Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Variation Interpretation Predictors: Principles, Types, Performance, and Choice
Abhishek Niroula, Mauno Vihinen
Human Mutation (2016) Vol. 37, Iss. 6, pp. 579-597
Open Access | Times Cited: 124

Showing 26-50 of 124 citing articles:

A base measure of precision for protein stability predictors: structural sensitivity
Octav Caldararu, Tom L. Blundell, Kasper P. Kepp
BMC Bioinformatics (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 35
Predicting Severity of Disease-Causing Variants
Abhishek Niroula, Mauno Vihinen
Human Mutation (2017) Vol. 38, Iss. 4, pp. 357-364
Open Access | Times Cited: 43
Investigating DNA-, RNA-, and protein-based features as a means to discriminate pathogenic synonymous variants
Mark Livingstone, Lukas Folkman, Yuedong Yang, et al.
Human Mutation (2017) Vol. 38, Iss. 10, pp. 1336-1347
Open Access | Times Cited: 43
Real-world clinical applicability of pathogenicity predictors assessed onSERPINA1mutations in alpha-1-antitrypsin deficiency
Edoardo Giacopuzzi, Mattia Laffranchi, Romina Berardelli, et al.
Human Mutation (2018) Vol. 39, Iss. 9, pp. 1203-1213
Open Access | Times Cited: 41
How Functional Genomics Can Keep Pace With VUS Identification
Corey L. Anderson, Saba Munawar, Louise Reilly, et al.
Frontiers in Cardiovascular Medicine (2022) Vol. 9
Open Access | Times Cited: 18
Data set and fitting dependencies when estimating protein mutant stability: Toward simple, balanced, and interpretable models
Kristoffer T. Bæk, Kasper P. Kepp
Journal of Computational Chemistry (2022) Vol. 43, Iss. 8, pp. 504-518
Open Access | Times Cited: 17
A Bibliometric Analysis of the Use of Machine Learning Methods in Variant Effect Prediction
Gülbahar Merve Şilbir, Burçin Kurt
Osmaniye Korkut Ata Üniversitesi Fen Bilimleri Enstitüsü Dergisi (2025) Vol. 8, Iss. 2, pp. 632-651
Closed Access
Blind prediction of deleterious amino acid variations with SNPs&GO
Emidio Capriotti, Pier Luigi Martelli, Piero Fariselli, et al.
Human Mutation (2017) Vol. 38, Iss. 9, pp. 1064-1071
Open Access | Times Cited: 30
Computational Design To Reduce Conformational Flexibility and Aggregation Rates of an Antibody Fab Fragment
Cheng Zhang, Maariyah Samad, Haoran Yu, et al.
Molecular Pharmaceutics (2018) Vol. 15, Iss. 8, pp. 3079-3092
Open Access | Times Cited: 28
Solution structure and functional investigation of human guanylate kinase reveals allosteric networking and a crucial role for the enzyme in cancer
Nazimuddin Khan, Parag P. Shah, David Ban, et al.
Journal of Biological Chemistry (2019) Vol. 294, Iss. 31, pp. 11920-11933
Open Access | Times Cited: 27
The DBSAV Database: Predicting Deleteriousness of Single Amino Acid Variations in the Human Proteome
Jimin Pei, Nick V. Grishin
Journal of Molecular Biology (2021) Vol. 433, Iss. 11, pp. 166915-166915
Open Access | Times Cited: 21
REEV: review, evaluate and explain variants
Dzmitry Hramyka, Henrike L. Sczakiel, Max Zhao, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. W1, pp. W148-W158
Open Access | Times Cited: 3
Functional analysis of rare variants in mismatch repair proteins augments results from computation-based predictive methods
Sanjeevani Arora, Peter J. Huwe, Rahmat K. Sikder, et al.
Cancer Biology & Therapy (2017) Vol. 18, Iss. 7, pp. 519-533
Open Access | Times Cited: 25
Prediction of disease-associated mutations in the transmembrane regions of proteins with known 3D structure
Petr Popov, Ilya V. Bizin, M. Michael Gromiha, et al.
PLoS ONE (2019) Vol. 14, Iss. 7, pp. e0219452-e0219452
Open Access | Times Cited: 25
PhD-SNPg: updating a webserver and lightweight tool for scoring nucleotide variants
Emidio Capriotti, Piero Fariselli
Nucleic Acids Research (2023) Vol. 51, Iss. W1, pp. W451-W458
Open Access | Times Cited: 8
How to Define Pathogenicity, Health, and Disease?
Mauno Vihinen
Human Mutation (2016) Vol. 38, Iss. 2, pp. 129-136
Open Access | Times Cited: 23
Large differences in proportions of harmful and benign amino acid substitutions between proteins and diseases
Gerard C. P. Schaafsma, Mauno Vihinen
Human Mutation (2017) Vol. 38, Iss. 7, pp. 839-848
Open Access | Times Cited: 22
Comparison of Bioinformatics Prediction, Molecular Modeling, and Functional Analyses ofFOXC1Mutations in Patients with Axenfeld-Rieger Syndrome
Morteza Seifi, Tim Footz, Sherry Taylor, et al.
Human Mutation (2016) Vol. 38, Iss. 2, pp. 169-179
Open Access | Times Cited: 21
Representativeness of variation benchmark datasets
Gerard C. P. Schaafsma, Mauno Vihinen
BMC Bioinformatics (2018) Vol. 19, Iss. 1
Open Access | Times Cited: 19
Benchmarking subcellular localization and variant tolerance predictors on membrane proteins
Tommaso Orioli, Mauno Vihinen
BMC Genomics (2019) Vol. 20, Iss. S8
Open Access | Times Cited: 18
Problems in variation interpretation guidelines and in their implementation in computational tools
Mauno Vihinen
Molecular Genetics & Genomic Medicine (2020) Vol. 8, Iss. 9
Open Access | Times Cited: 18
Mutation severity spectrum of rare alleles in the human genome is predictive of disease type
Jimin Pei, Lisa N. Kinch, Zbyszek Otwinowski, et al.
PLoS Computational Biology (2020) Vol. 16, Iss. 5, pp. e1007775-e1007775
Open Access | Times Cited: 17
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
A Comprehensive Evaluation of the Performance of Prediction Algorithms on Clinically Relevant Missense Variants
Erda Qorri, Bertalan Takács, Alexandra Gráf, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 14, pp. 7946-7946
Open Access | Times Cited: 10
Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI
Marco Carraro, Giovanni Minervini, Manuel Giollo, et al.
Human Mutation (2017) Vol. 38, Iss. 9, pp. 1042-1050
Open Access | Times Cited: 16

Scroll to top