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Rare coding variants in CHRNB2 reduce the likelihood of smoking.
Nat Genet. 2023 Jul;55(7):1138-1148. doi: 10.1038/s41588-023-01417-8. Epub 2023 Jun 12.
Nat Genet. 2023.
PMID: 37308787
Free PMC article.
Population-scale analysis of common and rare genetic variation associated with hearing loss in adults.
Praveen K, Dobbyn L, Gurski L, Ayer AH, Staples J, Mishra S, Bai Y, Kaufman A, Moscati A, Benner C, Chen E, Chen S, Popov A, Smith J; GHS-REGN DiscovEHR collaboration; Regeneron Genetics Center; Decibel-REGN collaboration; Melander O, Jones MB, Marchini J, Balasubramanian S, Zambrowicz B, Drummond MC, Baras A, Abecasis GR, Ferreira MA, Stahl EA, Coppola G.
Praveen K, et al.
Commun Biol. 2022 Jun 3;5(1):540. doi: 10.1038/s42003-022-03408-7.
Commun Biol. 2022.
PMID: 35661827
Free PMC article.
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