Lista de obras - Jana Strohmaier - 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 contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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

Adverse reactions to antidepressants

artículo científico publicado en 2009

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder

article

Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample

artículo científico publicado en 2012

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

artículo científico publicado en 2016

Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder

artículo científico publicado en 2012

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

Attitudes toward the right to autonomous decision-making in psychiatric genetic testing: Controversial and context-dependent

scientific article published on 26 March 2019

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

scientific article published on 11 November 2019

Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin

artículo científico publicado en 2008

Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders.

artículo científico publicado en 2017

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

artículo científico publicado en 2016

Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis

artículo científico publicado en 2015

Copy number variants in German patients with schizophrenia

artículo científico publicado en 2013

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

Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium

artículo científico publicado en 2017

Effect of copy number variant burden on Global Assessment of Functioning in schizophrenia

artículo científico publicado en 2016

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

scientific article published on 29 November 2018

Epigenetic alteration of the dopamine transporter gene in alcohol-dependent patients is associated with age.

artículo científico publicado en 2012

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

G72 and its association with major depression and neuroticism in large population-based groups from Germany

artículo científico publicado en 2008

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

artículo científico publicado en 2017

Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders

artículo científico publicado en 2012

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 G72 correlates with brain activation in the right middle temporal gyrus in a verbal fluency task in healthy individuals

artículo científico publicado en 2011

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

artículo científico publicado en 2016

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

artículo científico publicado en 2018

Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder

artículo científico publicado en 2012

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

artículo científico publicado en 2019

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

artículo científico publicado en 2011

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

artículo científico publicado en 2016

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

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

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

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

article

Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1.

artículo científico publicado en 2016

Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2.

scientific article published on 23 September 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2018

Implication of a rare deletion at distal 16p11.2 in schizophrenia

artículo científico publicado en 2013

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

artículo científico publicado en 2014

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

artículo científico publicado en 2022

Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study

Investigation of SHANK3 in schizophrenia

artículo científico publicado en 2017

Investigation of the role of TCF4 rare sequence variants in schizophrenia

artículo científico publicado en 2015

Longer telomere length in patients with schizophrenia

artículo científico publicado en 2013

Low Birth Weight in MZ Twins Discordant for Birth Weight is Associated with Shorter Telomere Length and lower IQ, but not Anxiety/Depression in Later Life

artículo científico publicado en 2015

Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.

artículo científico publicado en 2010

Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder

artículo científico publicado en 2012

No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

artículo científico publicado en 2016

No association between genetic variants at the DGCR2 gene and schizophrenia in a German sample

article

No association between the serine racemase gene (SRR) and bipolar disorder in a German case-control sample

artículo científico publicado en 2007

No association between the serine racemase gene (SRR) and schizophrenia in a German case-control sample

artículo científico publicado en 2007

No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder

artículo científico publicado en 2013

Parents' Attitudes toward Clinical Genetic Testing for Autism Spectrum Disorder-Data from a Norwegian Sample

artículo científico publicado en 2017

Perceived stress and hair cortisol: Differences in bipolar disorder and schizophrenia

artículo científico publicado en 2016

Premorbid adjustment: a phenotype highlighting a distinction rather than an overlap between schizophrenia and bipolar disorder

artículo científico publicado en 2009

Response to the letter by Esteves et al

artículo científico publicado en 2018

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

Studies in humans and mice implicate neurocan in the etiology of mania

artículo científico publicado en 2012

Suicidal ideation during treatment of depression with escitalopram and nortriptyline in genome-based therapeutic drugs for depression (GENDEP): a clinical trial

artículo científico publicado en 2009

Telomere Length in Newborns is Related to Maternal Stress During Pregnancy.

artículo científico publicado en 2017

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 opioid peptides enkephalin and beta-endorphin in alcohol dependence

artículo científico publicado en 2008

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

Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families

scientific article published on 04 February 2020

Lista de obras de Jana Strohmaier

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

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

Adverse reactions to antidepressants

Analysis of shared heritability in common disorders of the brain

Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder

Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample

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

Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar 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

Attitudes toward the right to autonomous decision-making in psychiatric genetic testing: Controversial and context-dependent

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

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

Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin

Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders.

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

Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis

Copy number variants in German patients with schizophrenia

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

Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium

Effect of copy number variant burden on Global Assessment of Functioning in schizophrenia

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

Epigenetic alteration of the dopamine transporter gene in alcohol-dependent patients is associated with age.

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

G72 and its association with major depression and neuroticism in large population-based groups from Germany

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

Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders

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 G72 correlates with brain activation in the right middle temporal gyrus in a verbal fluency task in healthy individuals

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

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

Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder

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

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

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

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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

Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1.

Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2.

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

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

Implication of a rare deletion at distal 16p11.2 in schizophrenia

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

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study

Investigation of SHANK3 in schizophrenia

Investigation of the role of TCF4 rare sequence variants in schizophrenia

Longer telomere length in patients with schizophrenia

Low Birth Weight in MZ Twins Discordant for Birth Weight is Associated with Shorter Telomere Length and lower IQ, but not Anxiety/Depression in Later Life

Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.

Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder

No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

No association between genetic variants at the DGCR2 gene and schizophrenia in a German sample

No association between the serine racemase gene (SRR) and bipolar disorder in a German case-control sample

No association between the serine racemase gene (SRR) and schizophrenia in a German case-control sample

No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder

Parents' Attitudes toward Clinical Genetic Testing for Autism Spectrum Disorder-Data from a Norwegian Sample

Perceived stress and hair cortisol: Differences in bipolar disorder and schizophrenia

Premorbid adjustment: a phenotype highlighting a distinction rather than an overlap between schizophrenia and bipolar disorder

Response to the letter by Esteves et al

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

Studies in humans and mice implicate neurocan in the etiology of mania

Suicidal ideation during treatment of depression with escitalopram and nortriptyline in genome-based therapeutic drugs for depression (GENDEP): a clinical trial

Telomere Length in Newborns is Related to Maternal Stress During Pregnancy.

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 opioid peptides enkephalin and beta-endorphin in alcohol dependence

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

Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families