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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:

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

Showing 1-25 of 57 citing articles:

The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource
Elliot Sollis, Abayomi Mosaku, Ala Abid, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D977-D985
Open Access | Times Cited: 954
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
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
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
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
Protein-altering variants at copy number-variable regions influence diverse human phenotypes
Margaux L.A. Hujoel, Robert E. Handsaker, Maxwell A. Sherman, et al.
Nature Genetics (2024) Vol. 56, Iss. 4, pp. 569-578
Open Access | Times Cited: 14
Functional characterization of human genomic variation linked to polygenic diseases
Tania Fabo, Paul A. Khavari
Trends in Genetics (2023) Vol. 39, Iss. 6, pp. 462-490
Open Access | Times Cited: 18
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
Chromosomal deletions on 16p11.2 encompassing SH2B1 are associated with accelerated metabolic disease
Ruth Hanßen, Chiara Auwerx, Maarja Jõeloo, et al.
Cell Reports Medicine (2023) Vol. 4, Iss. 8, pp. 101155-101155
Open Access | Times Cited: 16
Genome-wide association testing beyond SNPs
Laura Harris, Ellen M. McDonagh, Xiaolei Zhang, et al.
Nature Reviews Genetics (2024)
Closed Access | Times Cited: 5
Reciprocal and non-reciprocal effects of clinically relevant SETBP1 protein dosage changes
Lilit Antonyan, Xin Zhang, Anjie Ni, et al.
Human Molecular Genetics (2025)
Open Access
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
Exome Sequencing Has a High Diagnostic Rate in Sporadic Congenital Hypopituitarism and Reveals Novel Candidate Genes
Julian Martinez-Mayer, Sebastián Vishnopolska, Catalina Perticarari, et al.
The Journal of Clinical Endocrinology & Metabolism (2024) Vol. 109, Iss. 12, pp. 3196-3210
Open Access | Times Cited: 4
Genetic ancestry in Population Pharmacogenomics unravels distinct geographical patterns related to drug toxicity
Kariofyllis Karamperis, Sonja Katz, Federico Melograna, et al.
iScience (2024) Vol. 27, Iss. 10, pp. 110916-110916
Open Access | Times Cited: 4
From Biobanking to Personalized Medicine: the journey of the Estonian Biobank
Lili Milani, Maris Alver, Sven Laur, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4
Disrupted transcriptional networks regulated by CHD1L during neurodevelopment underlie the mirrored neuroanatomical and growth phenotypes of the 1q21.1 copy number variant
Marianne Victoria Lemée, Maria Nicla Loviglio, Ye Tao, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Gene dosage architecture across complex traits
Sayeh Kazem, Kuldeep Kumar, Martineau Jean‐Louis, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
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
Buffering and non-monotonic behavior of gene dosage response curves for human complex traits
Nikhil Milind, Courtney J. Smith, Huisheng Zhu, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
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
GATK-gCNV: A Rare Copy Number Variant Discovery Algorithm and Its Application to Exome Sequencing in the UK Biobank
Mehrtash Babadi, Jack Fu, Samuel K. Lee, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 13
Microdeletions and microduplications linked to severe congenital disorders in infertile men
Triin Kikas, Anna Maria Punab, Laura Kasak, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 7
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
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