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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:

Can Animal Models of Copy Number Variants That Predispose to Schizophrenia Elucidate Underlying Biology?
Annika Forsingdal, Trine N. Jørgensen, Line Olsen, et al.
Biological Psychiatry (2018) Vol. 85, Iss. 1, pp. 13-24
Closed Access | Times Cited: 39

Showing 1-25 of 39 citing articles:

The contribution of copy number variants to psychiatric symptoms and cognitive ability
Josephine Mollon, Laura Almasy, Sébastien Jacquemont, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 4, pp. 1480-1493
Open Access | Times Cited: 46
Translating insights from neuropsychiatric genetics and genomics for precision psychiatry
Elliott Rees, Michael J. Owen
Genome Medicine (2020) Vol. 12, Iss. 1
Open Access | Times Cited: 74
Copy number variation and neuropsychiatric illness
Elliott Rees, George Kirov
Current Opinion in Genetics & Development (2021) Vol. 68, pp. 57-63
Open Access | Times Cited: 72
Advantages and Limitations of Animal Schizophrenia Models
Magdalena Białoń, Agnieszka Wąsik
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 11, pp. 5968-5968
Open Access | Times Cited: 67
Toward recovery in schizophrenia: Current concepts, findings, and future research directions
Toshiaki Onitsuka, Yoji Hirano, Takanobu Nakazawa, et al.
Psychiatry and Clinical Neurosciences (2022) Vol. 76, Iss. 7, pp. 282-291
Closed Access | Times Cited: 45
Advances in Zebrafish as a Comprehensive Model of Mental Disorders
Lei Wang, Fan Liu, Yimeng Fang, et al.
Depression and Anxiety (2023) Vol. 2023, pp. 1-48
Open Access | Times Cited: 24
Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders
Zhonghua Hu, Xiao Xiao, Zhuohua Zhang, et al.
Molecular Psychiatry (2019) Vol. 24, Iss. 10, pp. 1400-1414
Closed Access | Times Cited: 74
Comprehensive analysis of a novel mouse model of the 22q11.2 deletion syndrome: a model with the most common 3.0-Mb deletion at the human 22q11.2 locus
Ryo� Saito, Michinori Koebis, Taku Nagai, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 44
Unravelling the genetic basis of Schizophrenia
Clara Casey, John F. Fullard, Roy D. Sleator
Gene (2024) Vol. 902, pp. 148198-148198
Open Access | Times Cited: 5
Transcriptomic networks implicate neuronal energetic abnormalities in three mouse models harboring autism and schizophrenia-associated mutations
Aaron Gordon, Annika Forsingdal, Ib Vestergaard Klewe, et al.
Molecular Psychiatry (2019) Vol. 26, Iss. 5, pp. 1520-1534
Open Access | Times Cited: 34
Behavioral Tasks Evaluating Schizophrenia-like Symptoms in Animal Models: A Recent Update
Mary Jasmin Ang, Sueun Lee, Jong-Choon Kim, et al.
Current Neuropharmacology (2020) Vol. 19, Iss. 5, pp. 641-664
Open Access | Times Cited: 31
Implications of germline copy-number variations in psychiatric disorders: review of large-scale genetic studies
Masahiro Nakatochi, Itaru Kushima, Norio Ozaki
Journal of Human Genetics (2020) Vol. 66, Iss. 1, pp. 25-37
Closed Access | Times Cited: 27
A Case for Thalamic Mechanisms of Schizophrenia: Perspective From Modeling 22q11.2 Deletion Syndrome
Yanbo Jiang, Mary H. Patton, Stanislav S. Zakharenko
Frontiers in Neural Circuits (2021) Vol. 15
Open Access | Times Cited: 20
Neuroimaging Findings in Neurodevelopmental Copy Number Variants: Identifying Molecular Pathways to Convergent Phenotypes
Ana Isabel Silva, Friederike Ehrhart, Magnús Ö. Úlfarsson, et al.
Biological Psychiatry (2022) Vol. 92, Iss. 5, pp. 341-361
Open Access | Times Cited: 14
Neurexin1α knockout rats display oscillatory abnormalities and sensory processing deficits back-translating key endophenotypes of psychiatric disorders
Philipp Janz, Marie Bainier, Samuel Marashli, et al.
Translational Psychiatry (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 14
Mechanisms of copy number variants in neuropsychiatric disorders: From genes to therapeutics
Marc P. Forrest, Peter Penzes
Current Opinion in Neurobiology (2023) Vol. 82, pp. 102750-102750
Closed Access | Times Cited: 8
Mice with deficiency in Pcdh15, a gene associated with bipolar disorders, exhibit significantly elevated diurnal amplitudes of locomotion and body temperature
Daisuke Mori, Chihiro Inami, Ryosuke Ikeda, et al.
Translational Psychiatry (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 2
Use of mouse models to investigate the contributions of CNVs associated with schizophrenia and autism to disease mechanisms
Steven E. Hyman
Current Opinion in Genetics & Development (2021) Vol. 68, pp. 99-105
Open Access | Times Cited: 17
Innovative screening models for the discovery of new schizophrenia drug therapies: an integrated approach
Marinos G. Sotiropoulos, Eleni Poulogiannopoulou, Foteini Delis, et al.
Expert Opinion on Drug Discovery (2021) Vol. 16, Iss. 7, pp. 791-806
Closed Access | Times Cited: 16
Copy Number Variations and Schizophrenia
Kamila Szecówka, Błażej Misiak, Izabela Łaczmańska, et al.
Molecular Neurobiology (2022) Vol. 60, Iss. 4, pp. 1854-1864
Open Access | Times Cited: 12
Social behavior in 16p11.2 and 22q11.2 copy number variations: Insights from mice and humans
Arianna Benedetti, Cinzia Molent, Weronika Barcik, et al.
Genes Brain & Behavior (2021) Vol. 21, Iss. 5
Open Access | Times Cited: 15
Zebrafish as a tool to study schizophrenia-associated copy number variants
Philip D. Campbell, Michael Granato
Disease Models & Mechanisms (2020) Vol. 13, Iss. 4
Open Access | Times Cited: 15
Application of animal experimental models in the research of schizophrenia
Pengjie Wang, Manling Li, Aizhen Zhao, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2021) Vol. 186, Iss. 4, pp. 209-227
Closed Access | Times Cited: 11
Copy Number Variations in Neuropsychiatric Disorders
Gergely Büki, Kinga Hadzsiev, Judit Bene
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 18, pp. 13671-13671
Open Access | Times Cited: 4
The abiding relevance of mouse models of rare mutations to psychiatric neuroscience and therapeutics
Joseph A. Gogos, Gregg W. Crabtree, Anastasia Diamantopoulou
Schizophrenia Research (2019) Vol. 217, pp. 37-51
Open Access | Times Cited: 11
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