskay Liston, et al.
Genetics in Medicine (2020) Vol. 22, Iss. 6, pp. 1015-1024
Open Access | Times Cited: 74
Clinical features and complications of Loeys-Dietz syndrome: A systematic review
Pishoy Gouda, Robert Kay, Marina Habib, et al.
International Journal of Cardiology (2022) Vol. 362, pp. 158-167
Open Access | Times Cited: 56
Pregnancy in patients with the Fontan operation
Claudia Montanaro, Siobhán Boyle, Gurleen Wander, et al.
European Journal of Preventive Cardiology (2024) Vol. 31, Iss. 11, pp. 1336-1344
Closed Access | Times Cited: 9
Cardiovascular Management of Aortopathy in Children: A Scientific Statement From the American Heart Association
Shaine A. Morris, Jonathan N. Flyer, Anji T. Yetman, et al.
Circulation (2024) Vol. 150, Iss. 11
Closed Access | Times Cited: 8
Deep learning-derived 12-lead electrocardiogram-based genotype prediction for hypertrophic cardiomyopathy: a pilot study
Laite Chen, Xia Sheng, Chenyang Jiang
Annals of Medicine (2023) Vol. 55, Iss. 1
Open Access | Times Cited: 17
Clinical Decision Analysis of Genetic Evaluation and Testing in 1013 Intensive Care Unit Infants with Congenital Heart Defects Supports Universal Genetic Testing
Benjamin M. Helm, Stephanie M. Ware
Genes (2024) Vol. 15, Iss. 4, pp. 505-505
Open Access | Times Cited: 6
The Role of Genetic Testing in Patients with Heritable Thoracic Aortic Diseases
Emanuele Monda, Michele Lioncino, Federica Verrillo, et al.
Diagnostics (2023) Vol. 13, Iss. 4, pp. 772-772
Open Access | Times Cited: 14
The role of genetic testing in Marfan syndrome
Emanuele Monda, Martina Caiazza, Giuseppe Limongelli
Current Opinion in Cardiology (2024) Vol. 39, Iss. 3, pp. 162-169
Closed Access | Times Cited: 4
Outcomes and experiences of genetic testing in children with congenital heart disease
A. Morrish, B. O’Malley, D. Hilton, et al.
Journal of Medical Genetics (2025), pp. jmg-110553
Closed Access
Current and future diagnostics of congenital heart disease (CHD)
Marc‐Phillip Hitz, Gregor Dombrowsky, Н А Мельник, et al.
Medizinische Genetik (2025) Vol. 37, Iss. 2, pp. 95-102
Closed Access
Thoracic Aortic Dilation: Implications for Physical Activity and Sport Participation
Emanuele Monda, Federica Verrillo, Marta Rubino, et al.
Diagnostics (2022) Vol. 12, Iss. 6, pp. 1392-1392
Open Access | Times Cited: 17
Current approach to genetic testing and genetic evaluation referrals for adults with congenital heart disease
Laura B. Oehlman, Alexander R. Opotowsky, K. Nicole Weaver, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 3
A cell and transcriptome atlas of the human arterial vasculature
Quanyi Zhao, Albert J. Pedroza, Disha Sharma, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access | Times Cited: 3
Genetic counseling for congenital heart disease – Practice resource of the National Society of Genetic Counselors
Hannah E. Ison, Emily Griffin, A. Parrott, et al.
Journal of Genetic Counseling (2021) Vol. 31, Iss. 1, pp. 9-33
Open Access | Times Cited: 23
The genetic workup for structural congenital heart disease
Teodoro Jerves, Andrea Beaton, Paul Kruszka
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2019) Vol. 184, Iss. 1, pp. 178-186
Closed Access | Times Cited: 24
Cardiopatías congénitas del adulto en España: estructura, actividad y características clínicas
José María Oliver Ruiz, Laura Dos, Ana González García, et al.
Revista Española de Cardiología (2020) Vol. 73, Iss. 10, pp. 804-811
Closed Access | Times Cited: 23
Genetic Testing in Patients With Congenital Heart Disease: You Do No Harm When Using the Right Tools!
Julie De Backer, Laura Muiño Mosquera
Circulation Genomic and Precision Medicine (2023) Vol. 16, Iss. 2
Closed Access | Times Cited: 7
Current state and future directions of genomic medicine in aortic dissection: A path to prevention and personalized care
Alana C. Cecchi, Madeline Drake, Chrisanne S. Campos, et al.
Seminars in Vascular Surgery (2022) Vol. 35, Iss. 1, pp. 51-59
Open Access | Times Cited: 12
WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation
Lili Hao, Jing Ma, Feizhen Wu, et al.
Clinical and Translational Medicine (2022) Vol. 12, Iss. 7
Open Access | Times Cited: 12
Peripheral microRNA panels to guide the diagnosis of familial cardiomyopathy
Thalía Belmonte, Alipio Mangas, María Calderón‐Domínguez, et al.
Translational research (2020) Vol. 218, pp. 1-15
Closed Access | Times Cited: 18
Uncovering the Genetic Basis of Congenital Heart Disease: Recent Advancements and Implications for Clinical Management
Karanjot Chhatwal, J J Smith, Harroop Bola, et al.
CJC Pediatric and Congenital Heart Disease (2023) Vol. 2, Iss. 6, pp. 464-480
Open Access | Times Cited: 6
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