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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:

RBM20 phosphorylation and its role in nucleocytoplasmic transport and cardiac pathogenesis
Yanghai Zhang, Chunyan Wang, Mingming Sun, et al.
The FASEB Journal (2022) Vol. 36, Iss. 5
Open Access | Times Cited: 24

Showing 24 citing articles:

Precise genomic editing of pathogenic mutations in RBM20 rescues dilated cardiomyopathy
Takahiko Nishiyama, Yu Zhang, Miao Cui, et al.
Science Translational Medicine (2022) Vol. 14, Iss. 672
Open Access | Times Cited: 96
RNA-binding proteins in cardiovascular biology and disease: the beat goes on
Mirko Völkers, Thomas Preiß, Matthias W. Hentze
Nature Reviews Cardiology (2024) Vol. 21, Iss. 6, pp. 361-378
Closed Access | Times Cited: 14
Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy
Ana Töpf, Dan Cox, Irina Zaharieva, et al.
Nature Genetics (2024) Vol. 56, Iss. 3, pp. 395-407
Open Access | Times Cited: 13
Mechanisms of RBM20 Cardiomyopathy: Insights From Model Systems
Zachery R. Gregorich, Yanghai Zhang, Timothy J. Kamp, et al.
Circulation Genomic and Precision Medicine (2024) Vol. 17, Iss. 1
Closed Access | Times Cited: 12
Striated muscle-specific base editing enables correction of mutations causing dilated cardiomyopathy
Markus Grosch, Laura Schraft, Adrian Chan, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 20
Mislocalization of pathogenic RBM20 variants in dilated cardiomyopathy is caused by loss-of-interaction with Transportin-3
Julia Kornienko, Marta Rodríguez‐Martínez, Kai Fenzl, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 18
Regulation of plant resistance to salt stress by the SnRK1‐dependent splicing factor SRRM1L
Qi Sun, Yixin Sun, X. Liu, et al.
New Phytologist (2024) Vol. 242, Iss. 5, pp. 2093-2114
Closed Access | Times Cited: 5
Discovery of Titin and Its Role in Heart Function and Disease
Henk Granzier, Siegfried Labeit
Circulation Research (2025) Vol. 136, Iss. 1, pp. 135-157
Closed Access
Alternative splicing factors and cardiac disease: more than just mis-splicing?
Zachery R. Gregorich, Wei Guo
RNA (2025), pp. rna.080332.124-rna.080332.124
Closed Access
Reducing Granules Without Splicing Restoration Alleviates RBM20 Cardiomyopathy
Mei Methawasin, Yanghai Zhang, Zachery R. Gregorich, et al.
Circulation Research (2025)
Closed Access
Disruption of the nuclear localization signal in RBM20 is causative in dilated cardiomyopathy
Yanghai Zhang, Zachery R. Gregorich, Yujuan Wang, et al.
JCI Insight (2023) Vol. 8, Iss. 13
Open Access | Times Cited: 8
Comprehensive review on gene mutations contributing to dilated cardiomyopathy
Shipeng Wang, Zhiyu Zhang, Jiahuan He, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 8
Risk Assessment and Personalized Treatment Options in Inherited Dilated Cardiomyopathies: A Narrative Review
Diana-Aurora Arnăutu, Dragoş Cozma, Ioan-Radu Lala, et al.
Biomedicines (2024) Vol. 12, Iss. 8, pp. 1643-1643
Open Access | Times Cited: 2
Sorafenib induces cardiotoxicity through RBM20-mediated alternative splicing of sarcomeric and mitochondrial genes
Songming Liu, Shanshan Yue, Yuxuan Guo, et al.
Pharmacological Research (2023) Vol. 198, pp. 107017-107017
Open Access | Times Cited: 5
Screening and identification of key biomarkers associated with endometriosis using bioinformatics and next generation sequencing data analysis
Basavaraj Vastrad, Chanabasayya Vastrad
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Integrated proteomics and transcriptomics analysis reveals insights into differences in premature mortality associated with disparate pathogenic RBM20 variants
Zachery R. Gregorich, Eli J. Larson, Yanghai Zhang, et al.
Journal of Molecular and Cellular Cardiology (2024) Vol. 197, pp. 78-89
Closed Access | Times Cited: 1
Rbm20 ablation is associated with changes in the expression of titin-interacting and metabolic proteins
Eli J. Larson, Zachery R. Gregorich, Yanghai Zhang, et al.
Molecular Omics (2022) Vol. 18, Iss. 7, pp. 627-634
Open Access | Times Cited: 7
Deep phenotyping of two preclinical mouse models and a cohort of RBM20 mutation carriers reveals no sex-dependent disease severity in RBM20 cardiomyopathy
David C. Lennermann, Mark E. Pepin, Markus Grosch, et al.
AJP Heart and Circulatory Physiology (2022) Vol. 323, Iss. 6, pp. H1296-H1310
Closed Access | Times Cited: 7
SR Protein Kinases Regulate the Splicing of Cardiomyopathy-Relevant Genes via Phosphorylation of the RSRSP Stretch in RBM20
Mingming Sun, Yutong Jin, Yanghai Zhang, et al.
Genes (2022) Vol. 13, Iss. 9, pp. 1526-1526
Open Access | Times Cited: 6
SPAG6 c.900 T>C affects boar semen quality and blood–testis barrier function by creating a new splice acceptor site
Rong Bai, Dake Chen, Hao Xiong, et al.
Animal Genetics (2023) Vol. 54, Iss. 4, pp. 446-456
Closed Access | Times Cited: 3
Integrated Proteomics and Transcriptomics Analysis Reveals Insights into Differences in Premature Mortality Associated with Disparate Pathogenic Rbm20 Variants
Zachery R. Gregorich, Eli J. Larson, Yanghai Zhang, et al.
(2024)
Closed Access
Screening and identification of key biomarkers associated with endometriosis using bioinformatics and next-generation sequencing data analysis
Basavaraj Vastrad, Chanabasayya Vastrad
Egyptian Journal of Medical Human Genetics (2024) Vol. 25, Iss. 1
Open Access
[Research progress on the expression of the RBM20 gene in dilated cardiomyopathy].
Xin Lin
PubMed (2023) Vol. 25, Iss. 10, pp. 1084-1088
Closed Access
Digenic Inheritance Involving a Muscle Specific Protein Kinase and the Giant Titin Protein Causes a Skeletal Muscle Myopathy

SSRN Electronic Journal (2021)
Open Access
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