Systematic common and rare variant association testing in 392,030 whole genomes in All of Us.

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Title: Systematic common and rare variant association testing in 392,030 whole genomes in All of Us.
Authors: Lu W, Carroll RJ, Solomonson M, Guez J, He MK, Marten DJ, Martinez-Carrasco A, Wang Y, Dowd CS, Kanai M, Gorissen BL, Kouame AJS, Brogan J, Waxse BJ, Samarakoon R, Cook JA, Qian J, Zhou Y, Choi KW, Basford M, Lyons M, Linder JE, Stewart S, Gupta N, Schultz P, Goldstein D, Llanwarne C, Goldstein JI, Higham EGC, King DC, Palmer DS, Elenbaas JS, Rohlicek GK, He Q, Goodrich JK, Smoller JW, Lichtenstein L, Gabriel SB, Martin AR, Karnes JH, Hebbring SJ, Daly MJ, Dutka T, Musick A, Denny JC, Zhou W, Roden DM, Neale BM, Karczewski KJ
Corporate Authors: All of Us Research Program Genomics Investigators
Source: MedRxiv : the preprint server for health sciences [medRxiv] 2026 May 12. Date of Electronic Publication: 2026 May 12.
Publication Type: Journal Article; Preprint
Journal Info: Country of Publication: United States NLM ID: 101767986 Publication Model: Electronic Cited Medium: Internet NLM ISO Abbreviation: medRxiv Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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DbLabel: MEDLINE Ultimate
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PubType: Academic Journal
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  Data: <i>Country of Publication: </i>United States <i>NLM ID: </i>101767986 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>NLM ISO Abbreviation: </i>medRxiv <i>Subsets: </i>PubMed not MEDLINE
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