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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:

In Silico Study of Rett Syndrome Treatment-Related Genes, MECP2, CDKL5, and FOXG1, by Evolutionary Classification and Disordered Region Assessment
Muhamad Fahmi, Gen Yasui, Kaito Seki, et al.
International Journal of Molecular Sciences (2019) Vol. 20, Iss. 22, pp. 5593-5593
Open Access | Times Cited: 15

Showing 15 citing articles:

CDKL Family Kinases Have Evolved Distinct Structural Features and Ciliary Function
Peter Canning, Kwangjin Park, João Gonçalves, et al.
Cell Reports (2018) Vol. 22, Iss. 4, pp. 885-894
Open Access | Times Cited: 69
Cyclin-Dependent Kinase-Like 5 (CDKL5): Possible Cellular Signalling Targets and Involvement in CDKL5 Deficiency Disorder
Syouichi Katayama, Noriyuki Sueyoshi, T. INAZU, et al.
Neural Plasticity (2020) Vol. 2020, pp. 1-14
Open Access | Times Cited: 35
A mutation-led search for novel functional domains in MeCP2
Jacky Guy, Beatrice Alexander-Howden, Laura FitzPatrick, et al.
Human Molecular Genetics (2018) Vol. 27, Iss. 14, pp. 2531-2545
Open Access | Times Cited: 28
Clinical gene therapy development for the central nervous system: Candidates and challenges for AAVs
Tiffany W. Leong, Arindam Pal, Qi Cai, et al.
Journal of Controlled Release (2023) Vol. 357, pp. 511-530
Open Access | Times Cited: 5
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
The Functional Classification of ORF8 in SARS-CoV-2 Replication, Immune Evasion, and Viral Pathogenesis Inferred through Phylogenetic Profiling
Muhamad Fahmi, Hiromu Kitagawa, Gen Yasui, et al.
Evolutionary Bioinformatics (2021) Vol. 17
Open Access | Times Cited: 12
Genome-Wide Analysis of Whole Human Glycoside Hydrolases by Data-Driven Analysis in Silico
Takahiro Nakamura, Muhamad Fahmi, Jun Tanaka, et al.
International Journal of Molecular Sciences (2019) Vol. 20, Iss. 24, pp. 6290-6290
Open Access | Times Cited: 11
Active human full-length CDKL5 produced in the Antarctic bacterium Pseudoalteromonas haloplanktis TAC125
Andrea Colarusso, Concetta Lauro, Marzia Calvanese, et al.
Microbial Cell Factories (2022) Vol. 21, Iss. 1
Open Access | Times Cited: 7
Soluble Recombinant Protein Production in Pseudoalteromonas haloplanktis TAC125: The Case Study of the Full-Length Human CDKL5 Protein
Marzia Calvanese, Andrea Colarusso, Concetta Lauro, et al.
Methods in molecular biology (2022), pp. 219-232
Closed Access | Times Cited: 6
Macromolecular Interactions of Disordered Proteins
István Simon
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 2, pp. 504-504
Open Access | Times Cited: 6
Unusual double mutation in MECP2 and CDKL5 genes in Rett-like syndrome: Correlation with phenotype and genes expression
Marwa Ben Jdila, Chahnez Triki, Rania Ghorbel, et al.
Clinica Chimica Acta (2020) Vol. 508, pp. 287-294
Closed Access | Times Cited: 5
Genotype-phenotype implications from three representative clinical FOXG1 variants associated with FOXG1 syndrome
Yan Bai, Aiwen Yi, Xin Jing, et al.
Seizure (2021) Vol. 89, pp. 45-47
Open Access | Times Cited: 3
Zinc finger protein 483 (ZNF483) regulates neuronal differentiation and methyl-CpG-binding protein 2 (MeCP2) intracellular localization
Gen Yasui, Syouichi Katayama, Yukihiko Kubota, et al.
Biochemical and Biophysical Research Communications (2021) Vol. 568, pp. 68-75
Closed Access | Times Cited: 2
Evolutionary Analysis of Rett Syndrome-Causing Proteins and Their Pathogenic Missense Point Mutations: Structural Order–Disorder, Post-Translational Modifications, Evolutionary Rates, and Interacting Proteins
Muhamad Fahmi, Gen Yasui, Kaito Seki, et al.
(2019)
Open Access | Times Cited: 1
Induced pluripotent stem cells for modeling of Rett Syndrome
Bipin Raj Shekhar, Dhanjit Kumar Das
Elsevier eBooks (2021), pp. 171-216
Closed Access
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