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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.

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Showing 1-25 of 35 citing articles:

Repetitive Restricted Behaviors in Autism Spectrum Disorder: From Mechanism to Development of Therapeutics
Junbin Tian, Xuping Gao, Li Yang
Frontiers in Neuroscience (2022) Vol. 16
Open Access | Times Cited: 60
Region-based analysis of rare genomic variants in whole-genome sequencing datasets reveal two novel Alzheimer’s disease-associated genes: DTNB and DLG2
Dmitry Prokopenko, Sanghun Lee, Julian Hecker, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 4, pp. 1963-1969
Open Access | Times Cited: 22
Reduced expression of the psychiatric risk gene DLG2 (PSD93) impairs hippocampal synaptic integration and plasticity
Simonas Griesius, Cian O’Donnell, Sophie Waldron, et al.
Neuropsychopharmacology (2022) Vol. 47, Iss. 7, pp. 1367-1378
Open Access | Times Cited: 19
Brain-derived tau oligomer polymorphs: distinct aggregations, stability profiles, and biological activities
Filippa Lo Cascio, S.J. Park, Urmi Sengupta, et al.
Communications Biology (2025) Vol. 8, Iss. 1
Open Access
DLG2 rs11607886 polymorphism associated with schizophrenia and precuneus functional changes
Hanyu Zhu, Zhaoyang Wu, Junxiao Wang, et al.
Schizophrenia Research (2025) Vol. 280, pp. 50-58
Closed Access
From social effort to social behavior: An integrated neural model for social motivation
Alisa Kanterman, Simone Shamay‐Tsoory
Neuroscience & Biobehavioral Reviews (2025), pp. 106170-106170
Closed Access
Actionable Genomics in Clinical Practice: Paradigmatic Case Reports of Clinical and Therapeutic Strategies Based upon Genetic Testing
Merlin G. Butler, Daniel Moreno‐De‐Luca, Antonio M. Persico
Genes (2022) Vol. 13, Iss. 2, pp. 323-323
Open Access | Times Cited: 13
Differential Methylation Profile in Fragile X Syndrome-Prone Offspring Mice after in Utero Exposure to Lactobacillus Reuteri
Reem Rafik AlOlaby, Marwa Zafarullah, Mariana Barboza, et al.
Genes (2022) Vol. 13, Iss. 8, pp. 1300-1300
Open Access | Times Cited: 11
Selective behavioural impairments in mice heterozygous for the cross disorder psychiatric risk gene DLG2
Rachel Pass, Niels Haan, Trevor Humby, et al.
Genes Brain & Behavior (2022) Vol. 21, Iss. 4
Open Access | Times Cited: 11
A mild impairment in reversal learning in a bowl‐digging substrate deterministic task but not other cognitive tests in the Dlg2+/− rat model of genetic risk for psychiatric disorder
Simonas Griesius, Sophie Waldron, Katie Kamenish, et al.
Genes Brain & Behavior (2023) Vol. 22, Iss. 6
Open Access | Times Cited: 6
Maintenance of a narrow hybrid zone between native and introduced red foxes (Vulpes vulpes) despite conspecificity and high dispersal capabilities
Sophie Preckler‐Quisquater, Cate B. Quinn, Benjamin N. Sacks
Molecular Ecology (2024) Vol. 33, Iss. 13
Open Access | Times Cited: 1
Rapid motor progression of Parkinson’s disease associates with clinical and genetic variants
LingXiao Cao, Yong Jiang, Ying‐shan Piao, et al.
Frontiers in Bioscience-Landmark (2021) Vol. 26, Iss. 12
Open Access | Times Cited: 9
Enhancing DLG2 Implications in Neuropsychiatric Disorders: Analysis of a Cohort of Eight Patients with 11q14.1 Imbalances
Veronica Bertini, Roberta Milone, Paola Cristofani, et al.
Genes (2022) Vol. 13, Iss. 5, pp. 859-859
Open Access | Times Cited: 6
From Hyposociability to Hypersociability—The Effects of PSD-95 Deficiency on the Dysfunctional Development of Social Behavior
Wen‐Jun Gao, Nancy R. Mack
Frontiers in Behavioral Neuroscience (2021) Vol. 15
Open Access | Times Cited: 8
Genetic alterations in the neuronal development genes are associated with changes of the tumor immune microenvironment in pancreatic cancer
Kaiyi Mu, Juan Fu, Jessica Gai, et al.
Annals of Pancreatic Cancer (2023) Vol. 6, pp. 10-10
Open Access | Times Cited: 3
Selection Signatures in Italian Livestock Guardian and Herding Shepherd Dogs
Arianna Bionda, Matteo Cortellari, Daniele Bigi, et al.
Veterinary Sciences (2022) Vol. 10, Iss. 1, pp. 3-3
Open Access | Times Cited: 5
A Genome-Wide Interaction Study of Erythrocyte ω-3 Polyunsaturated Fatty Acid Species and Memory in the Framingham Heart Study Offspring Cohort
Carmen Annevelink, Jason Westra, Aleix Sala‐Vila, et al.
Journal of Nutrition (2023) Vol. 154, Iss. 5, pp. 1640-1651
Closed Access | Times Cited: 2
Behavioural and molecular characterisation of the Dlg2 haploinsufficiency rat model of genetic risk for psychiatric disorder
Sophie Waldron, Rachel Pass, Simonas Griesius, et al.
Genes Brain & Behavior (2022) Vol. 21, Iss. 4
Open Access | Times Cited: 4
Region-based analysis of rare genomic variants in whole-genome sequencing datasets reveal two novel Alzheimer’s disease-associated genes: DTNB and DLG2
Dmitry Prokopenko, Sanghun Lee, Julian Hecker, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 5
K369I Tau Mice Demonstrate a Shift Towards Striatal Neuron Burst Firing and Goal-directed Behaviour
Max Mo, Marie E. Jönsson, Miranda A. Mathews, et al.
Neuroscience (2020) Vol. 449, pp. 46-62
Open Access | Times Cited: 4
Genetic Diversity and Selection Signatures of Lvliang Black Goat Using Genome-Wide SNP Data
Ke Cai, Wannian Wang, Xu Wang, et al.
Animals (2024) Vol. 14, Iss. 21, pp. 3154-3154
Open Access
Unveiling genetic insights: Array-CGH and WES discoveries in a cohort of 122 children with essential autism spectrum disorder
Paola Granata, Alessandra Zito, Dario Cocciadiferro, et al.
BMC Genomics (2024) Vol. 25, Iss. 1
Closed Access
Exonic mutations in cell–cell adhesion may contribute to CADASIL-related CSVD pathology
Paul J. Dunn, Rod A. Lea, Neven Maksemous, et al.
Human Genetics (2023) Vol. 142, Iss. 9, pp. 1361-1373
Open Access | Times Cited: 1
DLG2 intragenic exonic deletions reinforce the link to neurodevelopmental disorders and suggest a potential association with congenital anomalies and dysmorphism
Yunjia Chen, Ender Karaca, Nathaniel H. Robin, et al.
Genetics in Medicine (2023) Vol. 26, Iss. 1, pp. 101010-101010
Closed Access | Times Cited: 1
Dorsal Striatal Functional Connectivity and Repetitive Behavior Dimensions in Children and Youths With Neurodevelopmental Disorders
Eun Jung Choi, Marlee M. Vandewouw, Margot J. Taylor, et al.
Biological Psychiatry Cognitive Neuroscience and Neuroimaging (2023) Vol. 9, Iss. 4, pp. 387-397
Closed Access | Times Cited: 1
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