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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 26-50 of 91 citing articles:

New Insights into Kleefstra Syndrome: Report of Two Novel Cases with Previously Unreported Features and Literature Review
Claudia Ciaccio, Giulietta Scuvera, Arianna Tucci, et al.
Cytogenetic and Genome Research (2018) Vol. 156, Iss. 3, pp. 127-133
Closed Access | Times Cited: 33
The neuronal stimulation–transcription coupling map
Kelsey M. Tyssowski, Jesse Gray
Current Opinion in Neurobiology (2019) Vol. 59, pp. 87-94
Open Access | Times Cited: 30
RAI1 Regulates Activity-Dependent Nascent Transcription and Synaptic Scaling
Patricia M. Garay, Alex Chen, Takao Tsukahara, et al.
Cell Reports (2020) Vol. 32, Iss. 6, pp. 108002-108002
Open Access | Times Cited: 28
Sleep Disturbance as a Precursor of Severe Regression in Kleefstra Syndrome Suggests a Need for Firm and Rapid Pharmacological Treatment
Karlijn Vermeulen, Wouter Staal, Joost Janzing, et al.
Clinical Neuropharmacology (2017) Vol. 40, Iss. 4, pp. 185-188
Closed Access | Times Cited: 31
Targeted next generation sequencing of a panel of autism-related genes identifies an EHMT1 mutation in a Kleefstra syndrome patient with autism and normal intellectual performance
István Bock, Krisztina Németh, Klára Pentelényi, et al.
Gene (2016) Vol. 595, Iss. 2, pp. 131-141
Closed Access | Times Cited: 30
Effects of traumatic stress in adolescence on PTSD-like behaviors, dendrite development, and H3K9me2/BDNF expression in the amygdala of male rats
Mingyue Zhao, Zemeng Zhu, Haonan Li, et al.
Journal of Affective Disorders (2021) Vol. 296, pp. 388-399
Closed Access | Times Cited: 21
TCF4 Mutations Disrupt Synaptic Function Through Dysregulation of RIMBP2 in Patient-Derived Cortical Neurons
Brittany A. Davis, Huei-Ying Chen, Zengyou Ye, et al.
Biological Psychiatry (2023) Vol. 95, Iss. 7, pp. 662-675
Open Access | Times Cited: 9
Haploinsufficiency of EHMT1 improves pattern separation and increases hippocampal cell proliferation
Marco Benevento, Charlotte A. Oomen, Alexa E. Horner, et al.
Scientific Reports (2017) Vol. 7, Iss. 1
Open Access | Times Cited: 28
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: 27
Histone demethylase KDM5C is a SAHA-sensitive central hub at the crossroads of transcriptional axes involved in multiple neurodevelopmental disorders
Loredana Poeta, Agnese Padula, Benedetta Attianese, et al.
Human Molecular Genetics (2019) Vol. 28, Iss. 24, pp. 4089-4102
Open Access | Times Cited: 24
Epigenetic Signaling in Glia Controls Presynaptic Homeostatic Plasticity
Tingting Wang, Danielle T. Morency, Nathan Harris, et al.
Neuron (2019) Vol. 105, Iss. 3, pp. 491-505.e3
Open Access | Times Cited: 23
Alzheimer’s Disease: the Potential of Epigenetic Treatments and Current Clinical Candidates
Rachel Coneys, Ian Wood
Neurodegenerative Disease Management (2020) Vol. 10, Iss. 3, pp. 543-558
Open Access | Times Cited: 22
A Novel Kleefstra Syndrome-associated Variant That Affects the Conserved TPLX Motif within the Ankyrin Repeat of EHMT1 Leads to Abnormal Protein Folding
Patrick R. Blackburn, Alexander Tischer, Michael T. Zimmermann, et al.
Journal of Biological Chemistry (2017) Vol. 292, Iss. 9, pp. 3866-3876
Open Access | Times Cited: 24
Epigenetics and memory: Emerging role of histone lysine methyltransferase G9a/GLP complex as bidirectional regulator of synaptic plasticity
Karen Ka Lam Pang, Mahima Sharma, Sreedharan Sajikumar
Neurobiology of Learning and Memory (2019) Vol. 159, pp. 1-5
Closed Access | Times Cited: 21
Adaptive Synaptic Scaling in Spiking Networks for Continual Learning and Enhanced Robustness
Mingkun Xu, Faqiang Liu, Yifan Hu, et al.
IEEE Transactions on Neural Networks and Learning Systems (2024) Vol. 36, Iss. 3, pp. 5151-5165
Closed Access | Times Cited: 2
NRSF/REST lies at the intersection between epigenetic regulation, miRNA-mediated gene control and neurodevelopmental pathways associated with Intellectual disability (ID) and Schizophrenia
Mouhamed Alsaqati, Brittany A. Davis, Jamie L. Wood, et al.
Translational Psychiatry (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 10
Glial Sphingosine-Mediated Epigenetic Regulation Stabilizes Synaptic Function inDrosophilaModels of Alzheimer's Disease
Pengqi Yin, Yimei Cai, Tao Cui, et al.
Journal of Neuroscience (2023) Vol. 43, Iss. 42, pp. 6954-6971
Open Access | Times Cited: 6
9q34.3 microduplications lead to neurodevelopmental disorders through EHMT1 overexpression
Maria Teresa Bonati, Chiara Castronovo, Alessandra Sironi, et al.
Neurogenetics (2019) Vol. 20, Iss. 3, pp. 145-154
Open Access | Times Cited: 17
Firing Rate Homeostasis Can Occur in the Absence of Neuronal Activity-Regulated Transcription
Kelsey M. Tyssowski, Katherine C. Letai, Samuel D. Rendall, et al.
Journal of Neuroscience (2019) Vol. 39, Iss. 50, pp. 9885-9899
Open Access | Times Cited: 16
Bioinformatics enrichment analysis of genes and pathways related to maternal type 1 diabetes associated with adverse fetal outcomes
Ravi Bhushan, Anjali Rani, Akhtar Ali, et al.
Journal of Diabetes and its Complications (2020) Vol. 34, Iss. 5, pp. 107556-107556
Closed Access | Times Cited: 16
EHMT1 regulates Parvalbumin-positive interneuron development and GABAergic input in sensory cortical areas
Moritz Negwer, Karol Piera, Rick Hesen, et al.
Brain Structure and Function (2020) Vol. 225, Iss. 9, pp. 2701-2716
Open Access | Times Cited: 12
Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder
Hidekazu Kato, Itaru Kushima, Daisuke Mori, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 12
Cell consequences of loss of function of the epigenetic factor EHMT1
Lucía Iglesias-Ortega, Clara Megías-Fernández, Paloma Domínguez-Giménez, et al.
Cellular Signalling (2023) Vol. 108, pp. 110734-110734
Open Access | Times Cited: 4
A human in vitro neuronal model for studying homeostatic plasticity at the network level
Xiuming Yuan, Sofía Puvogel, Jon-Ruben van Rhijn, et al.
Stem Cell Reports (2023) Vol. 18, Iss. 11, pp. 2222-2239
Open Access | Times Cited: 4
Establishment of human pluripotent stem cell-derived cortical neurosphere model to study pathomechanisms and chemical toxicity in Kleefstra syndrome
Andrea Balogh, Mária Bódi-Jakus, Vivien Réka Karl, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1

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