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:

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: 26

Showing 1-25 of 26 citing articles:

The Role of the Notch Signaling Pathway in the Differentiation of Human Umbilical Cord-Derived Mesenchymal Stem Cells
Wanhong Xing, Jianxin Yang, Ying Zheng, et al.
Frontiers in Bioscience-Landmark (2024) Vol. 29, Iss. 2
Open Access | Times Cited: 8

Abnormal Progenitor Cell Differentiation and Cardiomyocyte Proliferation in Hypoplastic Right Heart Syndrome
Yang Yu, Cankun Wang, Shiqiao Ye, et al.
Circulation (2024) Vol. 149, Iss. 11, pp. 888-891
Closed Access | Times Cited: 4

Advances and challenges in the diagnosis and management of left ventricular noncompaction in adults: A literature review
Jordan Llerena-Velastegui, Sebastian Velastegui‐Zurita, Carolina Santander-Fuentes, et al.
Current Problems in Cardiology (2024) Vol. 49, Iss. 6, pp. 102571-102571
Open Access | Times Cited: 4

Decoding Hearts: Genetic Insights and Clinical Strategies in Congenital Heart Disease
Christopher M. Stark, Brian N. Hughes, John P. Schacht, et al.
NeoReviews (2025) Vol. 26, Iss. 2, pp. e73-e88
Closed Access

Cirrhosis Promotes Cardiac Fibrosis Development by Inhibiting Notch1 in Cardiac Fibroblasts
He Sun, Kai Song, Zeyu Zhou, et al.
JACC Basic to Translational Science (2025)
Open Access

Genetics of single ventricle congenital heart disease
Sarah U. Morton, Tina O. Findley
Elsevier eBooks (2025), pp. 13-28
Closed Access

Aspirin and Celecoxib Regulate Notch1/Hes1 Pathway to Prevent Pressure Overload-Induced Myocardial Hypertrophy
Wei Minghui, Ziyu Lu, Haifeng Zhang, et al.
International Heart Journal (2024) Vol. 65, Iss. 3, pp. 475-486
Open Access | Times Cited: 3

The new era of cardiovascular research: revolutionizing cardiovascular research with 3D models in a dish
Yuan Yang, Hao Yang, Fedir N. Kiskin, et al.
Medical Review (2024) Vol. 4, Iss. 1, pp. 68-85
Open Access | Times Cited: 2

NOTCH1 Gene as a Novel Cause of Thoracic Aortic Aneurysm in Patients with Tricuspid Aortic Valve: Two Cases Reported
Laura Torres‐Juan, Yolanda Rico, Elena Fortuny, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 10, pp. 8644-8644
Open Access | Times Cited: 6

Inhibition of SUV39H1 reduces tumor angiogenesis via Notch1 in oral squamous cell carcinoma
Yan Chen, Xiuhong Weng, Chuanjie Zhang, et al.
PeerJ (2024) Vol. 12, pp. e17222-e17222
Open Access | Times Cited: 1

Cardiomyocyte proliferation and regeneration in congenital heart disease
Jialiang Liang, Xingyu He, Yigang Wang
Pediatric Discovery (2024) Vol. 2, Iss. 3
Open Access | Times Cited: 1

A Contemporary Review of the Genomic Associations of Coronary Artery Myocardial Bridging
Peyton Moore, Paul R. Murdock, Akash Ramanathan, et al.
Genes (2023) Vol. 14, Iss. 12, pp. 2175-2175
Open Access | Times Cited: 2

Exploring the Multiple Roles of Notch1 in Biological Development: An Analysis and Study Based on Phylogenetics and Transcriptomics
Yuesi Zhou, Zihao Yan, Ya Pang, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 1, pp. 611-611
Open Access

The Addis Ababa Lions: Whole-Genome Sequencing of a Rare and Precious Population
Marjan Barazandeh, Divya Kriti, Jörns Fickel, et al.
Genome Biology and Evolution (2024) Vol. 16, Iss. 2
Open Access

Deciphering Congenital Heart Disease Using Human Induced Pluripotent Stem Cells
Hao Zhang, Joseph C Wu
Advances in experimental medicine and biology (2024), pp. 239-252
Closed Access

Integrated multi-omics analysis identifies features that predict human pluripotent stem cell-derived progenitor differentiation to cardiomyocytes
Aaron D. Simmons, Claudia Baumann, Xiangyu Zhang, et al.
Journal of Molecular and Cellular Cardiology (2024) Vol. 196, pp. 52-70
Closed Access

In Vivo and In Vitro Approaches to Modeling Hypoplastic Left Heart Syndrome
Matthew Alonzo, Javier Contreras, Jakob Bering, et al.
Current Cardiology Reports (2024)
Open Access

Genetic Insights into Congenital Cardiac Septal Defects—A Narrative Review
Jorge L. Cervantes‐Salazar, Nonanzit Pérez‐Hernández, Juan Calderón‐Colmenero, et al.
Biology (2024) Vol. 13, Iss. 11, pp. 911-911
Open Access

Characterization of genomic variants associated with congenital heart disease in patients from southwestern Colombian
Angie Lizeth Grueso Cerón, Daniela Arturo-Terranova, José Soto
Heliyon (2023) Vol. 10, Iss. 1, pp. e23678-e23678
Open Access | Times Cited: 1

hiPSCs as a Unique Platform to Model Cardiogenesis in NOTCH1-Associated HLHS: hiPSCs to Model Complex Congenital Heart Defects
Fabrice Jaffré
Circulation Research (2023) Vol. 132, Iss. 2, pp. 205-207
Closed Access

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