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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:

LYRUS: a machine learning model for predicting the pathogenicity of missense variants
Jiaying Lai, Jordan Yang, Ece D. Gamsiz Uzun, et al.
Bioinformatics Advances (2021) Vol. 2, Iss. 1
Open Access | Times Cited: 9

Showing 9 citing articles:

Predicting the Pathogenic Effects of Non-Synonymous Single Nucleotide Variants in Human Diseases
Nismabi A Nisamudheen, Prachi Balyan, A. Najitha Banu, et al.
Elsevier eBooks (2025), pp. 197-225
Closed Access
Mutually beneficial confluence of structure-based modeling of protein dynamics and machine learning methods
Anupam Banerjee, Satyaki Saha, Nathan C. Tvedt, et al.
Current Opinion in Structural Biology (2022) Vol. 78, pp. 102517-102517
Open Access | Times Cited: 17
A review of genetic variant databases and machine learning tools for predicting the pathogenicity of breast cancer
Rahaf M. Ahmad, Bassam R. Ali, Fatma Al‐Jasmi, et al.
Briefings in Bioinformatics (2023) Vol. 25, Iss. 1
Open Access | Times Cited: 9
Variant Impact Predictor database (VIPdb), version 2: trends from three decades of genetic variant impact predictors
Yu-Jen Lin, Arul S. Menon, Zhiqiang Hu, et al.
Human Genomics (2024) Vol. 18, Iss. 1
Open Access | Times Cited: 3
Cutting-Edge AI Technologies Meet Precision Medicine to Improve Cancer Care
Peng‐Chan Lin, Yi-Shan Tsai, Yu‐Min Yeh, et al.
Biomolecules (2022) Vol. 12, Iss. 8, pp. 1133-1133
Open Access | Times Cited: 9
Variant Impact Predictor database (VIPdb), version 2: Trends from 25 years of genetic variant impact predictors
Yu-Jen Lin, Arul S. Menon, Zhiqiang Hu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
AI-derived comparative assessment of the performance of pathogenicity prediction tools on missense variants of breast cancer genes
Rahaf M. Ahmad, Bassam R. Ali, Fatma Al‐Jasmi, et al.
Human Genomics (2024) Vol. 18, Iss. 1
Open Access
A multitask neural network trained on embeddings from ESMFold can accurately rank order clinical outcomes for different cystic fibrosis mutations
Erik Drysdale
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
An integrative framework for clinical diagnosis and knowledge discovery from exome sequencing data
M. Shojaei, Navid Mohammadvand, Tunca Doğan, et al.
Computers in Biology and Medicine (2023) Vol. 169, pp. 107810-107810
Closed Access
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