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:

Loss-of-function variants in the schizophrenia risk gene SETD1A alter neuronal network activity in human neurons through the cAMP/PKA pathway
Shan Wang, Jon-Ruben van Rhijn, Ibrahim A. Akkouh, et al.
Cell Reports (2022) Vol. 39, Iss. 5, pp. 110790-110790
Open Access | Times Cited: 46

Showing 1-25 of 46 citing articles:

The molecular pathology of schizophrenia: an overview of existing knowledge and new directions for future research
Takumi Nakamura, Atsushi Takata
Molecular Psychiatry (2023) Vol. 28, Iss. 5, pp. 1868-1889
Open Access | Times Cited: 27

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

Rare diseases of epigenetic origin: Challenges and opportunities
Maggie P. Fu, Sarah M. Merrill, Mehul Sharma, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 20

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

Rare genetic brain disorders with overlapping neurological and psychiatric phenotypes
Kathryn J. Peall, Michael J. Owen, Jérémy Hall
Nature Reviews Neurology (2023) Vol. 20, Iss. 1, pp. 7-21
Closed Access | Times Cited: 13

miRNA profiling of hiPSC-derived neurons from monozygotic twins discordant for schizophrenia
Noora Räsänen, Jari Tiihonen, Marja Koskuvi, et al.
Schizophrenia (2025) Vol. 11, Iss. 1
Open Access

Metabolic contributions to neuronal deficits caused by genomic disruption of schizophrenia risk gene SETD1A
Zheng‐Shan Chong, Zi Jian Khong, Shermaine Huiping Tay, et al.
Schizophrenia (2022) Vol. 8, Iss. 1
Open Access | Times Cited: 20

Generation of glutamatergic/GABAergic neuronal co-cultures derived from human induced pluripotent stem cells for characterizing E/I balance in vitro
Shan Wang, Rick Hesen, Britt Mossink, et al.
STAR Protocols (2023) Vol. 4, Iss. 1, pp. 101967-101967
Open Access | Times Cited: 12

Breaking the Burst: Unveiling Mechanisms Behind Fragmented Network Bursts in Patient-derived Neurons
Nina Doorn, Eva J.H.F. Voogd, Marloes Levers, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4

Epigenetic maintenance of adult neural stem cell quiescence in the mouse hippocampus via Setd1a
Ting Zhao, Yan Hong, Bowen Yan, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 4

Human Pluripotent Stem Cell-Derived Astrocyte Functionality Compares Favorably with Primary Rat Astrocytes
Bas Lendemeijer, Maurits Unkel, Hilde Smeenk, et al.
eNeuro (2024) Vol. 11, Iss. 9, pp. ENEURO.0148-24.2024
Open Access | Times Cited: 4

Morphological and transcriptomic analyses of stem cell-derived cortical neurons reveal mechanisms underlying synaptic dysfunction in schizophrenia
Annie Kathuria, Kara Lopez-Lengowski, Bradley Watmuff, et al.
Genome Medicine (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 9

O-GlcNAc Transferase Congenital Disorder of Glycosylation (OGT-CDG): Potential mechanistic targets revealed by evaluating the OGT interactome
Johnathan M. Mayfield, Naomi L. Hitefield, Ignacy Czajewski, et al.
Journal of Biological Chemistry (2024) Vol. 300, Iss. 9, pp. 107599-107599
Open Access | Times Cited: 3

The role of histone methyltransferases in neurocognitive disorders associated with brain size abnormalities
Foster D. Ritchie, Sofia B. Lizarraga
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 8

SETD1A variant-associated psychosis: A systematic review of the clinical literature and description of two new cases
Mark A. Colijn, Prescilla Carrion, Guillaume Poirier‐Morency, et al.
Progress in Neuro-Psychopharmacology and Biological Psychiatry (2023) Vol. 129, pp. 110888-110888
Open Access | Times Cited: 7

CACNA1Ahaploinsufficiency leads to reduced synaptic function and increased intrinsic excitability
Marina P. Hommersom, Nina Doorn, Sofía Puvogel, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2

Developmental disruption to the cortical transcriptome and synaptosome in a model of SETD1A loss-of-function
Nicholas E. Clifton, Matthew L. Bosworth, Niels Haan, et al.
Human Molecular Genetics (2022) Vol. 31, Iss. 18, pp. 3095-3106
Open Access | Times Cited: 8

Rapid specification of human pluripotent stem cells to functional astrocytes
Bas Lendemeijer, Maurits Unkel, Britt Mossink, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Closed Access | Times Cited: 8

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

Defined co-cultures of glutamatergic and GABAergic neurons with a mutation in DISC1 reveal aberrant phenotypes in GABAergic neurons
Johanna Heider, Aaron Stahl, Denise Sperlich, et al.
BMC Neuroscience (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 1

Sex-dependent effects of Setd1a haploinsufficiency on development and adult behaviour
Matthew L. Bosworth, Anthony R Isles, Lawrence S. Wilkinson, et al.
PLoS ONE (2024) Vol. 19, Iss. 8, pp. e0298717-e0298717
Open Access | Times Cited: 1

Genetic Diversity in Schizophrenia: Developmental Implications of Ultra-Rare, Protein-Truncating Mutations
Jacob D. Clarin, Nadia N. Bouras, Wen‐Jun Gao
Genes (2024) Vol. 15, Iss. 9, pp. 1214-1214
Open Access | Times Cited: 1

Integrated bioinformatics and interaction analysis to advance chronotherapies for mental disorders
Apoorva Bhatnagar, Gupta Raj, Sandip Das, et al.
Frontiers in Pharmacology (2024) Vol. 15
Open Access | Times Cited: 1

Page 1 - Next Page

Scroll to top