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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:

Genotype–phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study
Samuel J. R. A. Chawner, Michael J. Owen, Peter Holmans, et al.
The Lancet Psychiatry (2019) Vol. 6, Iss. 6, pp. 493-505
Open Access | Times Cited: 110

Showing 1-25 of 110 citing articles:

Anxiety disorders
Brenda W.J.H. Penninx, Daniel S. Pine, Emily A. Holmes, et al.
The Lancet (2021) Vol. 397, Iss. 10277, pp. 914-927
Open Access | Times Cited: 418
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
Genetic Advances in Autism
Anita Thapar, Michael Rutter
Journal of Autism and Developmental Disorders (2020) Vol. 51, Iss. 12, pp. 4321-4332
Open Access | Times Cited: 119
A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants
Samuel J. R. A. Chawner, Joanne Doherty, Richard Anney, et al.
American Journal of Psychiatry (2021) Vol. 178, Iss. 1, pp. 77-86
Open Access | Times Cited: 83
Translating insights from neuropsychiatric genetics and genomics for precision psychiatry
Elliott Rees, Michael J. Owen
Genome Medicine (2020) Vol. 12, Iss. 1
Open Access | Times Cited: 74
16p11.2 deletion syndrome
Wendy K. Chung, Timothy P. L. Roberts, Elliott H. Sherr, et al.
Current Opinion in Genetics & Development (2021) Vol. 68, pp. 49-56
Open Access | Times Cited: 65
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: 56
Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology
Sébastien Jacquemont, Guillaume Huguet, Marieke Klein, et al.
American Journal of Psychiatry (2022) Vol. 179, Iss. 3, pp. 189-203
Open Access | Times Cited: 47
Examining the role of common variants in rare neurodevelopmental conditions
Qin Qin Huang, Emilie M. Wigdor, Daniel Malawsky, et al.
Nature (2024)
Open Access | Times Cited: 10
Detecting microstructural deviations in individuals with deep diffusion MRI tractometry
Maxime Chamberland, Sila Genc, Chantal M. W. Tax, et al.
Nature Computational Science (2021) Vol. 1, Iss. 9, pp. 598-606
Open Access | Times Cited: 49
Recent advances in anxiety disorders: Focus on animal models and pathological mechanisms
Hongqing Zhao, Mi Zhou, Yang Liu, et al.
Animal Models and Experimental Medicine (2023) Vol. 6, Iss. 6, pp. 559-572
Open Access | Times Cited: 16
Dissecting the contribution of common variants to risk of rare neurodevelopmental conditions
Qin Qin Huang, Emilie M. Wigdor, Patrick Campbell, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 6
Psychiatric Genetics Begins to Find Its Footing
Jordan W. Smoller
American Journal of Psychiatry (2019) Vol. 176, Iss. 8, pp. 609-614
Open Access | Times Cited: 46
Childhood intellectual disability and parents' mental health: integrating social, psychological and genetic influences
Kate Baker, Rory T. Devine, Elise Ng‐Cordell, et al.
The British Journal of Psychiatry (2020) Vol. 218, Iss. 6, pp. 315-322
Open Access | Times Cited: 46
Reciprocal Copy Number Variations at 22q11.2 Produce Distinct and Convergent Neurobehavioral Impairments Relevant for Schizophrenia and Autism Spectrum Disorder
Amy Lin, Ariana Vajdi, Leila Kushan, et al.
Biological Psychiatry (2020) Vol. 88, Iss. 3, pp. 260-272
Open Access | Times Cited: 42
Diagnostic genetic testing for neurodevelopmental psychiatric disorders: closing the gap between recommendation and clinical implementation
Brenda Finucane, David H. Ledbetter, Jacob Vorstman
Current Opinion in Genetics & Development (2021) Vol. 68, pp. 1-8
Open Access | Times Cited: 40
Novel treatments for autism spectrum disorder based on genomics and systems biology
Danielle Baribeau, Evdokia Anagnostou
Pharmacology & Therapeutics (2021) Vol. 230, pp. 107939-107939
Open Access | Times Cited: 34
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
Comparison of autism domains across thirty rare variant genotypes
Nabila M.H. Ali, Samuel J. R. A. Chawner, Leila Kushan, et al.
EBioMedicine (2025) Vol. 112, pp. 105521-105521
Open Access
Early manifestations of neurodevelopmental copy number variants in children: A population-based investigation
Charlotte Dennison, Joanna Martin, Amy Shakeshaft, et al.
Biological Psychiatry (2025)
Open Access
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans
Ida E. Sønderby, Dennis van der Meer, Clara Moreau, et al.
Translational Psychiatry (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 32
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
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
Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome
Ania Fiksinski, Maude Schneider, Janneke Zinkstok, et al.
Current Psychiatry Reports (2021) Vol. 23, Iss. 3
Open Access | Times Cited: 29
Longitudinal trajectories of cortical development in 22q11.2 copy number variants and typically developing controls
Maria Jalbrzikowski, Amy Lin, Ariana Vajdi, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 10, pp. 4181-4190
Open Access | Times Cited: 19
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