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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:

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

Showing 22 citing articles:

The Cerebellar Involvement in Autism Spectrum Disorders: From the Social Brain to Mouse Models
Lisa Mapelli, Teresa Soda, Egidio D’Angelo, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 7, pp. 3894-3894
Open Access | Times Cited: 77
The cerebellum and its connections to other brain structures involved in motor and non-motor functions: A comprehensive review
José Mário Prati, André Pontes‐Silva, Anna Carolyna Gianlorenço
Behavioural Brain Research (2024) Vol. 465, pp. 114933-114933
Closed Access | Times Cited: 17
Rett Syndrome and MECP2 Duplication Syndrome: Disorders of MeCP2 Dosage
Bridget E. Collins, Jeffrey L. Neul
Neuropsychiatric Disease and Treatment (2022) Vol. Volume 18, pp. 2813-2835
Open Access | Times Cited: 47
Advanced genetic therapies for the treatment of Rett syndrome: state of the art and future perspectives
Michela Palmieri, Diego Pozzer, Nicoletta Landsberger
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 31
Converging and Diverging Cerebellar Pathways for Motor and Social Behaviors in Mice
Meike E. van der Heijden
The Cerebellum (2024) Vol. 23, Iss. 5, pp. 1754-1767
Open Access | Times Cited: 6
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
P-sort: an open-source software for cerebellar neurophysiology
Ehsan Sedaghat-Nejad, Mohammad Amin Fakharian, Jay S. Pi, et al.
Journal of Neurophysiology (2021) Vol. 126, Iss. 4, pp. 1055-1075
Open Access | Times Cited: 32
Identification of M4 muscarinic acetylcholine receptor expressing astrocytes that regulate locomotion and survival in murine prion disease
Gonzalo S. Tejeda, Colin Molloy, Carrie K. Jones, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Closed Access
Neural Connections and Molecular Mechanisms Underlying Motor Skill Deficits in Genetic Models of Autism Spectrum Disorders
Jingwen Duan, Deyang Zeng, Tong Wu, et al.
Progress in Neurobiology (2025), pp. 102759-102759
Closed Access
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
A comprehensive longitudinal study of magnetic resonance imaging identifies novel features of the Mecp2 deficient mouse brain
Sara Carli, Linda Chaabane, Giuseppina De Rocco, et al.
Neurobiology of Disease (2023) Vol. 180, pp. 106083-106083
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
Modulation of Brain Cholesterol Metabolism through CYP46A1 Overexpression for Rett Syndrome
Emilie Audouard, Nicolas Khefif, Béatrix Gillet-Legrand, et al.
Pharmaceutics (2024) Vol. 16, Iss. 6, pp. 756-756
Open Access | Times Cited: 2
Movement disorders in patients with Rett syndrome: A systematic review of evidence and associated clinical considerations
Jatinder Singh, Evamaria Lanzarini, Nardo Nardocci, et al.
Psychiatry and Clinical Neurosciences (2021) Vol. 75, Iss. 12, pp. 369-393
Open Access | Times Cited: 15
Mitochondrial modulation with leriglitazone as a potential treatment for Rett syndrome
Uliana Musokhranova, C. J. Alejos Grau, Cristina Vergara, et al.
Journal of Translational Medicine (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 6
MeCP2 loss‐of‐function dysregulates microRNAs regionally and disrupts excitatory/inhibitory synaptic transmission balance
Patricia M. Horvath, Michelle K. Piazza, Ege T. Kavalali, et al.
Hippocampus (2022) Vol. 32, Iss. 8, pp. 610-623
Open Access | Times Cited: 4
Deficits in Cerebellum-Dependent Learning and Cerebellar Morphology in Male and Female BTBR Autism Model Mice
Elizabeth A. Kiffmeyer, Jameson A. Cosgrove, Jenna K. Siganos, et al.
NeuroSci (2022) Vol. 3, Iss. 4, pp. 624-644
Open Access | Times Cited: 3
Loss of the MeCP2 gene in parvalbumin interneurons leads to an inhibitory deficit in the amygdala and affects its functional connectivity.
Maj Liiwand, Joni Haikonen, Bojana Kokinovic, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Cerebellar Impairments in Genetic Models of Autism Spectrum Disorders: A Neurobiological Perspective
Konstantin Yenkoyan, Artem Grigoryan, Viera Kútna, et al.
Progress in Neurobiology (2024) Vol. 242, pp. 102685-102685
Closed Access
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.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
Deficits in cerebellum-dependent learning and cerebellar morphology in male and female BTBR autism model mice
Elizabeth A. Kiffmeyer, Jameson A. Cosgrove, Jenna K. Siganos, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
Imitative and contagious behaviors in animals and their potential roles in the study of neurodevelopmental disorders
Amtul-Noor Rana, Rodrigo Gonzales‐Rojas, Hye Young Lee
Neuroscience & Biobehavioral Reviews (2022) Vol. 143, pp. 104876-104876
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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