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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:

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

Showing 1-25 of 107 citing articles:

Alternative Splicing Regulatory Networks: Functions, Mechanisms, and Evolution
Jernej Ule, Benjamin J. Blencowe
Molecular Cell (2019) Vol. 76, Iss. 2, pp. 329-345
Open Access | Times Cited: 618
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
Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease
Hernán Gonorazky, Sergey Naumenko, Arun Ramani, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 3, pp. 466-483
Open Access | Times Cited: 208
Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease
Hernán Gonorazky, Sergey Naumenko, Arun Ramani, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 5, pp. 1007-1007
Open Access | Times Cited: 193
Clinical sequencing: From raw data to diagnosis with lifetime value
Sylvan M. Caspar, Nicolo Dubacher, Anna M. Kopps, et al.
Clinical Genetics (2017) Vol. 93, Iss. 3, pp. 508-519
Open Access | Times Cited: 92
Benchmarking deep learning splice prediction tools using functional splice assays
Tabea Riepe, Mubeen Khan, Susanne Roosing, et al.
Human Mutation (2021) Vol. 42, Iss. 7, pp. 799-810
Open Access | Times Cited: 78
Applications of artificial intelligence in clinical laboratory genomics
Swaroop Aradhya, Flavia M. Facio, Hillery C. Metz, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023) Vol. 193, Iss. 3
Open Access | Times Cited: 29
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
Computational Methods for the Pharmacogenetic Interpretation of Next Generation Sequencing Data
Yitian Zhou, Kohei Fujikura, Souren Mkrtchian, et al.
Frontiers in Pharmacology (2018) Vol. 9
Open Access | Times Cited: 65
Structural and functional modularity of the U2 snRNP in pre-mRNA splicing
Clarisse van der Feltz, Aaron A. Hoskins
Critical Reviews in Biochemistry and Molecular Biology (2019) Vol. 54, Iss. 5, pp. 443-465
Open Access | Times Cited: 56
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: 32
Messenger RNA Life-Cycle in Cancer Cells: Emerging Role of Conventional and Non-Conventional RNA-Binding Proteins?
Lucie Coppin, Julie Leclerc, Audrey Vincent, et al.
International Journal of Molecular Sciences (2018) Vol. 19, Iss. 3, pp. 650-650
Open Access | Times Cited: 54
Alternative splicing patterns of hnrnp genes in gill tissues of rainbow trout (Oncorhynchus mykiss) during salinity changes
Dazhi Liu, Han Yu, Na Xue, et al.
Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology (2024) Vol. 271, pp. 110948-110948
Closed Access | Times Cited: 6
Escaping from CRISPR–Cas-mediated knockout: the facts, mechanisms, and applications
Ying Wang, Yujing Zhai, Mingzhe Zhang, et al.
Cellular & Molecular Biology Letters (2024) Vol. 29, Iss. 1
Open Access | Times Cited: 5
The Emerging Role of the RBM20 and PTBP1 Ribonucleoproteins in Heart Development and Cardiovascular Diseases
Stefania Fochi, Pamela Lorenzi, Marilisa Galasso, et al.
Genes (2020) Vol. 11, Iss. 4, pp. 402-402
Open Access | Times Cited: 33
Mutations in cis that affect mRNA synthesis, processing and translation
Dirk Roos, Martin de Boer
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2021) Vol. 1867, Iss. 9, pp. 166166-166166
Open Access | Times Cited: 30
Pseudoexon activation in disease by non‐splice site deep intronic sequence variation — wild type pseudoexons constitute high‐risk sites in the human genome
Ulrika Simone Spangsberg Petersen, Thomas Koed Doktor, Brage Storstein Andresen
Human Mutation (2021) Vol. 43, Iss. 2, pp. 103-127
Open Access | Times Cited: 30
Understanding human DNA variants affecting pre-mRNA splicing in the NGS era
Luiz Gustavo Dufner‐Almeida, Ramon Torreglosa do Carmo, Cibele Masotti, et al.
Advances in genetics (2019), pp. 39-90
Closed Access | Times Cited: 30
Introme accurately predicts the impact of coding and noncoding variants on gene splicing, with clinical applications
Patricia J. Sullivan, Velimir Gayevskiy, Ryan L. Davis, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 10
A dual‐subcellular localized β‐glucosidase confers pathogen and insect resistance without a yield penalty in maize
Chuang Liu, Sheng-Feng He, Junbin Chen, et al.
Plant Biotechnology Journal (2023) Vol. 22, Iss. 4, pp. 1017-1032
Open Access | Times Cited: 10
Deep learning-based prediction of tissue-specific splice sites in the human neural retina
Tabea Riepe, Suzanne E. de Bruijn, Susanne Roosing, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Genome-wide Association Study Reveals the Genetic Mechanism of Wing Bone Strength in Cornish White
Longyu Zhuang, Yi-Xiang Shi, Xuefeng Shi, et al.
Poultry Science (2025), pp. 105324-105324
Open Access
Aberrant expression of alternative splicing variants in multiple sclerosis – A systematic review
Michael Hecker, Annelen Rüge, Elena Putscher, et al.
Autoimmunity Reviews (2019) Vol. 18, Iss. 7, pp. 721-732
Closed Access | Times Cited: 29
Extensive Alternative Splicing of KIR Transcripts
Jesse Bruijnesteijn, Marit K. H. van der Wiel, Nanine de Groot, et al.
Frontiers in Immunology (2018) Vol. 9
Open Access | Times Cited: 25
Genetic risk variants for multiple sclerosis are linked to differences in alternative pre-mRNA splicing
Elena Putscher, Michael Hecker, Brit Fitzner, et al.
Frontiers in Immunology (2022) Vol. 13
Open Access | Times Cited: 13
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