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Items: 1 to 20 of 111

1.

Complex variation in measures of general intelligence and cognitive change.

Rowe SJ, Rowlatt A, Davies G, Harris SE, Porteous DJ, Liewald DC, McNeill G, Starr JM, Deary IJ, Tenesa A.

PLoS One. 2013 Dec 12;8(12):e81189. doi: 10.1371/journal.pone.0081189. eCollection 2013.

2.

Genetic contributions to stability and change in intelligence from childhood to old age.

Deary IJ, Yang J, Davies G, Harris SE, Tenesa A, Liewald D, Luciano M, Lopez LM, Gow AJ, Corley J, Redmond P, Fox HC, Rowe SJ, Haggarty P, McNeill G, Goddard ME, Porteous DJ, Whalley LJ, Starr JM, Visscher PM.

Nature. 2012 Jan 18;482(7384):212-5. doi: 10.1038/nature10781.

PMID:
22258510
3.

Genome-wide association studies establish that human intelligence is highly heritable and polygenic.

Davies G, Tenesa A, Payton A, Yang J, Harris SE, Liewald D, Ke X, Le Hellard S, Christoforou A, Luciano M, McGhee K, Lopez L, Gow AJ, Corley J, Redmond P, Fox HC, Haggarty P, Whalley LJ, McNeill G, Goddard ME, Espeseth T, Lundervold AJ, Reinvang I, Pickles A, Steen VM, Ollier W, Porteous DJ, Horan M, Starr JM, Pendleton N, Visscher PM, Deary IJ.

Mol Psychiatry. 2011 Oct;16(10):996-1005. doi: 10.1038/mp.2011.85. Epub 2011 Aug 9.

4.

Genome-wide association study of intelligence: additive effects of novel brain expressed genes.

Loo SK, Shtir C, Doyle AE, Mick E, McGough JJ, McCracken J, Biederman J, Smalley SL, Cantor RM, Faraone SV, Nelson SF.

J Am Acad Child Adolesc Psychiatry. 2012 Apr;51(4):432-440.e2. doi: 10.1016/j.jaac.2012.01.006. Epub 2012 Feb 28.

PMID:
22449649
5.
6.

Replication study of candidate genes for cognitive abilities: the Lothian Birth Cohort 1936.

Houlihan LM, Harris SE, Luciano M, Gow AJ, Starr JM, Visscher PM, Deary IJ.

Genes Brain Behav. 2009 Mar;8(2):238-47. doi: 10.1111/j.1601-183X.2008.00470.x. Epub 2008 Dec 10.

7.

Analysis of the genetics of boar taint reveals both single SNPs and regional effects.

Rowe SJ, Karacaören B, de Koning DJ, Lukic B, Hastings-Clark N, Velander I, Haley CS, Archibald AL.

BMC Genomics. 2014 Jun 3;15:424. doi: 10.1186/1471-2164-15-424.

8.

A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence.

Spain SL, Pedroso I, Kadeva N, Miller MB, Iacono WG, McGue M, Stergiakouli E, Smith GD, Putallaz M, Lubinski D, Meaburn EL, Plomin R, Simpson MA.

Mol Psychiatry. 2016 Aug;21(8):1145-51. doi: 10.1038/mp.2015.108. Epub 2015 Aug 4.

9.

Genome-wide association study of tick resistance in South African Nguni cattle.

Mapholi NO, Maiwashe A, Matika O, Riggio V, Bishop SC, MacNeil MD, Banga C, Taylor JF, Dzama K.

Ticks Tick Borne Dis. 2016 Apr;7(3):487-97. doi: 10.1016/j.ttbdis.2016.02.005. Epub 2016 Feb 17.

PMID:
26897394
10.

Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).

