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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:

Copy number variation and neuropsychiatric problems in females and males in the general population
Joanna Martin, Kristiina Tammimies, Robert Karlsson, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2018) Vol. 180, Iss. 6, pp. 341-350
Open Access | Times Cited: 33

Showing 1-25 of 33 citing articles:

Why are females less likely to be diagnosed with ADHD in childhood than males?
Joanna Martin
The Lancet Psychiatry (2024) Vol. 11, Iss. 4, pp. 303-310
Open Access | Times Cited: 24
Association of Rare Copy Number Variants With Risk of Depression
Kimberley Kendall, Elliott Rees, Matthew Bracher‐Smith, et al.
JAMA Psychiatry (2019) Vol. 76, Iss. 8, pp. 818-818
Open Access | Times Cited: 123
Quality control and analytic best practices for testing genetic models of sex differences in large populations
Ekaterina Khramtsova, Melissa A. Wilson, Joanna Martin, et al.
Cell (2023) Vol. 186, Iss. 10, pp. 2044-2061
Open Access | Times Cited: 26
Gene copy number variation and pediatric mental health/neurodevelopment in a general population
Mehdi Zarrei, Christie L. Burton, Worrawat Engchuan, et al.
Human Molecular Genetics (2023) Vol. 32, Iss. 15, pp. 2411-2421
Open Access | Times Cited: 17
Copy Number Variation: Methods and Clinical Applications
Ondrej Pös, Ján Radvánszky, Jakub Styk, et al.
Applied Sciences (2021) Vol. 11, Iss. 2, pp. 819-819
Open Access | Times Cited: 40
Chromosomal and environmental contributions to sex differences in the vulnerability to neurological and neuropsychiatric disorders: Implications for therapeutic interventions
Patrick N. Pallier, Maria Ferrara, Francesca Romagnolo, et al.
Progress in Neurobiology (2022) Vol. 219, pp. 102353-102353
Open Access | Times Cited: 22
Genetics of Pediatric-Onset Psychiatric Disorders
Tess Levy, Joseph D. Buxbaum
Oxford University Press eBooks (2025), pp. 827-838
Closed Access
Insights into attention-deficit/hyperactivity disorder from recent genetic studies
Isabell Brikell, Christie L. Burton, Nina Roth Mota, et al.
Psychological Medicine (2021) Vol. 51, Iss. 13, pp. 2274-2286
Open Access | Times Cited: 27
Genetics of child aggression, a systematic review
Emiko Koyama, Tuana Kant, Atsushi Takata, et al.
Translational Psychiatry (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 4
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
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: 16
Association of copy number variation across the genome with neuropsychiatric traits in the general population
Anna L. Guyatt, Evie Stergiakouli, Joanna Martin, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2018) Vol. 177, Iss. 5, pp. 489-502
Open Access | Times Cited: 30
From genetics to systems biology of stress-related mental disorders
Shareefa Dalvie, Chris Chatzinakos, Obada Al Zoubi, et al.
Neurobiology of Stress (2021) Vol. 15, pp. 100393-100393
Open Access | Times Cited: 20
Chromosome X-wide common variant association study in autism spectrum disorder
Marla Mendes de Aquino, D. Chen, Worrawat Engchuan, et al.
The American Journal of Human Genetics (2024)
Closed Access | Times Cited: 2
Association between Copy Number Variation and Response to Social Skills Training in Autism Spectrum Disorder
Kristiina Tammimies, Danyang Li, Ielyzaveta Rabkina, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 16
Genetic architecture of Tourette syndrome: our current understanding
Laura Domènech, Carolina Cappi, Matthew Halvorsen
Psychological Medicine (2021) Vol. 51, Iss. 13, pp. 2201-2209
Closed Access | Times Cited: 14
Chromosome X-Wide Common Variant Association Study (XWAS) in Autism Spectrum Disorder
Marla Mendes de Aquino, D. Chen, Worrawat Engchuan, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Examining sex differences in neurodevelopmental and psychiatric genetic risk in anxiety and depression
Joanna Martin, Kimiya Asjadi, Leon Hubbard, et al.
PLoS ONE (2021) Vol. 16, Iss. 9, pp. e0248254-e0248254
Open Access | Times Cited: 9
Genetics of Attention-Deficit Hyperactivity Disorder
K. Langley, Joanna Martin, Anita Thapar
Current topics in behavioral neurosciences (2022), pp. 243-268
Closed Access | Times Cited: 5
Investigating gender-specific effects of familial risk for attention-deficit hyperactivity disorder and other neurodevelopmental disorders in the Swedish population
Joanna Martin, Laura Ghirardi, Qi Chen, et al.
BJPsych Open (2020) Vol. 6, Iss. 4
Open Access | Times Cited: 7
Sex differences in anxiety and depression in children with attention deficit hyperactivity disorder: Investigating genetic liability and comorbidity
Joanna Martin, Sharifah Shameem Agha, Olga Eyre, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2021) Vol. 186, Iss. 7, pp. 412-422
Open Access | Times Cited: 6
A Density Peak-Based Method to Detect Copy Number Variations From Next-Generation Sequencing Data
Kun Xie, Ye Tian, Xiguo Yuan
Frontiers in Genetics (2021) Vol. 11
Open Access | Times Cited: 5
Rare copy number variation in posttraumatic stress disorder
Adam X. Maihofer, Worrawat Engchuan, Guillaume Huguet, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 12, pp. 5062-5069
Open Access | Times Cited: 3
2q13 Distal Microdeletion: Considering Evidence for an Emerging Syndrome Versus Susceptibility Locus: Twenty‐Five New Cases and Review of the Literature
Eyal Elron, Mordechai Shohat, Lina Basel‐Salmon, et al.
American Journal of Medical Genetics Part A (2024)
Open Access
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