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:

Decoding Genetics of Congenital Heart Disease Using Patient-Derived Induced Pluripotent Stem Cells (iPSCs)
Hui Lin, Kim L. McBride, Vidu Garg, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 29

Showing 1-25 of 29 citing articles:

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: 56

Molecular genetic mechanisms of congenital heart disease
Talita Zahin Choudhury, Vidu Garg
Current Opinion in Genetics & Development (2022) Vol. 75, pp. 101949-101949
Open Access | Times Cited: 20

The Alberta Congenital Anomalies Surveillance System: a 40-year review with prevalence and trends for selected congenital anomalies, 1997–2019
R. Brian Lowry, Tanya Bedard, Xin Grevers, et al.
Health Promotion and Chronic Disease Prevention in Canada (2023) Vol. 43, Iss. 1, pp. 40-48
Open Access | Times Cited: 7

Understanding the Genetic and Non-genetic Interconnections in the Aetiology of Isolated Congenital Heart Disease: An Updated Review: Part 1
Jyoti Maddhesiya, Bhagyalaxmi Mohapatra
Current Cardiology Reports (2024) Vol. 26, Iss. 3, pp. 147-165
Closed Access | Times Cited: 2

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

Personalized Genetic Diagnosis of Congenital Heart Defects in Newborns
Olga María Diz, Rocío Toro, Sergi César, et al.
Journal of Personalized Medicine (2021) Vol. 11, Iss. 6, pp. 562-562
Open Access | Times Cited: 13

Bioengineering Systems for Modulating Notch Signaling in Cardiovascular Development, Disease, and Regeneration
Angello Huerta Gomez, Sanika Joshi, Yong Yang, et al.
Journal of Cardiovascular Development and Disease (2021) Vol. 8, Iss. 10, pp. 125-125
Open Access | Times Cited: 11

Progresses in genetic testing in congenital heart disease
Han Gao, Ying Liu, Wei Sheng, et al.
Medicine Plus (2024) Vol. 1, Iss. 2, pp. 100028-100028
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

Probing single ventricle heart defects with patient‐derived induced pluripotent stem cells and emerging technologies
Bailey Hall, Matthew Alonzo, Karen Texter, et al.
Birth Defects Research (2022) Vol. 114, Iss. 16, pp. 959-971
Open Access | Times Cited: 6

Translational potential of hiPSCs in predictive modeling of heart development and disease
Corrin Mansfield, Ming‐Tao Zhao, Madhumita Basu
Birth Defects Research (2022) Vol. 114, Iss. 16, pp. 926-947
Open Access | Times Cited: 5

An evidence appraisal of heart organoids in a dish and commensurability to human heart development in vivo
Dilip Thomas, Vinicio A. de Jesús Pérez, Nazish Sayed
BMC Cardiovascular Disorders (2022) Vol. 22, Iss. 1
Open Access | Times Cited: 5

Biosensor-based profiling to track cellular signalling in patient-derived models of dilated cardiomyopathy
Kyla Bourque, Cara Hawey, Alyson Jiang, et al.
Cellular Signalling (2022) Vol. 91, pp. 110239-110239
Closed Access | Times Cited: 4

Generation of iPSC line NCHi015-A from a patient with truncus arteriosus carrying heterozygous variants in KMT2D and NOTCH1
Jerry Wang, Jakob Bering, Matthew Alonzo, et al.
Stem Cell Research (2024) Vol. 78, pp. 103457-103457
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

From genes to therapy: A comprehensive exploration of congenital heart disease through the lens of genetics and emerging technologies
Khalid Nawaz, Nur Alifah, Talib Hussain, et al.
Current Problems in Cardiology (2024) Vol. 49, Iss. 9, pp. 102726-102726
Closed Access

Current genetic models for studying congenital heart diseases: Advantages and disadvantages
Ayat M. Shorbaji, Peter Natesan Pushparaj, Sherin Bakhashab, et al.
Bioinformation (2024) Vol. 20, Iss. 5, pp. 415-429
Open Access

Le système de surveillance des anomalies congénitales de l’Alberta : compte rendu des données sur 40 ans avec prévalence et tendances de certaines anomalies congénitales entre 1997 et 2019
R. Brian Lowry, Tanya Bedard, Xin Grevers, et al.
Promotion de la santé et prévention des maladies chroniques au Canada (2023) Vol. 43, Iss. 1, pp. 42-51
Open Access | Times Cited: 1

Creation of iPSC line NCHi004-A from a patient with down syndrome and congenital heart defects
Matthew Alonzo, Shiqiao Ye, Brian R. Beckman, et al.
Stem Cell Research (2023) Vol. 71, pp. 103156-103156
Open Access | Times Cited: 1

Generation of Cardiomyocytes and Endothelial Cells from Human iPSCs by Chemical Modulation of Wnt Signaling
Arline Joachim, Shiqiao Ye, Ming‐Tao Zhao
Methods in molecular biology (2021), pp. 335-344
Closed Access | Times Cited: 3

Generation of an induced pluripotent stem cell line NCHi003-A from a 11-year-old male with pulmonary atresia with intact ventricular septum (PA-IVS)
Javier Contreras, Matthew Alonzo, Shiqiao Ye, et al.
Stem Cell Research (2022) Vol. 64, pp. 102893-102893
Open Access | Times Cited: 2

Generation and characterization of a human induced pluripotent stem cell (iPSC) line from a patient with congenital heart disease (CHD)
Hui Lin, Shiqiao Ye, Zhaohui Xu, et al.
Stem Cell Research (2022) Vol. 65, pp. 102958-102958
Open Access | Times Cited: 2

Quantitative Proteomic Profiling of Murine Embryonic Heart Development Reveals a Role for the Mevalonate Pathway in Cardiomyocyte Proliferation
W. Daniel Edwards, Todd M. Greco, Gregory E. Miner, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Closed Access | Times Cited: 1

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