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21 results

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Page 1
Plasma proteomic associations with genetics and health in the UK Biobank.
Sun BB, Chiou J, Traylor M, Benner C, Hsu YH, Richardson TG, Surendran P, Mahajan A, Robins C, Vasquez-Grinnell SG, Hou L, Kvikstad EM, Burren OS, Davitte J, Ferber KL, Gillies CE, Hedman ÅK, Hu S, Lin T, Mikkilineni R, Pendergrass RK, Pickering C, Prins B, Baird D, Chen CY, Ward LD, Deaton AM, Welsh S, Willis CM, Lehner N, Arnold M, Wörheide MA, Suhre K, Kastenmüller G, Sethi A, Cule M, Raj A; Alnylam Human Genetics; AstraZeneca Genomics Initiative; Biogen Biobank Team; Bristol Myers Squibb; Genentech Human Genetics; GlaxoSmithKline Genomic Sciences; Pfizer Integrative Biology; Population Analytics of Janssen Data Sciences; Regeneron Genetics Center; Burkitt-Gray L, Melamud E, Black MH, Fauman EB, Howson JMM, Kang HM, McCarthy MI, Nioi P, Petrovski S, Scott RA, Smith EN, Szalma S, Waterworth DM, Mitnaul LJ, Szustakowski JD, Gibson BW, Miller MR, Whelan CD. Sun BB, et al. Among authors: davitte j. Nature. 2023 Oct;622(7982):329-338. doi: 10.1038/s41586-023-06592-6. Epub 2023 Oct 4. Nature. 2023. PMID: 37794186 Free PMC article.
Whole-genome sequencing of 490,640 UK Biobank participants.
UK Biobank Whole-Genome Sequencing Consortium. UK Biobank Whole-Genome Sequencing Consortium. Nature. 2025 Sep;645(8081):692-701. doi: 10.1038/s41586-025-09272-9. Epub 2025 Aug 6. Nature. 2025. PMID: 40770095 Free PMC article.
Proteomic signatures improve risk prediction for common and rare diseases.
Carrasco-Zanini J, Pietzner M, Davitte J, Surendran P, Croteau-Chonka DC, Robins C, Torralbo A, Tomlinson C, Grünschläger F, Fitzpatrick N, Ytsma C, Kanno T, Gade S, Freitag D, Ziebell F, Haas S, Denaxas S, Betts JC, Wareham NJ, Hemingway H, Scott RA, Langenberg C. Carrasco-Zanini J, et al. Among authors: davitte j. Nat Med. 2024 Sep;30(9):2489-2498. doi: 10.1038/s41591-024-03142-z. Epub 2024 Jul 22. Nat Med. 2024. PMID: 39039249 Free PMC article.
Narcolepsy as a potential risk factor for Schizophrenia.
Eghtedarian R, Tervi AM, Jones SE; FinnGen; Partinen M, Viippola E, Ollila HM. Eghtedarian R, et al. Transl Psychiatry. 2025 Feb 17;15(1):55. doi: 10.1038/s41398-025-03259-w. Transl Psychiatry. 2025. PMID: 39962082 Free PMC article.
Monoallelic TYROBP deletion is a novel risk factor for Alzheimer's disease.
Martiskainen H, Willman RM, Harju P, Heikkinen S, Heiskanen M, Müller SA, Sinisalo R, Takalo M, Mäkinen P, Kuulasmaa T, Pekkala V, Galván Del Rey A, Juopperi SP, Jeskanen H, Kervinen I, Saastamoinen K; FinnGen; Niiranen M, Heikkinen SV, Kurki MI, Marttila J, Mäkinen PI, Rostalski H, Hietanen T, Ngandu T, Lehtisalo J, Bellenguez C, Lambert JC, Haass C, Rinne J, Hakumäki J, Rauramaa T, Krüger J, Soininen H, Haapasalo A, Lichtenthaler SF, Leinonen V, Solje E, Hiltunen M. Martiskainen H, et al. Mol Neurodegener. 2025 Apr 29;20(1):50. doi: 10.1186/s13024-025-00830-3. Mol Neurodegener. 2025. PMID: 40301889 Free PMC article.
Population-scale gene-based analysis of whole-genome sequencing provides insights into metabolic health.
Zhao Y, Lockhart S, Liu J, Li X, Cortes A, Hua X, Gardner EJ, Kentistou KA, Cañadas-Garre M, Fabian L, Ho K, Timpson N, Lo Y, Davitte J, Savage DB, Buser-Doepner C, Ong KK, Zhang H, Scott R, O'Rahilly S, Perry JRB. Zhao Y, et al. Among authors: davitte j. Nat Genet. 2025 Oct;57(10):2436-2444. doi: 10.1038/s41588-025-02364-2. Epub 2025 Oct 10. Nat Genet. 2025. PMID: 41073786 Free PMC article.
A computational framework for defining and validating reproducible phenotyping algorithms of 313 diseases in the UK Biobank.
Torralbo A, Davitte JM, Croteau-Chonka DC, Ytsma C, Tomlinson C, Fitzpatrick NK, Chung SC, Fatemifar G, Cortes AS, Richardson TG, Barclay M, Carrasco-Zanini J, Finan C, Hemingway H, Hingorani AD, Kuan V, Langenberg C, Lyratzopoulos G, Lumbers RT, Pietzner M, Shah AD, Thygesen JH, Zelenka N, Whittaker JC, Ehm MG, Denaxas S. Torralbo A, et al. Among authors: davitte jm. Sci Rep. 2025 Jul 9;15(1):24607. doi: 10.1038/s41598-025-05838-9. Sci Rep. 2025. PMID: 40634319 Free PMC article.
21 results