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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:

Mechanism and modeling of human disease-associated near-exon intronic variants that perturb RNA splicing
Hung‐Lun Chiang, Yi-Ting Chen, Jia-Ying Su, et al.
Nature Structural & Molecular Biology (2022) Vol. 29, Iss. 11, pp. 1043-1055
Closed Access | Times Cited: 23

Showing 23 citing articles:

From computational models of the splicing code to regulatory mechanisms and therapeutic implications
Charlotte Capitanchik, Oscar G. Wilkins, Nils Wagner, et al.
Nature Reviews Genetics (2024)
Closed Access | Times Cited: 4
Multiplexed Assays of Human Disease-relevant Mutations Reveal UTR Dinucleotide Composition as a Major Determinant of RNA Stability
Jia-Ying Su, Yun-Lin Wang, Yu-Tung Hsieh, et al.
(2025)
Open Access
Defects in mRNA splicing and implications for infertility: a comprehensive review and in silico analysis
Kuokuo Li, Yuge Chen, Yuying Sheng, et al.
Human Reproduction Update (2025)
Closed Access
Multiplexed assays of human disease-relevant mutations reveal UTR dinucleotide composition as a major determinant of RNA stability
Jia-Ying Su, Yun-Lin Wang, Yu-Tung Hsieh, et al.
eLife (2025) Vol. 13
Open Access
Association Analysis of ENPP1 Tissue Expression, Polymorphism, and Growth Traits in Xiangsu Pigs
Jiaqi Chen, Jiajin Huang, Houqiang Xu
Genes (2025) Vol. 16, Iss. 4, pp. 395-395
Open Access
To splice or not to splice: pseudoexons in neurological disease and opportunities for intervention
Sue Fletcher, Niall P. Keegan, Rita Mejzini, et al.
Current Opinion in Genetics & Development (2025) Vol. 92, pp. 102343-102343
Open Access
The Establishment of Artificial RNA Cascade Circuits for Gene Regulation Based on Doxycycline-Induced Pre-mRNA Alternative Splicing
Guimin Dai, Jiawen Cheng, Weiran Liu, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 3, pp. 1163-1163
Open Access
Regulation of alternative splicing and polyadenylation in neurons
Seungjae Lee, Joseph I Aubee, Eric C. Lai
Life Science Alliance (2023) Vol. 6, Iss. 12, pp. e202302000-e202302000
Open Access | Times Cited: 7
SpliceAPP: an interactive web server to predict splicing errors arising from human mutations
Ang-Chu Huang, Jia-Ying Su, Yu-Jen Hung, et al.
BMC Genomics (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 2
Prioritizing de novo potential non-canonical splicing variants in neurodevelopmental disorders
Kuokuo Li, Jifang Xiao, Zhengbao Ling, et al.
EBioMedicine (2023) Vol. 99, pp. 104928-104928
Open Access | Times Cited: 5
Computational prediction of human deep intronic variation
Pedro Barbosa, Rosina Savisaar, Maria Carmo‐Fonseca, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
The Next, Next-Generation of Sequencing, Promising to Boost Research and Clinical Practice
Kishore R. Kumar, Mark J. Cowley, Ryan L. Davis
Seminars in Thrombosis and Hemostasis (2024) Vol. 50, Iss. 07, pp. 1039-1046
Closed Access | Times Cited: 1
Multiplexed Assays of Human Disease-relevant Mutations Reveal UTR Dinucleotide Composition as a Major Determinant of RNA Stability
Jia-Ying Su, Yun-Lin Wang, Yu-Tung Hsieh, et al.
(2024)
Open Access | Times Cited: 1
Multiplexed Assays of Human Disease-relevant Mutations Reveal UTR Dinucleotide Composition as a Major Determinant of RNA Stability
Jia-Ying Su, Yun-Lin Wang, Yu-Tung Hsieh, et al.
eLife (2024) Vol. 13
Open Access | Times Cited: 1
ParSE-seq: a calibrated multiplexed assay to facilitate the clinical classification of putative splice-altering variants
Matthew J. O’Neill, Tao Yang, Julie Laudeman, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 1
Monoallelic loss-of-function variants in GSK3B lead to autism and developmental delay
Senwei Tan, Qiumeng Zhang, Rui Zhan, et al.
Molecular Psychiatry (2024)
Closed Access | Times Cited: 1
Identifying pleiotropic genes via the composite test amidst the complexity of polygenic traits
En‐Yu Lai, Yen‐Tsung Huang
Briefings in Bioinformatics (2024) Vol. 25, Iss. 4
Open Access
Massively Parallel Polyribosome Profiling Reveals Translation Defects of Human Disease-Relevant UTR Mutations
Weiping Li, Jia-Ying Su, Yu-Chi Chang, et al.
(2024)
Open Access
Massively Parallel Polyribosome Profiling Reveals Translation Defects of Human Disease-Relevant UTR Mutations
Weiping Li, Jia-Ying Su, Yu-Chi Chang, et al.
(2024)
Open Access
Multiplexed Assays of Human Disease-relevant Mutations Reveal UTR Dinucleotide Composition as a Major Determinant of RNA Stability
Jia-Ying Su, Yun-Lin Wang, Yu-Tung Hsieh, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Massively Parallel Polyribosome Profiling Reveals Translation Defects of Human Disease-Relevant UTR Mutations
Weiping Li, Jia-Ying Su, Yu-Chi Chang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Identification of deleterious variants in nine polycystic kidney disease affected families
Jing Yuan, Zhongmei Shao, Mingrong Lv, et al.
Gene (2024) Vol. 919, pp. 148505-148505
Closed Access
ParSE-seq: A Calibrated Multiplexed Assay to Facilitate the Clinical Classification of Putative Splice-altering Variants
Matthew J. O’Neill, Tao Yang, Julie Laudeman, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
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