All of Us Publications

There are currently 474 publications and counting

Inclusion on this list does not constitute endorsement by All of Us

Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height

Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height

Hawkes G, Beaumont RN, Li Z, Mandla R, Li X, Albert CM, Arnett DK, Ashley-Koch AE, Ashrani AA, Barnes KC, Boerwinkle E, Brody JA, Carson AP, Chami N, Chen YI, Chung MK, Curran JE, Darbar D, Ellinor PT, Fornage M, Gordeuk VR, Guo X, He J, Hwu CM, Kalyani RR, Kaplan R, Kardia SLR, Kooperberg C, Loos RJF, Lubitz SA, Minster RL, Naseri T, Viali S, Mitchell BD, Murabito JM, Palmer ND, Psaty BM, Redline S, Shoemaker MB, Silverman EK, Telen MJ, Weiss ST, Yanek LR, Zhou H; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium; Liu CT, North KE, Justice AE, Locke JM, Owens N, Murray A, Patel K, Frayling TM, Wright CF, Wood AR, Lin X, Manning A, Weedon MN. Nat Commun. 2024 Oct 3;15(1):8549. doi: 10.1038/s41467-024-52579-w. PMID: 39362880; PMCID: PMC11450065.

October 3, 2024

Proteogenomic analysis integrated with electronic health records data reveals disease-associated variants in Black Americans

Proteogenomic analysis integrated with electronic health records data reveals disease-associated variants in Black Americans

Tahir UA, Barber JL, Cruz DE, Kars ME, Deng S, Tuftin B, Gillman MG, Benson MD, Robbins JM, Chen ZZ, Rao P, Katz DH, Farrell L, Sofer T, Hall ME, Ekunwe L, Tracy RP, Durda P, Taylor KD, Liu Y, Johnson WC, Guo X, Chen YI, Manichaikul AW, Jain D, Wang TJ, Reiner AP, Natarajan P, Itan Y, Rich SS, Rotter JI, Wilson JG, Raffield LM, Gerszten RE. J Clin Invest. 2024 Sep 24:e181802. doi: 10.1172/JCI181802. Epub ahead of print. PMID: 39316441.

September 24, 2024

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