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The individual and global impact of copy-number variants on complex human traits.
Auwerx C, Lepamets M, Sadler MC, Patxot M, Stojanov M, Baud D, Mägi R; Estonian Biobank Research Team; Porcu E, Reymond A, Kutalik Z. Auwerx C, et al. Am J Hum Genet. 2022 Apr 7;109(4):647-668. doi: 10.1016/j.ajhg.2022.02.010. Epub 2022 Mar 2. Am J Hum Genet. 2022. PMID: 35240056 Free PMC article.
The pleiotropic spectrum of proximal 16p11.2 CNVs.
Auwerx C, Kutalik Z, Reymond A. Auwerx C, et al. Am J Hum Genet. 2024 Nov 7;111(11):2309-2346. doi: 10.1016/j.ajhg.2024.08.015. Epub 2024 Sep 26. Am J Hum Genet. 2024. PMID: 39332410 Free PMC article. Review.
Response to Bassett et al.
Zamariolli M, Auwerx C, Sadler MC, van der Graaf A, Lepik K, Schoeler T, Moysés-Oliveira M, Dantas AG, Melaragno MI, Kutalik Z. Zamariolli M, et al. Among authors: auwerx c. Am J Hum Genet. 2023 Jul 6;110(7):1219-1220. doi: 10.1016/j.ajhg.2023.05.017. Am J Hum Genet. 2023. PMID: 37419093 Free PMC article. No abstract available.
The impact of 22q11.2 copy-number variants on human traits in the general population.
Zamariolli M, Auwerx C, Sadler MC, van der Graaf A, Lepik K, Schoeler T, Moysés-Oliveira M, Dantas AG, Melaragno MI, Kutalik Z. Zamariolli M, et al. Among authors: auwerx c. Am J Hum Genet. 2023 Feb 2;110(2):300-313. doi: 10.1016/j.ajhg.2023.01.005. Epub 2023 Jan 26. Am J Hum Genet. 2023. PMID: 36706759 Free PMC article.
19 results