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Taal, HR; St Pourcain, B; Thiering, E; Das, S; Mook-Kanamori, DO; Warrington, NM; Kaakinen, M; Kreiner-Møller, E; Bradfield, JP; Freathy, RM; Geller, F; Guxens, M; Cousminer, DL; Kerkhof, M; Timpson, NJ; Ikram, MA; Beilin, LJ; Bønnelykke, K; Buxton, JL; Charoen, P; Chawes, BL; Eriksson, J; Evans, DM; Hofman, A; Kemp, JP; Kim, CE; Klopp, N; Lahti, J; Lye, SJ; McMahon, G; Mentch, FD; Müller-Nurasyid, M; O'Reilly, PF; Prokopenko, I; Rivadeneira, F; Steegers, EA; Sunyer, J; Tiesler, C; Yaghootkar, H; Cohorts for Heart and Aging Research in Genetic Epidemiology Consortium; Breteler, MM; Decarli, C; Breteler, MM; Debette, S; Fornage, M; Gudnason, V; Launer, LJ; van der Lugt, A; Mosley, TH; Seshadri, S; Smith, AV; Vernooij, MW; Early Genetics & Lifecourse Epidemiology Consortium; Blakemore, AI; Chiavacci, RM; Feenstra, B; Fernandez-Banet, J; Grant, SF; Hartikainen, AL; van der Heijden, AJ; Iñiguez, C; Lathrop, M; McArdle, WL; Mølgaard, A; Newnham, JP; Palmer, LJ; Palotie, A; Pouta, A; Ring, SM; Sovio, U; Standl, M; Uitterlinden, AG; Wichmann, HE; Vissing, NH; DeCarli, C; van Duijn, CM; McCarthy, MI; Koppelman, GH; Estivill, X; Hattersley, AT; Melbye, M; Bisgaard, H; Pennell, CE; Widen, E; Hakonarson, H; Smith, GD; Heinrich, J; Jarvelin, MR; Jaddoe, VW; Early Growth Genetics Consortium.
Common variants at 12q15 and 12q24 are associated with infant head circumference.
Nat Genet. 2012; 44(5):532-538 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Autor/innen der Med Uni Graz:
Ropele Stefan
Schmidt Helena
Schmidt Reinhold
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Abstract:
To 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.
Find related publications in this database (using NLM MeSH Indexing)
Chromosomes, Human, Pair 12 - genetics
European Continental Ancestry Group - genetics
Female -
Genetic Loci -
Genetic Markers -
Genome-Wide Association Study -
Head - growth & development
Humans -
Infant -
Male -
Meta-Analysis as Topic -
Polymorphism, Single Nucleotide - genetics
Pregnancy -
Pregnancy Complications - etiology

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