Lista de obras - Julien Bryois - Dominio Público Uruguay

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

Author Correction: Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk

scientific article published on 01 March 2020

Automated protein-DNA interaction screening of Drosophila regulatory elements

artículo científico publicado en 2011

Biological annotation of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals.

artículo científico publicado en 2018

Building a schizophrenia genetic network: Transcription Factor 4 regulates genes involved in neuronal development and schizophrenia risk

Building a schizophrenia genetic network: transcription factor 4 regulates genes involved in neuronal development and schizophrenia risk

scientific article published on 01 September 2018

Cis and trans effects of human genomic variants on gene expression.

artículo científico publicado en 2014

Comparative genetic architectures of schizophrenia in East Asian and European populations

artículo científico publicado en 2019

Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders

artículo científico publicado en 2020

Coordinated effects of sequence variation on DNA binding, chromatin structure, and transcription

artículo científico publicado en 2013

Correction: Passive and active DNA methylation and the interplay with genetic variation in gene regulation

artículo científico publicado en 2013

Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophrenia

artículo científico publicado en 2018

Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder.

artículo científico publicado en 2018

Functional consequences of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals

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

article

Genetic identification of brain cell types underlying schizophrenia

scientific article published on 21 May 2018

Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease

artículo científico publicado en 2020

Genetic meta-analysis identifies 9 novel loci and functional pathways for Alzheimers disease risk

Genome-wide Analysis of Insomnia (N=1,331,010) Identifies Novel Loci and Functional Pathways

artículo científico publicado en 2018

Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income

artículo científico publicado en 2019

Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways

scientific article published on 25 February 2019

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 association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.

artículo científico publicado en 2019

Genome-wide association study of post-traumatic stress disorder reexperiencing symptoms in >165,000 US veterans

scientific article published on 29 July 2019

Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk

scholarly article by Iris E Jansen et al published March 2019 in Nature Genetics

Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk

Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia

artículo científico publicado en 2020

Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders

artículo científico publicado en 2017

Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways

scientific article published on 25 June 2018

Obesity remodels activity and transcriptional state of a lateral hypothalamic brake on feeding

scientific article published on 27 June 2019

Passive and active DNA methylation and the interplay with genetic variation in gene regulation

artículo científico publicado en 2013

Reproducible Genetic Risk Loci for Anxiety: Results From ∼200,000 Participants in the Million Veteran Program

scientific article published on 07 January 2020

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

artículo científico publicado en 2020

Single cell analysis of autism patient with bi-allelic NRXN1-alpha deletion reveals skewed fate choice in neural progenitors and impaired neuronal functionality

scientific article published on 12 July 2019

Single nuclei RNAseq stratifies multiple sclerosis patients into distinct white matter glial responses

artículo científico publicado en 2022

The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls

scientific article published on 01 November 2019

Time-dependent genetic effects on gene expression implicate aging processes

artículo científico publicado en 2017

Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicing

artículo científico publicado en 2015

Whole exome sequencing of a dominant retinitis pigmentosa family identifies a novel deletion in PRPF31

scientific article published on 07 April 2014

Lista de obras de Julien Bryois

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

Author Correction: Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk

Automated protein-DNA interaction screening of Drosophila regulatory elements

Biological annotation of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals.

Building a schizophrenia genetic network: Transcription Factor 4 regulates genes involved in neuronal development and schizophrenia risk

Building a schizophrenia genetic network: transcription factor 4 regulates genes involved in neuronal development and schizophrenia risk

Cis and trans effects of human genomic variants on gene expression.

Comparative genetic architectures of schizophrenia in East Asian and European populations

Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders

Coordinated effects of sequence variation on DNA binding, chromatin structure, and transcription

Correction: Passive and active DNA methylation and the interplay with genetic variation in gene regulation

Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophrenia

Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder.

Functional consequences of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals

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

Genetic identification of brain cell types underlying schizophrenia

Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease

Genetic meta-analysis identifies 9 novel loci and functional pathways for Alzheimers disease risk

Genome-wide Analysis of Insomnia (N=1,331,010) Identifies Novel Loci and Functional Pathways

Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income

Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways

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 association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.

Genome-wide association study of post-traumatic stress disorder reexperiencing symptoms in >165,000 US veterans

Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk

Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk

Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia

Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders

Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways

Obesity remodels activity and transcriptional state of a lateral hypothalamic brake on feeding

Passive and active DNA methylation and the interplay with genetic variation in gene regulation

Reproducible Genetic Risk Loci for Anxiety: Results From ∼200,000 Participants in the Million Veteran Program

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

Single cell analysis of autism patient with bi-allelic NRXN1-alpha deletion reveals skewed fate choice in neural progenitors and impaired neuronal functionality

Single nuclei RNAseq stratifies multiple sclerosis patients into distinct white matter glial responses

The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls

Time-dependent genetic effects on gene expression implicate aging processes

Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicing

Whole exome sequencing of a dominant retinitis pigmentosa family identifies a novel deletion in PRPF31