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A genome-wide association study identifies five loci influencing facial morphology in EuropeansThe ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligenceSubcortical brain alterations in major depressive disorder: findings from the ENIGMA Major Depressive Disorder working groupThe ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic dataCommon Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adultsDyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sampleMeta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking.Genetic influences on handedness: data from 25,732 Australian and Dutch twin familiesCommon variants in the trichohyalin gene are associated with straight hair in EuropeansNovel genetic loci underlying human intracranial volume identified through genome-wide associationDyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutationGenome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis ConsortiumThe genetic correlation between height and IQ: shared genes or assortative mating?Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficitsCognitive function in adolescence: testing for interactions between breast-feeding and FADS2 polymorphismsA haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling abilityThe Brisbane Systems Genetics Study: genetical genomics meets complex trait geneticsAssessing Variations in Areal Organization for the Intrinsic Brain: From Fingerprints to ReliabilityGenetic imaging consortium for addiction medicine: From neuroimaging to genesGenetic and Environmental Contributions to Functional Connectivity Architecture of the Human BrainCommon genetic variants associated with cognitive performance identified using the proxy-phenotype methodMulti-site study of additive genetic effects on fractional anisotropy of cerebral white matter: Comparing meta and megaanalytical approaches for data poolingGenome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption.Genetic basis of a cognitive complexity metricDevelopment of brain structural connectivity between ages 12 and 30: a 4-Tesla diffusion imaging study in 439 adolescents and adults.Harmonization of Neuroticism and Extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of Item Response Theory.Investigating brain connectivity heritability in a twin study using diffusion imaging data.ENIGMA and the individual: Predicting factors that affect the brain in 35 countries worldwide.Robust Identification of Partial-Correlation Based Networks with Applications to Cortical Thickness Data.Handedness in twins: joint analysis of data from 35 samples.Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control.Genotype by environment interactions in cognitive ability: a survey of 14 studies from four countries covering four age groups.Development of insula connectivity between ages 12 and 30 revealed by high angular resolution diffusion imaging.DEVELOPMENT OF THE "RICH CLUB" IN BRAIN CONNECTIVITY NETWORKS FROM 438 ADOLESCENTS & ADULTS AGED 12 TO 30Short telomere length is associated with impaired cognitive performance in European ancestry cohorts.Genetic contribution to individual variation in binocular rivalry rateA commonly carried genetic variant in the delta opioid receptor gene, OPRD1, is associated with smaller regional brain volumes: replication in elderly and young populationsCortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group.A variant in LIN28B is associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure.Automatic clustering and population analysis of white matter tracts using maximum density paths.
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P50
description
hulumtuese
@sq
researcher
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wetenschapper
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հետազոտող
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name
Margaret J Wright
@nl
Margaret J Wright
@sl
Margaret J. Wright
@en
Margaret J. Wright
@es
type
label
Margaret J Wright
@nl
Margaret J Wright
@sl
Margaret J. Wright
@en
Margaret J. Wright
@es
altLabel
M J Wright
@en
Margaret J Wright
@en
Margaret Wright
@en
Margie
@en
Wright MJ
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prefLabel
Margaret J Wright
@nl
Margaret J Wright
@sl
Margaret J. Wright
@en
Margaret J. Wright
@es
P1053
A-4560-2016
P106
P1153
57204537248
7401558228
P21
P2456
P31
P3829
P496
0000-0001-7133-4970