Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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 eight neuropsychiatric copy number variants on human brain structure
Claudia Modenato, Kuldeep Kumar, Clara Moreau, et al.
Translational Psychiatry (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 32

Showing 1-25 of 32 citing articles:

Genetic Heterogeneity Shapes Brain Connectivity in Psychiatry
Clara Moreau, Annabelle Harvey, Kuldeep Kumar, et al.
Biological Psychiatry (2022) Vol. 93, Iss. 1, pp. 45-58
Open Access | Times Cited: 22
Reciprocal and non-reciprocal effects of clinically relevant SETBP1 protein dosage changes
Lilit Antonyan, Xin Zhang, Anjie Ni, et al.
Human Molecular Genetics (2025)
Open Access
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
Lessons Learned From Neuroimaging Studies of Copy Number Variants: A Systematic Review
Claudia Modenato, Sandra Martin‐Brevet, Clara Moreau, et al.
Biological Psychiatry (2021) Vol. 90, Iss. 9, pp. 596-610
Open Access | Times Cited: 31
Subcortical Brain Alterations in Carriers of Genomic Copy Number Variants
Kuldeep Kumar, Claudia Modenato, Clara Moreau, et al.
American Journal of Psychiatry (2023) Vol. 180, Iss. 9, pp. 685-698
Open Access | Times Cited: 12
Convergence and Divergence of Rare Genetic Disorders on Brain Phenotypes
Armin Raznahan, Hyejung Won, David C. Glahn, et al.
JAMA Psychiatry (2022) Vol. 79, Iss. 8, pp. 818-818
Closed Access | Times Cited: 17
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
Increased Prevalence of Rare Copy Number Variants in Treatment-Resistant Psychosis
Martilias S. Farrell, Tyler Dietterich, Matthew K. Harner, et al.
Schizophrenia Bulletin (2022) Vol. 49, Iss. 4, pp. 881-892
Open Access | Times Cited: 14
Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants
Jente Verbesselt, Cynthia Solot, Ellen Van Den Heuvel, et al.
Genes (2023) Vol. 14, Iss. 3, pp. 679-679
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
Pervasive alterations of intra-axonal volume and network organization in young children with a 16p11.2 deletion
Anne Maillard, David Romascano, Julio E. Villalón‐Reina, et al.
Translational Psychiatry (2024) Vol. 14, Iss. 1
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
Motor difficulties in 16p11.2 copy number variation
Amandeep Jutla, Loraine Harvey, Jeremy Veenstra‐VanderWeele, et al.
Autism Research (2024) Vol. 17, Iss. 5, pp. 906-916
Closed Access | Times Cited: 2
Structural deviations of the posterior fossa and the cerebellum and their cognitive links in a neurodevelopmental deletion syndrome
Esra Sefik, Kuaikuai Duan, Yiheng Li, et al.
Molecular Psychiatry (2024) Vol. 29, Iss. 11, pp. 3395-3411
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
Association of behavioural and social–communicative profiles in children with 16p11.2 copy number variants: a multi‐site study
Jente Verbesselt, Louisa Walsh, Marissa W Mitchel, et al.
Journal of Intellectual Disability Research (2024) Vol. 68, Iss. 8, pp. 969-984
Closed Access | Times Cited: 1
Molecular signatures of cortical expansion in the human foetal brain
Gareth Ball, Stuart Oldham, Vanessa Kyriakopoulou, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 1
The Variegation of Human Brain Vulnerability to Rare Genetic Disorders and Convergence With Behaviorally Defined Disorders
Elizabeth Levitis, Siyuan Liu, Ethan T. Whitman, et al.
Biological Psychiatry (2023) Vol. 95, Iss. 2, pp. 136-146
Open Access | Times Cited: 3
Structural deviations of the posterior fossa and the cerebellum and their cognitive links in a neurodevelopmental deletion syndrome
Esra Sefik, Yiheng Li, Brittney Sholar, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 5
Subcortical Anatomy in Neurogenetic Disorders: New Findings and Future Questions
Konrad Wagstyl, Armin Raznahan
American Journal of Psychiatry (2023) Vol. 180, Iss. 9, pp. 634-635
Closed Access | Times Cited: 2
Rare CNVs and phenome-wide profiling: a tale of brain-structural divergence and phenotypical convergence
Jakub Kopál, Kuldeep Kumar, Karin Saltoun, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Closed Access | Times Cited: 3
Language Profiles of School-Age Children With 16p11.2 Copy Number Variants in a Clinically Ascertained Cohort
Jente Verbesselt, Jeroen Breckpot, Inge Zink, et al.
Journal of Speech Language and Hearing Research (2024) Vol. 67, Iss. 11, pp. 4487-4503
Closed Access
Unraveling the link between CNVs, cognition and individual neuroimaging deviation scores from a population-based reference cohort
Charlotte Fraza, Ida E. Sønderby, Rune Bøen, et al.
Nature Mental Health (2024)
Closed Access
Translational Study of Copy Number Variations in Schizophrenia
Min-Chih Cheng, Wei‐Hsien Chien, Yu‐Shu Huang, et al.
International Journal of Molecular Sciences (2021) Vol. 23, Iss. 1, pp. 457-457
Open Access | Times Cited: 4
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
Page 1 - Next Page

Scroll to top