Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

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

Showing 1-25 of 38 citing articles:

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
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
The potential of in vitro neuronal networks cultured on micro electrode arrays for biomedical research
Marta Cerina, Maria Carla Piastra, Monica Frega
Progress in Biomedical Engineering (2023) Vol. 5, Iss. 3, pp. 032002-032002
Open Access | Times Cited: 18
Vitamin D deficiency: infertility and neurodevelopmental diseases (attention deficit hyperactivity disorder, autism, and schizophrenia)
Michael J. Berridge
AJP Cell Physiology (2017) Vol. 314, Iss. 2, pp. C135-C151
Open Access | Times Cited: 61
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
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
TAF1, associated with intellectual disability in humans, is essential for embryogenesis and regulates neurodevelopmental processes in zebrafish
Sanna Gudmundsson, Maria Wilbe, Beata Filipek‐Górniok, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 39
Potential link between copy number variation and abnormal genome wide DNA methylation profile in an individual with severe ADHD and a strong response to micronutrient treatment
Aaron J. Stevens, Martin A. Kennedy, Kit Doudney, et al.
Psychiatry Research Case Reports (2025), pp. 100254-100254
Open Access
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
Past, Present, and Future of Neuronal Models In Vitro
Jason M. Keller, Monica Frega
Advances in neurobiology (2019), pp. 3-17
Closed Access | Times Cited: 35
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
Convergence of spectrums: neuronal gene network states in autism spectrum disorder
Josefa M. Sullivan, Silvia De Rubeis, Anne Schaefer
Current Opinion in Neurobiology (2019) Vol. 59, pp. 102-111
Open Access | Times Cited: 29
Epigenetic regulation of craniofacial development and disease
Lomeli C. Shull, Kristin Artinger
Birth Defects Research (2023) Vol. 116, Iss. 1
Closed Access | Times Cited: 8
A loss-of-function variant in SUV39H2 identified in autism-spectrum disorder causes altered H3K9 trimethylation and dysregulation of protocadherin β-cluster genes in the developing brain
Shabeesh Balan, Yoshimi Iwayama, Tetsuo Ohnishi, et al.
Molecular Psychiatry (2021) Vol. 26, Iss. 12, pp. 7550-7559
Closed Access | Times Cited: 18
Identification and Characterizations of Novel, Selective Histone Methyltransferase SET7 Inhibitors by Scaffold Hopping- and 2D-Molecular Fingerprint-Based Similarity Search
Hong Ding, Wenchao Lu, Jun Hu, et al.
Molecules (2018) Vol. 23, Iss. 3, pp. 567-567
Open Access | Times Cited: 15
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
Human-Derived Cortical Neurospheroids Coupled to Passive, High-Density and 3D MEAs: A Valid Platform for Functional Tests
Lorenzo Muzzi, Donatella Di Lisa, Matteo Falappa, et al.
Bioengineering (2023) Vol. 10, Iss. 4, pp. 449-449
Open Access | Times Cited: 4
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
Following Excitation/Inhibition Ratio Homeostasis from Synapse to EEG in Monogenetic Neurodevelopmental Disorders
Lisa Geertjens, Torben W. van Voorst, Arianne Bouman, et al.
Genes (2022) Vol. 13, Iss. 2, pp. 390-390
Open Access | Times Cited: 6
Defensive and offensive behaviours in a Kleefstra syndrome mouse model
Alejandra Alonso, Anumita Samanta, Jacqueline van der Meij, et al.
Animal Cognition (2023) Vol. 26, Iss. 4, pp. 1131-1140
Open Access | Times Cited: 3
The Object Space Task reveals increased expression of cumulative memory in a mouse model of Kleefstra syndrome
Evelien H. S. Schut, Alejandra Alonso, Steven Smits, et al.
Neurobiology of Learning and Memory (2020) Vol. 173, pp. 107265-107265
Open Access | Times Cited: 7
Reactive Sputtered Silicon Nitride as an Alternative Passivation Layer for Microelectrode Arrays in Sensitive Bioimpedimetric Cell Monitoring
Sabine Schmidt, Tobias Haensch, Ronny Frank, et al.
ACS Applied Materials & Interfaces (2021) Vol. 13, Iss. 49, pp. 59185-59195
Closed Access | Times Cited: 6
Neuronal network dysfunction in a human model for Kleefstra syndrome mediated by enhanced NMDAR signaling
Monica Frega, Katrin Linda, Jason M. Keller, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2019)
Open Access | Times Cited: 5
Page 1 - Next Page

Scroll to top