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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:

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

Showing 20 citing articles:

Rigor and reproducibility in human brain organoid research: Where we are and where we need to go
Soraya O. Sandoval, Gerarda Cappuccio, Karina Kruth, et al.
Stem Cell Reports (2024) Vol. 19, Iss. 6, pp. 796-816
Open Access | Times Cited: 14
Potential for New Therapeutic Approaches by Targeting Lactate and pH Mediated Epigenetic Dysregulation in Major Mental Diseases
Shabnam Nohesara, Hamid M. Abdolmaleky, Sam Thiagalingam
Biomedicines (2024) Vol. 12, Iss. 2, pp. 457-457
Open Access | Times Cited: 7
Scaled and efficient derivation of loss-of-function alleles in risk genes for neurodevelopmental and psychiatric disorders in human iPSCs
Hanwen Zhang, Ada McCarroll, Lilia Peyton, et al.
Stem Cell Reports (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
Schizophrenia, a disease of impaired dynamic metabolic flexibility: A new mechanistic framework
Zoltán Sarnyai, Dorit Ben‐Shachar
Psychiatry Research (2024) Vol. 342, pp. 116220-116220
Open Access | Times Cited: 3
SETD1A variant-associated psychosis: A systematic review of the clinical literature and description of two new cases
Mark Ainsley 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
Parkinson’s disease risk enhancers in microglia
Alix Booms, Steven Pierce, Edwin J. C. Van der Schans, et al.
iScience (2024) Vol. 27, Iss. 2, pp. 108921-108921
Open Access | Times Cited: 2
A Hybrid 2D‐to‐3D in vitro Differentiation Platform Improves Outcomes of Cerebral Cortical Organoid Generation in hiPSCs
Dosh Whye, Erika M. Norabuena, Gayathri Srinivasan, et al.
Current Protocols (2024) Vol. 4, Iss. 10
Closed Access | Times Cited: 2
Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion
Ryan H. Purcell, Esra Sefik, Erica Werner, et al.
Science Advances (2023) Vol. 9, Iss. 33
Open Access | Times Cited: 5
What have genetic studies of rare sequence variants taught us about the aetiology of schizophrenia?
Lea Heinzer, David Curtis
Journal of Translational Genetics and Genomics (2024) Vol. 8, Iss. 1, pp. 1-12
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
Histone post-translational modification and heterochromatin alterations in neurodegeneration: revealing novel disease pathways and potential therapeutics
Raven M. A. Fisher, Mariana P. Torrente
Frontiers in Molecular Neuroscience (2024) Vol. 17
Open Access | Times Cited: 1
Cross-species transcriptomic analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion
Ryan H. Purcell, Esra Sefik, Erica Werner, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
WITHDRAWN: Sex-dependent effects ofSetd1ahaploinsufficiency on development and adult behaviour
Matthew L. Bosworth, Anthony R Isles, Lawrence S. Wilkinson, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Scaled and Efficient Derivation of Loss of Function Alleles in Risk Genes for Neurodevelopmental and Psychiatric Disorders in Human iPSC
Hanwen Zhang, Lilia Peyton, Ada McCarroll, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Genetics and Schizophrenia
Hayley Seltzberg, Jarrod Ehrie, Eric L. Goldwaser
Current Behavioral Neuroscience Reports (2024) Vol. 11, Iss. 2, pp. 57-63
Closed Access
Mutations of schizophrenia risk gene SETD1A dysregulate synaptic function in human neurons
Xiao Su, Hanwen Zhang, Hong Yan, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Sex-dependent effects ofSetd1ahaploinsufficiency on development and adult behaviour
Matthew L. Bosworth, Anthony R Isles, Lawrence S. Wilkinson, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 2
Metabolic and Molecular Aspects of Schizophrenia: A Review
Sharique Ahmad, Pushpendra D. Pratap, Silky Rai, et al.
Saudi Journal of Medicine (2023) Vol. 8, Iss. 04, pp. 145-151
Open Access
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