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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:

Effects of pathogenic CNVs on physical traits in participants of the UK Biobank
David Owen, Mathew Bracher-Smith, Kimberley Kendall, et al.
BMC Genomics (2018) Vol. 19, Iss. 1
Open Access | Times Cited: 73

Showing 1-25 of 73 citing articles:

A structural variation reference for medical and population genetics
Ryan L. Collins, Harrison Brand, Konrad J. Karczewski, et al.
Nature (2020) Vol. 581, Iss. 7809, pp. 444-451
Open Access | Times Cited: 817
A cross-disorder dosage sensitivity map of the human genome
Ryan L. Collins, Joseph Glessner, Eleonora Porcu, et al.
Cell (2022) Vol. 185, Iss. 16, pp. 3041-3055.e25
Open Access | Times Cited: 221
GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data
Mehrtash Babadi, Jack Fu, Samuel K. Lee, et al.
Nature Genetics (2023) Vol. 55, Iss. 9, pp. 1589-1597
Open Access | Times Cited: 47
Rare copy-number variants as modulators of common disease susceptibility
Chiara Auwerx, Maarja Jõeloo, Marie C. Sadler, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 23
Phenome-wide Burden of Copy-Number Variation in the UK Biobank
Matthew Aguirre, Manuel A. Rivas, James R. Priest
The American Journal of Human Genetics (2019) Vol. 105, Iss. 2, pp. 373-383
Open Access | Times Cited: 78
Copy number variation and neuropsychiatric illness
Elliott Rees, George Kirov
Current Opinion in Genetics & Development (2021) Vol. 68, pp. 57-63
Open Access | Times Cited: 72
The individual and global impact of copy-number variants on complex human traits
Chiara Auwerx, Maarja Lepamets, Marie C. Sadler, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 4, pp. 647-668
Open Access | Times Cited: 57
Influences of rare copy-number variation on human complex traits
Margaux L.A. Hujoel, Maxwell A. Sherman, Alison R. Barton, et al.
Cell (2022) Vol. 185, Iss. 22, pp. 4233-4248.e27
Open Access | Times Cited: 39
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: 54
Large mosaic copy number variations confer autism risk
Maxwell A. Sherman, Rachel E. Rodin, Giulio Genovese, et al.
Nature Neuroscience (2021) Vol. 24, Iss. 2, pp. 197-203
Open Access | Times Cited: 48
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
Genome-wide association testing beyond SNPs
Laura Harris, Ellen M. McDonagh, Xiaolei Zhang, et al.
Nature Reviews Genetics (2024)
Closed Access | Times Cited: 5
Immune-developmental processes contribute to schizophrenia risk: insights from a genetic overlap study with height
Cato Romero, Christiaan de Leeuw, Marijn Schipper, 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
Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models
Derek J.C. Tai, Parisa Razaz, Serkan Erdin, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 10, pp. 1789-1813
Open Access | Times Cited: 25
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
Diversity and consequences of structural variation in the human genome
Ryan L. Collins, Michael E. Talkowski
Nature Reviews Genetics (2025)
Closed 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
MicroRNAs and their delivery in diabetic fibrosis
Alexa Wonnacott, Laura Denby, Richard J. Coward, et al.
Advanced Drug Delivery Reviews (2021) Vol. 182, pp. 114045-114045
Open Access | Times Cited: 31
A cross-disorder dosage sensitivity map of the human genome
Ryan L. Collins, Joseph Glessner, Eleonora Porcu, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 29
CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank
Tomas Fitzgerald, Ewan Birney
Cell Genomics (2022) Vol. 2, Iss. 8, pp. 100167-100167
Open Access | Times Cited: 21
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
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
The impact of 22q11.2 copy-number variants on human traits in the general population
Malú Zamariolli, Chiara Auwerx, Marie C. Sadler, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 2, pp. 300-313
Open Access | Times Cited: 7
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
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