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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:

The Potential of Single Nucleotide Polymorphisms (SNPs) as Biomarkers and Their Association with the Increased Risk of Coronary Heart Disease: A Systematic Review
Bernap Dwi Putra Sitinjak, Niky Murdaya, Tiara Anisya Rachman, et al.
Vascular Health and Risk Management (2023) Vol. Volume 19, pp. 289-301
Open Access | Times Cited: 18

Showing 18 citing articles:

Evaluation of single nucleotide polymorphisms in the human norepinephrine transporter (hNET) gene for structural, functional, and pathogenic significance
Orçun Avşar
Nucleosides Nucleotides & Nucleic Acids (2025), pp. 1-16
Closed Access | Times Cited: 1
Genetic, lifestyle and metabolic factors contributing to cardiovascular disease in the Italian population: a literature review
Claudia Ojeda‐Granados, E Campisi, Martina Barchitta, et al.
Frontiers in Nutrition (2024) Vol. 11
Open Access | Times Cited: 4
Targeting senescence and GATA4 in age-related cardiovascular disease: a comprehensive approach
Mohd Imran, Abdulmalik Saleh Alfawaz Altamimi, Muhammad Afzal, et al.
Biogerontology (2025) Vol. 26, Iss. 1
Closed Access
Association of functional variants in miRNA genes with the risk of coronary heart disease
Taqweem Ul Haq, Muhammad Riaz Khan, Sajjad Ali, et al.
Egyptian Journal of Medical Human Genetics (2025) Vol. 26, Iss. 1
Open Access
Clinical Application of Artificial Intelligence in the Diagnosis, Prediction, and Classification of Coronary Heart Disease
Mahbuba Ferdowsi, Choon‐Hian Goh, Haipeng Liu, et al.
Cardiovascular Innovations and Applications (2025) Vol. 10, Iss. 1
Open Access
In Silico Functional and Structural Analysis of Non-synonymous Single Nucleotide Polymorphisms (nsSNPs) in Human Paired Box 4 Gene
Md. Mostafa Kamal, Md. Numan Islam, Md. Golam Rabby, et al.
Biochemical Genetics (2023) Vol. 62, Iss. 4, pp. 2975-2998
Closed Access | Times Cited: 5
From Cells to Plaques: The Molecular Pathways of Coronary Artery Calcification and Disease
Andreas Mitsis, Elina Khattab, Evi Christodoulou, et al.
Journal of Clinical Medicine (2024) Vol. 13, Iss. 21, pp. 6352-6352
Open Access | Times Cited: 1
ANRIL's Epigenetic Regulation and Its Implications for Cardiovascular Disorders
Ehssan Moglad, Parjinder Kaur, Soumya V. Menon, et al.
Journal of Biochemical and Molecular Toxicology (2024) Vol. 38, Iss. 12
Open Access | Times Cited: 1
Pangenomics of the cichlid species (Oreochromis niloticus) reveals genetic admixture ancestry with potential for aquaculture improvement in Kenya
John Gitau Mwaura, Clabe Wekesa, Kiprotich Kelvin, et al.
The Journal of Basic and Applied Zoology (2023) Vol. 84, Iss. 1
Open Access | Times Cited: 2
Moving from GWAS signals to rare functional variation in inflammatory bowel disease through application of GenePy2 as a potential DNA biomarker
Guo Cheng, James J. Ashton, Andrew Collins, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Examining treatment targets and equity in bone-active medication use within secondary fracture prevention: a systematic review and meta-analysis
Anum Ali, Ella Huszti, Shahryar Noordin, et al.
Osteoporosis International (2024) Vol. 35, Iss. 9, pp. 1497-1511
Closed Access
Tackling the role of rare functional variation in inflammatory bowel disease through application of GenePy2 as a potential DNA biomarker
Sarah Ennis, Guo Cheng, James J. Ashton, et al.
Research Square (Research Square) (2024)
Open Access
The Relationship Between GAPDH Gene Polymorphism and Risk of Acute Coronary Syndrome in South Indians with Type 2 Diabetes Mellitus
Sushmita Bora, Prashant Shankarrao Adole, Kolar Vishwanath Vinod, et al.
Biochemical Genetics (2024)
Closed Access
Functional Genomics and Human Diseases
Shuvomoy Banerjee, Juni Banerjee, Anand Krishna Tiwari
(2024), pp. 141-166
Closed Access
Correlation of Osteocalcin with Vitamin D Level in Postmenopausal Women Concerning CYP24A1 and VDR Gene Polymorphisms
Noor Mohammed Abdulrahman, Shatha Hussein Ali
AL-Kindy College Medical Journal (2024) Vol. 20, Iss. 2, pp. 135-144
Open Access
Impact of missense mutations on the structure–function relationship of human succinyl-CoA synthetase using in silico analysis
Sarra El-Abed, Olfa Alila Fersi, Abdelaziz Tlili, et al.
Mitochondrion (2024) Vol. 80, pp. 101978-101978
Closed Access
Gene expression & biochemical analysis in alkaptonuria caused by a founder pathogenic variant across different age groups from India
S. Abraham, Anitha Barney, Sony Mohan, et al.
The Indian Journal of Medical Research (2024) Vol. 160, pp. 448-456
Open Access
Lack of association between the −2549 insertion/deletion variant of vascular endothelial growth factor and coronary artery disease in the Turkish population
Serbülent Yığıt, Ayşe Feyda Nursal, Ataç ÇELİK, et al.
Revista da Associação Médica Brasileira (2024) Vol. 70, Iss. 10
Open Access
The Genotypic Imperative: Unraveling Disease-Permittivity in Functional Modules of Complex Diseases
Abdoul K. Kaba, Kelly L. Vomo-Donfack, Ian Morilla
Mathematics (2023) Vol. 11, Iss. 24, pp. 4916-4916
Open Access
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