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Chromosomal deletions on 16p11.2 encompassing SH2B1 are associated with accelerated metabolic disease.
Cell Rep Med. 2023 Aug 15;4(8):101155. doi: 10.1016/j.xcrm.2023.101155.
Cell Rep Med. 2023.
PMID: 37586323
Free PMC article.
GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer.
Koel M, Võsa U, Jõeloo M, Läll K, Gualdo NP, Laivuori H, Lemmelä S; Estonian Biobank Research Team; FinnGen; Daly M, Palta P, Mägi R, Laisk T.
Koel M, et al. Among authors: joeloo m.
Hum Mol Genet. 2023 Jun 5;32(12):2103-2116. doi: 10.1093/hmg/ddad043.
Hum Mol Genet. 2023.
PMID: 36929174
Free PMC article.
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Genetic determinants of plasma protein levels in the Estonian population.
Kalnapenkis A, Jõeloo M, Lepik K, Kukuškina V, Kals M, Alasoo K; Estonian Biobank Research Team; Mägi R, Esko T, Võsa U.
Kalnapenkis A, et al. Among authors: joeloo m.
Sci Rep. 2024 Apr 2;14(1):7694. doi: 10.1038/s41598-024-57966-3.
Sci Rep. 2024.
PMID: 38565889
Free PMC article.
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Rare copy-number variants as modulators of common disease susceptibility.
Auwerx C, Jõeloo M, Sadler MC, Tesio N, Ojavee S, Clark CJ, Mägi R; Estonian Biobank Research Team; Reymond A, Kutalik Z.
Auwerx C, et al. Among authors: joeloo m.
Genome Med. 2024 Jan 8;16(1):5. doi: 10.1186/s13073-023-01265-5.
Genome Med. 2024.
PMID: 38185688
Free PMC article.
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