Lista de obras - Jens Treutlein - Dominio Público Uruguay

A common risk variant in CACNA1C supports a sex-dependent effect on longitudinal functioning and functional recovery from episodes of schizophrenia-spectrum but not bipolar disorder

artículo científico publicado en 2015

A mega-analysis of genome-wide association studies for major depressive disorder

artículo científico publicado en 2012

A putative high risk diplotype of the G72 gene is in healthy individuals associated with better performance in working memory functions and altered brain activity in the medial temporal lobe

artículo científico publicado en 2009

A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry

artículo científico publicado en 2010

Analysis of Rare Variants in the Alcohol Dependence Candidate Gene GATA4

scientific article published on 04 July 2016

Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder

artículo científico publicado en 2014

Association between dopa decarboxylase gene variants and borderline personality disorder

artículo científico publicado en 2014

Association between neuropeptide Y receptor Y2 promoter variant rs6857715 and major depressive disorder

artículo científico publicado en 2016

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 of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts

artículo científico publicado en 2015

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics

article

Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter

artículo científico publicado en 2009

Effect of the G72 (DAOA) putative risk haplotype on cognitive functions in healthy subjects

artículo científico publicado en 2009

Effects of the circadian rhythm gene period 1 (per1) on psychosocial stress-induced alcohol drinking

artículo científico publicado en 2011

Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder

scientific article published on 29 November 2018

Expert and self-assessment of lifetime symptoms and diagnosis of major depressive disorder in large-scale genetic studies in the general population: comparison of a clinical interview and a self-administered checklist

artículo científico

Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder

artículo científico publicado en 2017

Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis

artículo científico

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia

artículo científico publicado en 2012

Genetic variation in the G72 gene is associated with increased frontotemporal fiber tract integrity

artículo científico publicado en 2014

Genetic variation in the schizophrenia-risk gene neuregulin 1 correlates with brain activation and impaired speech production in a verbal fluency task in healthy individuals

artículo científico

Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with differences in frontal brain activation in a working memory task in healthy individuals

artículo científico publicado en 2008

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

artículo científico publicado en 2018

Genome-wide association study identifies 30 loci associated with bipolar disorder.

artículo científico publicado en 2019

Genome-wide association study of alcohol dependence

scientific journal article

Genome-wide association study reveals two new risk loci for bipolar disorder

artículo científico publicado en 2014

Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression

artículo científico publicado en 2010

Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster

artículo científico publicado en 2011

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genotype-phenotype association mining in bipolar disorder: market research meets complex genetics

article

Glutamate receptor δ 1 (GRID1) genetic variation and brain structure in schizophrenia

artículo científico publicado en 2012

Identification of shared risk loci and pathways for bipolar disorder and schizophrenia

artículo científico publicado en 2017

Impact of schizophrenia-risk gene dysbindin 1 on brain activation in bilateral middle frontal gyrus during a working memory task in healthy individuals

artículo científico publicado en 2010

Impact on birth weight of maternal smoking throughout pregnancy mediated by DNA methylation

artículo científico publicado en 2018

Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia

artículo científico publicado en 2014

NCAN Cross-Disorder Risk Variant Is Associated With Limbic Gray Matter Deficits in Healthy Subjects and Major Depression

artículo científico publicado en 2015

No association between a common haplotype of the 6 and 10-repeat alleles in intron 8 and the 3'UTR of the DAT1 gene and adult attention deficit hyperactivity disorder

artículo científico publicado en 2007

Shared genetic etiology between alcohol dependence and major depressive disorder.

