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The UK Biobank resource with deep phenotyping and genomic data.
Bycroft C, Freeman C, Petkova D, Band G, Elliott LT, Sharp K, Motyer A, Vukcevic D, Delaneau O, O'Connell J, Cortes A, Welsh S, Young A, Effingham M, McVean G, Leslie S, Allen N, Donnelly P, Marchini J. Bycroft C, et al. Among authors: sharp k. Nature. 2018 Oct;562(7726):203-209. doi: 10.1038/s41586-018-0579-z. Epub 2018 Oct 10. Nature. 2018. PMID: 30305743 Free PMC article.
Haplotype estimation for biobank-scale data sets.
O'Connell J, Sharp K, Shrine N, Wain L, Hall I, Tobin M, Zagury JF, Delaneau O, Marchini J. O'Connell J, et al. Among authors: sharp k. Nat Genet. 2016 Jul;48(7):817-20. doi: 10.1038/ng.3583. Epub 2016 Jun 6. Nat Genet. 2016. PMID: 27270105 Free PMC article.
Genome-wide association studies of brain imaging phenotypes in UK Biobank.
Elliott LT, Sharp K, Alfaro-Almagro F, Shi S, Miller KL, Douaud G, Marchini J, Smith SM. Elliott LT, et al. Among authors: sharp k. Nature. 2018 Oct;562(7726):210-216. doi: 10.1038/s41586-018-0571-7. Epub 2018 Oct 10. Nature. 2018. PMID: 30305740 Free PMC article.
A reference panel of 64,976 haplotypes for genotype imputation.
McCarthy S, Das S, Kretzschmar W, Delaneau O, Wood AR, Teumer A, Kang HM, Fuchsberger C, Danecek P, Sharp K, Luo Y, Sidore C, Kwong A, Timpson N, Koskinen S, Vrieze S, Scott LJ, Zhang H, Mahajan A, Veldink J, Peters U, Pato C, van Duijn CM, Gillies CE, Gandin I, Mezzavilla M, Gilly A, Cocca M, Traglia M, Angius A, Barrett JC, Boomsma D, Branham K, Breen G, Brummett CM, Busonero F, Campbell H, Chan A, Chen S, Chew E, Collins FS, Corbin LJ, Smith GD, Dedoussis G, Dorr M, Farmaki AE, Ferrucci L, Forer L, Fraser RM, Gabriel S, Levy S, Groop L, Harrison T, Hattersley A, Holmen OL, Hveem K, Kretzler M, Lee JC, McGue M, Meitinger T, Melzer D, Min JL, Mohlke KL, Vincent JB, Nauck M, Nickerson D, Palotie A, Pato M, Pirastu N, McInnis M, Richards JB, Sala C, Salomaa V, Schlessinger D, Schoenherr S, Slagboom PE, Small K, Spector T, Stambolian D, Tuke M, Tuomilehto J, Van den Berg LH, Van Rheenen W, Volker U, Wijmenga C, Toniolo D, Zeggini E, Gasparini P, Sampson MG, Wilson JF, Frayling T, de Bakker PI, Swertz MA, McCarroll S, Kooperberg C, Dekker A, Altshuler D, Willer C, Iacono W, Ripatti S, Soranzo N, Walter K, Swaroop A, Cucca F, Anderson CA, Myers RM, Boehnke M, McCarthy MI, Durbi… See abstract for full author list ➔ McCarthy S, et al. Among authors: sharp k. Nat Genet. 2016 Oct;48(10):1279-83. doi: 10.1038/ng.3643. Epub 2016 Aug 22. Nat Genet. 2016. PMID: 27548312 Free PMC article.
Altered steady state and activity-dependent de novo protein expression in fragile X syndrome.
Bowling H, Bhattacharya A, Zhang G, Alam D, Lebowitz JZ, Bohm-Levine N, Lin D, Singha P, Mamcarz M, Puckett R, Zhou L, Aryal S, Sharp K, Kirshenbaum K, Berry-Kravis E, Neubert TA, Klann E. Bowling H, et al. Among authors: sharp k. Nat Commun. 2019 Apr 12;10(1):1710. doi: 10.1038/s41467-019-09553-8. Nat Commun. 2019. PMID: 30979884 Free PMC article.
Identification of rfk-1, a Meiotic Driver Undergoing RNA Editing in Neurospora.
Rhoades NA, Harvey AM, Samarajeewa DA, Svedberg J, Yusifov A, Abusharekh A, Manitchotpisit P, Brown DW, Sharp KJ, Rehard DG, Peters J, Ostolaza-Maldonado X, Stephenson J, Shiu PKT, Johannesson H, Hammond TM. Rhoades NA, et al. Among authors: sharp kj. Genetics. 2019 May;212(1):93-110. doi: 10.1534/genetics.119.302122. Epub 2019 Mar 27. Genetics. 2019. PMID: 30918007 Free PMC article.
462 results