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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:

Expanding the MECP2 network using comparative genomics reveals potential therapeutic targets for Rett syndrome
Irene Unterman, Idit Bloch, Simona Cazacu, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 13

Showing 13 citing articles:

State‐of‐the‐art therapies for Rett syndrome
Nicolas Panayotis, Yann Ehinger, Marie‐Solenne Félix, et al.
Developmental Medicine & Child Neurology (2022) Vol. 65, Iss. 2, pp. 162-170
Open Access | Times Cited: 24
Propofol Inhibits Glioma Stem Cell Growth and Migration and Their Interaction with Microglia via BDNF-AS and Extracellular Vesicles
Rephael Nizar, Simona Cazacu, Cunli Xiang, et al.
Cells (2023) Vol. 12, Iss. 15, pp. 1921-1921
Open Access | Times Cited: 9
KW-2449 and VPA exert therapeutic effects on human neurons and cerebral organoids derived from MECP2-null hESCs
Yajie Xu, Peipei Liu, Zhong-Ze Yan, et al.
Stem Cell Research & Therapy (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 11
BIOCHEMICAL AND MOLECULAR DETERMINANTS OF THE SUBCLINICAL INFLAMMATORY MECHANISMS IN RETT SYNDROME
Valeria Cordone
Archives of Biochemistry and Biophysics (2024) Vol. 757, pp. 110046-110046
Open Access | Times Cited: 2
Using multi-scale genomics to associate poorly annotated genes with rare diseases
Christina Canavati, Dana Sherill-Rofe, Lara Kamal, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 1
Methyl-CpG Binding Protein 2 as a Potential Diagnostic and Prognostic Marker Facilitates Glioma Progression Through Activation of Wnt/β-Catenin Pathway
Guanyou Huang, Yujuan Wu, DU Yong-gui, et al.
World Neurosurgery (2022) Vol. 171, pp. e560-e571
Closed Access | Times Cited: 7
Machine-learning of complex evolutionary signals improves classification of SNVs
Sapir Labes, Doron Stupp, Naama Wagner, et al.
NAR Genomics and Bioinformatics (2022) Vol. 4, Iss. 2
Open Access | Times Cited: 4
Abolished clustering of MeCP2T158M can be partially reverted with small molecules
Rodrigo Lata, Liesbeth Steegmans, Ranie Kellens, et al.
Translational Medicine Communications (2024) Vol. 9, Iss. 1
Open Access
Role of histone deacetylase inhibitors in non-neoplastic diseases
Chunxiao Zhou, Dengke Zhao, Chunyan Wu, et al.
Heliyon (2024) Vol. 10, Iss. 13, pp. e33997-e33997
Open Access
IRSF 2023 - Rett Syndrome Scientific Meeting Report
Nupur Garg, Zhaolan Zhou, Eric D. Marsh, et al.
Translational Science of Rare Diseases (2023) Vol. 6, Iss. 4, pp. 137-150
Open Access | Times Cited: 1
HDAC inhibitors rescue MeCP2T158Mspeckles in a high content screen
Rodrigo Lata, Liesbeth Steegmans, Ranie Kellens, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
DEPCOD: a tool to detect and visualize co-evolution of protein domains
Fei Ji, Gracia Bonilla, Rustem Krykbaev, et al.
Nucleic Acids Research (2022) Vol. 50, Iss. W1, pp. W246-W253
Open Access | Times Cited: 2
KW-2449 and VPA exert therapeutic effects on human neurons and cerebral organoids derived from MECP2-null hESCs
Yajie Xu, Peipei Liu, Zhong-Ze Yan, et al.
Research Square (Research Square) (2022)
Open Access
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