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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:

Missense variant pathogenicity predictors generalize well across a range of function‐specific prediction challenges
Vikas Pejaver, Sean D. Mooney, Predrag Radivojac
Human Mutation (2017) Vol. 38, Iss. 9, pp. 1092-1108
Open Access | Times Cited: 52

Showing 1-25 of 52 citing articles:

Translating cancer genomics into precision medicine with artificial intelligence: applications, challenges and future perspectives
Jia Xu, Pengwei Yang, Shang Xue, et al.
Human Genetics (2019) Vol. 138, Iss. 2, pp. 109-124
Open Access | Times Cited: 227
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
Comprehensive characterization of amino acid positions in protein structures reveals molecular effect of missense variants
Sumaiya Iqbal, Eduardo Pérez‐Palma, Jakob Berg Jespersen, et al.
Proceedings of the National Academy of Sciences (2020) Vol. 117, Iss. 45, pp. 28201-28211
Open Access | Times Cited: 99
Crowdsourcing assessment of maternal blood multi-omics for predicting gestational age and preterm birth
Adi L. Tarca, Bálint Pataki, Roberto Romero, et al.
Cell Reports Medicine (2021) Vol. 2, Iss. 6, pp. 100323-100323
Open Access | Times Cited: 75
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: 59
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
LAMA2gene mutation update: Toward a more comprehensive picture of the laminin-α2 variome and its related phenotypes
Jorge Oliveira, Angela Gruber, Márcio Cardoso, et al.
Human Mutation (2018) Vol. 39, Iss. 10, pp. 1314-1337
Open Access | Times Cited: 83
Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment
Angélique Quartier, Jérémie Courraud, Thuong Ha, et al.
Human Mutation (2019) Vol. 40, Iss. 11, pp. 2021-2032
Open Access | Times Cited: 55
Reports from CAGI: The Critical Assessment of Genome Interpretation
Roger A. Hoskins, Susanna Repo, Daniel Barsky, et al.
Human Mutation (2017) Vol. 38, Iss. 9, pp. 1039-1041
Open Access | Times Cited: 42
Evolution of the regulation of developmental gene expression in blind Mexican cavefish
Julien Leclercq, Jorge Torres‐Paz, Maxime Policarpo, et al.
Development (2024) Vol. 151, Iss. 20
Open Access | Times Cited: 4
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
Analyzing genetic and epigenetic HORMAD alterations in breast cancer resistance and metastatic events
Adam Hermawan, Herwandhani Putri
Journal of Research in Pharmacy (2025) Vol. 29, Iss. 1, pp. 137-150
Open Access
Evaluation of enzyme activity predictions for variants of unknown significance in Arylsulfatase A
Shantanu Jain, Marena Trinidad, Thanh Nguyen, et al.
Human Genetics (2025)
Open Access
A comprehensive in silico investigation unravels the structural and functional consequences of non-synonymous single-nucleotide polymorphisms in human OXTR gene
Pranab Behari Mazumder, Shuvo Chandra Das, Sobuj Mondol, et al.
Egyptian Journal of Medical Human Genetics (2025) Vol. 26, Iss. 1
Open Access
Accurate identification and mechanistic evaluation of pathogenic missense variants with Rhapsody-2
Anupam Banerjee, Anthony T. Bogetti, İvet Bahar
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 18
Open Access
RheoScale: A tool to aggregate and quantify experimentally determined substitution outcomes for multiple variants at individual protein positions
Abby M. Hodges, Aron W. Fenton, Larissa L Dougherty, et al.
Human Mutation (2018) Vol. 39, Iss. 12, pp. 1814-1826
Open Access | Times Cited: 29
InMeRF: prediction of pathogenicity of missense variants by individual modeling for each amino acid substitution
Jun‐ichi Takeda, Kentaro Nanatsue, Ryosuke Yamagishi, et al.
NAR Genomics and Bioinformatics (2020) Vol. 2, Iss. 2
Open Access | Times Cited: 25
Evaluation of enzyme activity predictions for variants of unknown significance in Arylsulfatase A
Shantanu Jain, Marena Trinidad, Thanh Nguyen, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
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
Assessment of methods for predicting the effects of PTEN and TPMT protein variants
Vikas Pejaver, Giulia Babbi, Rita Casadio, et al.
Human Mutation (2019) Vol. 40, Iss. 9, pp. 1495-1506
Open Access | Times Cited: 21
The Melanocortin 4 Receptor p.Ile269Asn Mutation Is Associated with Childhood and Adult Obesity in Mexicans
Miguel Vázquez‐Moreno, Helen Zeng, Daniel Locia‐Morales, et al.
The Journal of Clinical Endocrinology & Metabolism (2019) Vol. 105, Iss. 4, pp. e1468-e1477
Open Access | Times Cited: 18
Novel gene-specific Bayesian Gaussian mixture model to predict the missense variants pathogenicity of Sanfilippo syndrome
Eman Mohammed, Alaaeldin Fayez, Nabil M. Abdelfattah, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 2
Evolution of Human Brain Size-Associated NOTCH2NL Genes Proceeds toward Reduced Protein Levels
Gerrald A. Lodewijk, Diana Pereira Fernandes, Iraklis Vretzakis, et al.
Molecular Biology and Evolution (2020) Vol. 37, Iss. 9, pp. 2531-2548
Open Access | Times Cited: 15
Prediction and evaluation of deleterious and disease causing non-synonymous SNPs (nsSNPs) in human NF2 gene responsible for neurofibromatosis type 2 (NF2)
Brandon Havranek, Shahidul M. Islam
Journal of Biomolecular Structure and Dynamics (2020) Vol. 39, Iss. 18, pp. 7044-7055
Closed Access | Times Cited: 15
ADGRL3 genomic variation implicated in neurogenesis and ADHD links functional effects to the incretin polypeptide GIP
Oscar M. Vidal, Jorge I. Vélez, Mauricio Arcos‐Burgos
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 7
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