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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:

Clinical Characterization of Copy Number Variants Associated With Neurodevelopmental Disorders in a Large-scale Multiancestry Biobank
Rebecca Birnbaum, Behrang Mahjani, Ruth J. F. Loos, et al.
JAMA Psychiatry (2022) Vol. 79, Iss. 3, pp. 250-250
Open Access | Times Cited: 33

Showing 1-25 of 33 citing articles:

Candidate biomarkers in psychiatric disorders: state of the field
Anissa Abi‐Dargham, Scott J. Moeller, Farzana Ali, et al.
World Psychiatry (2023) Vol. 22, Iss. 2, pp. 236-262
Open Access | Times Cited: 156
The Genesis of Schizophrenia: An Origin Story
Rebecca Birnbaum, Daniel R. Weinberger
American Journal of Psychiatry (2024) Vol. 181, Iss. 6, pp. 482-492
Closed Access | Times Cited: 10
Population-Based Risk of Psychiatric Disorders Associated With Recurrent Copy Number Variants
Morteza Vaez, Simone Montalbano, Xabier Calle Sánchez, et al.
JAMA Psychiatry (2024) Vol. 81, Iss. 10, pp. 957-957
Open Access | Times Cited: 9
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
Mapping recurrent mosaic copy number variation in human neurons
Chen Sun, Kunal Kathuria, Sarah B. Emery, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5
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
Disentangling mechanisms behind the pleiotropic effects of proximal 16p11.2 BP4-5 CNVs
Chiara Auwerx, Samuel Moix, Zoltán Kutalik, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 11, pp. 2347-2361
Open Access | Times Cited: 3
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: 3
Genome-Wide Sequencing Modalities for Children with Unexplained Global Developmental Delay and Intellectual Disabilities—A Narrative Review
Mary Ko, Hui-Ju Chen
Children (2023) Vol. 10, Iss. 3, pp. 501-501
Open Access | Times Cited: 8
Disentangling mechanisms behind the pleiotropic effects of proximal 16p11.2 BP4-5 CNVs
Chiara Auwerx, Samuel Moix, Zoltán Kutalik, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11–q13 imprinting region
Rabeya Akter Mim, Anjana Soorajkumar, Noor Kosaji, et al.
Brain and Behavior (2024) Vol. 14, Iss. 4
Open Access | Times Cited: 2
A systematic review and pooled analysis of penetrance estimates of copy number variants associated with neurodevelopment
Shuxiang Goh, Lavvina Thiyagarajan, Tracy Dudding‐Byth, et al.
Genetics in Medicine (2024) Vol. 27, Iss. 1, pp. 101227-101227
Closed Access | Times Cited: 2
Adult-onset obstructive sleep apnea and pediatric pharyngoplasty in 22q11.2 deletion syndrome
Sabrina Cancelliere, Tracy Heung, Simone Fischbach, et al.
Sleep Medicine (2023) Vol. 104, pp. 49-55
Open Access | Times Cited: 4
Mapping the Complex Genetic Landscape of Human Neurons
Chen Sun, Kunal Kathuria, Sarah B. Emery, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
Approaches to studying the impact of 22q11.2 copy number variants
Anne S. Bassett, Donna M. McDonald‐McGinn, Erik Boot, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 7, pp. 1216-1218
Open Access | Times Cited: 4
Copy number variants differ in frequency across genetic ancestry groups
Laura M. Schultz, Alexys Knighton, Guillaume Huguet, et al.
Human Genetics and Genomics Advances (2024) Vol. 5, Iss. 4, pp. 100340-100340
Open Access | Times Cited: 1
Contribution of copy number variations to education, socioeconomic status and cognition from a genome-wide study of 305,401 subjects
Xinrui Wu, Bang‐Sheng Wu, Jujiao Kang, et al.
Molecular Psychiatry (2024)
Closed Access | Times Cited: 1
Trends in Body Mass Index Among Individuals With Neurodevelopmental Disorders
Miguel Garcia‐Argibay, Sebastian Lundström, Samuele Cortese, et al.
JAMA Network Open (2024) Vol. 7, Iss. 9, pp. e2431543-e2431543
Open Access | Times Cited: 1
Evaluating the Joint Effects of Recurrent Copy Number Variants and Polygenic Scores on the Risk of Psychiatric Disorders in the iPSYCH2015 Case-Cohort Sample
Morteza Vaez, Simone Montalbano, Ryan K. Waples, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access | Times Cited: 1
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
The Phenotypic variability of 16p11.2 distal BP2–BP3 deletion in a transgenerational family and in neurodevelopmentally ascertained samples
Marc Woodbury‐Smith, Lia D’Abate, Dimitri J. Stavropoulos, et al.
Journal of Medical Genetics (2023) Vol. 60, Iss. 12, pp. 1153-1160
Open Access | Times Cited: 2
Improving CNV Detection Performance in Microarray Data Using a Machine Learning-Based Approach
Chul Jun Goh, Hyuk‐Jung Kwon, Yoonhee Kim, et al.
Diagnostics (2023) Vol. 14, Iss. 1, pp. 84-84
Open Access | Times Cited: 2
The hallmarks of autism
Bernard J. Crespi
Frontiers in Psychiatry (2022) Vol. 13
Open Access | Times Cited: 4
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis
David Curtis
Psychiatric Genetics (2022) Vol. 32, Iss. 4, pp. 156-161
Open Access | Times Cited: 3
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
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