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:

Novel SF3B1 in-frame deletions result in aberrant RNA splicing in CLL patients
Anant A. Agrawal, Michael Seiler, Lindsey T. Brinton, et al.
Blood Advances (2017) Vol. 1, Iss. 15, pp. 995-1000
Open Access | Times Cited: 16

Showing 16 citing articles:

Alternative splicing of its 5′-UTR limits CD20 mRNA translation and enables resistance to CD20-directed immunotherapies
Zhiwei Ang, Luca Paruzzo, Katharina E. Hayer, et al.
Blood (2023) Vol. 142, Iss. 20, pp. 1724-1739
Open Access | Times Cited: 24

Splicing modulation sensitizes chronic lymphocytic leukemia cells to venetoclax by remodeling mitochondrial apoptotic dependencies
Elisa ten Hacken, Rebecca Valentin, Fara Faye Regis, et al.
JCI Insight (2018) Vol. 3, Iss. 19
Open Access | Times Cited: 48

U2-2 snRNA Mutations Alter the Transcriptome
Zhongxuan Chi, Varun Gupta, Charles C. Query
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Closed Access

Multi-omics reveals mitochondrial metabolism proteins susceptible for drug discovery in AML
Mika Caplan, Karli J. Wittorf, Kasidy Weber, et al.
Leukemia (2022) Vol. 36, Iss. 5, pp. 1296-1305
Open Access | Times Cited: 14

UBR5 HECT domain mutations identified in mantle cell lymphoma control maturation of B cells
Samantha Swenson, Tyler J. Gilbreath, Heather Vahle, et al.
Blood (2020) Vol. 136, Iss. 3, pp. 299-312
Open Access | Times Cited: 21

Rare and private spliceosomal gene mutations drive partial, complete, and dual phenocopies of hotspot alterations
Joseph Pangallo, Jean‐Jacques Kiladjian, Bruno Cassinat, et al.
Blood (2020)
Open Access | Times Cited: 15

SF3B1 mutation predicts unfavorable treatment-free survival in Chinese chronic lymphocytic leukemia patients
Yi Miao, Yixin Zou, Danling Gu, et al.
Annals of Translational Medicine (2019) Vol. 7, Iss. 8, pp. 176-176
Open Access | Times Cited: 12

CtIP-mediated alternative mRNA splicing fine-tunes the DNA damage response
Rosario Prados‐Carvajal, Guillermo Rodríguez‐Real, Gabriel Gutiérrez, et al.
RNA (2020) Vol. 27, Iss. 3, pp. 303-323
Open Access | Times Cited: 8

Degenerate minigene library analysis enables identification of altered branch point utilization by mutant splicing factor 3B1 (SF3B1)
Abhishek Gupta, Tushar Murthy, Kiran Paul, et al.
Nucleic Acids Research (2018) Vol. 47, Iss. 2, pp. 970-980
Open Access | Times Cited: 8

Alternative splicing of its 5’-UTR limits CD20 mRNA translation and enables resistance to CD20-directed immunotherapies
Zhiwei Ang, Luca Paruzzo, Katharina E. Hayer, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2

The role of SF3B1 and NOTCH1 in the pathogenesis of leukemia
Shiva Abolhasani, Seyyed Sina Hejazian, Vahid Karpisheh, et al.
IUBMB Life (2022) Vol. 75, Iss. 3, pp. 257-278
Closed Access | Times Cited: 3

CtIP -mediated alternative mRNA splicing finetunes the DNA damage response
Rosario Prados‐Carvajal, Guillermo Rodríguez‐Real, Gabriel Gutiérrez, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2019)
Open Access | Times Cited: 3

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