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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:

Machine learning-based reclassification of germline variants of unknown significance: The RENOVO algorithm
Valentina Favalli, Giulia Tini, Emanuele Bonetti, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 4, pp. 682-695
Open Access | Times Cited: 32

Showing 1-25 of 32 citing articles:

Analysis of missense variants in the human genome reveals widespread gene-specific clustering and improves prediction of pathogenicity
Mathieu Quinodoz, Virginie G. Peter, Katarina Cisarova, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 3, pp. 457-470
Open Access | Times Cited: 58
An ensemble machine learning-based performance evaluation identifies top In-Silico pathogenicity prediction methods that best classify driver mutations in cancer
Subrata Das, Vatsal Patel, Shouvik Chakravarty, et al.
BioData Mining (2025) Vol. 18, Iss. 1
Open Access | Times Cited: 1
Unlocking precision medicine: clinical applications of integrating health records, genetics, and immunology through artificial intelligence
Yiming Chen, Tzu‐Hung Hsiao, Ching‐Heng Lin, et al.
Journal of Biomedical Science (2025) Vol. 32, Iss. 1
Open Access | Times Cited: 1
Artificial intelligence and database for NGS-based diagnosis in rare disease
Yee Wen Choon, Yee Fan Choon, Nurul Athirah Nasarudin, et al.
Frontiers in Genetics (2024) Vol. 14
Open Access | Times Cited: 8
WilsonGenAI a deep learning approach to classify pathogenic variants in Wilson Disease
Aastha Vatsyayan, Mukesh Kumar, Bhaskar Jyoti Saikia, et al.
PLoS ONE (2024) Vol. 19, Iss. 5, pp. e0303787-e0303787
Open Access | Times Cited: 4
Advances in Breast Cancer Risk Modeling: Integrating Clinics, Imaging, Pathology and Artificial Intelligence for Personalized Risk Assessment
Filippo Pesapane, Ottavia Battaglia, Giuseppe Pellegrino, et al.
Future Oncology (2023) Vol. 19, Iss. 38, pp. 2547-2564
Closed Access | Times Cited: 10
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: 10
Improved Q-Learning-Based Motion Control for Basketball Intelligent Robots Under Multi-Sensor Data Fusion
Lan Jianping, Xiujuan Dong
IEEE Access (2024) Vol. 12, pp. 57059-57070
Open Access | Times Cited: 3
A novel seven-tier framework for the classification of MEFV missense variants using adaptive and rigid classifiers
Mustafa Tarık Alay
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
A series of reviews in familial cancer: genetic cancer risk in context variants of uncertain significance in MMR genes: which procedures should be followed?
Morghan C. Lucas, T. Keßler, Florentine Scharf, et al.
Familial Cancer (2025) Vol. 24, Iss. 2
Closed Access
Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach
Sandrine M. Caputo, Lisa Golmard, Mélanie Léoné, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 10, pp. 1907-1923
Open Access | Times Cited: 23
Variant classification changes over time in the clinical molecular diagnostic laboratory setting
Elan Hahn, Chloe Mighton, Yael Fisher, et al.
Journal of Medical Genetics (2024) Vol. 61, Iss. 8, pp. 788-793
Closed Access | Times Cited: 2
Rare disease genomics and precision medicine
Juhyeon Hong, D. Lee, A. Hwang, et al.
Genomics & Informatics (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 2
Current Status of Next-Generation Sequencing Approaches for Candidate Gene Discovery in Familial Parkinson´s Disease
Nikita Simone Pillay, Owen A. Ross, Alan Christoffels, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 9
CHEK2 Alterations in Pediatric Malignancy: A Single-Institution Experience
Eman Abdelghani, Kathleen M. Schieffer, Catherine E. Cottrell, et al.
Cancers (2023) Vol. 15, Iss. 6, pp. 1649-1649
Open Access | Times Cited: 5
Germline CDH1 G212E Missense Variant: Combining Clinical, In Vitro and In Vivo Strategies to Unravel Disease Burden
Joana Figueiredo, Fátima Mercadillo, Soraia Melo, et al.
Cancers (2021) Vol. 13, Iss. 17, pp. 4359-4359
Open Access | Times Cited: 11
Applying Artificial Intelligence for Phenotyping of Inherited Arrhythmia Syndromes
Sophie Sigfstead, River Jiang, Robert Avram, et al.
Canadian Journal of Cardiology (2024) Vol. 40, Iss. 10, pp. 1841-1851
Closed Access | Times Cited: 1
Generative AI models in time varying biomedical data: a systematic review (Preprint)
Rosemary He, Varuni Sarwal, Xinru Qiu, et al.
(2024)
Open Access | Times Cited: 1
From diagnostic testing to precision medicine: the evolving role of genomics in cardiac channelopathies and cardiomyopathies in children
Minu‐Tshyeto Bidzimou, Andrew P. Landstrom
Current Opinion in Genetics & Development (2022) Vol. 76, pp. 101978-101978
Open Access | Times Cited: 5
MARGINAL: An Automatic Classification of Variants in BRCA1 and BRCA2 Genes Using a Machine Learning Model
Vasiliki Karalidou, Despoina Kalfakakou, Αθανάσιος Παπαθανασίου, et al.
Biomolecules (2022) Vol. 12, Iss. 11, pp. 1552-1552
Open Access | Times Cited: 5
Validation and Data-Integration of Yeast-Based Assays for Functional Classification of BRCA1 Missense Variants
Francesca Bellè, Alberto Mercatanti, Samuele Lodovichi, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 7, pp. 4049-4049
Open Access | Times Cited: 4
Blockchain-based data sharing algorithm in distributed network data storage
Shuguang Cui, Haixia Wang
Journal of Computational Methods in Sciences and Engineering (2024) Vol. 24, Iss. 1, pp. 427-444
Closed Access
Breast Cancer High-Penetrance Genes BRCA1 and BRCA2 Mutations Using Next-Generation Sequencing Among Iraqi Kurdish Women
Ahmad N Hassan, Mustafa S Mustafa
Cureus (2024)
Open Access
Accuracy of renovo predictions on variants reclassified over time
Emanuele Bonetti, Giulia Tini, Luca Mazzarella
Journal of Translational Medicine (2024) Vol. 22, Iss. 1
Open Access
Identification of Novel Potential Predisposing Variants in Familial Acute Myeloid Leukemia
Chiara Ronchini, Federica Gigli, Martina Fontanini, et al.
Cancer Reports (2024) Vol. 7, Iss. 8
Open Access
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