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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:

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

Showing 13 citing articles:

Rare copy-number variants as modulators of common disease susceptibility
Chiara Auwerx, Maarja Jõeloo, Marie C. Sadler, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 23
Genetic and phenotypic similarity across major psychiatric disorders: a systematic review and quantitative assessment
Vincent-Raphaël Bourque, Cécile Poulain, Catherine Proulx, et al.
Translational Psychiatry (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 6
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
Potential link between copy number variation and abnormal genome wide DNA methylation profile in an individual with severe ADHD and a strong response to micronutrient treatment
Aaron J. Stevens, Martin A. Kennedy, Kit Doudney, et al.
Psychiatry Research Case Reports (2025), pp. 100254-100254
Open Access
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
The pleiotropic spectrum of proximal 16p11.2 CNVs
Chiara Auwerx, Zoltán Kutalik, Alexandre Reymond
The American Journal of Human Genetics (2024)
Open Access | Times Cited: 2
CNV-Profile Regression: A New Approach for Copy Number Variant Association Analysis in Whole Genome Sequencing Data
Yaqin Si, Wenbin Lu, Shannon T. Holloway, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Using rare genetic mutations to revisit structural brain asymmetry
Jakub Kopál, Kuldeep Kumar, Kimia Shafighi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
Genome-wide CNV analysis uncovers novel pathogenic regions in cohort of five multiplex families with neurodevelopmental disorders
Behjat Ul Mudassir, Mashael Alhumaidi Alotaibi, Nadeem Kizilbash, et al.
Heliyon (2023) Vol. 9, Iss. 9, pp. e19718-e19718
Open Access | Times Cited: 2
On the Neurobiological Basis of Chronotype: Insights from a Multimodal Population Neuroscience Study
L Zhou, Karin Saltoun, Julie Carrier, et al.
Research Square (Research Square) (2024)
Open Access
High-effect gene-coding variants impact cognition, mental well-being, and neighborhood safety substrates in brain morphology
Jakub Kopál, Guillaume Huguet, Justin Marotta, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Knowledge-Based Prioritization of Genomic Variations: A Quest for Detailed Understanding the Genetic Architecture of Diseases
Ivan Y. Iourov
(2023)
Open Access | Times Cited: 1
Brain signatures of rare variants hint at cardiovascular risk
Laura Dattaro
The Transmitter (2023)
Open Access
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