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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 x 10(-9)) and rs1042725 on chromosome 12q15 (P = 2.8 x 10(-10)) were robustly associated with head circumference in infancy. Although these loci have previously been associated with adult height(1), their effects on infant head circumference were largely independent of height (P = 3.8 x 10(-7) for rs7980687 and P = 1.3 x 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 x 10(-6)). SNPs correlated to the 17q21 signal have shown genome-wide association with adult intracranial volume(2), Parkinson's disease and other neurodegenerative diseases(3-5), indicating that a common genetic variant in this region might link early brain growth with neurological disease in later life.
Birth weight within the normal range is associated with a variety of adult-onset diseases, but the mechanisms behind these associations are poorly understood(1). Previous genome-wide association studies of birth weight identified a variant in the ADCY5 gene associated both with birth weight and type 2 diabetes and a second variant, near CCNL1, with no obvious link to adult traits(2). In an expanded genome-wide association metaanalysis and follow-up study of birth weight (of up to 69,308 individuals of European descent from 43 studies), we have now extended the number of loci associated at genome-wide significance to 7, accounting for a similar proportion of variance as maternal smoking. Five of the loci are known to be associated with other phenotypes: ADCY5 and CDKAL1 with type 2 diabetes, ADRB1 with adult blood pressure and HMGA2 and LCORL with adult height. Our findings highlight genetic links between fetal growth and postnatal growth and metabolism.
Geothermobarometric, radiogenic isotopic and thermochronologic data are used to track the influence of an ancient continental margin (Western Province) on development of an adjacent Carboniferous-Cretaceous magmatic arc (Outboard Median Batholith) in Fiordland, New Zealand. The data show a record of complicated Mesozoic Gondwana margin growth. Paragneiss within the Outboard Median Batholith is of Carboniferous to Jurassic age and records burial to middle crustal depths in Late Jurassic-Early Cretaceous during subduction-related plutonism and arc thickening. In contrast, Western Province metasedimentary rocks in the area of study immediately west of the Outboard Median Batholith are Late Cambrian-Early Ordovician in age, recrystallized at the amphibolite facies in the Late Devonian-Early Carboniferous and exhibit no evidence for Mesozoic textural or isotopic reequilibration. A phase of deformation, between 128 and 116 Ma deformed, exhumed, and cooled the Outboard Median Batholith to greenschist facies temperatures, while large parts of the Western Province underwent >= 9 kbar metamorphic conditions. Zircon grains from Mesozoic inboard plutons are isotopically more evolved (epsilon Hf(t) = +2.3 to +4.0) than those in the Outboard Median Batholith (epsilon Hf(t) = +9.4 to +11.1). The contrasting zircon Hf isotope ratios, absence of S-type plutons or Proterozoic-Early Paleozoic inherited zircon, and the apparent absence of Early Paleozoic metasedimentary rocks indicates that the Outboard Median Batholith is unlikely to be underlain by the Western Province continental lithosphere. The new data are consistent with the Outboard Median Batholith representing an allochthonous (although not necessarily exotic) arc that was juxtaposed onto the Gondwana continental margin along the intervening Grebe Mylonite Zone.