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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:

Regulation, diversity and function of MECP2 exon and 3′UTR isoforms
Deivid C. Rodrigues, Marat Mufteev, James Ellis
Human Molecular Genetics (2020) Vol. 29, Iss. R1, pp. R89-R99
Open Access | Times Cited: 14

Showing 14 citing articles:

MeCP2: The Genetic Driver of Rett Syndrome Epigenetics
Katrina Good, John B. Vincent, Juan Ausió
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 99
Rare variants in the MECP2 gene in girls with central precocious puberty: a translational cohort study
Ana Pinheiro Machado Canton, Flávia Rezende Tinano, Leonardo Guasti, et al.
The Lancet Diabetes & Endocrinology (2023) Vol. 11, Iss. 8, pp. 545-554
Open Access | Times Cited: 21
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
MECP2 and the biology of MECP2 duplication syndrome
Santosh R. D’Mello
Journal of Neurochemistry (2021) Vol. 159, Iss. 1, pp. 29-60
Open Access | Times Cited: 29
Transcriptional Inhibition of the Mecp2 Promoter by MeCP2E1 and MeCP2E2 Isoforms Suggests Negative Auto-Regulatory Feedback that can be Moderated by Metformin
Sandhini Lockman, Matthew Genung, Kimia Sheikholeslami, et al.
Journal of Molecular Neuroscience (2024) Vol. 74, Iss. 1
Closed Access | Times Cited: 3
Meta-Analysis Identifies BDNF and Novel Common Genes Differently Altered in Cross-Species Models of Rett Syndrome
Florencia Haase, Rachna Singh, Brian Gloss, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 19, pp. 11125-11125
Open Access | Times Cited: 10
Zebrafish in understanding molecular pathophysiology, disease modeling, and developing effective treatments for Rett syndrome
Subrata Pramanik, Asis Bala, Ajay Pradhan
The Journal of Gene Medicine (2024) Vol. 26, Iss. 2
Closed Access | Times Cited: 1
Site-Blocking Antisense Oligonucleotides as a Mechanism to Fine-Tune MECP2 Expression
Amanda M. Vanderplow, Grace E. Dodis, Yewon Rhee, et al.
RNA (2024) Vol. 30, Iss. 12, pp. 1554-1571
Open Access | Times Cited: 1
The Chromatin Structure at the MECP2 Gene and In Silico Prediction of Potential Coding and Non-Coding MECP2 Splice Variants
Danilo Shevkoplyas, Yen My Vuu, James Davie, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 24, pp. 15643-15643
Open Access | Times Cited: 6
Meta-Analysis Identifies Novel Common Genes Differently Altered in Cross-Species Models of Rett Syndrome
Florencia Dagmar Haase, Rachna Singh, Brian Gloss, et al.
(2022)
Open Access | Times Cited: 4
Alternative polyadenylation quantitative trait methylation mapping in human cancers provides clues into the molecular mechanisms of APA
Yige Li, Jingwen Gong, Sun Qing-rong, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 3, pp. 562-583
Open Access
Role of MeCP2 in oligodendrocyte lineage cells in Rett syndrome: review and inference
Zhen Zhang, Peng Li, Yongchang Chen
Ageing and Neurodegenerative Diseases (2023) Vol. 3, Iss. 3
Open Access
Comparative analysis of the mitochondrial proteome in a mouse model of Rett syndrome
Gocha Golubiani
(2023)
Open Access
Transcriptomic and epigenetic changes after the phenotypic rescue of a Rett Syndrome mouse model
Dulce B. Vargas-Landín
(2021)
Closed Access
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