Publication Directory

Explore 709 peer-reviewed journal articles based on All of Us data

Looking for other kinds of publications? Our expanded catalog also includes news, pre-prints, abstracts, and other articles related to the program.

Inclusion on these pages does not constitute endorsement by All of Us

Improving follow-up survey completion rates through pilot interventions in the All of Us Research Program: Results from a non-randomized intervention study

Improving follow-up survey completion rates through pilot interventions in the All of Us Research Program: Results from a non-randomized intervention study

Cronin RM, Feng X, Able A, Sutherland S, Givens B, Johnston R, Depry C, Le Blanc KW, Caro O, Mapes B, Denny J, Couper MP, Chen Q, Prabhu Das I. PLoS One. 2024 Oct 15;19(10):e0308995. doi: 10.1371/journal.pone.0308995. PMID: 39405295; PMCID: PMC11478879.

October 15, 2024

Racial and ethnic differences in healthcare access and utilization among U.S. adults with melanoma and keratinocyte carcinomas in the NIH All of Us Research Program

Racial and ethnic differences in healthcare access and utilization among U.S. adults with melanoma and keratinocyte carcinomas in the NIH All of Us Research Program

Juarez MC, Shah JT, Lee N, Stevenson ML, Carucci JA, Criscito MC. Arch Dermatol Res. 2024 Oct 14;316(10):686. doi: 10.1007/s00403-024-03383-5. PMID: 39400730.

October 14, 2024

Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genes

Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genes

Huerta-Chagoya A, Schroeder P, Mandla R, Li J, Morris L, Vora M, Alkanaq A, Nagy D, Szczerbinski L, Madsen JGS, Bonàs-Guarch S, Mollandin F, Cole JB, Porneala B, Westerman K, Li JH, Pollin TI, Florez JC, Gloyn AL, Carey DJ, Cebola I, Mirshahi UL, Manning AK, Leong A, Udler M, Mercader JM. Nat Genet. 2024 Nov;56(11):2370-2379. doi: 10.1038/s41588-024-01947-9. Epub 2024 Oct 8. Erratum in: Nat Genet. 2024 Nov;56(11):2576. doi: 10.1038/s41588-024-01986-2. Erratum in: Nat Genet. 2025 Apr;57(4):1060. doi: 10.1038/s41588-025-02175-5. PMID: 39379762; PMCID: PMC11549050.

October 8, 2024

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

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