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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:

Treating Rett syndrome: from mouse models to human therapies
Neeti Vashi, Monica J. Justice
Mammalian Genome (2019) Vol. 30, Iss. 5-6, pp. 90-110
Open Access | Times Cited: 91

Showing 1-25 of 91 citing articles:

Image-based profiling for drug discovery: due for a machine-learning upgrade?
Srinivas Niranj Chandrasekaran, Hugo Ceulemans, Justin D. Boyd, et al.
Nature Reviews Drug Discovery (2020) Vol. 20, Iss. 2, pp. 145-159
Open Access | Times Cited: 321
Multiplex epigenome editing of MECP2 to rescue Rett syndrome neurons
Junming Qian, Xiaonan Guan, Bing Xie, et al.
Science Translational Medicine (2023) Vol. 15, Iss. 679
Open Access | Times Cited: 51
MeCP2: The Genetic Driver of Rett Syndrome Epigenetics
Katrina Good, John B. Vincent, Juan Ausió
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 99
Role of DNA Methyl-CpG-Binding Protein MeCP2 in Rett Syndrome Pathobiology and Mechanism of Disease
Shervin Pejhan, Mojgan Rastegar
Biomolecules (2021) Vol. 11, Iss. 1, pp. 75-75
Open Access | Times Cited: 62
Drug Studies on Rett Syndrome: From Bench to Bedside
Gomathi Mohan, S. Padmapriya, Balachandar Vellingiri
Journal of Autism and Developmental Disorders (2020) Vol. 50, Iss. 8, pp. 2740-2764
Closed Access | Times Cited: 51
Calcium-Dependent Hyperexcitability in Human Stem Cell–Derived Rett Syndrome Neuronal Networks
Kartik S. Pradeepan, Fraser P. McCready, Wei Wei, et al.
Biological Psychiatry Global Open Science (2024) Vol. 4, Iss. 2, pp. 100290-100290
Open Access | Times Cited: 8
State‐of‐the‐art therapies for Rett syndrome
Nicolas Panayotis, Yann Ehinger, Marie‐Solenne Félix, et al.
Developmental Medicine & Child Neurology (2022) Vol. 65, Iss. 2, pp. 162-170
Open Access | Times Cited: 24
Sex Differences in Brain Disorders
Małgorzata Ziemka‐Nałęcz, Paulina Pawelec, Karolina Ziąbska, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 19, pp. 14571-14571
Open Access | Times Cited: 15
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
Compromised immune/inflammatory responses in Rett syndrome
Alessandra Pecorelli, Carlo Cervellati, Valeria Cordone, et al.
Free Radical Biology and Medicine (2020) Vol. 152, pp. 100-106
Open Access | Times Cited: 38
Changes in the Cerebrospinal Fluid and Plasma Lipidome in Patients with Rett Syndrome
Martina Zandl‐Lang, Thomas Züllig, Martin Trötzmüller, et al.
Metabolites (2022) Vol. 12, Iss. 4, pp. 291-291
Open Access | Times Cited: 20
MeCP2 dysfunction prevents proper BMP signaling and neural progenitor expansion in brain organoid
Hyowon Hong, Sae‐Bom Yoon, Jung Eun Park, et al.
Annals of Clinical and Translational Neurology (2023) Vol. 10, Iss. 7, pp. 1170-1185
Open Access | Times Cited: 11
Variable expression of MECP2, CDKL5, and FMR1 in the human brain: Implications for gene restorative therapies
Antonino Zito, Jeannie T. Lee
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 9
Open Access | Times Cited: 4
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
Steatotic liver disease diagnosed in a 24-year-old woman with Rett syndrome: a case report
Larissa Albino, Adil Adatia, Aducio Thiesen, et al.
Journal of International Medical Research (2025) Vol. 53, Iss. 1
Open Access
Use of poly adenosine tail mimetics to enhance mRNA expression from genes associated with haploinsufficiency disorders
Bahareh Torkzaban, Yining Zhu, Christian Lopez, et al.
Molecular Therapy — Nucleic Acids (2025) Vol. 36, Iss. 1, pp. 102453-102453
Open Access
Therapeutic effects of CGS21680, a selective A2A receptor agonist, via BDNF-related pathways in R106W mutation Rett syndrome model
Youngin Jeong, Min Woo Kim, Seulgi Lee, et al.
Biomedicine & Pharmacotherapy (2025) Vol. 183, pp. 117821-117821
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
Broadening the Phenotype Spectrum of MECP2 Variants in Men
Johannes Lötjönen, Venla Kurra, Hannele Laivuori, et al.
Molecular Genetics & Genomic Medicine (2025) Vol. 13, Iss. 2
Open Access
Women With Genetic Epilepsies
Paula Marques, Nagham Kaka, Quratulain Zulfiqar Ali, et al.
Neurology Genetics (2025) Vol. 11, Iss. 1
Open Access
Advances of deep Neural Networks (DNNs) in the development of peptide drugs
Yuzhen Niu, Pingyang Qin, Ping Lin
Future Medicinal Chemistry (2025), pp. 1-15
Closed Access
Potentiation of the M1 muscarinic acetylcholine receptor normalizes neuronal activation patterns and improves apnea severity in Mecp2 mice
Mackenzie Smith, Grace E. Dodis, Amanda M. Vanderplow, et al.
Neurobiology of Disease (2025), pp. 106859-106859
Open Access
Neuroglia pathology in genetic and epigenetic disorders of the central nervous system
Harvey B. Sarnat, Vijayaraghava T.S. Rao
Handbook of clinical neurology (2025), pp. 87-99
Closed Access
Autistic-like behaviors and impaired chronic inflammatory pain in primary nociceptive neuron-specific deletion of Mecp2 or Fmr1 knockout male mice
Peng-Bo Jing, Youhang Zhou, Feng‐Ming Zhang, et al.
Behavioural Brain Research (2025), pp. 115570-115570
Closed Access
Loss of MeCP2 leads to sleep deficits that are time-of-day dependent and worsen with sleep deprivation
Abrar Al Maghribi, Michael J. Rempe, E Medina, et al.
(2025)
Open Access
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