메뉴 건너뛰기




Volumn 44, Issue 5, 2012, Pages 539-544

Common variants at 6q22 and 17q21 are associated with intracranial volume

(129)  Ikram, M Arfan a,b,ag   Fornage, Myriam c,d,ag   Smith, Albert V e,f,ag   Seshadri, Sudha g,h,i,ag   Schmidt, Reinhold j,al   Debette, Stéphanie g,h,k   Vrooman, Henri A a   Sigurdsson, Sigurdur e   Ropele, Stefan j   Taal, H Rob a   Mook Kanamori, Dennis O a,l   Coker, Laura H m   Longstreth, W T n   Niessen, Wiro J a,o   Destefano, Anita L g,h,i   Beiser, Alexa g,h,i   Zijdenbos, Alex P p   Struchalin, Maksim a   Jack, Clifford R q   Rivadeneira, Fernando a   more..


Author keywords

[No Author keywords available]

Indexed keywords

AGED; ARTICLE; BRAIN SIZE; CEPHALOMETRY; CHROMOSOME 17Q; CHROMOSOME 17Q21; CHROMOSOME 6Q; CHROMOSOME 6Q22; FEMALE; GENE LOCUS; GENETIC ASSOCIATION; GENETIC VARIABILITY; HUMAN; MALE; PRIORITY JOURNAL;

EID: 84860342407     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.2245     Document Type: Article
Times cited : (98)

