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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:

Genome interpretation using in silico predictors of variant impact
Panagiotis Katsonis, Kevin Wilhelm, Amanda M. Williams, et al.
Human Genetics (2022) Vol. 141, Iss. 10, pp. 1549-1577
Open Access | Times Cited: 54

Showing 1-25 of 54 citing articles:

CADD v1.7: using protein language models, regulatory CNNs and other nucleotide-level scores to improve genome-wide variant predictions
Max Schubach, Thorben Maaß, Lusiné Nazaretyan, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. D1, pp. D1143-D1154
Open Access | Times Cited: 132
CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods
Shantanu Jain, Constantina Bakolitsa, Steven E. Brenner, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 38
Guidelines for releasing a variant effect predictor
Benjamin Livesey, Mihaly Badonyi, Mafalda Dias, et al.
Genome biology (2025) Vol. 26, Iss. 1
Open Access | Times Cited: 2
Critical assessment of missense variant effect predictors on disease-relevant variant data
Ruchir Rastogi, Ryan Chung, Sindy Li, et al.
Human Genetics (2025)
Open Access | Times Cited: 2
Evaluating predictors of kinase activity of STK11 variants identified in primary human non-small cell lung cancers
Yile Chen, Kyoungyeul Lee, Junwoo Woo, et al.
Human Genetics (2025)
Open Access | Times Cited: 1
Computational approaches for predicting variant impact: An overview from resources, principles to applications
Ye Liu, William S.B. Yeung, Philip C.N. Chiu, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 31
Benchmarking computational variant effect predictors by their ability to infer human traits
Daniel Tabet, Da Kuang, Megan Lancaster, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 7
Critical assessment of missense variant effect predictors on disease-relevant variant data
Ruchir Rastogi, Ryan Chung, Sindy Li, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 6
Variant effect predictors: a systematic review and practical guide
Cristian Riccio, Max L. Jansen, Linlin Guo, et al.
Human Genetics (2024) Vol. 143, Iss. 5, pp. 625-634
Open Access | Times Cited: 4
Meta-EA: a gene-specific combination of available computational tools for predicting missense variant effects
Panagiotis Katsonis, Olivier Lichtarge
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
NAVIP: Unraveling the influence of neighboring small sequence variants on functional impact prediction
Jan-Simon Baasner, Andreas Rempel, Dakota Howard, et al.
PLoS Computational Biology (2025) Vol. 21, Iss. 2, pp. e1012732-e1012732
Open Access
A cellular assay to determine the fusion capacity of MFN2 variants linked to Charcot–Marie-Tooth disease of type 2 A
Chloe Barsa, Julian Perrin, Claudine David, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Identification of novel variants in carbamoyl phosphate synthetase 1 gene and comparative pathogenicity assessments of CPS1 missense variants following ACMG/AMP-ClinGen recommendation for computational tools
Li Fei, Qin Cai, Wei Ji, et al.
Molecular Genetics and Metabolism Reports (2025) Vol. 43, pp. 101208-101208
Closed Access
DTreePred: an online viewer based on machine learning for pathogenicity prediction of genomic variants
Daniel H. F. Gomes, Inácio Gomes Medeiros, Tirzah Braz Petta Lajus, et al.
BMC Bioinformatics (2025) Vol. 26, Iss. 1
Open Access
Resources and tools for rare disease variant interpretation
Luana Licata, Allegra Via, Paola Turina, et al.
Frontiers in Molecular Biosciences (2023) Vol. 10
Open Access | Times Cited: 9
Machine learning and phylogenetic analysis allow for predicting antibiotic resistance in M. tuberculosis
Alper Yurtseven, Sofia Buyanova, Amay Ajaykumar Agrawal, et al.
BMC Microbiology (2023) Vol. 23, Iss. 1
Open Access | Times Cited: 9
Translating pharmacogenomic sequencing data into drug response predictions—How to interpret variants of unknown significance
Roman Tremmel, Sebastian Pirmann, Yitian Zhou, et al.
British Journal of Clinical Pharmacology (2023)
Open Access | Times Cited: 8
Bioinformatics characterization of variants of uncertain significance in pediatric sensorineural hearing loss
Sloane Clay, Adele K. Evans, Regina M. Zambrano, et al.
Frontiers in Pediatrics (2024) Vol. 12
Open Access | Times Cited: 3
Prioritization of genes associated with type 2 diabetes mellitus for functional studies
Wei Xuan Tan, Xueling Sim, Chin Meng Khoo, et al.
Nature Reviews Endocrinology (2023) Vol. 19, Iss. 8, pp. 477-486
Closed Access | Times Cited: 7
Pathogenic variants of human GABRA1 gene associated with epilepsy: A computational approach
Ayla Arslan
Heliyon (2023) Vol. 9, Iss. 9, pp. e20218-e20218
Open Access | Times Cited: 7
Menke-Hennekam syndrome; delineation of domain-specific subtypes with distinct clinical and DNA methylation profiles
Sadegheh Haghshenas, Hidde J. Bout, Josephine Schijns, et al.
Human Genetics and Genomics Advances (2024) Vol. 5, Iss. 3, pp. 100287-100287
Open Access | Times Cited: 2
Understanding the heterogeneous performance of variant effect predictors across human protein-coding genes
Fawzy Mohamed, Joseph A. Marsh
Scientific Reports (2024) Vol. 14, Iss. 1
Closed Access | Times Cited: 2
Making sense of missense: challenges and opportunities in variant pathogenicity prediction
Ivan Molotkov, Elaine R. Mardis, Mykyta Artomov
Disease Models & Mechanisms (2024) Vol. 17, Iss. 12
Open Access | Times Cited: 2
Genetic testing for diffuse lung diseases in children
Aaron Hamvas, Bimal P. Chaudhari, Lawrence M. Nogee
Pediatric Pulmonology (2023) Vol. 59, Iss. 9, pp. 2286-2297
Closed Access | Times Cited: 5
Simultaneous Occurrence of Hypospadias and Bilateral Cleft Lip and Jaw in a Crossbred Calf: Clinical, Computer Tomographic, and Genomic Characterization
Simona Marc, Alexandru Eugeniu Mizeranschi, Cristina Paul, et al.
Animals (2023) Vol. 13, Iss. 10, pp. 1709-1709
Open Access | Times Cited: 5
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