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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:

RNA mis-splicing in disease
Marina M. Scotti, Maurice S. Swanson
Nature Reviews Genetics (2015) Vol. 17, Iss. 1, pp. 19-32
Open Access | Times Cited: 1046

Showing 1-25 of 1046 citing articles:

Opportunities and obstacles for deep learning in biology and medicine
Travers Ching, Daniel Himmelstein, Brett K. Beaulieu‐Jones, et al.
Journal of The Royal Society Interface (2018) Vol. 15, Iss. 141, pp. 20170387-20170387
Open Access | Times Cited: 1857
Alternative splicing as a regulator of development and tissue identity
Francisco E. Baralle, Jimena Giudice
Nature Reviews Molecular Cell Biology (2017) Vol. 18, Iss. 7, pp. 437-451
Open Access | Times Cited: 1106
Single-cell RNA counting at allele and isoform resolution using Smart-seq3
Michael Hagemann-Jensen, Christoph Ziegenhain, Ping Chen, et al.
Nature Biotechnology (2020) Vol. 38, Iss. 6, pp. 708-714
Open Access | Times Cited: 546
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: 536
Circular RNAs: Biogenesis, Function and Role in Human Diseases
John Greene, Anne‐Marie Baird, Lauren Brady, et al.
Frontiers in Molecular Biosciences (2017) Vol. 4
Open Access | Times Cited: 497
Genetic diagnosis of Mendelian disorders via RNA sequencing
Laura S. Kremer, Daniel M. Bader, Christian Mertes, et al.
Nature Communications (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 496
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: 468
An atlas of alternative splicing profiles and functional associations reveals new regulatory programs and genes that simultaneously express multiple major isoforms
Javier Tapial, Kevin Ha, Timothy Sterne-Weiler, et al.
Genome Research (2017) Vol. 27, Iss. 10, pp. 1759-1768
Open Access | Times Cited: 398
Deep intronic mutations and human disease
Rita Vaz‐Drago, Noélia Custódio, Maria Carmo‐Fonseca
Human Genetics (2017) Vol. 136, Iss. 9, pp. 1093-1111
Closed Access | Times Cited: 380
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: 318
The Emerging Role of RNA as a Therapeutic Target for Small Molecules
Colleen M. Connelly, Michelle H. Moon, John S. Schneekloth
Cell chemical biology (2016) Vol. 23, Iss. 9, pp. 1077-1090
Open Access | Times Cited: 287
Lessons from non-canonical splicing
Christopher R. Sibley, Lorea Blázquez, Jernej Ule
Nature Reviews Genetics (2016) Vol. 17, Iss. 7, pp. 407-421
Open Access | Times Cited: 284
Aberrant RNA Splicing in Cancer
Luisa F. Escobar‐Hoyos, Katherine Knorr, Omar Abdel‐Wahab
Annual Review of Cancer Biology (2018) Vol. 3, Iss. 1, pp. 167-185
Open Access | Times Cited: 284
A road map for understanding molecular and genetic determinants of osteoporosis
Tie‐Lin Yang, Hui Shen, Anqi Liu, et al.
Nature Reviews Endocrinology (2019) Vol. 16, Iss. 2, pp. 91-103
Open Access | Times Cited: 279
Splicing regulation by long noncoding RNAs
Natali Romero-Barrios, María Florencia Legascue, Moussa Benhamed, et al.
Nucleic Acids Research (2018) Vol. 46, Iss. 5, pp. 2169-2184
Open Access | Times Cited: 254
Transcriptome Profiling in Human Diseases: New Advances and Perspectives
Amelia Casamassimi, Antonio Federico, Monica Rienzo, et al.
International Journal of Molecular Sciences (2017) Vol. 18, Iss. 8, pp. 1652-1652
Open Access | Times Cited: 243
Precise temporal regulation of alternative splicing during neural development
Sebastien M. Weyn‐Vanhentenryck, Huijuan Feng, Dmytro Ustianenko, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 238
TimeLapse-seq: adding a temporal dimension to RNA sequencing through nucleoside recoding
Jeremy A. Schofield, Erin E. Duffy, Lea Kiefer, et al.
Nature Methods (2018) Vol. 15, Iss. 3, pp. 221-225
Open Access | Times Cited: 233
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
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: 202
The Cancer Spliceome: Reprograming of Alternative Splicing in Cancer
Ettaib El Marabti, Ihab Younis
Frontiers in Molecular Biosciences (2018) Vol. 5
Open Access | Times Cited: 201
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: 192
Transcriptome variation in human tissues revealed by long-read sequencing
Dafni A. Glinos, Garrett Garborcauskas, Paul Hoffman, et al.
Nature (2022) Vol. 608, Iss. 7922, pp. 353-359
Open Access | Times Cited: 191
Alternative splicing and the evolution of phenotypic novelty
Stephen J. Bush, Lu Chen, Jaime M. Tovar-Corona, et al.
Philosophical Transactions of the Royal Society B Biological Sciences (2016) Vol. 372, Iss. 1713, pp. 20150474-20150474
Open Access | Times Cited: 187
The roles of RNA processing in translating genotype to phenotype
Kassie S. Manning, Thomas A. Cooper
Nature Reviews Molecular Cell Biology (2016) Vol. 18, Iss. 2, pp. 102-114
Open Access | Times Cited: 186
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