Lista de obras - Bradley T Webb - Dominio Público Uruguay

(1)H nuclear magnetic resonance metabolomics analysis identifies novel urinary biomarkers for lung function

artículo científico publicado en 2010

A Genome-Wide Analysis of Liberal and Conservative Political Attitudes

article

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A genome-wide scan for modifier loci in schizophrenia

artículo científico publicado en 2007

A genome-wide significant linkage for severe depression on chromosome 3: the depression network study

artículo científico publicado en 2011

A joint genomewide linkage analysis of symptoms of alcohol dependence and conduct disorder

artículo científico publicado en 2006

A large-scale genome-wide association study meta-analysis of cannabis use disorder

artículo científico publicado en 2020

A multi-dimensional evidence-based candidate gene prioritization approach for complex diseases-schizophrenia as a case

artículo científico publicado en 2009

A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity.

artículo científico publicado en 1995

A schizophrenia locus may be located in region 10p15-p11 ⬇️

artículo científico publicado el 10 de julio de 1998

A simple yet accurate correction for winner's curse can predict signals discovered in much larger genome scans

artículo científico publicado en 2016

ACSL6 is associated with the number of cigarettes smoked and its expression is altered by chronic nicotine exposure

artículo científico publicado en 2011

ALDH2*2 and peer drinking in East Asian college students

artículo científico publicado en 2017

Age of onset and family history as indicators of polygenic risk for major depression.

artículo científico publicado en 2017

An epigenome-wide association study of early-onset major depression in monozygotic twins

artículo científico publicado en 2020

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Association 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).

artículo científico publicado en 2010

Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

scholarly article by Miruna C. Barbu et al published July 2018 in Biological Psychiatry: Cognitive Neuroscience and Neuroimaging

Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis

artículo científico publicado en 2013

CHRONICITY OF DEPRESSION AND MOLECULAR MARKERS IN A LARGE SAMPLE OF HAN CHINESE WOMEN.

artículo científico publicado en 2016

Catechol-O-methyltransferase and the clinical features of psychosis.

artículo científico publicado en 2006

Clinical features of psychotic disorders and polymorphisms in HT2A, DRD2, DRD4, SLC6A3 (DAT1), and BDNF: a family based association study

artículo científico publicado en 2004

Comprehensive gene-based association study of a chromosome 20 linked region implicates novel risk loci for depressive symptoms in psychotic illness

artículo científico publicado en 2011

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

artículo científico publicado en 2016

Copy number variation accuracy in genome-wide association studies

artículo científico publicado en 2011

Efficient calculation of empirical P-values for genome-wide linkage analysis through weighted permutation

artículo científico publicado en 2008

Expanding the phenotype for the recurrent p.Ala391Glu variant in FGFR3: Beyond crouzon syndrome and acanthosis nigricans

artículo científico publicado en 2019

GWAS meta-analysis (N=279,930) identifies new genes and functional links to intelligence

article

Genetic effects influencing risk for major depressive disorder in China and Europe

artículo científico publicado en 2017

Genetic risk sum score comprised of common polygenic variation is associated with body mass index

artículo científico publicado en 2010

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

artículo científico publicado en 2018

Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence

article

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

artículo científico publicado en 2002

Genomewide association study of movement-related adverse antipsychotic effects

artículo científico publicado en 2009

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.

artículo científico publicado en 2006

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

artículo científico publicado en 2017

High-resolution mass spectrometry proteomics for the identification of candidate plasma protein biomarkers for chronic obstructive pulmonary disease

artículo científico publicado en 2010

Identification of quantitative trait loci and candidate genes for an anxiolytic-like response to ethanol in BXD recombinant inbred strains

artículo científico publicado en 2016

Identification of susceptibility loci for alcohol-related traits in the Irish Affected Sib Pair Study of Alcohol Dependence

artículo científico publicado en 2006

In silico whole genome association scan for murine prepulse inhibition

artículo científico publicado en 2009

Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium

artículo científico publicado en 2020

Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity

artículo científico publicado en 2018

Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes

artículo científico publicado en 2012

Model-based gene selection shows engrailed 1 is associated with antipsychotic response

artículo científico publicado en 2008

Molecular Genetic Analysis Subdivided by Adversity Exposure Suggests Etiologic Heterogeneity in Major Depression

artículo científico publicado en 2018

Molecular Genetic Influences on Normative and Problematic Alcohol Use in a Population-Based Sample of College Students

artículo científico publicado en 2017

Molecular validation of the schizophrenia spectrum.

