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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:

Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot
Donna J. Page, Matthieu J. Miossec, Simon G. Williams, et al.
Circulation Research (2019) Vol. 124, Iss. 4, pp. 553-563
Open Access | Times Cited: 161

Showing 1-25 of 161 citing articles:

Heart Disease and Stroke Statistics—2021 Update
Salim S. Virani, Álvaro Alonso, Hugo J. Aparicio, et al.
Circulation (2021) Vol. 143, Iss. 8
Open Access | Times Cited: 4765
Heart Disease and Stroke Statistics—2022 Update: A Report From the American Heart Association
Connie W. Tsao, Aaron W. Aday, Zaid Almarzooq, et al.
Circulation (2022) Vol. 145, Iss. 8
Open Access | Times Cited: 4330
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: 4309
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: 979
The impact of VEGF on cancer metastasis and systemic disease
Yunlong Yang, Yihai Cao
Seminars in Cancer Biology (2022) Vol. 86, pp. 251-261
Open Access | Times Cited: 171
Genomic frontiers in congenital heart disease
Sarah U. Morton, Daniel Quiat, Jonathan G. Seidman, et al.
Nature Reviews Cardiology (2021) Vol. 19, Iss. 1, pp. 26-42
Open Access | Times Cited: 160
Molecular Genetics and Complex Inheritance of Congenital Heart Disease
Nicholas S. Diab, Syndi Barish, Weilai Dong, et al.
Genes (2021) Vol. 12, Iss. 7, pp. 1020-1020
Open Access | Times Cited: 85
Lifespan Perspective on Congenital Heart Disease Research
Gerhard‐Paul Diller, Alexandra Arvanitaki, Alexander R. Opotowsky, et al.
Journal of the American College of Cardiology (2021) Vol. 77, Iss. 17, pp. 2219-2235
Open Access | Times Cited: 79
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
Cardiomyocyte Proliferation and Maturation: Two Sides of the Same Coin for Heart Regeneration
Ming‐Tao Zhao, Shiqiao Ye, Juan Su, et al.
Frontiers in Cell and Developmental Biology (2020) Vol. 8
Open Access | Times Cited: 72
Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH
Na Zhu, Emilia M. Swietlik, Carrie L. Welch, et al.
Genome Medicine (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 65
Genetics of congenital heart disease: a narrative review of recent advances and clinical implications
Jun Yasuhara, Vidu Garg
Translational Pediatrics (2021) Vol. 10, Iss. 9, pp. 2366-2386
Open Access | Times Cited: 58
Analyzing exosomal miRNA profiles in tetralogy of fallot fetuses’ amniotic fluid
Hainan Yang, Yadan Li, Qiuyue Chen, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access | Times Cited: 1
Enigmatic Vessel: The Persistent Hypoglossal Artery in a Tetralogy of Fallot Patient with brain abscess- Report of a rare case
Amina Hameed, Ranam Akhtar, Khurram Khaliq Bhinder, et al.
Medical Reports (2025), pp. 100167-100167
Open Access | Times Cited: 1
Congenital heart disease risk loci identified by genome-wide association study in European patients
Harald Lahm, Meiwen Jia, Martina Dreßen, et al.
Journal of Clinical Investigation (2020) Vol. 131, Iss. 2
Open Access | Times Cited: 70
Genetic Basis of Human Congenital Heart Disease
Shannon N. Nees, Wendy K. Chung
Cold Spring Harbor Perspectives in Biology (2019) Vol. 12, Iss. 9, pp. a036749-a036749
Open Access | Times Cited: 61
Genetic counselling and testing in adults with congenital heart disease: A consensus document of the ESC Working Group of Grown-Up Congenital Heart Disease, the ESC Working Group on Aorta and Peripheral Vascular Disease and the European Society of Human Genetics
Julie De Backer, Antoine Bondue, Werner Budts, et al.
European Journal of Preventive Cardiology (2019) Vol. 27, Iss. 13, pp. 1423-1435
Open Access | Times Cited: 55
PIWI-interacting RNA sequencing profiles in maternal plasma-derived exosomes reveal novel non-invasive prenatal biomarkers for the early diagnosis of nonsyndromic cleft lip and palate
Shanshan Jia, Qiang Zhang, Yu Wang, et al.
EBioMedicine (2021) Vol. 65, pp. 103253-103253
Open Access | Times Cited: 33
Impaired Human Cardiac Cell Development due to NOTCH1 Deficiency
Shiqiao Ye, Cankun Wang, Zhaohui Xu, et al.
Circulation Research (2022) Vol. 132, Iss. 2, pp. 187-204
Open Access | Times Cited: 27
Contribution of NOTCH1 genetic variants to bicuspid aortic valve and other congenital lesions
Radosław Dębiec, Stephen E. Hamby, Peter D. Jones, et al.
Heart (2022) Vol. 108, Iss. 14, pp. 1114-1120
Open Access | Times Cited: 24
Dysregulation of Lymphatic Endothelial VEGFR3 Signaling in Disease
Kevin Kuonqui, Adana-Christine Campbell, Ananta Sarker, et al.
Cells (2023) Vol. 13, Iss. 1, pp. 68-68
Open Access | Times Cited: 16
In-Depth Genomic Analysis: The New Challenge in Congenital Heart Disease
Francesco Nappi
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 3, pp. 1734-1734
Open Access | Times Cited: 6
FLT4 causes developmental disorders of the cardiovascular and lymphovascular systems via pleiotropic molecular mechanisms
Richard M. Monaghan, Richard W. Naylor, Daisy Flatman, et al.
Cardiovascular Research (2024) Vol. 120, Iss. 10, pp. 1164-1176
Open Access | Times Cited: 5
The Notch pathway: a novel therapeutic target for cardiovascular diseases?
Giorgio Aquila, Aleksandra Kostina, Francesco Vieceli Dalla Sega, et al.
Expert Opinion on Therapeutic Targets (2019) Vol. 23, Iss. 8, pp. 695-710
Open Access | Times Cited: 41
Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants
Gavin Chapman, Julie Moreau, I P Eddie, et al.
Human Molecular Genetics (2019) Vol. 29, Iss. 4, pp. 566-579
Open Access | Times Cited: 40
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