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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:

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

Showing 1-25 of 31 citing articles:

Pharmacogenomics: A Genetic Approach to Drug Development and Therapy
Rowaid Qahwaji, Ibraheem Ashankyty, Naif S. Sannan, et al.
Pharmaceuticals (2024) Vol. 17, Iss. 7, pp. 940-940
Open Access | Times Cited: 9
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: 1
Identifying and Overcoming the Sampling Challenges in Relative Binding Free Energy Calculations of a Model Protein:Protein Complex
Ivy Zhang, Dominic A. Rufa, Iván Pulido, et al.
Journal of Chemical Theory and Computation (2023) Vol. 19, Iss. 15, pp. 4863-4882
Open Access | Times Cited: 13
Navigating Uncertainty: Assessing Variants of Uncertain Significance in the CDKL5 Gene for Developmental and Epileptic Encephalopathy Using In Silico Prediction Tools and Computational Analysis
Özlem Yalçın Çapan
Journal of Molecular Neuroscience (2025) Vol. 75, Iss. 1
Closed Access
Knowledge of the genetics of human pain gained over the last decade from next-generation sequencing
Dario Kringel, Jörn Lötsch
Pharmacological Research (2025), pp. 107667-107667
Open Access
MOLGENIS VIP: an open-source and modular pipeline for high-throughput and integrated DNA variant analysis
W Maassen, Lennart Johansson, Bart Charbon, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
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
Functional validation of EIF2AK4 (GCN2) missense variants associated with pulmonary arterial hypertension
Giulia Emanuelli, Jiayi Zhu, Wei Li, et al.
Human Molecular Genetics (2024)
Open Access | Times Cited: 2
APF2: an improved ensemble method for pharmacogenomic variant effect prediction
Yitian Zhou, Sebastian Pirmann, Volker M. Lauschke
The Pharmacogenomics Journal (2024) Vol. 24, Iss. 3
Open Access | Times Cited: 2
Assessment of variant effect predictors unveils variants difficulty as a critical performance indicator
Ragousandirane Radjasandirane, Julien Diharce, Jean‐Christophe Gelly, et al.
(2024)
Closed Access | Times Cited: 2
NAVIP: Unraveling the Influence of Neighboring Small Sequence Variants on Functional Impact Prediction
Jan-Simon Baasner, Andreas Rempel, Dakota Howard, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2019)
Open Access | Times Cited: 14
Basic science methods for the characterization of variants of uncertain significance in hypertrophic cardiomyopathy
Chang Yoon Doh, Thomas Kampourakis, Kenneth S. Campbell, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 4
Functional validation ofEIF2AK4(GCN2) missense variants associated with pulmonary arterial hypertension
Giulia Emanuelli, Jiayi Zhu, Nicolas W Morell, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
MLe-KCNQ2: An Artificial Intelligence Model for the Prognosis of Missense KCNQ2 Gene Variants
Alba Saez-Matia, Markel G. Ibarluzea, Sara M‐Alicante, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 5, pp. 2910-2910
Open Access | Times Cited: 1
Using computational approaches to enhance the interpretation of missense variants in the PAX6 gene
Nadya S. Andhika, Susmito Biswas, Claire Hardcastle, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 8, pp. 1005-1013
Open Access | Times Cited: 1
INDELpred: Improving the prediction and interpretation of indel pathogenicity within the clinical genome
Yilin Wei, Tongda Zhang, Bangyao Wang, et al.
Human Genetics and Genomics Advances (2024) Vol. 5, Iss. 4, pp. 100325-100325
Open Access | Times Cited: 1
Functional analysis of ESRP1/2 gene variants and CTNND1 isoforms in orofacial cleft pathogenesis
Caroline Caetano da Silva, Claudio Macias-Treviño, Jason W. Mitchell, et al.
Communications Biology (2024) Vol. 7, Iss. 1
Open Access | Times Cited: 1
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: 1
Identifying and overcoming the sampling challenges in relative binding free energy calculations of a model protein:protein complex
Ivy Zhang, Dominic A. Rufa, Iván Pulido, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Bioinformatic analysis of the effect of SNPs in the pig TERT gene on the structural and functional characteristics of the enzyme to develop new genetic markers of productivity traits
Mykyta Peka, Viktor Balatsky, Artem Saienko, et al.
BMC Genomics (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 2
Constructing and interpreting a large-scale variant effect map for an ultrarare disease gene: Comprehensive prediction of the functional impact of PSAT1 genotypes
Michael J. Xie, Gareth A. Cromie, Katherine Owens, et al.
PLoS Genetics (2023) Vol. 19, Iss. 10, pp. e1010972-e1010972
Open Access | Times Cited: 2
Towards More Accurate Pharmacogenomic Variant Effect Predictions
Yoomi Park, Volker M. Lauschke
Pharmacogenomics (2023) Vol. 24, Iss. 16, pp. 841-844
Closed Access | Times Cited: 2
Reply: Follow the allosteric transitions to predict variant pathogenicity: a channel-specific approach
Ludovica Montanucci, Tobias Brünger, Dennis Lal
Brain (2024) Vol. 147, Iss. 5, pp. e41-e42
Closed Access
Bioinformatics in Primary Immunodeficiencies: Towards a “Computational Immunology” Era
Jairo Rivera, Alexios‐Fotios A. Mentis
Rare diseases of the immune system (2024), pp. 23-65
Closed Access
Understanding the heterogeneous performance of variant effect predictors across human protein-coding genes
Fawzy Mohamed, Joseph A. Marsh
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
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