artículo científico publicado en 2013

Multi-species data integration and gene ranking enrich significant results in an alcoholism genome-wide association study

artículo científico publicado en 2012

No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF).

artículo científico publicado en 2004

Novel linkage to chromosome 20p using latent classes of psychotic illness in 270 Irish high-density families

artículo científico publicado en 2008

On the association of common and rare genetic variation influencing body mass index: a combined SNP and CNV analysis

artículo científico publicado en 2014

Polygenic Risk Score Prediction of Alcohol Dependence Symptoms Across Population-Based and Clinically Ascertained Samples

artículo científico publicado en 2018

Polygenic prediction of the phenome, across ancestry, in emerging adulthood.

artículo científico publicado en 2017

Polygenic risk for severe psychopathology among Europeans is associated with major depressive disorder in Han Chinese women

artículo científico publicado en 2017

Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss

artículo científico publicado en 2003

Prioritization and association analysis of murine-derived candidate genes in anxiety-spectrum disorders

artículo científico publicado en 2011

Proteomic biomarkers in plasma that differentiate rapid and slow decline in lung function in adult cigarette smokers with chronic obstructive pulmonary disease (COPD).

artículo científico publicado en 2010

Quantitative linkage genome scan for atopy in a large collection of Caucasian families

artículo científico publicado en 2006

RETRACTED ARTICLE: 11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project

retracted scholarly article

Relationship between polygenic risk scores and symptom dimensions of schizophrenia and schizotypy in multiplex families with schizophrenia

artículo científico publicado en 2022

Replication of the Interaction of PRKG1 and Trauma Exposure on Alcohol Misuse in an Independent African American Sample

artículo científico publicado en 2018

SNP-based heritability estimates of the personality dimensions and polygenic prediction of both neuroticism and major depression: findings from CONVERGE.

scientific article published on 25 October 2016

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

artículo científico publicado en 2020

Significant correlation in linkage signals from genome-wide scans of schizophrenia and schizotypy

artículo científico publicado en 2007

TWAS pathway method greatly enhances the number of leads for uncovering the molecular underpinnings of psychiatric disorders

scientific article published on 21 September 2020

The Genetic Architecture of Major Depressive Disorder in Han Chinese Women

artículo científico publicado en 2016

The utility of empirically assigning ancestry groups in cross-population genetic studies of addiction

artículo científico

Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

scholarly article published 10 March 2018

Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

artículo científico publicado en 2018

Using genetic information from candidate gene and genome-wide association studies in risk prediction for alcohol dependence

artículo científico publicado en 2013

Lista de obras de Bradley T Webb

(1)H nuclear magnetic resonance metabolomics analysis identifies novel urinary biomarkers for lung function

A Genome-Wide Analysis of Liberal and Conservative Political Attitudes

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A genome-wide scan for modifier loci in schizophrenia

A genome-wide significant linkage for severe depression on chromosome 3: the depression network study

A joint genomewide linkage analysis of symptoms of alcohol dependence and conduct disorder

A large-scale genome-wide association study meta-analysis of cannabis use disorder

A multi-dimensional evidence-based candidate gene prioritization approach for complex diseases-schizophrenia as a case

A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity.

A schizophrenia locus may be located in region 10p15-p11 ⬇️

A simple yet accurate correction for winner's curse can predict signals discovered in much larger genome scans

ACSL6 is associated with the number of cigarettes smoked and its expression is altered by chronic nicotine exposure

ALDH2*2 and peer drinking in East Asian college students

Age of onset and family history as indicators of polygenic risk for major depression.

