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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:

Histone Methylation by the Kleefstra Syndrome Protein EHMT1 Mediates Homeostatic Synaptic Scaling
Marco Benevento, Giovanni Iacono, Martijn Selten, et al.
Neuron (2016) Vol. 91, Iss. 2, pp. 341-355
Open Access | Times Cited: 91

Showing 1-25 of 91 citing articles:

Rapid Neuronal Differentiation of Induced Pluripotent Stem Cells for Measuring Network Activity on Micro-electrode Arrays
Monica Frega, Sebastianus H. C. van Gestel, Katrin Linda, et al.
Journal of Visualized Experiments (2017), Iss. 119
Open Access | Times Cited: 147
How the epigenome integrates information and reshapes the synapse
Rianne R. Campbell, Marcelo A. Wood
Nature reviews. Neuroscience (2019) Vol. 20, Iss. 3, pp. 133-147
Open Access | Times Cited: 142
Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder
Tom S. Koemans, Tjitske Kleefstra, Melissa C. Chubak, et al.
PLoS Genetics (2017) Vol. 13, Iss. 10, pp. e1006864-e1006864
Open Access | Times Cited: 135
Inhibition of EHMT1/2 rescues synaptic and cognitive functions for Alzheimer’s disease
Yan Zheng, Aiyi Liu, Zijun Wang, et al.
Brain (2019) Vol. 142, Iss. 3, pp. 787-807
Open Access | Times Cited: 132
Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling
Monica Frega, Katrin Linda, Jason M. Keller, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 121
Epigenetic Etiology of Intellectual Disability
Shigeki Iwase, Nathalie G. Bérubé, Zhaolan Zhou, et al.
Journal of Neuroscience (2017) Vol. 37, Iss. 45, pp. 10773-10782
Open Access | Times Cited: 120
All for One But Not One for All: Excitatory Synaptic Scaling and Intrinsic Excitability Are Coregulated by CaMKIV, Whereas Inhibitory Synaptic Scaling Is Under Independent Control
Annelise Joseph, Gina G. Turrigiano
Journal of Neuroscience (2017) Vol. 37, Iss. 28, pp. 6778-6785
Open Access | Times Cited: 97
SETD5 Regulates Chromatin Methylation State and Preserves Global Transcriptional Fidelity during Brain Development and Neuronal Wiring
Alessandro Sessa, Luca Fagnocchi, Giuseppina Mastrototaro, et al.
Neuron (2019) Vol. 104, Iss. 2, pp. 271-289.e13
Open Access | Times Cited: 89
The emerging role of chromatin remodelers in neurodevelopmental disorders: a developmental perspective
Britt Mossink, Moritz Negwer, Dirk Schubert, et al.
Cellular and Molecular Life Sciences (2020) Vol. 78, Iss. 6, pp. 2517-2563
Open Access | Times Cited: 80
Smith-Magenis Syndrome—Clinical Review, Biological Background and Related Disorders
Berardo Rinaldi, Roberta Villa, Alessandra Sironi, et al.
Genes (2022) Vol. 13, Iss. 2, pp. 335-335
Open Access | Times Cited: 43
Neuron-specific alternative splicing of transcriptional machineries: Implications for neurodevelopmental disorders
Robert S. Porter, Farris Jaamour, Shigeki Iwase
Molecular and Cellular Neuroscience (2017) Vol. 87, pp. 35-45
Open Access | Times Cited: 73
Amelioration of autism-like social deficits by targeting histone methyltransferases EHMT1/2 in Shank3-deficient mice
Zijun Wang, Ping Zhong, Kaijie Ma, et al.
Molecular Psychiatry (2019) Vol. 25, Iss. 10, pp. 2517-2533
Open Access | Times Cited: 66
Stable Encoding of Visual Cues in the Mouse Retrosplenial Cortex
Anna Powell, William M. Connelly, Asta Vasalauskaite, et al.
Cerebral Cortex (2020) Vol. 30, Iss. 8, pp. 4424-4437
Open Access | Times Cited: 60
Epigenetic regulation of autophagy-related genes: Implications for neurodevelopmental disorders
Elly Lewerissa, Nael Nadif Kasri, Katrin Linda
Autophagy (2023) Vol. 20, Iss. 1, pp. 15-28
Open Access | Times Cited: 22
Histone Lysine Methylation and Neurodevelopmental Disorders
Jeong‐Hoon Kim, Jang Yong Lee, Im‐Soon Lee, et al.
International Journal of Molecular Sciences (2017) Vol. 18, Iss. 7, pp. 1404-1404
Open Access | Times Cited: 60
Distinct Pathogenic Genes Causing Intellectual Disability and Autism Exhibit a Common Neuronal Network Hyperactivity Phenotype
Monica Frega, Martijn Selten, Britt Mossink, et al.
Cell Reports (2020) Vol. 30, Iss. 1, pp. 173-186.e6
Open Access | Times Cited: 49
The phenomenal epigenome in neurodevelopmental disorders
Ummi Ciptasari, Hans van Bokhoven
Human Molecular Genetics (2020) Vol. 29, Iss. R1, pp. R42-R50
Open Access | Times Cited: 48
Intellectual disability and autism spectrum disorders ‘on the fly’: insights from Drosophila
Mireia Coll-Tané, Alina Krebbers, Anna Castells‐Nobau, et al.
Disease Models & Mechanisms (2019) Vol. 12, Iss. 5
Open Access | Times Cited: 45
Inhibition of EHMT1/2 rescues synaptic damage and motor impairment in a PD mouse model
Zhixiong Zhang, Rui Wang, Hui Zhou, et al.
Cellular and Molecular Life Sciences (2024) Vol. 81, Iss. 1
Open Access | Times Cited: 5
Targeting EHMT2/ G9a for cancer therapy: Progress and perspective
Suraya Jan, Mohd Ishaq Dar, Rubiada Wani, et al.
European Journal of Pharmacology (2020) Vol. 893, pp. 173827-173827
Closed Access | Times Cited: 39
Probing disrupted neurodevelopment in autism using human stem cell‐derived neurons and organoids: An outlook into future diagnostics and drug development
Guang Yang, Aleksandr Shcheglovitov
Developmental Dynamics (2019) Vol. 249, Iss. 1, pp. 6-33
Open Access | Times Cited: 38
Novel Phenotypes and Genotype–Phenotype Correlations in a Large Clinical Cohort of Patients With Kleefstra Syndrome
Zoë J. Frazier, Seyda Kilic, Hailey Osika, et al.
Clinical Genetics (2025)
Closed Access
DOT1L in neural development and neurological and psychotic disorders
Fang Shen, Linghui Zeng, Yanpan Gao
Neurochemistry International (2025) Vol. 185, pp. 105955-105955
Closed Access
Euchromatin histone methyltransferase 1 regulates cortical neuronal network development
Marijn B. Martens, Monica Frega, Jessica Classen, et al.
Scientific Reports (2016) Vol. 6, Iss. 1
Open Access | Times Cited: 38
Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome
Giovanni Iacono, Aline Dubos, Hamid Méziane, et al.
Nucleic Acids Research (2018) Vol. 46, Iss. 10, pp. 4950-4965
Open Access | Times Cited: 36
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