References (27)
  • 1
    • 33750111464 scopus 로고    scopus 로고
    • The influence of head growth in fetal life, infancy, and childhood on intelligence at the ages of 4 and 8 years
    • DOI 10.1542/peds.2005-2629
    • Gale, C.R., O'Callaghan, F.J., Bredow, M. & Martyn, C.N. The influence of head growth in fetal life, infancy, and childhood on intelligence at the ages of 4 and 8 years. Pediatrics 118, 1486-1492 (2006). (Pubitemid 46393794)
    • (2006) Pediatrics , vol.118 , Issue.4 , pp. 1486-1492
    • Gale, C.R.1    O'Callaghan, F.J.2    Bredow, M.3    Martyn, C.N.4
  • 2
    • 0742323508 scopus 로고    scopus 로고
    • Critical periods of brain growth and cognitive function in children
    • DOI 10.1093/brain/awh034
    • Gale, C.R., O'Callaghan, F.J., Godfrey, K.M., Law, C.M. & Martyn, C.N. Critical periods of brain growth and cognitive function in children. Brain 127, 321-329 (2004). (Pubitemid 38160317)
    • (2004) Brain , vol.127 , Issue.2 , pp. 321-329
    • Gale, C.R.1    O'Callaghan, F.J.2    Godfrey, K.M.3    Law, C.M.4    Martyn, C.N.5
  • 3
    • 11844288889 scopus 로고    scopus 로고
    • Measures of brain morphology and infarction in the framingham heart study: Establishing what is normal
    • DeCarli, C. et al. Measures of brain morphology and infarction in the framingham heart study: establishing what is normal. Neurobiol. Aging 26, 491-510 (2005).
    • (2005) Neurobiol. Aging , vol.26 , pp. 491-510
    • Decarli, C.1
  • 5
    • 0031778072 scopus 로고    scopus 로고
    • Evidence for genetic variance in white matter hyperintensity volume in normal elderly male twins
    • Carmelli, D. et al. Evidence for genetic variance in white matter hyperintensity volume in normal elderly male twins. Stroke 29, 1177-1181 (1998). (Pubitemid 28265474)
    • (1998) Stroke , vol.29 , Issue.6 , pp. 1177-1181
    • Carmelli, D.1    DeCarli, C.2    Swan, G.E.3    Jack, L.M.4    Reed, T.5    Wolf, P.A.6    Miller, B.L.7
  • 7
    • 63449100039 scopus 로고    scopus 로고
    • Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. Design of prospective meta-analyses of genome-wide association studies from 5 cohorts
    • Psaty, B.M. et al. Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. Design of prospective meta-analyses of genome-wide association studies from 5 cohorts. Circ. Cardiovasc. Genet. 2, 73-80 (2009).
    • (2009) Circ. Cardiovasc. Genet. , vol.2 , pp. 73-80
    • Psaty, B.M.1
  • 8
    • 77952307991 scopus 로고    scopus 로고
    • Genome-wide analysis of genetic loci associated with Alzheimer disease
    • Seshadri, S. et al. Genome-wide analysis of genetic loci associated with Alzheimer disease. J. Am. Med. Assoc. 303, 1832-1840 (2010).
    • (2010) J. Am. Med. Assoc. , vol.303 , pp. 1832-1840
    • Seshadri, S.1
  • 9
    • 65949090748 scopus 로고    scopus 로고
    • Genomewide association studies of stroke
    • Ikram, M.A. et al. Genomewide association studies of stroke. N. Engl. J. Med. 360, 1718-1728 (2009).
    • (2009) N. Engl. J. Med. , vol.360 , pp. 1718-1728
    • Ikram, M.A.1
  • 10
    • 84860324077 scopus 로고    scopus 로고
    • Common variants at 12q15 and 12q24 are associated with infant head circumference
    • 15 April doi:10.1038/ng.2238
    • Taal, H.R. et al. Common variants at 12q15 and 12q24 are associated with infant head circumference. Nat. Genet. published online (15 April 2012); doi:10.1038/ng.2238.
    • (2012) Nat. Genet. Published Online
    • Taal, H.R.1
  • 11
    • 77957947562 scopus 로고    scopus 로고
    • Hundreds of variants clustered in genomic loci and biological pathways affect human height
    • Lango Allen, H. et al. Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature 467, 832-838 (2010).
    • (2010) Nature , vol.467 , pp. 832-838
    • Lango Allen, H.1
  • 12
    • 77149123320 scopus 로고    scopus 로고
    • The H1 haplotype of the tau gene (MAPT) is associated with mild cognitive impairment
    • Di Maria, E. et al. The H1 haplotype of the tau gene (MAPT) is associated with mild cognitive impairment. J. Alzheimers Dis. 19, 909-914 (2010).
    • (2010) J. Alzheimers Dis. , vol.19 , pp. 909-914
    • Di Maria, E.1
  • 13
    • 50449104624 scopus 로고    scopus 로고
    • Evolutionary toggling of the MAPT 17q21.31 inversion region
