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Volumn 169, Issue 2, 2012, Pages 186-194

Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD

(58)  Stergiakouli, Evangelia a,b,c,d   Hamshere, Marian a,b,c,d   Holmans, Peter a,b,c,d   Langley, Kate a,b,c,d   Zaharieva, Irina a,b,c,d   Hawi, Ziarah a,b,c,d   Kent, Lindsey a,b,c,d   Gill, Michael a,b,c,d   Williams, Nigel a,b,c,d   Owen, Michael J a,b,c,d   O'Donovan, Michael a,b,c,d   Thapar, Anita a,b,c,d   Faraone, Stephen V e   Neale, Benjamin M f,g   Ripke, Stephan f,g   Daly, Mark f,g   Medland, Sarah E g,h   Asherson, Philip i   Franke, Barbara j   Steinhausen, Hans Christoph k,l   more..


Author keywords

[No Author keywords available]

Indexed keywords

CHOLESTEROL; DNA; NICOTINIC RECEPTOR;

EID: 84863116416     PISSN: 0002953X     EISSN: 15357228     Source Type: Journal    
DOI: 10.1176/appi.ajp.2011.11040551     Document Type: Article
Times cited : (172)

References (40)
  • 2
    • 80053924932 scopus 로고    scopus 로고
    • Fitting the pieces together: Current research on the genetic basis of attention-deficit/hyperactivity disorder (ADHD)
    • Stergiakouli E, Thapar A: Fitting the pieces together: current research on the genetic basis of attention-deficit/hyperactivity disorder (ADHD). Neuropsychiatr Dis Treat 2010; 6:551-560
    • (2010) Neuropsychiatr Dis Treat , vol.6 , pp. 551-560
    • Stergiakouli, E.1    Thapar, A.2
  • 11
    • 45549110436 scopus 로고    scopus 로고
    • Genome-wide association studies in psychiatry: Lessons from early studies of non-psychiatric and psychiatric phenotypes
    • DOI 10.1038/mp.2008.45, PII MP200845
    • Craddock N, O'Donovan MC, Owen MJ: Genome-wide association studies in psychiatry: lessons from early studies of nonpsychiatric and psychiatric phenotypes. Mol Psychiatry 2008; 13:649-653 (Pubitemid 351861534)
    • (2008) Molecular Psychiatry , vol.13 , Issue.7 , pp. 649-653
    • Craddock, N.1    O'Donovan, M.C.2    Owen, M.J.3
  • 12
    • 67651113905 scopus 로고    scopus 로고
    • Genome-wide association studies in ADHD
    • Franke B, Neale BM, Faraone SV: Genome-wide association studies in ADHD. Hum Genet 2009; 126:13-50
    • (2009) Hum Genet , vol.126 , pp. 13-50
    • Franke, B.1    Neale, B.M.2    Faraone, S.V.3
  • 13
    • 34948877698 scopus 로고    scopus 로고
    • Prediction of individual genetic risk to disease from genome-wide association studies
    • Wray NR, Goddard ME, Visscher PM: Prediction of individual genetic risk to disease from genome-wide association studies. Genome Res 2007; 17:1520-158
    • (2007) Genome Res , vol.17 , pp. 1520-2158
    • Wray, N.R.1    Goddard, M.E.2    Visscher, P.M.3
  • 14
    • 13144265739 scopus 로고    scopus 로고
    • Genome-wide association studies: Theoretical and practical concerns
    • DOI 10.1038/nrg1522
    • Wang W, Barratt B, Clayton D, Todd J: Genome-wide association studies: theoretical and practical concerns. Nat Rev Genet 2005; 6:109-118 (Pubitemid 40179533)
    • (2005) Nature Reviews Genetics , vol.6 , Issue.2 , pp. 109-118
    • Wang, W.Y.S.1    Barratt, B.J.2    Clayton, D.G.3    Todd, J.A.4
  • 20
    • 84969213492 scopus 로고    scopus 로고
    • Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
    • The Wellcome Trust Case Control Consortium
    • The Wellcome Trust Case Control Consortium: Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 2007; 447:661-678
    • (2007) Nature , vol.447 , pp. 661-678
  • 21
    • 24944580962 scopus 로고    scopus 로고
    • Design of case-controls studies with unscreened controls
    • DOI 10.1111/j.1529-8817.2005.00175.x
    • Moskvina V, Holmans P, Schmidt KM, Craddock N: Design of case-controls studies with unscreened controls. Ann Hum Genet 2005; 69(part 5):566-576 (Pubitemid 41309434)
    • (2005) Annals of Human Genetics , vol.69 , Issue.5 , pp. 566-576
    • Moskvina, V.1    Holmans, P.2    Schmidt, K.M.3    Craddock, N.4
  • 24
    • 35948984173 scopus 로고    scopus 로고
    • PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
    • DOI 10.1101/gr.6861907
    • Wang K, Li M, Hadley D, Liu R, Glessner J, Grant SF, Hakonarson H, Bucan M: PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. Genome Res 2007; 17:1665-1674 (Pubitemid 350074862)
    • (2007) Genome Research , vol.17 , Issue.11 , pp. 1665-1674
    • Wang, K.1    Li, M.2    Hadley, D.3    Liu, R.4    Glessner, J.5    Grant, S.F.A.6    Hakonarson, H.7    Bucan, M.8
  • 25
    • 33746512512 scopus 로고    scopus 로고
    • Principal components analysis corrects for stratification in genome-wide association studies
    • DOI 10.1038/ng1847, PII NG1847
    • Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D: Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 2006; 38:904-909 (Pubitemid 44141658)
    • (2006) Nature Genetics , vol.38 , Issue.8 , pp. 904-909
    • Price, A.L.1    Patterson, N.J.2    Plenge, R.M.3    Weinblatt, M.E.4    Shadick, N.A.5    Reich, D.6
  • 26
    • 43249125992 scopus 로고    scopus 로고
    • Estimation of the multiple testing burden for genomewide association studies of nearly all common variants
    • DOI 10.1002/gepi.20303
    • Pe'er I, Yelensky R, Altshuler D, Daly MJ: Estimation of the multiple testing burden for genomewide association studies of nearly all common variants. Genet Epidemiol 2008; 32:381-385 (Pubitemid 351656309)
    • (2008) Genetic Epidemiology , vol.32 , Issue.4 , pp. 381-385
    • Pe'er, I.1    Yelensky, R.2    Altshuler, D.3    Daly, M.J.4
  • 27
    • 67649345185 scopus 로고
    • An improved Bonferroni procedure for multiple tests of significance
    • Simes RJ: An improved Bonferroni procedure for multiple tests of significance. Biometrika 1986; 73:751-754
    • (1986) Biometrika , vol.73 , pp. 751-754
    • Simes, R.J.1
  • 31
    • 75549084894 scopus 로고    scopus 로고
    • PANTHER version 7: Improved phylogenetic trees, orthologs and collaboration with the Gene Ontology Consortium
    • Mi H, Dong Q, Muruganujan A, Gaudet P, Lewis S, Thomas PD: PANTHER version 7: improved phylogenetic trees, orthologs and collaboration with the Gene Ontology Consortium. Nucleic Acids Res 2010; 38:D204-D210
    • (2010) Nucleic Acids Res , vol.38
    • Mi, H.1    Dong, Q.2    Muruganujan, A.3    Gaudet, P.4    Lewis, S.5    Thomas, P.D.6
  • 33
    • 78049450213 scopus 로고    scopus 로고
    • Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function
    • Raychaudhuri S, Korn JM, McCarroll SA, Altshuler D, Sklar P, Purcell S, Daly MJ: Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. PLoS Genet 2010; 6:e1001097
    • (2010) PLoS Genet , vol.6
    • Raychaudhuri, S.1    Korn, J.M.2    McCarroll, S.A.3    Altshuler, D.4    Sklar, P.5    Purcell, S.6    Daly, M.J.7
  • 34
    • 77955397870 scopus 로고    scopus 로고
    • Single particle tracking of alpha7 nicotinic AChR in hippocampal neurons reveals regulated confinement at glutamatergic and GABAergic perisynaptic sites
    • Burli T, Baer K, Ewers H, Sidler C, Fuhrer C, Fritschy JM: Single particle tracking of alpha7 nicotinic AChR in hippocampal neurons reveals regulated confinement at glutamatergic and GABAergic perisynaptic sites. PLoS One 2010; 5:e11507
    • (2010) PLoS One , vol.5
    • Burli, T.1    Baer, K.2    Ewers, H.3    Sidler, C.4    Fuhrer, C.5    Fritschy, J.M.6
  • 35
    • 29244456419 scopus 로고    scopus 로고
    • P50 sensory gating deficit in children with centrotemporal spikes and sharp waves in the EEG
    • DOI 10.1016/j.neulet.2005.09.071, PII S0304394005011316
    • Fiedler BJ, Debus OM, Neubauer BA, Kienle M, Kurlemann G: P50 sensory gating deficit in children with centrotemporal spikes and sharp waves in the EEG. Neurosci Lett 2006; 393:206-210 (Pubitemid 41821109)
    • (2006) Neuroscience Letters , vol.393 , Issue.2-3 , pp. 206-210
    • Fiedler, B.J.1    Debus, O.M.2    Neubauer, B.A.3    Kienle, M.4    Kurlemann, G.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.