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Typing myalgic encephalomyelitis by infection at onset: A DecodeME study.
Bretherick AD, McGrath SJ, Devereux-Cooke A, Leary S, Northwood E, Redshaw A, Stacey P, Tripp C, Wilson J, Chowdhury S, Lewis I, Almelid Ø, Baby SV, Baker T, Becher H, Boutin T, Clyde M, Garcia D, Ireland J, Kerr SM, McDowall E, Perry D, Samms GL, Vitart V, Wolfe JC, Ponting CP. Bretherick AD, et al. Among authors: boutin t. NIHR Open Res. 2023 Aug 21;3:20. doi: 10.3310/nihropenres.13421.4. eCollection 2023. NIHR Open Res. 2023. PMID: 37881452 Free PMC article.
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.
Nagy R, Boutin TS, Marten J, Huffman JE, Kerr SM, Campbell A, Evenden L, Gibson J, Amador C, Howard DM, Navarro P, Morris A, Deary IJ, Hocking LJ, Padmanabhan S, Smith BH, Joshi P, Wilson JF, Hastie ND, Wright AF, McIntosh AM, Porteous DJ, Haley CS, Vitart V, Hayward C. Nagy R, et al. Genome Med. 2017 Mar 7;9(1):23. doi: 10.1186/s13073-017-0414-4. Genome Med. 2017. PMID: 28270201 Free PMC article.
Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits.
Bretherick AD, Canela-Xandri O, Joshi PK, Clark DW, Rawlik K, Boutin TS, Zeng Y, Amador C, Navarro P, Rudan I, Wright AF, Campbell H, Vitart V, Hayward C, Wilson JF, Tenesa A, Ponting CP, Baillie JK, Haley C. Bretherick AD, et al. PLoS Genet. 2020 Jul 6;16(7):e1008785. doi: 10.1371/journal.pgen.1008785. eCollection 2020 Jul. PLoS Genet. 2020. PMID: 32628676 Free PMC article.
Variants associated with HHIP expression have sex-differential effects on lung function.
Fawcett KA, Obeidat M, Melbourne C, Shrine N, Guyatt AL, John C, Luan J, Richmond A, Moksnes MR, Granell R, Weiss S, Imboden M, May-Wilson S, Hysi P, Boutin TS, Portas L, Flexeder C, Harris SE, Wang CA, Lyytikäinen LP, Palviainen T, Foong RE, Keidel D, Minelli C, Langenberg C, Bossé Y, Van den Berge M, Sin DD, Hao K, Campbell A, Porteous D, Padmanabhan S, Smith BH, Evans DM, Ring S, Langhammer A, Hveem K, Willer C, Ewert R, Stubbe B, Pirastu N, Klaric L, Joshi PK, Patasova K, Massimo M, Polasek O, Starr JM, Karrasch S, Strauch K, Meitinger T, Rudan I, Rantanen T, Pietiläinen K, Kähönen M, Raitakari OT, Hall GL, Sly PD, Pennell CE, Kaprio J, Lehtimäki T, Vitart V, Deary IJ, Jarvis D, Wilson JF, Spector T, Probst-Hensch N, Wareham NJ, Völzke H, Henderson J, Strachan DP, Brumpton BM, Hayward C, Hall IP, Tobin MD, Wain LV. Fawcett KA, et al. Among authors: boutin ts. Wellcome Open Res. 2021 May 24;5:111. doi: 10.12688/wellcomeopenres.15846.2. eCollection 2020. Wellcome Open Res. 2021. PMID: 33728380 Free PMC article.
Parent of origin genetic effects on methylation in humans are common and influence complex trait variation.
Zeng Y, Amador C, Xia C, Marioni R, Sproul D, Walker RM, Morris SW, Bretherick A, Canela-Xandri O, Boutin TS, Clark DW, Campbell A, Rawlik K, Hayward C, Nagy R, Tenesa A, Porteous DJ, Wilson JF, Deary IJ, Evans KL, McIntosh AM, Navarro P, Haley CS. Zeng Y, et al. Nat Commun. 2019 Mar 27;10(1):1383. doi: 10.1038/s41467-019-09301-y. Nat Commun. 2019. PMID: 30918249 Free PMC article.
Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation.
Zeng Y, Amador C, Xia C, Marioni R, Sproul D, Walker RM, Morris SW, Bretherick A, Canela-Xandri O, Boutin TS, Clark DW, Campbell A, Rawlik K, Hayward C, Nagy R, Tenesa A, Porteous DJ, Wilson JF, Deary IJ, Evans KL, McIntosh AM, Navarro P, Haley CS. Zeng Y, et al. Nat Commun. 2019 May 1;10(1):2069. doi: 10.1038/s41467-019-10155-7. Nat Commun. 2019. PMID: 31043600 Free PMC article.
Insights into the genetic basis of retinal detachment.
Boutin TS, Charteris DG, Chandra A, Campbell S, Hayward C, Campbell A; UK Biobank Eye & Vision Consortium; Nandakumar P, Hinds D; 23andMe Research Team; Mitry D, Vitart V. Boutin TS, et al. Hum Mol Genet. 2020 Mar 13;29(4):689-702. doi: 10.1093/hmg/ddz294. Hum Mol Genet. 2020. PMID: 31816047 Free PMC article.
83 results