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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:

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

Showing 1-25 of 47 citing articles:

Astrocytes and brain-derived neurotrophic factor (BDNF)
Martina Albini, Alicja Krawczun-Rygmaczewska, Fabrizia Cesca
Neuroscience Research (2023) Vol. 197, pp. 42-51
Open Access | Times Cited: 45
Top caregiver concerns in Rett syndrome and related disorders: data from the US natural history study
Jeffrey L. Neul, Tim A. Benke, Eric D. Marsh, et al.
Journal of Neurodevelopmental Disorders (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 35
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
Trofinetide: First Approval
Susan J. Keam
Drugs (2023) Vol. 83, Iss. 9, pp. 819-824
Closed Access | Times Cited: 24
Nitrogen-Containing Heterocyclic Drug Products Approved by the FDA in 2023: Synthesis and biological activity
Weijiang Luo, Yiqi Liu, Hui Qin, et al.
European Journal of Medicinal Chemistry (2024) Vol. 279, pp. 116838-116838
Closed Access | Times Cited: 9
Trofinetide for Rett Syndrome: Highlights on the Development and Related Inventions of the First USFDA-Approved Treatment for Rare Pediatric Unmet Medical Need
Shuaibu Abdullahi Hudu, Fayig El-Migdadi, Aiman Al-Qtaitat, et al.
Journal of Clinical Medicine (2023) Vol. 12, Iss. 15, pp. 5114-5114
Open Access | Times Cited: 16
Trofinetide receives FDA approval as first drug for Rett syndrome
Zaib Un Nisa Mughal, Bisma Ahmed, Burhanuddin Sohail Rangwala, et al.
Annals of Medicine and Surgery (2024) Vol. 86, Iss. 5, pp. 2382-2385
Open Access | Times Cited: 5
The epigenetic modification of DNA methylation in neurological diseases
Linke Li, R Chen, Hui Zhang, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 5
Mecp2: An Important Role in the Pathogenesis of RETT Syndrome
Yujia Zhou
Theoretical and Natural Science (2025) Vol. 90, Iss. 1, pp. 24-31
Closed Access
Understanding Rett Syndrome: Genetic, clinical and therapeutic perspectives - literature review
Sylwia Urbańska, Aleksandra Witas, Martyna Borowska-Łygan, et al.
Journal of Education Health and Sport (2025) Vol. 77, pp. 57074-57074
Open Access
Unveiling Molecular Dynamics of MeCp2, CDKL5 and BDNF in the Hippocampus of Individuals With Intractable Mesial Temporal Lobe Epilepsy
NoorMohammad Meshkinkhood, Parastoo Barati Dowom, Farshid Noorbakhsh, et al.
Journal of Cellular and Molecular Medicine (2025) Vol. 29, Iss. 3
Open Access
Synthetic Approaches to the New Drugs Approved during 2023
Scott P. France, Erick A. Lindsey, Emma L. McInturff, et al.
Journal of Medicinal Chemistry (2025)
Closed Access
A novel approach to metabolic profiling in case models of MECP2-related disorders
Jessica A. Cooley Coleman, Bridgette A. Moffitt, William C. Bridges, et al.
Metabolic Brain Disease (2025) Vol. 40, Iss. 2
Open Access
Effectiveness of Art-Therapy-Based Intervention Programmes for Improving Social Communication in Children with Rett Syndrome
Olena Chebotariova, Oksana Kysla
Journal of Intellectual Disability - Diagnosis and Treatment (2025) Vol. 13, Iss. 1, pp. 1-11
Closed Access
MECP2 duplication syndrome—Typical EEG characteristics
Walter Otu, Ritu Sudhakaran, German Alfonso Garza-García, et al.
Epileptic Disorders (2025)
Open Access
SRSF9-Mediated Exon Recognition Promotes Exon 2 Inclusion in Mecp2 Pre-mRNA Alternative Splicing
Saya Oshizuki, So Masaki, Satoshi Tanaka, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 7, pp. 3319-3319
Open Access
Small SNPs, Big Effects: A Review of Single Nucleotide Variations and Polymorphisms in Key Genes Associated With Autism Spectrum Disorder
Srinath Satyanarayana, Akanksha A. Kalal, Priyanka Anand, et al.
International Journal of Developmental Neuroscience (2025) Vol. 85, Iss. 2
Closed Access
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
Potentiation of the muscarinic acetylcholine receptor 1 modulates neurophysiological features in a mouse model of Rett syndrome
Hong‐Wei Dong, Kelly Weiss, Kathryn Baugh, et al.
Neurotherapeutics (2024) Vol. 21, Iss. 4, pp. e00384-e00384
Open Access | Times Cited: 2
Developing AAV-delivered nonsense suppressor tRNAs for neurological disorders
Jiaming Wang, Guangping Gao, Dan Wang
Neurotherapeutics (2024) Vol. 21, Iss. 4, pp. e00391-e00391
Open Access | Times Cited: 2
Liquid-liquid phase separation: a new perspective on respiratory diseases
Li Wang, Yongjun Wang, Z. J. Ke, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 2
MECP2 Variants in Males: More Common Than Previously Appreciated
Amitha Ananth, Cary Fu, Jeffrey L. Neul, et al.
Pediatric Neurology (2024) Vol. 161, pp. 263-267
Closed Access | Times Cited: 2
Top Caregiver Concerns in Rett syndrome and related disorders: data from the US Natural History Study
Jeffrey L. Neul, Tim A. Benke, Eric D. Marsh, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 5
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
Preclinical milestones in MECP2 gene transfer for treating Rett syndrome
Indumathy Jagadeeswaran, Jiyoung Oh, Sarah E. Sinnett
Developmental Neuroscience (2024), pp. 1-10
Open Access | Times Cited: 1
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