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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:

Intermolecular insights into allosteric inhibition of histone lysine-specific demethylase 1
Xiangyu Zhang, Yixiang Sun, Ziheng Zhang, et al.
Biochimica et Biophysica Acta (BBA) - General Subjects (2021) Vol. 1865, Iss. 11, pp. 129990-129990
Closed Access | Times Cited: 10

Showing 10 citing articles:

SP2509 functions as a novel ferroptosis inhibitor by reducing intracellular iron level in vascular smooth muscle cells
Yi He, Xingbo Wang, Siqi Chen, et al.
Free Radical Biology and Medicine (2024) Vol. 219, pp. 49-63
Open Access | Times Cited: 10
Leveraging non-enzymatic functions of LSD1 for novel therapeutics
Yihui Song, Bin Yu
Trends in Pharmacological Sciences (2025)
Closed Access
Therapeutic potential of targeting LSD1/ KDM1A in cancers
Xiangyu Zhang, Xinran Wang, Tianxiao Wu, et al.
Pharmacological Research (2021) Vol. 175, pp. 105958-105958
Closed Access | Times Cited: 36
Pharmacological inhibition of LSD1 suppresses growth of hepatocellular carcinoma by inducing GADD45B
Na Sang, Xi Zhong, Kun Gou, et al.
MedComm (2023) Vol. 4, Iss. 3
Open Access | Times Cited: 9
Designing drugs when there is low data availability: one-shot learning and other approaches to face the issues of a long-term concern
Gabriel Corrêa Veríssimo, Mateus Sá Magalhães Serafim, Thales Kronenberger, et al.
Expert Opinion on Drug Discovery (2022) Vol. 17, Iss. 9, pp. 929-947
Closed Access | Times Cited: 14
Identification of novel indole derivatives as highly potent and efficacious LSD1 inhibitors
Xiangyu Zhang, Yixiang Sun, Hai‐Lan Huang, et al.
European Journal of Medicinal Chemistry (2022) Vol. 239, pp. 114523-114523
Closed Access | Times Cited: 12
Structure-based discovery of 1-(3-fluoro-5-(5-(3-(methylsulfonyl)phenyl)-1H-pyrazolo[3,4-b]pyridin-3-yl)phenyl)-3-(pyrimidin-5-yl)urea as a potent and selective nanomolar type-II PLK4 inhibitor
Yin Sun, Lin Wang, Yu Sun, et al.
European Journal of Medicinal Chemistry (2022) Vol. 243, pp. 114714-114714
Closed Access | Times Cited: 8
Uncovering New Conformational States of the Substrate Binding Pocket of LSD1 Potential for Inhibitor Design via Funnel Metadynamics
Kecheng Yang, Hong‐Min Liu
The Journal of Physical Chemistry B (2023) Vol. 128, Iss. 1, pp. 137-149
Closed Access | Times Cited: 3
Histone Demethylases
Stephen C. Kales, Anton Simeonov
Royal Society of Chemistry eBooks (2024), pp. 383-403
Closed Access
Drug Discovery for Chromatin Readers, Writers, Erasers, Remodelers and Epitranscriptomic Targets

Royal Society of Chemistry eBooks (2024)
Closed Access
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