Davies G, Armstrong N, Bis JC, Bressler J, Chouraki V, Giddaluru S, Hofer E, Ibrahim-Verbaas CA, Kirin M, Lahti J, van der Lee SJ, Le Hellard S, Liu T, Marioni RE, Oldmeadow C, Postmus I, Smith AV, Smith JA, Thalamuthu A, Thomson R, Vitart V, Wang J, Yu L, Zgaga L, Zhao W, Boxall R, Harris SE, Hill WD, Liewald DC, Luciano M, Adams H, Ames D, Amin N, Amouyel P, Assareh AA, Au R, Becker JT, Beiser A, Berr C, Bertram L, Boerwinkle E, Buckley BM, Campbell H, Corley J, De Jager PL, Dufouil C, Eriksson JG, Espeseth T, Faul JD, Ford I; Generation Scotland, Gottesman RF, Griswold ME, Gudnason V, Harris TB, Heiss G, Hofman A, Holliday EG, Huffman J, Kardia SL, Kochan N, Knopman DS, Kwok JB, Lambert JC, Lee T, Li G, Li SC, Loitfelder M, Lopez OL, Lundervold AJ, Lundqvist A, Mather KA, Mirza SS, Nyberg L, Oostra BA, Palotie A, Papenberg G, Pattie A, Petrovic K, Polasek O, Psaty BM, Redmond P, Reppermund S, Rotter JI, Schmidt H, Schuur M, Schofield PW, Scott RJ, Steen VM, Stott DJ, van Swieten JC, Taylor KD, Trollor J, Trompet S, Uitterlinden AG, Weinstein G, Widen E, Windham BG, Jukema JW, Wright AF, Wright MJ, Yang Q, Amieva H, Attia JR, Bennett DA, Brodaty H, de Craen AJ, Hayward C, Ikram MA, Lindenberger U, Nilsson LG, Porteous DJ, Räikkönen K, Reinvang I, Rudan I, Sachdev PS, Schmidt R, Schofield PR, Srikanth V, Starr JM, Turner ST, Weir DR, Wilson JF, van Duijn C, Launer L, Fitzpatrick AL, Seshadri S, Mosley TH Jr, Deary IJ.

Mol Psychiatry. 2015 Feb;20(2):183-92. doi: 10.1038/mp.2014.188. Epub 2015 Feb 3.

11.

Genome-wide association study for endocrine fertility traits using single nucleotide polymorphism arrays and sequence variants in dairy cattle.

Tenghe AMM, Bouwman AC, Berglund B, Strandberg E, de Koning DJ, Veerkamp RF.

J Dairy Sci. 2016 Jul;99(7):5470-5485. doi: 10.3168/jds.2015-10533. Epub 2016 May 4.

PMID:
27157577
12.

Methodological Considerations in Estimation of Phenotype Heritability Using Genome-Wide SNP Data, Illustrated by an Analysis of the Heritability of Height in a Large Sample of African Ancestry Adults.

Chen F, He J, Zhang J, Chen GK, Thomas V, Ambrosone CB, Bandera EV, Berndt SI, Bernstein L, Blot WJ, Cai Q, Carpten J, Casey G, Chanock SJ, Cheng I, Chu L, Deming SL, Driver WR, Goodman P, Hayes RB, Hennis AJ, Hsing AW, Hu JJ, Ingles SA, John EM, Kittles RA, Kolb S, Leske MC, Millikan RC, Monroe KR, Murphy A, Nemesure B, Neslund-Dudas C, Nyante S, Ostrander EA, Press MF, Rodriguez-Gil JL, Rybicki BA, Schumacher F, Stanford JL, Signorello LB, Strom SS, Stevens V, Van Den Berg D, Wang Z, Witte JS, Wu SY, Yamamura Y, Zheng W, Ziegler RG, Stram AH, Kolonel LN, Le Marchand L, Henderson BE, Haiman CA, Stram DO.

PLoS One. 2015 Jun 30;10(6):e0131106. doi: 10.1371/journal.pone.0131106. eCollection 2015.

13.

Estimation of Genetic Relationships Between Individuals Across Cohorts and Platforms: Application to Childhood Height.

Fedko IO, Hottenga JJ, Medina-Gomez C, Pappa I, van Beijsterveldt CE, Ehli EA, Davies GE, Rivadeneira F, Tiemeier H, Swertz MA, Middeldorp CM, Bartels M, Boomsma DI.

Behav Genet. 2015 Sep;45(5):514-28. doi: 10.1007/s10519-015-9725-7. Epub 2015 Jun 3.

14.

Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins.

