about
A population-specific HTR2B stop codon predisposes to severe impulsivityReplication of association between working memory and Reelin, a potential modifier gene in schizophreniaGenome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopiaReplication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia familiesNine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive errorGenome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohortsGenome-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.Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraineRole of nicotine dependence in the association between the dopamine receptor gene DRD3 and major depressive disorderMeta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder.Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortiumAnalysis of detailed phenotype profiles reveals CHRNA5-CHRNA3-CHRNB4 gene cluster association with several nicotine dependence traits.Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2.Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality ConsortiumMeta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error.Association of a nonsynonymous variant of DAOA with visuospatial ability in a bipolar family sample.Association of AKT1 with verbal learning, verbal memory, and regional cortical gray matter density in twins.Genome-wide association study on detailed profiles of smoking behavior and nicotine dependence in a twin sample.Does originating from a genetic isolate affect the level of cognitive impairments in schizophrenia families?Mixture model clustering of phenotype features reveals evidence for association of DTNBP1 to a specific subtype of schizophrenia.Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 (NLRP3) Gene.Analysis of shared heritability in common disorders of the brainErratum: A population-specific HTR2B stop codon predisposes to severe impulsivityGenome-wide association meta-analysis highlights light-induced signaling as a driver for refractive errorGenome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
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հետազոտող
@hy
name
Juho Wedenoja
@ast
Juho Wedenoja
@en
Juho Wedenoja
@es
Juho Wedenoja
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Juho Wedenoja
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Juho Wedenoja
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type
label
Juho Wedenoja
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Juho Wedenoja
@en
Juho Wedenoja
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Juho Wedenoja
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Juho Wedenoja
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Juho Wedenoja
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altLabel
Juho Olavi Wedenoja
@en
prefLabel
Juho Wedenoja
@ast
Juho Wedenoja
@en
Juho Wedenoja
@es
Juho Wedenoja
@fr
Juho Wedenoja
@nl
Juho Wedenoja
@sl
P106
P21
P31
P496
0000-0002-6155-0378