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:

MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing
Matthew Mort, Timothy Sterne-Weiler, Biao Li, et al.
Genome biology (2014) Vol. 15, Iss. 1
Open Access | Times Cited: 154

Showing 1-25 of 154 citing articles:

The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies
Peter D. Stenson, Matthew Mort, Edward V. Ball, et al.
Human Genetics (2017) Vol. 136, Iss. 6, pp. 665-677
Open Access | Times Cited: 1290
The human splicing code reveals new insights into the genetic determinants of disease
Hui Xiong, Babak Alipanahi, Leo J. Lee, et al.
Science (2014) Vol. 347, Iss. 6218
Open Access | Times Cited: 1195
Roles for retrotransposon insertions in human disease
Dustin C. Hancks, Haig H. Kazazian
Mobile DNA (2016) Vol. 7, Iss. 1
Open Access | Times Cited: 611
Splicing mutations in human genetic disorders: examples, detection, and confirmation
Anna Abramowicz, Monika Goś
Journal of Applied Genetics (2018) Vol. 59, Iss. 3, pp. 253-268
Open Access | Times Cited: 540
CADD-Splice—improving genome-wide variant effect prediction using deep learning-derived splice scores
Philipp Rentzsch, Max Schubach, Jay Shendure, et al.
Genome Medicine (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 540
In silico prediction of splice-altering single nucleotide variants in the human genome
Xueqiu Jian, Eric Boerwinkle, Xiaoming Liu
Nucleic Acids Research (2014) Vol. 42, Iss. 22, pp. 13534-13544
Open Access | Times Cited: 500
Neoantigens: promising targets for cancer therapy
Na Xie, Guobo Shen, Wei Gao, et al.
Signal Transduction and Targeted Therapy (2023) Vol. 8, Iss. 1
Open Access | Times Cited: 483
Saturation editing of genomic regions by multiplex homology-directed repair
Gregory M. Findlay, Evan A. Boyle, Ronald J. Hause, et al.
Nature (2014) Vol. 513, Iss. 7516, pp. 120-123
Open Access | Times Cited: 349
The Expanding Landscape of Alternative Splicing Variation in Human Populations
Eddie Park, Zhicheng Pan, Zijun Zhang, et al.
The American Journal of Human Genetics (2018) Vol. 102, Iss. 1, pp. 11-26
Open Access | Times Cited: 319
Alternative tumour-specific antigens
Christof C. Smith, Sara R. Selitsky, Shengjie Chai, et al.
Nature reviews. Cancer (2019) Vol. 19, Iss. 8, pp. 465-478
Open Access | Times Cited: 278
Systematic Analysis of Splice-Site-Creating Mutations in Cancer
Reyka G. Jayasinghe, Song Cao, Qingsong Gao, et al.
Cell Reports (2018) Vol. 23, Iss. 1, pp. 270-281.e3
Open Access | Times Cited: 223
Pathogenic variants that alter protein code often disrupt splicing
Rachel Soemedi, Kamil J. Cygan, Christy L. Rhine, et al.
Nature Genetics (2017) Vol. 49, Iss. 6, pp. 848-855
Open Access | Times Cited: 213
MMSplice: modular modeling improves the predictions of genetic variant effects on splicing
Jun Cheng, Thi Yen Duong Nguyen, Kamil J. Cygan, et al.
Genome biology (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 204
GWASdb v2: an update database for human genetic variants identified by genome-wide association studies
Mulin Jun Li, Zipeng Liu, Panwen Wang, et al.
Nucleic Acids Research (2015) Vol. 44, Iss. D1, pp. D869-D876
Open Access | Times Cited: 182
Alternative Splicing in Neurogenesis and Brain Development
Chun-Hao Su, D Dhananjaya, Woan‐Yuh Tarn
Frontiers in Molecular Biosciences (2018) Vol. 5
Open Access | Times Cited: 171
The pathogenicity of splicing defects: mechanistic insights into pre‐ mRNA processing inform novel therapeutic approaches
Élisabeth Daguenet, Gwendal Dujardin, Juan Valcárcel
EMBO Reports (2015) Vol. 16, Iss. 12, pp. 1640-1655
Open Access | Times Cited: 135
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
Novel genetic and epigenetic factors of importance for inter-individual differences in drug disposition, response and toxicity
Volker M. Lauschke, Yitian Zhou, Magnus Ingelman‐Sundberg
Pharmacology & Therapeutics (2019) Vol. 197, pp. 122-152
Open Access | Times Cited: 114
Rules and tools to predict the splicing effects of exonic and intronic mutations
Kinji Ohno, Jun‐ichi Takeda, Akio Masuda
Wiley Interdisciplinary Reviews - RNA (2017) Vol. 9, Iss. 1
Closed Access | Times Cited: 107
Exome sequencing explained: a practical guide to its clinical application
Eleanor G. Seaby, Reuben J. Pengelly, Sarah Ennis
Briefings in Functional Genomics (2015) Vol. 15, Iss. 5, pp. 374-384
Open Access | Times Cited: 93
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
All exons are not created equal—exon vulnerability determines the effect of exonic mutations on splicing
Lise Lolle Holm, Thomas Koed Doktor, Katharina Kirkegaard Flugt, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. 8, pp. 4588-4603
Open Access | Times Cited: 9
Interpretation of mRNA splicing mutations in genetic disease: review of the literature and guidelines for information-theoretical analysis
Natasha Caminsky, Eliseos J. Mucaki, Peter K. Rogan
F1000Research (2014) Vol. 3, pp. 282-282
Open Access | Times Cited: 89
Genomic HEXploring allows landscaping of novel potential splicing regulatory elements
Steffen Erkelenz, Stephan Theiss, Marianne Otte, et al.
Nucleic Acids Research (2014) Vol. 42, Iss. 16, pp. 10681-10697
Open Access | Times Cited: 83
S-CAP extends pathogenicity prediction to genetic variants that affect RNA splicing
Karthik A. Jagadeesh, Joseph M. Paggi, James Ye, et al.
Nature Genetics (2019) Vol. 51, Iss. 4, pp. 755-763
Open Access | Times Cited: 67
Page 1 - Next Page

Scroll to top