    • Zody, M.C. et al. Evolutionary toggling of the MAPT 17q21.31 inversion region. Nat. Genet. 40, 1076-1083 (2008).
    • (2008) Nat. Genet. , vol.40 , pp. 1076-1083
    • Zody, M.C.1
  • 16
    • 56749171877 scopus 로고    scopus 로고
    • Granulin mutations associated with frontotemporal lobar degeneration and related disorders: An update
    • DOI 10.1002/humu.20785
    • Gijselinck, I., Van Broeckhoven, C. & Cruts, M. Granulin mutations associated with frontotemporal lobar degeneration and related disorders: an update. Hum. Mutat. 29, 1373-1386 (2008). (Pubitemid 352774891)
    • (2008) Human Mutation , vol.29 , Issue.12 , pp. 1373-1386
    • Gijselinck, I.1    Van Broeckhoven, C.2    Cruts, M.3
  • 17
    • 38149123302 scopus 로고    scopus 로고
    • Progranulin locus deletion in frontotemporal dementia
    • Gijselinck, I. et al. Progranulin locus deletion in frontotemporal dementia. Hum. Mutat. 29, 53-58 (2008).
    • (2008) Hum. Mutat. , vol.29 , pp. 53-58
    • Gijselinck, I.1
  • 18
    • 77149126400 scopus 로고    scopus 로고
    • Corticotropin-releasing hormone receptor-1 in cerebral microvessels changes during development and influences urocortin transport across the blood-brain barrier
    • Hsuchou, H., Kastin, A.J., Wu, X., Tu, H. & Pan, W. Corticotropin-releasing hormone receptor-1 in cerebral microvessels changes during development and influences urocortin transport across the blood-brain barrier. Endocrinology 151, 1221-1227 (2010).
    • (2010) Endocrinology , vol.151 , pp. 1221-1227
    • Hsuchou, H.1    Kastin, A.J.2    Wu, X.3    Tu, H.4    Pan, W.5
  • 21
    • 56049085381 scopus 로고    scopus 로고
    • Clinical and molecular delineation of the 17q21.31 microdeletion syndrome
    • Koolen, D.A. et al. Clinical and molecular delineation of the 17q21.31 microdeletion syndrome. J. Med. Genet. 45, 710-720 (2008).
    • (2008) J. Med. Genet. , vol.45 , pp. 710-720
    • Koolen, D.A.1
  • 22
    • 13944278863 scopus 로고    scopus 로고
    • A common inversion under selection in Europeans
    • Stefansson, H. et al. A common inversion under selection in Europeans. Nat. Genet. 37, 129-137 (2005).
    • (2005) Nat. Genet. , vol.37 , pp. 129-137
    • Stefansson, H.1
  • 23
    • 76349117214 scopus 로고    scopus 로고
    • The distribution and most recent common ancestor of the 17q21 inversion in humans
    • Donnelly, M.P. et al. The distribution and most recent common ancestor of the 17q21 inversion in humans. Am. J. Hum. Genet. 86, 161-171 (2010).
    • (2010) Am. J. Hum. Genet. , vol.86 , pp. 161-171
    • Donnelly, M.P.1
  • 24
    • 18144382265 scopus 로고    scopus 로고
    • Evolution of the brain and intelligence
    • DOI 10.1016/j.tics.2005.03.005
    • Roth, G. & Dicke, U. Evolution of the brain and intelligence. Trends Cogn. Sci. 9, 250-257 (2005). (Pubitemid 40615113)
    • (2005) Trends in Cognitive Sciences , vol.9 , Issue.5 , pp. 250-257
    • Roth, G.1    Dicke, U.2
  • 25
    • 0034074901 scopus 로고    scopus 로고
    • The thrombospondin type 1 repeat (TSR) superfamily: Diverse proteins with related roles in neuronal development
    • DOI 10.1002/(SICI)1097-0177(200006)218:2<280::AID-DVDY4>3.0.CO;2-0
    • Adams, J.C. & Tucker, R.P. The thrombospondin type 1 repeat (TSR) superfamily: diverse proteins with related roles in neuronal development. Dev. Dyn. 218, 280-299 (2000). (Pubitemid 30349640)
    • (2000) Developmental Dynamics , vol.218 , Issue.2 , pp. 280-299
    • Adams, J.C.1    Tucker, R.P.2
  • 26
    • 17144378894 scopus 로고    scopus 로고
    • The novel cytosolic RING finger protein dactylidin is up-regulated in brains of patients with Alzheimer's disease
    • DOI 10.1111/j.1460-9568.2005.03977.x
    • Von Rotz, R.C., Kins, S., Hipfel, R., von der Kammer, H. & Nitsch, R.M. The novel cytosolic RING finger protein dactylidin is up-regulated in brains of patients with Alzheimer's disease. Eur. J. Neurosci. 21, 1289-1298 (2005). (Pubitemid 40516627)
    • (2005) European Journal of Neuroscience , vol.21 , Issue.5 , pp. 1289-1298
    • Von Rotz, R.C.1    Kins, S.2    Hipfel, R.3    Von Der Kammer, H.4    Nitsch, R.M.5
  • 27
    • 33746512512 scopus 로고    scopus 로고
    • Price, A.L. et al. Nat. Genet. 38, 904-909 (2006).
    • (2006) Nat Genet. , vol.38 , pp. 904-909
    • Price, A.L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.