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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 51-75 of 145 citing articles:

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
SETD1A variant-associated psychosis: A systematic review of the clinical literature and description of two new cases
Mark Ainsley Colijn, Prescilla Carrion, Guillaume Poirier‐Morency, et al.
Progress in Neuro-Psychopharmacology and Biological Psychiatry (2023) Vol. 129, pp. 110888-110888
Open Access | Times Cited: 7
Purkinje-cell-specific MeCP2 deficiency leads to motor deficits and autistic-like behavior due to aberrations in PTP1B-TrkB-SK signaling
Fang‐Xiao Xu, Xin‐Tai Wang, Xinyu Cai, et al.
Cell Reports (2023) Vol. 42, Iss. 12, pp. 113559-113559
Open Access | Times Cited: 7
Overcoming genetic and cellular complexity to study the pathophysiology of X-linked intellectual disabilities
Dayne Martinez, Evan Jiang, Zhaolan Zhou
Journal of Neurodevelopmental Disorders (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 2
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
Clinical Features and Disease Progression in Older Individuals with Rett Syndrome
Jeffrey L. Neul, Tim A. Benke, Eric D. Marsh, et al.
Genes (2024) Vol. 15, Iss. 8, pp. 1107-1107
Open Access | Times Cited: 2
Safety and efficacy of genetic MECP2 supplementation in the R294X mouse model of Rett syndrome
Bridget E. Collins, Jonathan K. Merritt, Kirsty R. Erickson, et al.
Genes Brain & Behavior (2021) Vol. 21, Iss. 1
Open Access | Times Cited: 17
Inhibition of Elevated Ras-MAPK Signaling Normalizes Enhanced Motor Learning and Excessive Clustered Dendritic Spine Stabilization in the MECP2-Duplication Syndrome Mouse Model of Autism
Ryan T. Ash, Shelly A. Buffington, Jiyoung Park, et al.
eNeuro (2021) Vol. 8, Iss. 4, pp. ENEURO.0056-21.2021
Open Access | Times Cited: 17
Rett Syndrome Spectrum in Monogenic Developmental-Epileptic Encephalopathies and Epilepsies: A Review
Carlotta Spagnoli, Carlo Fusco, F Pisani
Genes (2021) Vol. 12, Iss. 8, pp. 1157-1157
Open Access | Times Cited: 17
Multimodal Neuroimaging in Rett Syndrome With MECP2 Mutation
Yu Kong, Qiu-bo Li, Yuan Zhao-hong, et al.
Frontiers in Neurology (2022) Vol. 13
Open Access | Times Cited: 11
Systemic proteome phenotypes reveal defective metabolic flexibility in Mecp2 mutants
Stephanie A. Zlatic, Erica Werner, Veda Surapaneni, et al.
Human Molecular Genetics (2023) Vol. 33, Iss. 1, pp. 12-32
Open Access | Times Cited: 6
POMC-specific knockdown of MeCP2 leads to adverse phenotypes in mice chronically exposed to high fat diet
Priscila Frayre, Karen Ponce-Rubio, Jessica Frayre, et al.
Behavioural Brain Research (2024) Vol. 461, pp. 114863-114863
Open Access | Times Cited: 2
Sensory experiences questionnaire unravels differences in sensory profiles between MECP2‐related disorders
Bernhard Suter, Davut Pehli̇van, Muharrem Ak, et al.
Autism Research (2024) Vol. 17, Iss. 4, pp. 775-784
Open Access | Times Cited: 2
CRL4DCAF13 E3 ubiquitin ligase targets MeCP2 for degradation to prevent DNA hypermethylation and ensure normal transcription in growing oocytes
Peipei Ren, Xiaomei Tong, Junjian Li, et al.
Cellular and Molecular Life Sciences (2024) Vol. 81, Iss. 1
Open Access | Times Cited: 2
MeCP2 gene therapy ameliorates disease phenotype in mouse model for Pitt Hopkins syndrome
Cassandra N. Dennys, Sheryl Anne D. Vermudez, Robert J.M. Deacon, et al.
Neurotherapeutics (2024), pp. e00376-e00376
Open Access | Times Cited: 2
Kdm4a is an activity downregulated barrier to generate engrams for memory separation
Xiuxian Guo, Pengfei Hong, Songhai Xiong, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 2
The promise of low-tech intervention in a high-tech era: Remodeling pathological brain circuits using behavioral reverse engineering
Daniel B. Polley, Daniela Schiller
Neuroscience & Biobehavioral Reviews (2022) Vol. 137, pp. 104652-104652
Open Access | Times Cited: 10
Exploring the characteristics and most bothersome symptoms in MECP2 duplication syndrome to pave the path toward developing parent‐oriented outcome measures
Muharrem Ak, Bernhard Suter, Zekeriya Aktürk, et al.
Molecular Genetics & Genomic Medicine (2022) Vol. 10, Iss. 8
Open Access | Times Cited: 10
Ca2+ imaging of self and other in medial prefrontal cortex during social dominance interactions in a tube test
Nuria García-Font, Rufus Mitchell‐Heggs, Kapil Saxena, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 31
Open Access | Times Cited: 10
Reversibility and therapeutic development for neurodevelopmental disorders, insights from genetic animal models
Platon Megagiannis, Rahul Suresh, Guy A. Rouleau, et al.
Advanced Drug Delivery Reviews (2022) Vol. 191, pp. 114562-114562
Closed Access | Times Cited: 10
Rett Syndrome: A Timely Review From Recognition to Current Clinical Approaches and Clinical Study Updates
Autumn S. Ivy, SM Standridge
Seminars in Pediatric Neurology (2021) Vol. 37, pp. 100881-100881
Closed Access | Times Cited: 14
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
Influence of the disordered domain structure of MeCP2 on its structural stability and dsDNA interaction
David Ortega-Alarcón, Rafael Claveria‐Gimeno, Sonia Vega, et al.
International Journal of Biological Macromolecules (2021) Vol. 175, pp. 58-66
Open Access | Times Cited: 11
Evidence Synthesis of Gene Therapy and Gene Editing from Different Disorders—Implications for Individuals with Rett Syndrome: A Systematic Review
Jatinder Singh, Ella Goodman-Vincent, Paramala Santosh
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 10, pp. 9023-9023
Open Access | Times Cited: 4
“Why don't they talk to our daughter?”: Eye-tracking AAC and medical communication in Rett syndrome
Usree Bhattacharya, Wisnu A. Pradana, Xing Wei, et al.
Language and Health (2023) Vol. 1, Iss. 1, pp. 32-43
Open Access | Times Cited: 4

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