Open Access Helper

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:

Congenital heart defects caused by FOXJ1
Maria B. Padua, Benjamin M. Helm, John R Wells, et al.
Human Molecular Genetics (2023) Vol. 32, Iss. 14, pp. 2335-2346
Closed Access | Times Cited: 10

Showing 10 citing articles:

Application of copy number variation sequencing combined with whole exome sequencing in prenatal left–right asymmetry disorders
Yu Qin, Muon Senglong, Koksear Touch, et al.
BMC Genomics (2025) Vol. 26, Iss. 1
Open Access
Genetics of single ventricle congenital heart disease
Sarah U. Morton, Tina O. Findley
Elsevier eBooks (2025), pp. 13-28
Closed Access
Identification and Functional Characterization of a Novel SOX4 Mutation Predisposing to Coffin–Siris Syndromic Congenital Heart Disease
Zi Yan, Binbin Dong, Yan-Jie Li, et al.
Children (2025) Vol. 12, Iss. 5, pp. 608-608
Open Access
Study on Potential Differentially Expressed Genes in Idiopathic Pulmonary Fibrosis by Bioinformatics and Next-Generation Sequencing Data Analysis
Muttanagouda Giriyappagoudar, Basavaraj Vastrad, Rajeshwari Horakeri, et al.
Biomedicines (2023) Vol. 11, Iss. 12, pp. 3109-3109
Open Access | Times Cited: 7
Zebrafish as a Model Organism for Congenital Hydrocephalus: Characteristics and Insights
Kaiyue Wang, Zhi Tang, Yijian Yang, et al.
Zebrafish (2024)
Closed Access | Times Cited: 2
<i>FOXJ1</i> Variants Causing Primary Ciliary Dyskinesia with Hydrocephalus: A Case Report from Japan
Masashi Ito, Kozo Morimoto, Takashi Ohfuji, et al.
Internal Medicine (2023) Vol. 63, Iss. 10, pp. 1433-1437
Open Access | Times Cited: 4
Discovery and functional investigation of BMP4 as a new causative gene for human congenital heart disease
Zhi Wang
American Journal of Translational Research (2024) Vol. 16, Iss. 5, pp. 2034-2048
Open Access | Times Cited: 1
Ectopic MYBL2-Mediated Regulation of Androglobin Gene Expression
A. Herwig, Carina Osterhof, Anna Keppner, et al.
Cells (2024) Vol. 13, Iss. 10, pp. 826-826
Open Access | Times Cited: 1
Study on potential differentially expressed genes in idiopathic pulmonary fibrosis by bioinformatics and next generation sequencing data analysis
Basavaraj Vastrad, Chanabasayya Vastrad
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
The role of primary cilia in congenital heart defect-associated neurological impairments
Nemanja Sarić, Nobuyuki Ishibashi
Frontiers in Genetics (2024) Vol. 15
Open Access
Non-coding cause of congenital heart defects: Abnormal RNA splicing with multiple isoforms as a mechanism for heterotaxy
John R Wells, Maria B. Padua, Allison Haaning, et al.
Human Genetics and Genomics Advances (2024) Vol. 5, Iss. 4, pp. 100353-100353
Open Access
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