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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:

MECP2 and the biology of MECP2 duplication syndrome
Santosh R. D’Mello
Journal of Neurochemistry (2021) Vol. 159, Iss. 1, pp. 29-60
Open Access | Times Cited: 29

Showing 1-25 of 29 citing articles:

The Role of Recombinant AAV in Precise Genome Editing
Swati Bijlani, Ka Ming Pang, Venkatesh Sivanandam, et al.
Frontiers in Genome Editing (2022) Vol. 3
Open Access | Times Cited: 42
Activation of recombinases at specific DNA loci by zinc-finger domain insertions
L. R. Mukhametzyanova, Lukas Theo Schmitt, Julia Torres-Rivera, et al.
Nature Biotechnology (2024)
Open Access | Times Cited: 5
Nodding syndrome: A role for environmental biotoxins that dysregulate MECP2 expression?
Peter S. Spencer, Raquel Valdes Angues, Valerie S. Palmer
Journal of the Neurological Sciences (2024) Vol. 462, pp. 123077-123077
Closed Access | Times Cited: 5
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
Auditory Dysfunction in Animal Models of Autism Spectrum Disorder
Ana Carolina Castro, Patrícia Monteiro
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 20
Nuclease-free precise genome editing corrects MECP2 mutations associated with Rett syndrome
Swati Bijlani, Ka Ming Pang, Lakshmi Bugga, et al.
Frontiers in Genome Editing (2024) Vol. 6
Open Access | Times Cited: 4
Next-generation strategies for gene-targeted therapies of central nervous system disorders: A workshop summary
Jill A. Morris, Chris Boshoff, Nina F. Schor, et al.
Molecular Therapy (2021) Vol. 29, Iss. 12, pp. 3332-3344
Open Access | Times Cited: 15
Rett and Rett-related disorders: Common mechanisms for shared symptoms?
Santosh R. D’Mello
Experimental Biology and Medicine (2023)
Open Access | Times Cited: 6
The autism-associated Meis2 gene is necessary for cardiac baroreflex regulation in mice
Julien Roussel, Romaric Larcher, Pierre Sicard, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 9
Clinical application of long‐read nanopore sequencing in a preimplantation genetic testing pre‐clinical workup to identify the junction for complex Xq chromosome rearrangement‐related disease
Tasuku Mariya, Yui Shichiri, Takeshi Sugimoto, et al.
Prenatal Diagnosis (2023) Vol. 43, Iss. 3, pp. 304-313
Closed Access | Times Cited: 5
Circular RNA CircDHRS3 Aggravates IL-1β-induced ECM Degradation, Apoptosis, and Inflammatory Response via Mediating MECP2 Expression
Xiao Ouyang, Yunzhi Ding, Yu Li, et al.
Inflammation (2023) Vol. 46, Iss. 5, pp. 1670-1683
Closed Access | Times Cited: 5
Mecp2 Deficiency in Peripheral Sensory Neuron Improves Cognitive Function by Enhancing Hippocampal Dendritic Spine Densities in Mice
Yuting Feng, Jingge Wang, Jun Liu, et al.
Cells (2024) Vol. 13, Iss. 11, pp. 988-988
Open Access | Times Cited: 1
An Irak1-Mecp2 tandem duplication mouse model for the study of MECP2 duplication syndrome
Eleonora Maino, Ori Scott, Samar Z. Rizvi, et al.
Disease Models & Mechanisms (2024) Vol. 17, Iss. 7
Open Access | Times Cited: 1
Deciphering the physiopathology of neurodevelopmental disorders using brain organoids
Olivier Dionne, Salomé Sabatié, Benoît Laurent
Brain (2024)
Open Access | Times Cited: 1
Site-Blocking Antisense Oligonucleotides as a Mechanism to Fine-Tune MECP2 Expression
Amanda M. Vanderplow, Grace E. Dodis, Yewon Rhee, et al.
RNA (2024) Vol. 30, Iss. 12, pp. 1554-1571
Open Access | Times Cited: 1
The Role of Genetics in Central Precocious Puberty: Confirmed and Potential Neuroendocrine Genetic and Epigenetic Contributors and Their Interactions with Endocrine Disrupting Chemicals (EDCs)
Andrea Mucci, Ethel G. Clemente
Endocrines (2022) Vol. 3, Iss. 3, pp. 433-451
Open Access | Times Cited: 5
An insertion mutation of the MECP2 gene in severe neonatal encephalopathy and ocular and oropharyngeal dyskinesia: a case report
Jianmin Liang, Cuijuan Xin, Meiying Xin, et al.
BMC Medical Genomics (2023) Vol. 16, Iss. 1
Open Access | Times Cited: 2
BDNF and Cerebellar Ataxia
Robert Lalonde, Magali Hernandez, C. Strazielle
Current Drug Research Reviews (2023) Vol. 16, Iss. 3, pp. 300-307
Closed Access | Times Cited: 2
Early life stress exacerbates behavioural and neuronal alterations in adolescent male mice lacking methyl-CpG binding protein 2 (Mecp2)
Jose Vicente Torres‐Perez, Elena Martínez-Rodríguez, Anabel Forte, et al.
Frontiers in Behavioral Neuroscience (2022) Vol. 16
Open Access | Times Cited: 3
MECP2-gén-duplikáció gyermekkori és praenatalis diagnózisa
Barbara Anna Bokor, Dóra Török, Emese Horváth, et al.
Orvosi Hetilap (2024) Vol. 165, Iss. 1, pp. 30-34
Open Access
A 10-Year Review on Advancements in Identifying and Treating Intellectual Disability Caused by Genetic Variations
Kexin Hou, Xinyan Zheng
Genes (2024) Vol. 15, Iss. 9, pp. 1118-1118
Open Access
Key Synaptic Pathology in Autism Spectrum Disorder: Genetic Mechanisms and Recent Advances
Yuan Zhang, Rui Tang, Zhimin Hu, et al.
Journal of Integrative Neuroscience (2024) Vol. 23, Iss. 10
Open Access
MeCP2 duplication causes hyperandrogenism by upregulating LHCGR and downregulating RORα
Yumeng Wang, Yu Wu, Yufang Zheng, et al.
Cell Death and Disease (2021) Vol. 12, Iss. 11
Open Access | Times Cited: 3
Finding meaning in chaos: a selection signature for functional interactions and its use in molecular biology
Lorin Weiner, Janice L. Brissette
FEBS Journal (2022) Vol. 290, Iss. 16, pp. 3914-3927
Open Access | Times Cited: 1
22q11 Copy Number Variations in a Brazilian Cohort of Children with Congenital Heart Disorders
Maiara Anschau Floriani, Andressa Schneiders Santos, Bruna Lixinski Diniz, et al.
Molecular Syndromology (2022) Vol. 14, Iss. 1, pp. 1-10
Open Access | Times Cited: 1
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