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Extreme evolutionary disparities seen in positive selection across seven complex diseasesehavioral GeneticsThe role of the Asn40Asp polymorphism of the mu opioid receptor gene (OPRM1) on alcoholism etiology and treatment: a critical reviewThe Status of Irritability in Psychiatry: A Conceptual and Quantitative ReviewAnnual Research Review: Transdiagnostic neuroscience of child and adolescent mental disorders--differentiating decision making in attention-deficit/hyperactivity disorder, conduct disorder, depression, and anxietyIs Schizotypy per se a Suitable Endophenotype of Schizophrenia? - Do Not Forget to Distinguish Positive from Negative FacetsThe role of sleep dysfunction in the occurrence of delusions and hallucinations: A systematic reviewChild development and molecular genetics: 14 years laterThe role of the catechol-O-methyltransferase (COMT) gene in personality and related psychopathological disordersFrom temporal processing to developmental language disorders: mind the gap.Genetic determinants of depression: recent findings and future directionsConnecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 MiceOmics-Based Strategies in Precision Medicine: Toward a Paradigm Shift in Inborn Errors of Metabolism InvestigationsMapping asthma-associated variants in admixed populationsNeuron-based heredity and human evolutionAdditional mechanisms conferring genetic susceptibility to Alzheimer's diseaseInvestigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysisA latent variable partial least squares path modeling approach to regional association and polygenic effect with applications to a human obesity studyRecent advances in the genetics of language impairmentGenetic variants on chromosome 1q41 influence ocular axial length and high myopiaExcess of rare variants in genes identified by genome-wide association study of hypertriglyceridemiaAttentional but not pre-attentive neural measures of auditory discrimination are atypical in children with developmental language disorder.The clinical implications of mouse models of enhanced anxiety.Childhood IQ and risk of bipolar disorder in adulthood: prospective birth cohort studyA unified method for detecting secondary trait associations with rare variants: application to sequence data.Pathological implications of Th1/Th2 cytokine genetic variants in Behçet's disease: Data from a pilot study in a Sicilian population.Polygenic risk and the development and course of asthma: an analysis of data from a four-decade longitudinal studyIntegrative Analysis of Transcriptomic and Epigenomic Data to Reveal Regulation Patterns for BMD Variation.A powerful latent variable method for detecting and characterizing gene-based gene-gene interaction on multiple quantitative traitsCopy number variations play important roles in heredity of common diseases: a novel method to calculate heritability of a polymorphism.Amygdala reactivity and negative emotionality: divergent correlates of antisocial personality and psychopathy traits in a community samplePaternal Age Alters Social Development in Offspring.Epistasis and natural selection shape the mutational architecture of complex traits.Genetic variants and their interactions in the prediction of increased pre-clinical carotid atherosclerosis: the cardiovascular risk in young Finns study.Nature, Nurture, and ExpertiseMapping complex traits as a dynamic system.A genome-wide association study identifies multiple loci associated with mathematics ability and disabilityCommon SNPs in FTO gene are associated with obesity related anthropometric traits in an island population from the eastern Adriatic coast of Croatia.Polygenic risk predicts obesity in both white and black young adults.UGT1A1 sequence variants and bilirubin levels in early postnatal life: a quantitative approach
P2860
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P2860
description
article
@en
im Oktober 2009 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в жовтні 2009
@uk
name
Common disorders are quantitative traits
@en
Common disorders are quantitative traits
@nl
type
label
Common disorders are quantitative traits
@en
Common disorders are quantitative traits
@nl
prefLabel
Common disorders are quantitative traits
@en
Common disorders are quantitative traits
@nl
P356
P1476
Common disorders are quantitative traits
@en
P2093
Claire M. A. Haworth
Oliver S. P. Davis
P2888
P304
P356
10.1038/NRG2670
P577
2009-10-27T00:00:00Z