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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:

Neurobiological perspective of 22q11.2 deletion syndrome
Janneke Zinkstok, Erik Boot, Anne S. Bassett, et al.
The Lancet Psychiatry (2019) Vol. 6, Iss. 11, pp. 951-960
Open Access | Times Cited: 97

Showing 1-25 of 97 citing articles:

Neuronal defects in a human cellular model of 22q11.2 deletion syndrome
Themasap A. Khan, Omer Revah, Aaron Gordon, et al.
Nature Medicine (2020) Vol. 26, Iss. 12, pp. 1888-1898
Open Access | Times Cited: 158
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
The Genetics and Epigenetics of 22q11.2 Deletion Syndrome
Qiumei Du, M. Teresa de la Morena, Nicolai S. C. van Oers
Frontiers in Genetics (2020) Vol. 10
Open Access | Times Cited: 88
A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome
Ania Fiksinski, Gil D. Hoftman, Jacob Vorstman, et al.
Molecular Psychiatry (2022) Vol. 28, Iss. 1, pp. 341-353
Open Access | Times Cited: 33
Unlocking Neural Function with 3D In Vitro Models: A Technical Review of Self-Assembled, Guided, and Bioprinted Brain Organoids and Their Applications in the Study of Neurodevelopmental and Neurodegenerative Disorders
Chiara D’Antoni, Lorenza Mautone, Caterina Sanchini, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 13, pp. 10762-10762
Open Access | Times Cited: 18
APOE expression and secretion are modulated by mitochondrial dysfunction
Meghan E. Wynne, Oluwaseun Ogunbona, Alicia R. Lane, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 16
Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence
Jakub Kopál, Kuldeep Kumar, Karin Saltoun, et al.
Nature Human Behaviour (2023) Vol. 7, Iss. 6, pp. 1001-1017
Open Access | Times Cited: 13
Untargeted metabolomic, and proteomic analysis identifies metabolic biomarkers and pathway alterations in individuals with 22q11.2 deletion syndrome
Marwa Zafarullah, Kathleen Angkustsiri, Austin Quach, et al.
Metabolomics (2024) Vol. 20, Iss. 2
Open Access | Times Cited: 5
Auditory evoked-potential abnormalities in a mouse model of 22q11.2 Deletion Syndrome and their interactions with hearing impairment
Lu Chen, Jennifer F. Linden
Translational Psychiatry (2025) Vol. 15, Iss. 1
Open Access
Comorbidity Between Mental and Physical Disorders in Children and Adolescents: Identification, Management, and Treatment
Daniele Marcotulli, Anna Salvalaggio, Anita Zardini, et al.
(2025), pp. 275-298
Closed Access
Cannabidiol and Neurodevelopmental Disorders in Children
Keith Cheung, Murray D. Mitchell, Helen Heussler
Frontiers in Psychiatry (2021) Vol. 12
Open Access | Times Cited: 29
Decoding microRNAs in autism spectrum disorder
Jinyu Li, Xiaohui Xu, Jiane Liu, et al.
Molecular Therapy — Nucleic Acids (2022) Vol. 30, pp. 535-546
Open Access | Times Cited: 19
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
The thalamic midline nucleus reuniens: potential relevance for schizophrenia and epilepsy
Margriet J. Dolleman-Van der Weel, Menno P. Witter
Neuroscience & Biobehavioral Reviews (2020) Vol. 119, pp. 422-439
Closed Access | Times Cited: 24
Criss‐crossing autism spectrum disorder and adult neurogenesis
Frank Bicker, Leonardo Nardi, Jannik Maier, et al.
Journal of Neurochemistry (2021) Vol. 159, Iss. 3, pp. 452-478
Closed Access | Times Cited: 22
The region‐selective regulation of endothelial claudin‐5 expression and signaling in brain health and disorders
Hideki Chiba, Naoki Ichikawa‐Tomikawa, Tetsuya Imura, et al.
Journal of Cellular Physiology (2021) Vol. 236, Iss. 10, pp. 7134-7143
Closed Access | Times Cited: 20
Mitochondrial protein synthesis and the bioenergetic cost of neurodevelopment
Pernille Bülow, Anupam Patgiri, Victor Faúndez
iScience (2022) Vol. 25, Iss. 9, pp. 104920-104920
Open Access | Times Cited: 15
Prevalence and incidence of psychotic disorders in 22q11.2 deletion syndrome: a meta-analysis
Umberto Provenzani, Stefano Damiani, Ilaria Bersano, et al.
International Review of Psychiatry (2022) Vol. 34, Iss. 7-8, pp. 676-688
Open Access | Times Cited: 15
The Genetics of Neurodevelopment in Congenital Heart Disease
Eli Patt, Asmita Singhania, Amy E. Roberts, et al.
Canadian Journal of Cardiology (2022) Vol. 39, Iss. 2, pp. 97-114
Open Access | Times Cited: 15
Trends in the prevalence, prenatal diagnosis, and outcomes of births with chromosomal abnormalities: a hospital-based study in Zhejiang Province, China during 2014–2020
Xinning Chen, Dan Lin, Yinghui Ye, et al.
Orphanet Journal of Rare Diseases (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 14
Microglial cannabinoid receptor type 1 mediates social memory deficits in mice produced by adolescent THC exposure and 16p11.2 duplication
Yuto Hasegawa, Juhyun Kim, Gianluca Ursini, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 8
Molecular Insights Into the Causes of Human Thymic Hypoplasia With Animal Models
Pratibha Bhalla, Christian Wysocki, Nicolai S. C. van Oers
Frontiers in Immunology (2020) Vol. 11
Open Access | Times Cited: 23
Tbx1, a gene encoded in 22q11.2 copy number variant, is a link between alterations in fimbria myelination and cognitive speed in mice
Takeshi Hiramoto, Akira Sumiyoshi, Takahira Yamauchi, et al.
Molecular Psychiatry (2021) Vol. 27, Iss. 2, pp. 929-938
Open Access | Times Cited: 19
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: 22
Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome
Maris Alver, Valentina Mancini, Kristi Läll, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 10, pp. 4191-4200
Open Access | Times Cited: 12
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