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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:

Sex differences in Mecp2-mutant Rett syndrome model mice and the impact of cellular mosaicism in phenotype development
Mayara C. Ribeiro, Jessica L. MacDonald
Brain Research (2020) Vol. 1729, pp. 146644-146644
Open Access | Times Cited: 40

Showing 1-25 of 40 citing articles:

Role of DNA Methyl-CpG-Binding Protein MeCP2 in Rett Syndrome Pathobiology and Mechanism of Disease
Shervin Pejhan, Mojgan Rastegar
Biomolecules (2021) Vol. 11, Iss. 1, pp. 75-75
Open Access | Times Cited: 62
Sex mechanisms as nonbinary influences on cognitive diversity
Nicola M. Grissom, Nic Glewwe, Cathy Chen, et al.
Hormones and Behavior (2024) Vol. 162, pp. 105544-105544
Open Access | Times Cited: 8
Using the tools of genetic epidemiology to understand sex differences in neuropsychiatric disorders
Alison Merikangas, Laura Almasy
Genes Brain & Behavior (2020) Vol. 19, Iss. 6
Open Access | Times Cited: 61
Perineuronal net degradation rescues CA2 plasticity in a mouse model of Rett syndrome
Kelly E. Carstens, Daniel J. Lustberg, Emma K. Shaughnessy, et al.
Journal of Clinical Investigation (2021) Vol. 131, Iss. 16
Open Access | Times Cited: 42
Excitation and Inhibition Imbalance in Rett Syndrome
Wei Li
Frontiers in Neuroscience (2022) Vol. 16
Open Access | Times Cited: 26
Rett syndrome
Wendy Gold, Alan K. Percy, Jeffrey L. Neul, et al.
Nature Reviews Disease Primers (2024) Vol. 10, Iss. 1
Closed Access | Times Cited: 5
Neural precursor cells rescue symptoms of Rett syndrome by activation of the Interferon γ pathway
Angelisa Frasca, Federica Miramondi, Erica Butti, et al.
EMBO Molecular Medicine (2024) Vol. 16, Iss. 12, pp. 3218-3246
Open Access | Times Cited: 4
Elucidating neuroepigenetic mechanisms to inform targeted therapeutics for brain disorders
Benjamin H. Weekley, Newaz I. Ahmed, Ian Maze
iScience (2025) Vol. 28, Iss. 3, pp. 112092-112092
Open Access
From womb to world: The interplay between maternal immune activation, neuroglia, and neurodevelopment
Daniele Mattei, Dilansu Güneykaya, Bilge Ugursu, et al.
Handbook of clinical neurology (2025), pp. 269-285
Closed Access
Vitamin D Supplementation Rescues Aberrant NF-κB Pathway Activation and Partially Ameliorates Rett Syndrome Phenotypes inMecp2Mutant Mice
Mayara C. Ribeiro, Seth M. Moore, Noriyuki Kishi, et al.
eNeuro (2020) Vol. 7, Iss. 3, pp. ENEURO.0167-20.2020
Open Access | Times Cited: 21
A Comprehensive and Integrative Approach to MeCP2 Disease Transcriptomics
Alexander J. Trostle, Lucian Li, Seon‐Young Kim, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 6, pp. 5122-5122
Open Access | Times Cited: 7
Multidimensional analysis of a social behavior identifies regression and phenotypic heterogeneity in a female mouse model for Rett syndrome
Michael Mykins, Benjamin B. Bridges, Angela Jo, et al.
Journal of Neuroscience (2024), pp. e1078232023-e1078232023
Open Access | Times Cited: 2
A small-molecule TrkB ligand improves dendritic spine phenotypes and atypical behaviors in female Rett syndrome mice
Destynie Medeiros, Karen Ayala-Baylon, Hailey X. Egido-Betancourt, et al.
Disease Models & Mechanisms (2024) Vol. 17, Iss. 6
Open Access | Times Cited: 2
Lateralized Expression of Cortical Perineuronal Nets during Maternal Experience is Dependent on MECP2
Billy Y. B. Lau, Dana E. Layo-Carris, Brett Addison Emery, et al.
eNeuro (2020) Vol. 7, Iss. 3, pp. ENEURO.0500-19.2020
Open Access | Times Cited: 16
Modeling Rett Syndrome with Human Pluripotent Stem Cells: Mechanistic Outcomes and Future Clinical Perspectives
Ana Rita Gomes, Tiago G. Fernandes, Joaquim M. S. Cabral, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 7, pp. 3751-3751
Open Access | Times Cited: 14
Profiling beneficial and potential adverse effects of MeCP2 overexpression in a hypomorphic Rett syndrome mouse model
Sheryl Anne D. Vermudez, Rocco G. Gogliotti, Bright Arthur, et al.
Genes Brain & Behavior (2021) Vol. 21, Iss. 1
Open Access | Times Cited: 12
Convergent cerebrospinal fluid proteomes and metabolic ontologies in humans and animal models of Rett syndrome
Stephanie A. Zlatic, Duc M. Duong, Kamal K.E. Gadalla, et al.
iScience (2022) Vol. 25, Iss. 9, pp. 104966-104966
Open Access | Times Cited: 8
MeCP2 ubiquitination and sumoylation, in search of a function
Ladan Kalani, Bo‐Hyun Kim, John B. Vincent, et al.
Human Molecular Genetics (2023) Vol. 33, Iss. 1, pp. 1-11
Closed Access | Times Cited: 4
Heterozygous Nexmif female mice demonstrate mosaic NEXMIF expression, autism-like behaviors, and abnormalities in dendritic arborization and synaptogenesis
Margaret O’Connor, Hui Qiao, Kathryn-Ann Odamah, et al.
Heliyon (2024) Vol. 10, Iss. 3, pp. e24703-e24703
Open Access | Times Cited: 1
Proteomic and transcriptional changes associated with MeCP2 dysfunction reveal nodes for therapeutic intervention in Rett syndrome
Ketan K. Marballi, Jessica L. MacDonald
Neurochemistry International (2021) Vol. 148, pp. 105076-105076
Open Access | Times Cited: 10
GENE TARGET: A framework for evaluating Mendelian neurodevelopmental disorders for gene therapy
Maya Chopra, Meera E. Modi, Kira A. Dies, et al.
Molecular Therapy — Methods & Clinical Development (2022) Vol. 27, pp. 32-46
Open Access | Times Cited: 7
Methyl‐CpG binding protein 2 dysfunction provides stress vulnerability with sex‐ and zygosity‐dependent outcomes
Livia Cosentino, Fabio Bellia, Nicole Pavoncello, et al.
European Journal of Neuroscience (2021) Vol. 55, Iss. 9-10, pp. 2766-2776
Closed Access | Times Cited: 8
Fluoxetine increases brain MeCP2 immuno-positive cells in a female Mecp2 heterozygous mouse model of Rett syndrome through endogenous serotonin
Claudia Villani, Mirjana Carli, Anna Maria Castaldo, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 8
Reversal of neurological deficits by painless nerve growth factor in a mouse model of Rett syndrome
Alexia Tiberi, Giulia Borgonovo, Giovanna Testa, et al.
Brain (2023) Vol. 147, Iss. 1, pp. 122-134
Open Access | Times Cited: 3
Dual synaptic inhibitions of brainstem neurons by GABA and glycine with impact on Rett syndrome
Hao Xing, Ningren Cui, Christopher M. Johnson, et al.
Journal of Cellular Physiology (2020) Vol. 236, Iss. 5, pp. 3615-3628
Closed Access | Times Cited: 6
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