Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Elongation factor ELOF1 drives transcription-coupled repair and prevents genome instability
Marit E. Geijer, Di Zhou, Kathiresan Selvam, et al.
Nature Cell Biology (2021) Vol. 23, Iss. 6, pp. 608-619
Open Access | Times Cited: 72

Showing 1-25 of 72 citing articles:

H3K4me3 regulates RNA polymerase II promoter-proximal pause-release
Hua Wang, Zheng Fan, Pavel V. Shliaha, et al.
Nature (2023) Vol. 615, Iss. 7951, pp. 339-348
Open Access | Times Cited: 208
Transcription-Coupled Nucleotide Excision Repair and the Transcriptional Response to UV-Induced DNA Damage
Nicolás Nieto Moreno, Anouk Olthof, Jesper Q. Svejstrup
Annual Review of Biochemistry (2023) Vol. 92, Iss. 1, pp. 81-113
Open Access | Times Cited: 57
Revolutionizing DNA repair research and cancer therapy with CRISPR–Cas screens
Samah W. Awwad, Almudena Serrano-Benítez, John C. Thomas, et al.
Nature Reviews Molecular Cell Biology (2023) Vol. 24, Iss. 7, pp. 477-494
Closed Access | Times Cited: 48
Structural basis for RNA polymerase II ubiquitylation and inactivation in transcription-coupled repair
Goran Kokić, George Yakoub, Diana van den Heuvel, et al.
Nature Structural & Molecular Biology (2024) Vol. 31, Iss. 3, pp. 536-547
Open Access | Times Cited: 31
Transcription-coupled repair of DNA–protein cross-links depends on CSA and CSB
Christopher J. Carnie, Aleida C. Acampora, Aldo S. Bader, et al.
Nature Cell Biology (2024) Vol. 26, Iss. 5, pp. 797-810
Open Access | Times Cited: 22
Transcription-coupled DNA–protein crosslink repair by CSB and CRL4CSA-mediated degradation
Marjolein van Sluis, Qing Yu, Melanie van der Woude, et al.
Nature Cell Biology (2024) Vol. 26, Iss. 5, pp. 770-783
Open Access | Times Cited: 21
Identifying candidate RNA-seq biomarkers for severity discrimination in chemical injuries: A machine learning and molecular dynamics approach
Masoud Arabfard, Esmaeil Behmard, Mazaher Maghsoudloo, et al.
International Immunopharmacology (2025) Vol. 148, pp. 114090-114090
Closed Access | Times Cited: 3
Molecular Mechanisms of Transcription-Coupled Repair
Christopher P. Selby, Laura A. Lindsey‐Boltz, Wentao Li, et al.
Annual Review of Biochemistry (2023) Vol. 92, Iss. 1, pp. 115-144
Open Access | Times Cited: 40
Elf1 promotes Rad26’s interaction with lesion-arrested Pol II for transcription-coupled repair
Reta D. Sarsam, Jun Xu, Indrajit Lahiri, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 3
Open Access | Times Cited: 13
STK19 positions TFIIH for cell-free transcription-coupled DNA repair
Tycho E.T. Mevissen, Maximilian Kümmecke, E. Schmid, et al.
Cell (2024)
Open Access | Times Cited: 10
STK19 is a transcription-coupled repair factor that participates in UVSSA ubiquitination and TFIIH loading
Yuanqing Tan, Meng Gao, Yanchao Huang, et al.
Nucleic Acids Research (2024)
Open Access | Times Cited: 9
STK19 facilitates the clearance of lesion-stalled RNAPII during transcription-coupled DNA repair
Diana van den Heuvel, Marta Rodríguez‐Martínez, Paula J. van der Meer, et al.
Cell (2024) Vol. 187, Iss. 25, pp. 7107-7125.e25
Open Access | Times Cited: 9
Transcription elongation factor ELOF1 is required for efficient somatic hypermutation and class switch recombination
Lizhen Wu, Anurupa Devi Yadavalli, Filip Šenigl, et al.
Molecular Cell (2025)
Open Access | Times Cited: 1
Transcription-coupled AID deamination damage depends on ELOF1-associated RNA polymerase II
Pengfei Dai, Yuanqing Tan, Yifeng Luo, et al.
Molecular Cell (2025)
Closed Access | Times Cited: 1
Dealing with transcription-blocking DNA damage: Repair mechanisms, RNA polymerase II processing and human disorders
Nan Jia, Chaowan Guo, Yuka Nakazawa, et al.
DNA repair (2021) Vol. 106, pp. 103192-103192
Open Access | Times Cited: 42
RNA polymerase pausing, stalling and bypass during transcription of damaged DNA: from molecular basis to functional consequences
Aleksei Agapov, A.A. Olina, Andrey Kulbachinskiy
Nucleic Acids Research (2022) Vol. 50, Iss. 6, pp. 3018-3041
Open Access | Times Cited: 35
STK19 drives transcription-coupled repair by stimulating repair complex stability, RNA Pol II ubiquitylation, and TFIIH recruitment
Anisha R. Ramadhin, Shun-Hsiao Lee, Di Zhou, et al.
Molecular Cell (2024)
Open Access | Times Cited: 8
Persistent TFIIH binding to non-excised DNA damage causes cell and developmental failure
Alba Muniesa-Vargas, Carlota Davó-Martínez, Cristina Ribeiro-Silva, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 6
Genomic Instability and Cancer Risk Associated with Erroneous DNA Repair
Kenichi Yoshioka, Rika Kusumoto‐Matsuo, Yusuke Matsuno, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 22, pp. 12254-12254
Open Access | Times Cited: 34
At the core of nucleotide excision repair
Jochen Kuper, Caroline Kisker
Current Opinion in Structural Biology (2023) Vol. 80, pp. 102605-102605
Closed Access | Times Cited: 16
A disease-associated XPA allele interferes with TFIIH binding and primarily affects transcription-coupled nucleotide excision repair
Diana van den Heuvel, Mihyun Kim, Annelotte P. Wondergem, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 11
Open Access | Times Cited: 14
TFIIH central activity in nucleotide excision repair to prevent disease
Arjan F. Theil, David Häckes, Hannes Lans
DNA repair (2023) Vol. 132, pp. 103568-103568
Open Access | Times Cited: 13
Live-cell imaging of endogenous CSB-mScarletI as a sensitive marker for DNA-damage-induced transcription stress
Di Zhou, Qing Yu, Roel C. Janssens, et al.
Cell Reports Methods (2024) Vol. 4, Iss. 1, pp. 100674-100674
Open Access | Times Cited: 5
RBM22 regulates RNA polymerase II 5′ pausing, elongation rate, and termination by coordinating 7SK-P-TEFb complex and SPT5
Xian Du, Wenying Qin, Chunyu Yang, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 5
Differential processing of RNA polymerase II at DNA damage correlates with transcription-coupled repair syndrome severity
Camila Gonzalo-Hansen, Barbara Steurer, Roel C. Janssens, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. 16, pp. 9596-9612
Open Access | Times Cited: 5
Page 1 - Next Page

Scroll to top