Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseasesAssumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblingsA genome-wide association study identifies five loci influencing facial morphology in EuropeansGenome-wide linkage and association analyses implicate FASN in predisposition to Uterine LeiomyomataMeta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorderGenetic studies of body mass index yield new insights for obesity biologySubcortical brain alterations in major depressive disorder: findings from the ENIGMA Major Depressive Disorder working groupReplicability and robustness of genome-wide-association studies for behavioral traitsGWAS of 126,559 individuals identifies genetic variants associated with educational attainmentThe ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic dataA genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personalityGenome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorderGenetic 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 associationGenome-wide association study reveals two new risk loci for bipolar disorderGenome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis ConsortiumGenetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficitsGenetic relationship between five psychiatric disorders estimated from genome-wide SNPsDirectional dominance on stature and cognition in diverse human populationsCommon genetic variants associated with cognitive performance identified using the proxy-phenotype methodGenome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architectureGenetic variants associated with disordered eatingA quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implicationsGenome-wide meta-analysis identifies new susceptibility loci for migraine.Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.Genome-wide analysis identifies 12 loci influencing human reproductive behavior.Genetic basis of a cognitive complexity metricAn integrated phenomic approach to multivariate allelic association.Whole-genome analyses of whole-brain data: working within an expanded search spaceENIGMA and the individual: Predicting factors that affect the brain in 35 countries worldwide.Handedness in twins: joint analysis of data from 35 samples.Multivariate genetic analyses of the 2D:4D ratio: examining the effects of hand and measurement technique in data from 757 twin families.ViewPoint and ViewDist: utilities for rapid graphing of linkage distributions and identification of outliers.Linkage analysis of a model quantitative trait in humans: finger ridge count shows significant multivariate linkage to 5q14.1.A note on the parameterization of Purcell's G x E model for ordinal and binary data.Modeling extended twin family data I: description of the Cascade model.Modeling extended twin family data II: power associated with different family structures.Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control.Does the sex of one's co-twin affect height and BMI in adulthood? A study of dizygotic adult twins from 31 cohorts
P50
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P50
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Sarah E Medland
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Sarah E Medland
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Sarah E. Medland
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Sarah E Medland
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Sarah E Medland
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Sarah E. Medland
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S E Medland
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Sarah E Medland
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Sarah Edkins
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Sarah Elizabeth Medland
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Sarah Medland
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Sarah E Medland
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Sarah E Medland
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Sarah E. Medland
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Sarah E. Medland
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P1053
C-7630-2013
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