Hill WD, Davies G, van de Lagemaat LN, Christoforou A, Marioni RE, Fernandes CP, Liewald DC, Croning MD, Payton A, Craig LC, Whalley LJ, Horan M, Ollier W, Hansell NK, Wright MJ, Martin NG, Montgomery GW, Steen VM, Le Hellard S, Espeseth T, Lundervold AJ, Reinvang I, Starr JM, Pendleton N, Grant SG, Bates TC, Deary IJ.

Transl Psychiatry. 2014 Jan 7;4:e341. doi: 10.1038/tp.2013.114.

15.

Childhood intelligence is heritable, highly polygenic and associated with FNBP1L.

Benyamin B, Pourcain B, Davis OS, Davies G, Hansell NK, Brion MJ, Kirkpatrick RM, Cents RA, Franić S, Miller MB, Haworth CM, Meaburn E, Price TS, Evans DM, Timpson N, Kemp J, Ring S, McArdle W, Medland SE, Yang J, Harris SE, Liewald DC, Scheet P, Xiao X, Hudziak JJ, de Geus EJ; Wellcome Trust Case Control Consortium 2 (WTCCC2), Jaddoe VW, Starr JM, Verhulst FC, Pennell C, Tiemeier H, Iacono WG, Palmer LJ, Montgomery GW, Martin NG, Boomsma DI, Posthuma D, McGue M, Wright MJ, Davey Smith G, Deary IJ, Plomin R, Visscher PM.

Mol Psychiatry. 2014 Feb;19(2):253-8. doi: 10.1038/mp.2012.184. Epub 2013 Jan 29.

16.

Genome-wide association of breast cancer: composite likelihood with imputed genotypes.

Politopoulos I, Gibson J, Tapper W, Ennis S, Eccles D, Collins A.

Eur J Hum Genet. 2011 Feb;19(2):194-9. doi: 10.1038/ejhg.2010.157. Epub 2010 Oct 20.

17.

Single Nucleotide Polymorphism Heritability of Behavior Problems in Childhood: Genome-Wide Complex Trait Analysis.

Pappa I, Fedko IO, Mileva-Seitz VR, Hottenga JJ, Bakermans-Kranenburg MJ, Bartels M, van Beijsterveldt CE, Jaddoe VW, Middeldorp CM, Rippe RC, Rivadeneira F, Tiemeier H, Verhulst FC, van IJzendoorn MH, Boomsma DI.

J Am Acad Child Adolesc Psychiatry. 2015 Sep;54(9):737-44. doi: 10.1016/j.jaac.2015.06.004. Epub 2015 Jun 20. Erratum in: J Am Acad Child Adolesc Psychiatry. 2015 Nov;54(11):965.

PMID:
26299295
18.

Localising loci underlying complex trait variation using Regional Genomic Relationship Mapping.

Nagamine Y, Pong-Wong R, Navarro P, Vitart V, Hayward C, Rudan I, Campbell H, Wilson J, Wild S, Hicks AA, Pramstaller PP, Hastie N, Wright AF, Haley CS.

PLoS One. 2012;7(10):e46501. doi: 10.1371/journal.pone.0046501. Epub 2012 Oct 15.

19.

Genome-wide analysis of the heritability of amyotrophic lateral sclerosis.

Keller MF, Ferrucci L, Singleton AB, Tienari PJ, Laaksovirta H, Restagno G, Chiò A, Traynor BJ, Nalls MA.

JAMA Neurol. 2014 Sep;71(9):1123-34. doi: 10.1001/jamaneurol.2014.1184. Erratum in: JAMA Neurol. 2014 Oct;71(10):1328.

20.

Genetic variations of human neuropsin gene and psychiatric disorders: polymorphism screening and possible association with bipolar disorder and cognitive functions.

Izumi A, Iijima Y, Noguchi H, Numakawa T, Okada T, Hori H, Kato T, Tatsumi M, Kosuga A, Kamijima K, Asada T, Arima K, Saitoh O, Shiosaka S, Kunugi H.

Neuropsychopharmacology. 2008 Dec;33(13):3237-45. doi: 10.1038/npp.2008.29. Epub 2008 Mar 19.

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