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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:

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

Showing 1-25 of 44 citing articles:

Transcriptional linkage analysis with in vivo AAV-Perturb-seq
António J. Santinha, Esther Klingler, Maria Kuhn, et al.
Nature (2023) Vol. 622, Iss. 7982, pp. 367-375
Open Access | Times Cited: 37
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
The genetic architecture of schizophrenia: review of large-scale genetic studies
Hidekazu Kato, Hiroki Kimura, Itaru Kushima, et al.
Journal of Human Genetics (2022) Vol. 68, Iss. 3, pp. 175-182
Closed Access | Times Cited: 36
The circadian system: A neglected player in neurodevelopmental disorders
Ahmed A. Bouteldja, Danae Penichet, Lalit K. Srivastava, et al.
European Journal of Neuroscience (2024) Vol. 60, Iss. 2, pp. 3858-3890
Open Access | Times Cited: 6
On-Target CRISPR/Cas9 Activity Can Cause Undesigned Large Deletion in Mouse Zygotes
Alexey Korablev, Varvara Lukyanchikova, Irina Serova, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 10, pp. 3604-3604
Open Access | Times Cited: 39
Touchscreen cognitive testing: Cross-species translation and co-clinical trials in neurodegenerative and neuropsychiatric disease
Daniel D. Palmer, Julie R. Dumont, Tyler D. Dexter, et al.
Neurobiology of Learning and Memory (2021) Vol. 182, pp. 107443-107443
Closed Access | Times Cited: 29
An antisense oligonucleotide-based strategy to ameliorate cognitive dysfunction in the 22q11.2 Deletion Syndrome
Pratibha Thakur, Martin Lackinger, Anastasia Diamantopoulou, et al.
(2025)
Open Access
Highly demarcated structural alterations in the brain and impaired social incentive learning in Tbx1 heterozygous mice
Takeshi Hiramoto, Akira Sumiyoshi, Risa Kato, et al.
Molecular Psychiatry (2024)
Open Access | Times Cited: 3
CRISPR/Cas9 Genome Editing Approaches for Psychiatric Research
Araceli Gutiérrez-Rodríguez, Carlos Cruz-Fuentes, Alma Delia Genis‐Mendoza, et al.
Brazilian Journal of Psychiatry (2023)
Open Access | Times Cited: 8
Review: Genes Involved in Mitochondrial Physiology Within 22q11.2 Deleted Region and Their Relevance to Schizophrenia
David Kolář, Branislav Krajčovič, Lenka Kletečková, et al.
Schizophrenia Bulletin (2023) Vol. 49, Iss. 6, pp. 1637-1653
Closed Access | Times Cited: 8
Modeling and Predicting Developmental Trajectories of Neuropsychiatric Dimensions Associated With Copy Number Variations
Noboru Hiroi, Takahira Yamauchi
The International Journal of Neuropsychopharmacology (2019) Vol. 22, Iss. 8, pp. 488-500
Open Access | Times Cited: 23
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
Chromosome 22q11.2 deletion causes PERK-dependent vulnerability in dopaminergic neurons
Yuko Arioka, Emiko Shishido, Itaru Kushima, et al.
EBioMedicine (2020) Vol. 63, pp. 103138-103138
Open Access | Times Cited: 20
Schizophrenia Risk Mediated by microRNA Target Genes Overlapped by Genome-Wide Rare Copy Number Variation in 22q11.2 Deletion Syndrome
Shengjie Ying, Tracy Heung, Zhaolei Zhang, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 12
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
Hyperactive mTORC1 in striatum dysregulates dopamine receptor expression and odor preference behavior
Lin Chen, Ryo� Saito, Shoko Noda‐Narita, et al.
Frontiers in Neuroscience (2024) Vol. 18
Open Access | Times Cited: 2
Mice carrying a schizophrenia-associated mutation of the Arhgap10 gene are vulnerable to the effects of methamphetamine treatment on cognitive function: association with morphological abnormalities in striatal neurons
Kazuhiro Hada, Bolati Wulaer, Taku Nagai, et al.
Molecular Brain (2021) Vol. 14, Iss. 1
Open Access | Times Cited: 15
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
Transcriptional coregulator Ess2 controls survival of post-thymic CD4+ T cells through the Myc and IL-7 signaling pathways
Ichiro Takada, Shinya Hidano, Sayuri Takahashi, et al.
Journal of Biological Chemistry (2022) Vol. 298, Iss. 9, pp. 102342-102342
Open Access | Times Cited: 10
Overexpression of astroglial major histocompatibility complex class I in the medial prefrontal cortex impairs visual discrimination learning in mice
Bolati Wulaer, Kazuhiro Hada, Akira Sobue, et al.
Molecular Brain (2020) Vol. 13, Iss. 1
Open Access | Times Cited: 12
Enhancement of mediodorsal thalamus rescues aberrant belief dynamics in a mouse model with schizophrenia-associated mutation
Tingting Zhou, Yi-Yun Ho, Ray X. Lee, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Consequences of 22q11.2 Microdeletion on the Genome, Individual and Population Levels
Małgorzata Karbarz
Genes (2020) Vol. 11, Iss. 9, pp. 977-977
Open Access | Times Cited: 11
Computational identification of variables in neonatal vocalizations predictive for postpubertal social behaviors in a mouse model of 16p11.2 deletion
Mitsuteru Nakamura, Kenny Ye, Mariel Barbachan e Silva, et al.
Molecular Psychiatry (2021) Vol. 26, Iss. 11, pp. 6578-6588
Open Access | Times Cited: 10
Mice with exonic RELN deletion identified from a patient with schizophrenia have impaired visual discrimination learning and reversal learning in touchscreen operant tasks
Jingzhu Liao, Geyao Dong, Bolati Wulaer, et al.
Behavioural Brain Research (2021) Vol. 416, pp. 113569-113569
Closed Access | Times Cited: 9
Shedding light on latent pathogenesis and pathophysiology of mental disorders: The potential of iPS cell technology
Yuko Arioka, Hiroki Okumura, Hideya Sakaguchi, et al.
Psychiatry and Clinical Neurosciences (2023) Vol. 77, Iss. 6, pp. 308-314
Open Access | Times Cited: 3
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