
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:
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
Sophie Waldron, Rachel Pass, Simonas Griesius, et al.
Genes Brain & Behavior (2022) Vol. 21, Iss. 4
Open Access | Times Cited: 4
Showing 4 citing articles:
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
Simonas Griesius, Cian O’Donnell, Sophie Waldron, et al.
Neuropsychopharmacology (2022) Vol. 47, Iss. 7, pp. 1367-1378
Open Access | Times Cited: 19
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
Simonas Griesius, Sophie Waldron, Katie Kamenish, et al.
Genes Brain & Behavior (2023) Vol. 22, Iss. 6
Open Access | Times Cited: 6
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
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