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5,101 results

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Page 1
Spectral clustering based on structural magnetic resonance imaging and its relationship with major depressive disorder and cognitive ability.
Yeung HW, Shen X, Stolicyn A, de Nooij L, Harris MA, Romaniuk L, Buchanan CR, Waiter GD, Sandu AL, McNeil CJ, Murray A, Steele JD, Campbell A, Porteous D, Lawrie SM, McIntosh AM, Cox SR, Smith KM, Whalley HC. Yeung HW, et al. Among authors: campbell a. Eur J Neurosci. 2021 Sep;54(6):6281-6303. doi: 10.1111/ejn.15423. Epub 2021 Sep 2. Eur J Neurosci. 2021. PMID: 34390586
Generation Scotland: Donor DNA Databank; A control DNA resource.
Kerr SM, Liewald DC, Campbell A, Taylor K, Wild SH, Newby D, Turner M, Porteous DJ. Kerr SM, et al. Among authors: campbell a. BMC Med Genet. 2010 Nov 23;11:166. doi: 10.1186/1471-2350-11-166. BMC Med Genet. 2010. PMID: 21092308 Free PMC article.
Cohort Profile: Generation Scotland: Scottish Family Health Study (GS:SFHS). The study, its participants and their potential for genetic research on health and illness.
Smith BH, Campbell A, Linksted P, Fitzpatrick B, Jackson C, Kerr SM, Deary IJ, Macintyre DJ, Campbell H, McGilchrist M, Hocking LJ, Wisely L, Ford I, Lindsay RS, Morton R, Palmer CN, Dominiczak AF, Porteous DJ, Morris AD. Smith BH, et al. Among authors: campbell h, campbell a. Int J Epidemiol. 2013 Jun;42(3):689-700. doi: 10.1093/ije/dys084. Epub 2012 Jul 10. Int J Epidemiol. 2013. PMID: 22786799
Molecular genetic contributions to socioeconomic status and intelligence.
Marioni RE, Davies G, Hayward C, Liewald D, Kerr SM, Campbell A, Luciano M, Smith BH, Padmanabhan S, Hocking LJ, Hastie ND, Wright AF, Porteous DJ, Visscher PM, Deary IJ. Marioni RE, et al. Among authors: campbell a. Intelligence. 2014 May;44(100):26-32. doi: 10.1016/j.intell.2014.02.006. Intelligence. 2014. PMID: 24944428 Free PMC article.
Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study.
Luciano M, Svinti V, Campbell A, Marioni RE, Hayward C, Wright AF, Taylor MS, Porteous DJ, Thomson P, Prendergast JG, Hastie ND, Farrington SM, Scotland G, Dunlop MG, Deary IJ. Luciano M, et al. Among authors: campbell a. Twin Res Hum Genet. 2015 Apr;18(2):117-25. doi: 10.1017/thg.2015.10. Epub 2015 Mar 6. Twin Res Hum Genet. 2015. PMID: 25744449 Free article. Clinical Trial.
Rare coding variants and X-linked loci associated with age at menarche.
Lunetta KL, Day FR, Sulem P, Ruth KS, Tung JY, Hinds DA, Esko T, Elks CE, Altmaier E, He C, Huffman JE, Mihailov E, Porcu E, Robino A, Rose LM, Schick UM, Stolk L, Teumer A, Thompson DJ, Traglia M, Wang CA, Yerges-Armstrong LM, Antoniou AC, Barbieri C, Coviello AD, Cucca F, Demerath EW, Dunning AM, Gandin I, Grove ML, Gudbjartsson DF, Hocking LJ, Hofman A, Huang J, Jackson RD, Karasik D, Kriebel J, Lange EM, Lange LA, Langenberg C, Li X, Luan J, Mägi R, Morrison AC, Padmanabhan S, Pirie A, Polasek O, Porteous D, Reiner AP, Rivadeneira F, Rudan I, Sala CF, Schlessinger D, Scott RA, Stöckl D, Visser JA, Völker U, Vozzi D, Wilson JG, Zygmunt M; EPIC-InterAct Consortium; Generation Scotland; Boerwinkle E, Buring JE, Crisponi L, Easton DF, Hayward C, Hu FB, Liu S, Metspalu A, Pennell CE, Ridker PM, Strauch K, Streeten EA, Toniolo D, Uitterlinden AG, Ulivi S, Völzke H, Wareham NJ, Wellons M, Franceschini N, Chasman DI, Thorsteinsdottir U, Murray A, Stefansson K, Murabito JM, Ong KK, Perry JR. Lunetta KL, et al. Nat Commun. 2015 Aug 4;6:7756. doi: 10.1038/ncomms8756. Nat Commun. 2015. PMID: 26239645 Free PMC article.
5,101 results