An epigenome-wide association study of early-onset major depression in monozygotic twins

Analysis of shared heritability in common disorders of the brain

Association 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).

Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis

CHRONICITY OF DEPRESSION AND MOLECULAR MARKERS IN A LARGE SAMPLE OF HAN CHINESE WOMEN.

Catechol-O-methyltransferase and the clinical features of psychosis.

Clinical features of psychotic disorders and polymorphisms in HT2A, DRD2, DRD4, SLC6A3 (DAT1), and BDNF: a family based association study

Comprehensive gene-based association study of a chromosome 20 linked region implicates novel risk loci for depressive symptoms in psychotic illness

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Copy number variation accuracy in genome-wide association studies

Efficient calculation of empirical P-values for genome-wide linkage analysis through weighted permutation

Expanding the phenotype for the recurrent p.Ala391Glu variant in FGFR3: Beyond crouzon syndrome and acanthosis nigricans

GWAS meta-analysis (N=279,930) identifies new genes and functional links to intelligence

Genetic effects influencing risk for major depressive disorder in China and Europe

Genetic risk sum score comprised of common polygenic variation is associated with body mass index

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence

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

Genomewide association study of movement-related adverse antipsychotic effects

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.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

High-resolution mass spectrometry proteomics for the identification of candidate plasma protein biomarkers for chronic obstructive pulmonary disease

Identification of quantitative trait loci and candidate genes for an anxiolytic-like response to ethanol in BXD recombinant inbred strains

Identification of susceptibility loci for alcohol-related traits in the Irish Affected Sib Pair Study of Alcohol Dependence

In silico whole genome association scan for murine prepulse inhibition

Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium

Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity

Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes

Model-based gene selection shows engrailed 1 is associated with antipsychotic response

Molecular Genetic Analysis Subdivided by Adversity Exposure Suggests Etiologic Heterogeneity in Major Depression

Molecular Genetic Influences on Normative and Problematic Alcohol Use in a Population-Based Sample of College Students

Molecular validation of the schizophrenia spectrum.

Multi-species data integration and gene ranking enrich significant results in an alcoholism genome-wide association study

No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF).

Novel linkage to chromosome 20p using latent classes of psychotic illness in 270 Irish high-density families

On the association of common and rare genetic variation influencing body mass index: a combined SNP and CNV analysis

Polygenic Risk Score Prediction of Alcohol Dependence Symptoms Across Population-Based and Clinically Ascertained Samples

Polygenic prediction of the phenome, across ancestry, in emerging adulthood.

Polygenic risk for severe psychopathology among Europeans is associated with major depressive disorder in Han Chinese women

Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss

Prioritization and association analysis of murine-derived candidate genes in anxiety-spectrum disorders

Proteomic biomarkers in plasma that differentiate rapid and slow decline in lung function in adult cigarette smokers with chronic obstructive pulmonary disease (COPD).

Quantitative linkage genome scan for atopy in a large collection of Caucasian families

RETRACTED ARTICLE: 11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project

Relationship between polygenic risk scores and symptom dimensions of schizophrenia and schizotypy in multiplex families with schizophrenia

Replication of the Interaction of PRKG1 and Trauma Exposure on Alcohol Misuse in an Independent African American Sample

SNP-based heritability estimates of the personality dimensions and polygenic prediction of both neuroticism and major depression: findings from CONVERGE.

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

Significant correlation in linkage signals from genome-wide scans of schizophrenia and schizotypy

TWAS pathway method greatly enhances the number of leads for uncovering the molecular underpinnings of psychiatric disorders

The Genetic Architecture of Major Depressive Disorder in Han Chinese Women

The utility of empirically assigning ancestry groups in cross-population genetic studies of addiction

Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

Using genetic information from candidate gene and genome-wide association studies in risk prediction for alcohol dependence