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000136503 0247_ $$2doi$$a10.1038/ng.2238
000136503 0247_ $$2pmid$$apmid:22504419
000136503 0247_ $$2pmc$$apmc:PMC3773913
000136503 0247_ $$2ISSN$$a1061-4036
000136503 0247_ $$2ISSN$$a1546-1718
000136503 0247_ $$2altmetric$$aaltmetric:698606
000136503 037__ $$aDZNE-2020-02825
000136503 041__ $$aEnglish
000136503 082__ $$a570
000136503 1001_ $$aTaal, H Rob$$b0
000136503 245__ $$aCommon variants at 12q15 and 12q24 are associated with infant head circumference.
000136503 260__ $$aLondon$$bMacmillan Publishers Limited, part of Springer Nature$$c2012
000136503 264_1 $$2Crossref$$3online$$bSpringer Science and Business Media LLC$$c2012-04-15
000136503 264_1 $$2Crossref$$3print$$bSpringer Science and Business Media LLC$$c2012-05-01
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000136503 3367_ $$2ORCID$$aJOURNAL_ARTICLE
000136503 3367_ $$00$$2EndNote$$aJournal Article
000136503 520__ $$aTo identify genetic variants associated with head circumference in infancy, we performed a meta-analysis of seven genome-wide association studies (GWAS) (N = 10,768 individuals of European ancestry enrolled in pregnancy and/or birth cohorts) and followed up three lead signals in six replication studies (combined N = 19,089). rs7980687 on chromosome 12q24 (P = 8.1 × 10(-9)) and rs1042725 on chromosome 12q15 (P = 2.8 × 10(-10)) were robustly associated with head circumference in infancy. Although these loci have previously been associated with adult height, their effects on infant head circumference were largely independent of height (P = 3.8 × 10(-7) for rs7980687 and P = 1.3 × 10(-7) for rs1042725 after adjustment for infant height). A third signal, rs11655470 on chromosome 17q21, showed suggestive evidence of association with head circumference (P = 3.9 × 10(-6)). SNPs correlated to the 17q21 signal have shown genome-wide association with adult intracranial volume, Parkinson's disease and other neurodegenerative diseases, indicating that a common genetic variant in this region might link early brain growth with neurological disease in later life.
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000136503 542__ $$2Crossref$$i2012-04-15$$uhttp://www.springer.com/tdm
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000136503 650_7 $$2NLM Chemicals$$aGenetic Markers
000136503 650_2 $$2MeSH$$aChromosomes, Human, Pair 12: genetics
000136503 650_2 $$2MeSH$$aEuropean Continental Ancestry Group: genetics
000136503 650_2 $$2MeSH$$aFemale
000136503 650_2 $$2MeSH$$aGenetic Loci
000136503 650_2 $$2MeSH$$aGenetic Markers
000136503 650_2 $$2MeSH$$aGenome-Wide Association Study
000136503 650_2 $$2MeSH$$aHead: growth & development
000136503 650_2 $$2MeSH$$aHead: pathology
000136503 650_2 $$2MeSH$$aHumans
000136503 650_2 $$2MeSH$$aInfant
000136503 650_2 $$2MeSH$$aMale
000136503 650_2 $$2MeSH$$aMeta-Analysis as Topic
000136503 650_2 $$2MeSH$$aPolymorphism, Single Nucleotide: genetics
000136503 650_2 $$2MeSH$$aPregnancy
000136503 650_2 $$2MeSH$$aPregnancy Complications: etiology
000136503 650_2 $$2MeSH$$aPregnancy Complications: pathology
000136503 7001_ $$aPourcain, Beate St$$b1
000136503 7001_ $$aThiering, Elisabeth$$b2
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000136503 7001_ $$aMook-Kanamori, Dennis O$$b4
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000136503 7001_ $$aKlopp, Norman$$b26
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000136503 7001_ $$aEpidemiology, Cohorts for Heart and Aging Research in Genetic$$b39
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000136503 7001_ $$aEpidemiology, Early Genetics & Lifecourse$$b50
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000136503 7001_ $$0P:(DE-HGF)0$$aSmith, George Davey$$b83$$eCorresponding author
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000136503 7001_ $$0P:(DE-HGF)0$$aJaddoe, Vincent W V$$b87$$eCorresponding author
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000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1001/archneur.65.11.1473$$o10.1001/archneur.65.11.1473
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1016/j.neuropsychologia.2003.11.022$$o10.1016/j.neuropsychologia.2003.11.022
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1001/archpsyc.1996.01830070053009$$o10.1001/archpsyc.1996.01830070053009
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1016/S0899-9007(00)00431-7$$o10.1016/S0899-9007(00)00431-7
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1093/aje/kwj108$$o10.1093/aje/kwj108
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1542/peds.2005-2629$$o10.1542/peds.2005-2629
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1093/brain/awh034$$o10.1093/brain/awh034
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1001/archpedi.1976.02120060027006$$o10.1001/archpedi.1976.02120060027006
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1375/twin.13.4.370$$o10.1375/twin.13.4.370
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1002/ajmg.a.32434$$o10.1002/ajmg.a.32434
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1016/j.pneurobio.2009.11.002$$o10.1016/j.pneurobio.2009.11.002
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1016/j.molmed.2006.06.006$$o10.1016/j.molmed.2006.06.006
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1016/j.ajhg.2009.01.017$$o10.1016/j.ajhg.2009.01.017
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1203/00006450-200003000-00006$$o10.1203/00006450-200003000-00006
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1371/journal.pgen.1000952$$o10.1371/journal.pgen.1000952
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1371/journal.pgen.1000214$$o10.1371/journal.pgen.1000214
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1371/journal.pone.0010693$$o10.1371/journal.pone.0010693
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1371/journal.pbio.0060107$$o10.1371/journal.pbio.0060107
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1128/MCB.20.17.6300-6307.2000$$o10.1128/MCB.20.17.6300-6307.2000
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1091/mbc.7.9.1455$$o10.1091/mbc.7.9.1455
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1080/03014460600742062$$o10.1080/03014460600742062
000136503 999C5 $$2Crossref$$oCA Coyle-Thompson 1993$$y1993
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1158/1535-7163.MCT-06-0659$$o10.1158/1535-7163.MCT-06-0659
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1038/nrc1186$$o10.1038/nrc1186
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1086/427565$$o10.1086/427565
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1038/376771a0$$o10.1038/376771a0
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1038/ng.446$$o10.1038/ng.446
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1210/en.2009-1039$$o10.1210/en.2009-1039
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1074/jbc.R800013200$$o10.1074/jbc.R800013200
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.3233/JAD-2010-101011$$o10.3233/JAD-2010-101011
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1046/j.1471-4159.2004.02320.x$$o10.1046/j.1471-4159.2004.02320.x
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1136/jnnp.2003.015750$$o10.1136/jnnp.2003.015750
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1002/humu.20785$$o10.1002/humu.20785
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1093/bioinformatics/btp420$$o10.1093/bioinformatics/btp420
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1111/j.0006-341X.1999.00997.x$$o10.1111/j.0006-341X.1999.00997.x
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1136/bmj.327.7414.557$$o10.1136/bmj.327.7414.557
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1002/uog.5225$$o10.1002/uog.5225
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1161/CIRCGENETICS.108.829747$$o10.1161/CIRCGENETICS.108.829747
000136503 999C5 $$2Crossref$$9-- missing cx lookup --$$a10.1016/j.neurobiolaging.2006.12.012$$o10.1016/j.neurobiolaging.2006.12.012