artículo científico publicado en 2018

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

artículo científico publicado en 2020

Smoking behaviour: investigation of the coaction of environmental and genetic risk factors

artículo científico publicado en 2014

Systematic analysis of glutamatergic neurotransmission genes in alcohol dependence and adolescent risky drinking behavior

artículo científico publicado en 2008

The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: findings from a large German case-control and family-based sample

artículo científico publicado en 2010

The effect of G72 genotype on neural correlates of memory encoding and retrieval

artículo científico publicado en 2009

The effect of Neuregulin 1 on neural correlates of episodic memory encoding and retrieval

artículo científico publicado en 2009

The impact of a Dysbindin schizophrenia susceptibility variant on fiber tract integrity in healthy individuals: a TBSS-based diffusion tensor imaging study

artículo científico publicado en 2011

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

Volition diminishes genetically mediated amygdala hyperreactivity

artículo científico publicado en 2009

XRCC5 as a risk gene for alcohol dependence: evidence from a genome-wide gene-set-based analysis and follow-up studies in Drosophila and humans

artículo científico publicado en 2014

αCaMKII autophosphorylation controls the establishment of alcohol drinking behavior

artículo científico publicado en 2013

Lista de obras de Jens Treutlein

A common risk variant in CACNA1C supports a sex-dependent effect on longitudinal functioning and functional recovery from episodes of schizophrenia-spectrum but not bipolar disorder

A mega-analysis of genome-wide association studies for major depressive disorder

A putative high risk diplotype of the G72 gene is in healthy individuals associated with better performance in working memory functions and altered brain activity in the medial temporal lobe

A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry

Analysis of Rare Variants in the Alcohol Dependence Candidate Gene GATA4

Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder

Association between dopa decarboxylase gene variants and borderline personality disorder

Association between neuropeptide Y receptor Y2 promoter variant rs6857715 and major depressive disorder

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 of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics

Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter

Effect of the G72 (DAOA) putative risk haplotype on cognitive functions in healthy subjects

Effects of the circadian rhythm gene period 1 (per1) on psychosocial stress-induced alcohol drinking

Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder

Expert and self-assessment of lifetime symptoms and diagnosis of major depressive disorder in large-scale genetic studies in the general population: comparison of a clinical interview and a self-administered checklist

Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder

Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia

Genetic variation in the G72 gene is associated with increased frontotemporal fiber tract integrity

Genetic variation in the schizophrenia-risk gene neuregulin 1 correlates with brain activation and impaired speech production in a verbal fluency task in healthy individuals

Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with differences in frontal brain activation in a working memory task in healthy individuals

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

Genome-wide association study identifies 30 loci associated with bipolar disorder.

Genome-wide association study of alcohol dependence

Genome-wide association study reveals two new risk loci for bipolar disorder

Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression

Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Genotype-phenotype association mining in bipolar disorder: market research meets complex genetics

Glutamate receptor δ 1 (GRID1) genetic variation and brain structure in schizophrenia

Identification of shared risk loci and pathways for bipolar disorder and schizophrenia

Impact of schizophrenia-risk gene dysbindin 1 on brain activation in bilateral middle frontal gyrus during a working memory task in healthy individuals

Impact on birth weight of maternal smoking throughout pregnancy mediated by DNA methylation

Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia

NCAN Cross-Disorder Risk Variant Is Associated With Limbic Gray Matter Deficits in Healthy Subjects and Major Depression

No association between a common haplotype of the 6 and 10-repeat alleles in intron 8 and the 3'UTR of the DAT1 gene and adult attention deficit hyperactivity disorder

Shared genetic etiology between alcohol dependence and major depressive disorder.

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

Smoking behaviour: investigation of the coaction of environmental and genetic risk factors

Systematic analysis of glutamatergic neurotransmission genes in alcohol dependence and adolescent risky drinking behavior

The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: findings from a large German case-control and family-based sample

The effect of G72 genotype on neural correlates of memory encoding and retrieval

The effect of Neuregulin 1 on neural correlates of episodic memory encoding and retrieval

The impact of a Dysbindin schizophrenia susceptibility variant on fiber tract integrity in healthy individuals: a TBSS-based diffusion tensor imaging study

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

Volition diminishes genetically mediated amygdala hyperreactivity

XRCC5 as a risk gene for alcohol dependence: evidence from a genome-wide gene-set-based analysis and follow-up studies in Drosophila and humans

αCaMKII autophosphorylation controls the establishment of alcohol drinking behavior