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"I'm quite proud of how we've handled it": health professionals' experiences of returning additional findings from the 100,000 genomes project.
Stafford-Smith B, Gurasashvili J, Peter M, Daniel M, Balasubramanian M, Bownass L, Brennan P, Cleaver R, Clowes V, Costello P, DeSouza B, Dubois L, Harrison R, Hawkes L, Jones EA, Kraus A, McEntagart M, Somarathi S, Taylor A, Tripathi V, Chitty LS, Hill M. Stafford-Smith B, et al. Among authors: taylor a. Eur J Hum Genet. 2024 Nov 5. doi: 10.1038/s41431-024-01716-6. Online ahead of print. Eur J Hum Genet. 2024. PMID: 39496896 Free article.
Impact of Social Stories on social and emotional health of autism spectrum primary school children: the ASSSIST2 RCT with economic evaluation.
Wright B, Bell KJ, Blackwell JE, Teige C, Mandefield L, Wang HI, Welch C, Scantlebury A, Watson J, McMillan D, Standley E, Attwell L, Carrick H, Taylor A, Taylor O, Hodkinson R, Edwards H, Pearson H, Parrott S, Marshall D, Varley D, Hargate R, Mclaren A, Elizabeth Hewitt C. Wright B, et al. Among authors: taylor a, taylor o. Health Technol Assess. 2024 Aug;28(39):1-121. doi: 10.3310/JBTM8017. Health Technol Assess. 2024. PMID: 39207130 Free article. Clinical Trial.
Radiation treatment of benign tumors in NF2-related-schwannomatosis: A national study of 266 irradiated patients showing a significant increase in malignancy/malignant progression.
Evans DG, Halliday D, Obholzer R, Afridi S, Forde C, Rutherford SA, Hammerbeck-Ward C, Lloyd SK, Freeman SM, Pathmanaban ON, Thomas OM, Laitt RD, Stivaros S, Kilday JP, Vassallo G, McBain C, Lavin T, Paterson C, Whitfield G, McCabe MG, Axon PR, Halliday J, Mackeith S, Parry A; English Specialist NF2 Research Group; Harkness EF, Buttimore J, King AT. Evans DG, et al. Neurooncol Adv. 2023 Mar 11;5(1):vdad025. doi: 10.1093/noajnl/vdad025. eCollection 2023 Jan-Dec. Neurooncol Adv. 2023. PMID: 37051330 Free PMC article.
Evaluation and deployment of isotype-specific salivary antibody assays for detecting previous SARS-CoV-2 infection in children and adults.
Thomas AC, Oliver E, Baum HE, Gupta K, Shelley KL, Long AE, Jones HE, Smith J, Hitchings B, di Bartolo N, Vasileiou K, Rabi F, Alamir H, Eghleilib M, Francis O, Oliver J, Morales-Aza B, Obst U, Shattock D, Barr R, Collingwood L, Duale K, Grace N, Livera GG, Bishop L, Downing H, Rodrigues F, Timpson N, Relton CL, Toye A, Woolfson DN, Berger I, Goenka A, Davidson AD, Gillespie KM, Williams AJK, Bailey M, Brooks-Pollock E, Finn A, Halliday A; CoMMinS Study Team. Thomas AC, et al. Commun Med (Lond). 2023 Mar 15;3(1):37. doi: 10.1038/s43856-023-00264-2. Commun Med (Lond). 2023. PMID: 36922542 Free PMC article.
Neoadjuvant atezolizumab + chemotherapy for resectable NSCLC: 3-year clinical update of phase II clinical trial results and translational findings.
Henick BS, Koch PD, Gainor JF, Awad MM, Chiuzan C, Izard S, Georgis Y, Mallick S, Garofano RF, Wong CV, Saqi A, Grindheim J, Schulze K, Sonett JR, Rizvi NA, Izar B, Taylor AM, Shu CA. Henick BS, et al. Among authors: taylor am. J Immunother Cancer. 2024 Dec 25;12(12):e009301. doi: 10.1136/jitc-2024-009301. J Immunother Cancer. 2024. PMID: 39721753 Free article. Clinical Trial.
Integrating vocational supports into a transition clinic: A pilot program.
Hale EW, Taylor A, Elton M, Honsbruch M, Rosenberg CR, Sanders JS. Hale EW, et al. Among authors: taylor a. Health Care Transit. 2024 Feb 27;2:100048. doi: 10.1016/j.hctj.2024.100048. eCollection 2024. Health Care Transit. 2024. PMID: 39712592 Free PMC article.
DNA methylation-based predictors of metabolic traits in Scottish and Singaporean cohorts.
Smith HM, Ng HK, Moodie JE, Gadd DA, McCartney DL, Bernabeu E, Campbell A, Redmond P, Taylor A, Page D, Corley J, Harris SE, Tay D, Deary IJ, Evans KL, Robinson MR, Chambers JC, Loh M, Cox SR, Marioni RE, Hillary RF. Smith HM, et al. Among authors: taylor a. Am J Hum Genet. 2024 Dec 13:S0002-9297(24)00421-X. doi: 10.1016/j.ajhg.2024.11.012. Online ahead of print. Am J Hum Genet. 2024. PMID: 39706196 Free article.
Eight-fold increased COVID-19 mortality in autosomal dominant tubulointerstitial kidney disease due to MUC1 mutations: an observational study.
Kidd KO, Williams AH, Taylor A, Martin L, Robins V, Sayer JA, Olinger E, Mabillard HR, Papagregoriou G, Deltas C, Stavrou C, Conlon PJ, Hogan RE, Elhassan EAE, Springer D, Zima T, Izzi C, Vrbacká A, Piherová L, Pohludka M, Radina M, Vylet'al P, Hodanova K, Zivna M, Kmoch S, Bleyer AJ Sr. Kidd KO, et al. Among authors: taylor a. BMC Nephrol. 2024 Dec 18;25(1):449. doi: 10.1186/s12882-024-03896-1. BMC Nephrol. 2024. PMID: 39696072 Free PMC article.
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