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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:

Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights
Itaru Kushima, Branko Aleksić, Masahiro Nakatochi, et al.
Cell Reports (2018) Vol. 24, Iss. 11, pp. 2838-2856
Open Access | Times Cited: 211

Showing 1-25 of 211 citing articles:

A large data resource of genomic copy number variation across neurodevelopmental disorders
Mehdi Zarrei, Christie L. Burton, Worrawat Engchuan, et al.
npj Genomic Medicine (2019) Vol. 4, Iss. 1
Open Access | Times Cited: 158
The role of GABAergic signalling in neurodevelopmental disorders
Xin Tang, Rudolf Jaenisch, Mriganka Sur
Nature reviews. Neuroscience (2021) Vol. 22, Iss. 5, pp. 290-307
Open Access | Times Cited: 131
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
Risk and Protective Environmental Factors Associated with Autism Spectrum Disorder: Evidence-Based Principles and Recommendations
Leonardo Emberti Gialloreti, Luigi Mazzone, Arianna Benvenuto, et al.
Journal of Clinical Medicine (2019) Vol. 8, Iss. 2, pp. 217-217
Open Access | Times Cited: 126
Dynamic functional connectivity in schizophrenia and autism spectrum disorder: Convergence, divergence and classification
Liron Rabany, Sophy Brocke, Vince D. Calhoun, et al.
NeuroImage Clinical (2019) Vol. 24, pp. 101966-101966
Open Access | Times Cited: 110
Genetic Associations between Voltage-Gated Calcium Channels and Psychiatric Disorders
Arturo Andrade, Ashton Brennecke, Shayna Mallat, et al.
International Journal of Molecular Sciences (2019) Vol. 20, Iss. 14, pp. 3537-3537
Open Access | Times Cited: 93
Autism spectrum disorder and schizophrenia: An updated conceptual review
Amandeep Jutla, Jennifer H. Foss‐Feig, Jeremy Veenstra‐VanderWeele
Autism Research (2021) Vol. 15, Iss. 3, pp. 384-412
Open Access | Times Cited: 85
Autism-like social deficit generated by Dock4 deficiency is rescued by restoration of Rac1 activity and NMDA receptor function
Daji Guo, Yinghui Peng, Laijian Wang, et al.
Molecular Psychiatry (2019) Vol. 26, Iss. 5, pp. 1505-1519
Open Access | Times Cited: 84
Schizophrenia in a genomic era: a review from the pathogenesis, genetic and environmental etiology to diagnosis and treatment insights
Mansour Zamanpoor
Psychiatric Genetics (2019) Vol. 30, Iss. 1, pp. 1-9
Closed Access | Times Cited: 77
The pediatric psychopharmacology of autism spectrum disorder: A systematic review - Part I: The past and the present
Antonio M. Persico, Arianna Ricciardello, Marco Lamberti, et al.
Progress in Neuro-Psychopharmacology and Biological Psychiatry (2021) Vol. 110, pp. 110326-110326
Closed Access | Times Cited: 76
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
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
Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions
Eduardo A. Maury, Maxwell A. Sherman, Giulio Genovese, et al.
Cell Genomics (2023) Vol. 3, Iss. 8, pp. 100356-100356
Open Access | Times Cited: 24
Gene Expression Profiling in the Cortex of Fabp4 Knockout Mice
Hinako Kirikae, Xiaofeng He, Tetsuo Ohnishi, et al.
Neuropsychopharmacology Reports (2025) Vol. 45, Iss. 1
Open Access | Times Cited: 1
The TMEM106B FTLD-protective variant, rs1990621, is also associated with increased neuronal proportion
Zeran Li, Fabiana Farias, Umber Dube, et al.
Acta Neuropathologica (2019) Vol. 139, Iss. 1, pp. 45-61
Open Access | Times Cited: 68
Reduced neonatal brain-derived neurotrophic factor is associated with autism spectrum disorders
Kristin Skogstrand, Christian M. Hagen, Nis Borbye‐Lorenzen, et al.
Translational Psychiatry (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 65
ARHGAP10, which encodes Rho GTPase-activating protein 10, is a novel gene for schizophrenia risk
Mariko Sekiguchi, Akira Sobue, Itaru Kushima, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 60
Diagnostic Classification and Prognostic Prediction Using Common Genetic Variants in Autism Spectrum Disorder: Genotype-Based Deep Learning
Haishuai Wang, Paul Avillach
JMIR Medical Informatics (2021) Vol. 9, Iss. 4, pp. e24754-e24754
Open Access | Times Cited: 47
Trends in big data analyses by multicenter collaborative translational research in psychiatry
Toshiaki Onitsuka, Yoji Hirano, Kiyotaka Nemoto, et al.
Psychiatry and Clinical Neurosciences (2021) Vol. 76, Iss. 1, pp. 1-14
Open Access | Times Cited: 45
Dissecting autism and schizophrenia through neuroimaging genomics
Clara Moreau, Armin Raznahan, Pierre Bellec, et al.
Brain (2021) Vol. 144, Iss. 7, pp. 1943-1957
Open Access | Times Cited: 43
Zbtb16 regulates social cognitive behaviors and neocortical development
Noriyoshi Usui, Stefano Berto, Ami Konishi, et al.
Translational Psychiatry (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 41
Cross-Disorder Analysis of Genic and Regulatory Copy Number Variations in Bipolar Disorder, Schizophrenia, and Autism Spectrum Disorder
Itaru Kushima, Masahiro Nakatochi, Branko Aleksić, et al.
Biological Psychiatry (2022) Vol. 92, Iss. 5, pp. 362-374
Open Access | Times Cited: 35
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: 34
Bringing machine learning to research on intellectual and developmental disabilities: taking inspiration from neurological diseases
Chirag Gupta, Pramod Chandrashekar, Ting Jin, et al.
Journal of Neurodevelopmental Disorders (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 32
The role of structural variations in Alzheimer’s disease and other neurodegenerative diseases
Hui Wang, Li‐San Wang, Gerard D. Schellenberg, et al.
Frontiers in Aging Neuroscience (2023) Vol. 14
Open Access | Times Cited: 18
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