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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:

Advances in understanding of Rett syndrome and MECP2 duplication syndrome: prospects for future therapies
Alexander J. Sandweiss, Vicky Brandt, Huda Y. Zoghbi
The Lancet Neurology (2020) Vol. 19, Iss. 8, pp. 689-698
Closed Access | Times Cited: 145

Showing 26-50 of 145 citing articles:

Targeted RNA editing in brainstem alleviates respiratory dysfunction in a mouse model of Rett syndrome
John R. Sinnamon, M. E. Jacobson, John F. Yung, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 33
Open Access | Times Cited: 21
Epilepsy: expert opinion on emerging drugs in phase 2/3 clinical trials
Amanda W. Pong, Jonathan Ross, Ivana Tyrlíková, et al.
Expert Opinion on Emerging Drugs (2022) Vol. 27, Iss. 1, pp. 75-90
Closed Access | Times Cited: 20
Comparison of evoked potentials across four related developmental encephalopathies
Joni N. Saby, Sarika U. Peters, Tim A. Benke, et al.
Journal of Neurodevelopmental Disorders (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 12
Brain Mitochondrial Bioenergetics in Genetic Neurodevelopmental Disorders: Focus on Down, Rett and Fragile X Syndromes
Daniela Valenti, Rosa Anna Vacca
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 15, pp. 12488-12488
Open Access | Times Cited: 11
Extending MeCP2 interactome: canonical nucleosomal histones interact with MeCP2
David Ortega-Alarcón, Rafael Claveria‐Gimeno, Sonia Vega, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. 7, pp. 3636-3653
Open Access | Times Cited: 4
X-Linked Epilepsies: A Narrative Review
Pia Bernardo, Claudia Cuccurullo, Marica Rubino, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 7, pp. 4110-4110
Open Access | Times Cited: 4
Gene therapy in pediatrics – Clinical studies and approved drugs (as of 2023)
Tahereh Mohammadian, Fatemeh Zahedipour, Paul Trosien, et al.
Life Sciences (2024) Vol. 348, pp. 122685-122685
Open Access | Times Cited: 4
Effects of MeCP2 on chronic seizures and cognitive function in mice with temporal lobe epilepsy
Yu Chen, Shu-Nan Yang, Guan-Ling Fu, et al.
Epilepsy Research (2025) Vol. 210, pp. 107512-107512
Closed Access
Intravenous esketamine in pediatric Rett syndrome: An open-label, early phase 1 pilot study
Huiping Li, Shuming Liu, Caimei Lin, et al.
Molecular Therapy — Methods & Clinical Development (2025) Vol. 33, Iss. 1, pp. 101413-101413
Open Access
Comprehensive assessment reveals numerous clinical and neurophysiological differences between MECP2‐allelic disorders
Davut Pehli̇van, Chengjun Huang, Holly K. Harris, et al.
Annals of Clinical and Translational Neurology (2025)
Open Access
Neurobiology of Autism Spectrum Disorder and Intellectual Disability
Alexandra Massa, Jesse Costales, Silvia De Rubeis, et al.
Oxford University Press eBooks (2025), pp. 855-864
Closed Access
Persistent Disruptions in Prefrontal Connectivity Despite Behavioral Rescue by Environmental Enrichment in a Mouse Model of Rett Syndrome
Sofie Ährlund‐Richter, Jonathan Harpe, Giselle Fernandes, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Synaptic disturbance in neurodevelopmental disorders: Perspectives from fragile X and Rett syndromes
Ruixiang Li, Mai Anzai, A. Shibata, et al.
Brain and Development (2025) Vol. 47, Iss. 3, pp. 104358-104358
Open Access
Gene-based therapeutics for rare genetic neurodevelopmental psychiatric disorders
Beverly L. Davidson, Guangping Gao, Elizabeth Berry‐Kravis, et al.
Molecular Therapy (2022) Vol. 30, Iss. 7, pp. 2416-2428
Open Access | Times Cited: 18
Improving clinical trial readiness to accelerate development of new therapeutics for Rett syndrome
Helen Leonard, Wendy Gold, Rodney C. Samaco, et al.
Orphanet Journal of Rare Diseases (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 16
C9orf72 poly(PR) aggregation in nucleus induces ALS/FTD-related neurodegeneration in cynomolgus monkeys
Lizhu Xu, Dan Wang, Lu Zhao, et al.
Neurobiology of Disease (2023) Vol. 184, pp. 106197-106197
Open Access | Times Cited: 9
The Efficacy of a Human-Ready miniMECP2 Gene Therapy in a Pre-Clinical Model of Rett Syndrome
Chanchal Sadhu, Christopher J. Lyons, Jiyoung Oh, et al.
Genes (2023) Vol. 15, Iss. 1, pp. 31-31
Open Access | Times Cited: 9
Multi‐omics in MECP2 duplication syndrome patients and carriers
Ainhoa Pascual‐Alonso, Clara Xiol, Dmitrii Smirnov, et al.
European Journal of Neuroscience (2024) Vol. 60, Iss. 2, pp. 4004-4018
Open Access | Times Cited: 3
MeCP2 Interacts with the Super Elongation Complex to Regulate Transcription
Jun Young Sonn, Wonho Kim, Marta Iwanaszko, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
Differential dynamics specify MeCP2 function at nucleosomes and methylated DNA
Gabriella N. L. Chua, John W. Watters, Paul Dominic B. Olinares, et al.
Nature Structural & Molecular Biology (2024) Vol. 31, Iss. 11, pp. 1789-1797
Open Access | Times Cited: 3
Deleting Mecp2 from the cerebellum rather than its neuronal subtypes causes a delay in motor learning in mice
Nathan P. Achilly, Ling-jie He, Olivia A. Kim, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 22
Early and Late Corrections in Mouse Models of Autism Spectrum Disorder
Changuk Chung, Wangyong Shin, Eunjoon Kim
Biological Psychiatry (2021) Vol. 91, Iss. 11, pp. 934-944
Closed Access | Times Cited: 22
MeCP2 Epigenetic Silencing of Oprm1 Gene in Primary Sensory Neurons Under Neuropathic Pain Conditions
Na Sun, Lina Yu, Yibo Gao, et al.
Frontiers in Neuroscience (2021) Vol. 15
Open Access | Times Cited: 18
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
Updated systematic-narrative review on communication intervention in Rett Syndrome: 2010–2022
Jeff Sigafoos, Laura Roche, Mark F. O’Reilly, et al.
Augmentative and Alternative Communication (2023) Vol. 39, Iss. 4, pp. 241-255
Open Access | Times Cited: 7

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