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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:

How does genetic variation modify ND-CNV phenotypes?
Thomas J. Dinneen, Fiana Ní Ghrálaigh, Ruth Walsh, et al.
Trends in Genetics (2021) Vol. 38, Iss. 2, pp. 140-151
Closed Access | Times Cited: 18

Showing 18 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
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
Bridging the translational gap: what can synaptopathies tell us about autism?
Ciara J. Molloy, Jennifer Cooke, Nicholas J. F. Gatford, et al.
Frontiers in Molecular Neuroscience (2023) Vol. 16
Open Access | Times Cited: 11
Mechanisms of copy number variants in neuropsychiatric disorders: From genes to therapeutics
Marc P. Forrest, Peter Penzes
Current Opinion in Neurobiology (2023) Vol. 82, pp. 102750-102750
Closed Access | Times Cited: 8
A review of the cognitive impact of neurodevelopmental and neuropsychiatric associated copy number variants
Ciara J. Molloy, Ciara Quigley, Áine McNicholas, et al.
Translational Psychiatry (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 7
A comprehensive review of deep learning-based variant calling methods
Ren Junjun, Zhang Zhengqian, Wu Ying, et al.
Briefings in Functional Genomics (2024) Vol. 23, Iss. 4, pp. 303-313
Closed Access | Times Cited: 2
Psychiatric patients with a de novo 17q12 deletion: Two case reports
Itaru Kushima, Mariko Uematsu, Kanako Ishizuka, et al.
Psychiatry and Clinical Neurosciences (2022) Vol. 76, Iss. 7, pp. 345-347
Open Access | Times Cited: 6
Clinical characterization of patients with schizophrenia and 16p13.11 duplication: A case series
Hiroki Kimura, Itaru Kushima, Masahiro Banno, et al.
Neuropsychopharmacology Reports (2023) Vol. 43, Iss. 2, pp. 267-271
Open Access | Times Cited: 3
Variable psychiatric manifestations in patients with 16p11.2 duplication: a case series of 4 patients
Yu Hayashi, Itaru Kushima, Branko Aleksić, et al.
Psychiatry and Clinical Neurosciences (2021) Vol. 76, Iss. 3, pp. 86-88
Open Access | Times Cited: 7
Accuratein silicoconfirmation of rare copy number variant calls from exome sequencing data using transfer learning
Renjie Tan, Yufeng Shen
Nucleic Acids Research (2022) Vol. 50, Iss. 21, pp. e123-e123
Open Access | Times Cited: 4
Neurodevelopmental disorder with dystonia due to SOX6 mutations
Susanne A. Schneider, Christine Mueller, Saskia Biskup, et al.
Molecular Genetics & Genomic Medicine (2022) Vol. 10, Iss. 12
Open Access | Times Cited: 3
Polygenic scores stratify ND-CNV carrier cognitive outcomes in the UK Biobank
Thomas J. Dinneen, Fiana Ní Ghrálaigh, Cathal Ormond, et al.
Research Square (Research Square) (2024)
Open Access
Prenatal diagnosis and family analysis of 17q12 microdeletion syndrome with fetal renal abnormalities
Fang Zhang, Qingqing Gu, Jiedong Song, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access
Polygenicity in a box: Copy number variants, neural circuit development, and neurodevelopmental disorders
Anthony‐Samuel LaMantia
Current Opinion in Neurobiology (2024) Vol. 89, pp. 102917-102917
Open Access
CNVs and Human Well-being: Integrating Psychiatric, Physical, and Socioeconomic Perspectives
Itaru Kushima, Masahiro Nakatochi, Norio Ozaki
Biological Psychiatry (2024)
Closed Access
Polygenic scores stratify neurodevelopmental copy number variant carrier cognitive outcomes in the UK Biobank
Thomas J. Dinneen, Fiana Ní Ghrálaigh, Cathal Ormond, et al.
npj Genomic Medicine (2024) Vol. 9, Iss. 1
Open Access
Accurate in silico confirmation of rare copy number variant calls from exome sequencing data using transfer learning
Renjie Tan, Yufeng Shen
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 1
Genetics of Childhood and Adolescent Anxiety and Obsessive-Compulsive Disorders
Paul Arnold, Lilit Antonyan, Francis Routledge, et al.
Springer eBooks (2022), pp. 73-96
Closed Access
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