Lista de obras - Per Qvist - Dominio Público Uruguay

Aberrant recombination and repair during immunoglobulin class switching in BRCA1-deficient human B cells

artículo científico publicado en 2015

Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder

artículo científico publicado en 2014

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

Brain proteome changes in female Brd1 mice unmask dendritic spine pathology and show enrichment for schizophrenia risk

scientific article published on 24 December 2018

Brain volumetric alterations accompanied with loss of striatal medium-sized spiny neurons and cortical parvalbumin expressing interneurons in Brd1 mice

artículo científico publicado en 2018

Circulating miRNAs as Potential Biomarkers for Patient Stratification in Bipolar Disorder: A Combined Review and Data Mining Approach

artículo científico publicado en 2022

Common risk variants identified in autism spectrum disorder

CtIP Mutations Cause Seckel and Jawad Syndromes

artículo científico publicado en 2011

DNA Methylation Analysis of BRD1 Promoter Regions and the Schizophrenia rs138880 Risk Allele

artículo científico publicado en 2017

Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq

artículo científico publicado en 2015

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 implicates CHRNA2 in cannabis use disorder

artículo científico publicado en 2019

Genome-wide association study implicatesCHRNA2in cannabis use disorder

Identification of common genetic risk variants for autism spectrum disorder

artículo científico publicado en 2019

Mice heterozygous for an inactivated allele of the schizophrenia associated Brd1 gene display selective cognitive deficits with translational relevance to schizophrenia

artículo científico publicado en 2017

Reduced Brd1 expression leads to reversible depression-like behaviors and gene-expression changes in female mice

artículo científico publicado en 2020

Size-Selective Phagocytic Clearance of Fibrillar α-Synuclein through Conformational Activation of Complement Receptor 4

artículo científico publicado en 2020

The Schizophrenia-Associated BRD1 Gene Regulates Behavior, Neurotransmission, and Expression of Schizophrenia Risk Enriched Gene Sets in Mice

artículo científico publicado en 2016

The effect of hypoxia on ZEB1 expression in a mimetic system of the blood-brain barrier

artículo científico publicado en 2018

The neurobiology of BRD1 implicates sex-biased dysregulation of nuclear receptor signaling in mental disorders

article

Lista de obras de Per Qvist

Aberrant recombination and repair during immunoglobulin class switching in BRCA1-deficient human B cells

Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes 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

Brain proteome changes in female Brd1 mice unmask dendritic spine pathology and show enrichment for schizophrenia risk

Brain volumetric alterations accompanied with loss of striatal medium-sized spiny neurons and cortical parvalbumin expressing interneurons in Brd1 mice

Circulating miRNAs as Potential Biomarkers for Patient Stratification in Bipolar Disorder: A Combined Review and Data Mining Approach

Common risk variants identified in autism spectrum disorder

CtIP Mutations Cause Seckel and Jawad Syndromes

DNA Methylation Analysis of BRD1 Promoter Regions and the Schizophrenia rs138880 Risk Allele

Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq

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

Genome-wide association study implicates CHRNA2 in cannabis use disorder

Genome-wide association study implicatesCHRNA2in cannabis use disorder

Identification of common genetic risk variants for autism spectrum disorder

Mice heterozygous for an inactivated allele of the schizophrenia associated Brd1 gene display selective cognitive deficits with translational relevance to schizophrenia

Reduced Brd1 expression leads to reversible depression-like behaviors and gene-expression changes in female mice

Size-Selective Phagocytic Clearance of Fibrillar α-Synuclein through Conformational Activation of Complement Receptor 4

The Schizophrenia-Associated BRD1 Gene Regulates Behavior, Neurotransmission, and Expression of Schizophrenia Risk Enriched Gene Sets in Mice

The effect of hypoxia on ZEB1 expression in a mimetic system of the blood-brain barrier

The neurobiology of BRD1 implicates sex-biased dysregulation of nuclear receptor signaling in mental disorders