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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:

Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from theENIGMAworking groups onCNVs
Ida E. Sønderby, Christopher R. K. Ching, Sophia I. Thomopoulos, et al.
Human Brain Mapping (2021) Vol. 43, Iss. 1, pp. 300-328
Open Access | Times Cited: 54

Showing 1-25 of 54 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
Cross disorder comparisons of brain structure in schizophrenia, bipolar disorder, major depressive disorder, and 22q11.2 deletion syndrome: A review of ENIGMA findings
Eun‐Jin Cheon, Carrie E. Bearden, Daqiang Sun, et al.
Psychiatry and Clinical Neurosciences (2022) Vol. 76, Iss. 5, pp. 140-161
Open Access | Times Cited: 53
The power of many brains: Catalyzing neuropsychiatric discovery through open neuroimaging data and large-scale collaboration
Bin Lü, Xiao Chen, F. Xavier Castellanos, et al.
Science Bulletin (2024) Vol. 69, Iss. 10, pp. 1536-1555
Open Access | Times Cited: 9
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
Discovering the gene-brain-behavior link in autism via generative machine learning
Shinjini Kundu, Haris I. Sair, Elliott H. Sherr, et al.
Science Advances (2024) Vol. 10, Iss. 24
Open Access | Times Cited: 6
The Enhancing NeuroImaging Genetics through Meta‐Analysis Consortium: 10 Years of Global Collaborations in Human Brain Mapping
Paul M. Thompson, Neda Jahanshad, Lianne Schmaal, et al.
Human Brain Mapping (2021) Vol. 43, Iss. 1, pp. 15-22
Open Access | Times Cited: 36
Mapping the genetic architecture of cortical morphology through neuroimaging: progress and perspectives
Dennis van der Meer, Tobias Kaufmann
Translational Psychiatry (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 23
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
Copy number variants and the tangential expansion of the cerebral cortex
Zhijie Liao, Kuldeep Kumar, Jakub Kopál, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Psychiatric Genetics in Clinical Practice: Essential Knowledge for Mental Health Professionals
Aaron D. Besterman, M.A. Alnor, Oscar M. Ramirez, et al.
American Journal of Psychiatry (2025)
Closed Access
Machine Learning in Electroconvulsive Therapy
Robert M. Lundin, Veronica Podence Falcao, Savani Kannangara, et al.
Journal of Ect (2024)
Closed Access | Times Cited: 3
Primary Psychosis: Risk and Protective Factors and Early Detection of the Onset
Claudio Brasso, Benedetta Giordano, Cristina Badino, et al.
Diagnostics (2021) Vol. 11, Iss. 11, pp. 2146-2146
Open Access | Times Cited: 22
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
Sleep EEG in young people with 22q11.2 deletion syndrome: A cross-sectional study of slow-waves, spindles and correlations with memory and neurodevelopmental symptoms
Nicholas Donnelly, Ullrich Bartsch, Hayley Moulding, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 12
Longitudinal Development of Thalamocortical Functional Connectivity in 22q11.2 Deletion Syndrome
Charles Schleifer, Kathleen O’Hora, Maria Jalbrzikowski, et al.
Biological Psychiatry Cognitive Neuroscience and Neuroimaging (2023) Vol. 9, Iss. 2, pp. 156-163
Open Access | Times Cited: 7
Distinct neurocognitive profiles and clinical phenotypes associated with copy number variation at the 22q11.2 locus
Kathleen O’Hora, Leila Kushan, Charles Schleifer, et al.
Autism Research (2023) Vol. 16, Iss. 12, pp. 2247-2262
Open Access | Times Cited: 7
Molecular signatures of cortical expansion in the human fetal brain
Gareth Ball, Stuart Oldham, Vanessa Kyriakopoulou, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
The effectiveness and tolerability of pharmacotherapy for psychosis in 22q11.2 Deletion Syndrome: A systematic review
Maya Tanham, Renee Chen, Nicola Warren, et al.
Australian & New Zealand Journal of Psychiatry (2024) Vol. 58, Iss. 5, pp. 393-403
Closed Access | Times Cited: 2
Effects of gene dosage and development on subcortical nuclei volumes in individuals with 22q11.2 copy number variations
Charles Schleifer, Kathleen O’Hora, Hoki Fung, et al.
Neuropsychopharmacology (2024) Vol. 49, Iss. 6, pp. 1024-1032
Open Access | Times Cited: 2
Using rare genetic mutations to revisit structural brain asymmetry
Jakub Kopál, Kuldeep Kumar, Kimia Shafighi, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 2
Understanding copy number variations through their genes: a molecular view on 16p11.2 deletion and duplication syndromes
Roberta Leone, Cecilia Zuglian, Riccardo Brambilla, et al.
Frontiers in Pharmacology (2024) Vol. 15
Open Access | Times Cited: 2
Challenges in multi-task learning for fMRI-based diagnosis: Benefits for psychiatric conditions and CNVs would likely require thousands of patients
Annabelle Harvey, Clara Moreau, Kuldeep Kumar, et al.
Imaging Neuroscience (2024) Vol. 2, pp. 1-20
Open Access | Times Cited: 2
Decoding the genetic landscape of autism: A comprehensive review
Mohammed Al‐Beltagi, Nermin Kamal Saeed, Adel Salah Bediwy, et al.
World Journal of Clinical Pediatrics (2024) Vol. 13, Iss. 3
Open Access | Times Cited: 2
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: 2
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