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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:

Neuronal regulation of pre-mRNA splicing by polypyrimidine tract binding proteins, PTBP1 and PTBP2
Niroshika Keppetipola, Shalini Sharma, Qin Li, et al.
Critical Reviews in Biochemistry and Molecular Biology (2012) Vol. 47, Iss. 4, pp. 360-378
Open Access | Times Cited: 176

Showing 26-50 of 176 citing articles:

Alternative splicing of a chromatin modifier alters the transcriptional regulatory programs of stem cell maintenance and neuronal differentiation
Mohammad Nazim, Chia-Ho Lin, An‐Chieh Feng, et al.
Cell stem cell (2024) Vol. 31, Iss. 5, pp. 754-771.e6
Open Access | Times Cited: 8
Raver1 links Ripk1 RNA splicing to caspase-8-mediated pyroptotic cell death, inflammation, and pathogen resistance
Boyao Zhang, Pontus Ørning, Jesse Lehman, et al.
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 7
Open Access | Times Cited: 1
The RNA-binding protein PTBP1 is necessary for B cell selection in germinal centers
Elisa Monzón‐Casanova, Michael Screen, Manuel D. Díaz‐Muñoz, et al.
Nature Immunology (2018) Vol. 19, Iss. 3, pp. 267-278
Open Access | Times Cited: 79
RNA‐binding proteins, neural development and the addictions
Camron D. Bryant, Narges Yazdani
Genes Brain & Behavior (2015) Vol. 15, Iss. 1, pp. 169-186
Open Access | Times Cited: 76
De Novo Prediction of PTBP1 Binding and Splicing Targets Reveals Unexpected Features of Its RNA Recognition and Function
Areum Han, Peter Stoilov, Anthony J. Linares, et al.
PLoS Computational Biology (2014) Vol. 10, Iss. 1, pp. e1003442-e1003442
Open Access | Times Cited: 74
Regulation of gene expression in mammalian nervous system through alternative pre-mRNA splicing coupled with RNA quality control mechanisms
Karen Yap, Eugene V. Makeyev
Molecular and Cellular Neuroscience (2013) Vol. 56, pp. 420-428
Closed Access | Times Cited: 72
In vitro iCLIP-based modeling uncovers how the splicing factor U2AF2 relies on regulation by cofactors
F.X. Reymond Sutandy, Stefanie Ebersberger, Lu Huang, et al.
Genome Research (2018) Vol. 28, Iss. 5, pp. 699-713
Open Access | Times Cited: 72
Discovery of physiological and cancer-related regulators of 3′ UTR processing with KAPAC
Andreas Gruber, Ralf Schmidt, Souvik Ghosh, et al.
Genome biology (2018) Vol. 19, Iss. 1
Open Access | Times Cited: 71
Uncovering the roles of long noncoding RNAs in neural development and glioma progression
Alexander Ramos, Frank J. Attenello, Daniel A. Lim
Neuroscience Letters (2015) Vol. 625, pp. 70-79
Open Access | Times Cited: 68
Ptbp2 Controls an Alternative Splicing Network Required for Cell Communication during Spermatogenesis
Molly M. Hannigan, Leah L. Zagore, Donny D. Licatalosi
Cell Reports (2017) Vol. 19, Iss. 12, pp. 2598-2612
Open Access | Times Cited: 67
The role of alternative splicing coupled to nonsense-mediated mRNA decay in human disease
Paulo J. da Costa, Juliane Menezes, Luı́sa Romão
The International Journal of Biochemistry & Cell Biology (2017) Vol. 91, pp. 168-175
Closed Access | Times Cited: 65
Developmental Attenuation of Neuronal Apoptosis by Neural-Specific Splicing of Bak1 Microexon
Lin Lin, Min Zhang, Peter Stoilov, et al.
Neuron (2020) Vol. 107, Iss. 6, pp. 1180-1196.e8
Open Access | Times Cited: 55
Tracking pre-mRNA maturation across subcellular compartments identifies developmental gene regulation through intron retention and nuclear anchoring
Kyu‐Hyeon Yeom, Zhicheng Pan, Chia-Ho Lin, et al.
Genome Research (2021) Vol. 31, Iss. 6, pp. 1106-1119
Open Access | Times Cited: 47
Crucial roles of different RNA-binding hnRNP proteins in Stem Cells
Wen Xie, Hecheng Zhu, Ming Zhao, et al.
International Journal of Biological Sciences (2021) Vol. 17, Iss. 3, pp. 807-817
Open Access | Times Cited: 43
Direct Neuronal Reprogramming: Bridging the Gap Between Basic Science and Clinical Application
Lakshmy Vasan, EunJee Park, Luke Ajay David, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 41
Long read sequencing reveals novel isoforms and insights into splicing regulation during cell state changes
David J. Wright, Nicola Hall, Naomi Irish, et al.
BMC Genomics (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 28
MAPP unravels frequent co-regulation of splicing and polyadenylation by RNA-binding proteins and their dysregulation in cancer
Maciej Bąk, Erik van Nimwegen, Ivan U. Kouzel, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 7
M6A-modified lncRNA FAM83H-AS1 promotes colorectal cancer progression through PTBP1
Xiaojing Luo, Yun‐Xin Lu, Yun Wang, et al.
Cancer Letters (2024) Vol. 598, pp. 217085-217085
Open Access | Times Cited: 7
RNA Binding Protein Ptbp2 Is Essential for Male Germ Cell Development
Leah L. Zagore, Sarah E. Grabinski, Thomas J. Sweet, et al.
Molecular and Cellular Biology (2015) Vol. 35, Iss. 23, pp. 4030-4042
Open Access | Times Cited: 63
PTBP1 and PTBP2 Repress Nonconserved Cryptic Exons
Jonathan P. Ling, Resham Chhabra, Jonathan Merran, et al.
Cell Reports (2016) Vol. 17, Iss. 1, pp. 104-113
Open Access | Times Cited: 59
MBNL expression in autoregulatory feedback loops
Patryk Konieczny, Ewa Stepniak-Konieczna, Krzysztof Sobczak
RNA Biology (2017) Vol. 15, Iss. 1, pp. 1-8
Open Access | Times Cited: 55
Polarizing the Neuron through Sustained Co-expression of Alternatively Spliced Isoforms
Karen Yap, Yixin Xiao, Brad A. Friedman, et al.
Cell Reports (2016) Vol. 15, Iss. 6, pp. 1316-1328
Open Access | Times Cited: 54
A network-based analysis of colon cancer splicing changes reveals a tumorigenesis-favoring regulatory pathway emanating from ELK1
Dror Hollander, Maya Donyo, Nir Atias, et al.
Genome Research (2016) Vol. 26, Iss. 4, pp. 541-553
Open Access | Times Cited: 53
Physiological and pathophysiological role of nonsense-mediated mRNA decay
Franziska Ottens, Niels H. Gehring
Pflügers Archiv - European Journal of Physiology (2016) Vol. 468, Iss. 6, pp. 1013-1028
Closed Access | Times Cited: 49
Alternative splicing and nonsense‐mediated mRNA decay enforce neural specific gene expression
Sika Zheng
International Journal of Developmental Neuroscience (2016) Vol. 55, Iss. 1, pp. 102-108
Open Access | Times Cited: 48

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