about
Prestin, a cochlear motor protein, is defective in non-syndromic hearing lossOn the association of common and rare genetic variation influencing body mass index: a combined SNP and CNV analysisACSL6 is associated with the number of cigarettes smoked and its expression is altered by chronic nicotine exposure.In silico whole genome association scan for murine prepulse inhibition.Identification of quantitative trait loci and candidate genes for an anxiolytic-like response to ethanol in BXD recombinant inbred strainsAssociation analysis of the PIP4K2A gene on chromosome 10p12 and schizophrenia in the Irish study of high density schizophrenia families (ISHDSF) and the Irish case-control study of schizophrenia (ICCSS).Genetic effects influencing risk for major depressive disorder in China and Europe.Age of onset and family history as indicators of polygenic risk for major depression.Comprehensive gene-based association study of a chromosome 20 linked region implicates novel risk loci for depressive symptoms in psychotic illness.Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis.Genomewide association study of movement-related adverse antipsychotic effects.Copy number variation accuracy in genome-wide association studies.Prioritization and association analysis of murine-derived candidate genes in anxiety-spectrum disorders.Genetic risk sum score comprised of common polygenic variation is associated with body mass indexMeta-analyses of genome-wide linkage scans of anxiety-related phenotypesUsing genetic information from candidate gene and genome-wide association studies in risk prediction for alcohol dependence.Molecular validation of the schizophrenia spectrum.SNP-based heritability estimates of the personality dimensions and polygenic prediction of both neuroticism and major depression: findings from CONVERGE.11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project.Molecular Genetic Influences on Normative and Problematic Alcohol Use in a Population-Based Sample of College Students.The utility of empirically assigning ancestry groups in cross-population genetic studies of addiction.The Genetic Architecture of Major Depressive Disorder in Han Chinese Women.ALDH2*2 and peer drinking in East Asian college students.Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.Efficient calculation of empirical P-values for genome-wide linkage analysis through weighted permutation.A simple yet accurate correction for winner's curse can predict signals discovered in much larger genome scans.CHRONICITY OF DEPRESSION AND MOLECULAR MARKERS IN A LARGE SAMPLE OF HAN CHINESE WOMEN.Novel linkage to chromosome 20p using latent classes of psychotic illness in 270 Irish high-density families.A multi-dimensional evidence-based candidate gene prioritization approach for complex diseases-schizophrenia as a case.(1)H nuclear magnetic resonance metabolomics analysis identifies novel urinary biomarkers for lung function.A genome-wide significant linkage for severe depression on chromosome 3: the depression network study.Clinical features of psychotic disorders and polymorphisms in HT2A, DRD2, DRD4, SLC6A3 (DAT1), and BDNF: a family based association study.Genome-wide scans of three independent sets of 90 Irish multiplex schizophrenia families and follow-up of selected regions in all families provides evidence for multiple susceptibility genes.No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF).Genomewide linkage study in the Irish affected sib pair study of alcohol dependence: evidence for a susceptibility region for symptoms of alcohol dependence on chromosome 4.Catechol-O-methyltransferase and the clinical features of psychosis.Identification of susceptibility loci for alcohol-related traits in the Irish Affected Sib Pair Study of Alcohol Dependence.Quantitative linkage genome scan for atopy in a large collection of Caucasian families.A joint genomewide linkage analysis of symptoms of alcohol dependence and conduct disorder.Model-based gene selection shows engrailed 1 is associated with antipsychotic response.
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description
hulumtues
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researcher
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wetenschapper
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հետազոտող
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name
Bradley T Webb
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Bradley T Webb
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Bradley T Webb
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Bradley T Webb
@nl
Bradley T Webb
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type
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Bradley T Webb
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Bradley T Webb
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Bradley T Webb
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Bradley T Webb
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Bradley T Webb
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Bradley T. Webb
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Webb BT
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Bradley T Webb
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Bradley T Webb
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Bradley T Webb
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Bradley T Webb
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Bradley T Webb
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P1053
B-1459-2009
P106
P21
P2456
P2798
P31
P3829
P496
0000-0002-0576-5366