List of works - Andrew A Brown

A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

scientific article published on 24 March 2017

A complete tool set for molecular QTL discovery and analysis

scientific article

Age-dependent changes in mean and variance of gene expression across tissues in a twin cohort

scientific article published on 8 December 2017

Age-dependent changes in mean and variance of gene expression across tissues in a twin cohort

article

Association analysis of ANK3 gene variants in nordic bipolar disorder and schizophrenia case-control samples

article

Associations between variants near a monoaminergic pathways gene (PHOX2B) and amygdala reactivity: a genome-wide functional imaging study

scientific article published in June 2012

CACNA1C risk variant and amygdala activity in bipolar disorder, schizophrenia and healthy controls

scientific article

Candidate gene analysis of the human natural killer-1 carbohydrate pathway and perineuronal nets in schizophrenia: B3GAT2 is associated with disease risk and cortical surface area

scientific article

Cell type-specific genetic regulation of gene expression across human tissues

scientific article published on 01 September 2020

Common genetic variants influence human subcortical brain structures

scientific article

Common sequence variants in the major histocompatibility complex region associate with cerebral ventricular size in schizophrenia

scientific article published on 22 April 2011

Cross-tissue eQTL enrichment of associations in schizophrenia

scientific article published in PLoS ONE

Effect of DISC1 SNPs on brain structure in healthy controls and patients with a history of psychosis

scientific article published on 19 July 2012

Estimating the causal tissues for complex traits and diseases

scientific article

Evaluation of PAX3 genetic variants and nevus number.

scientific article published on 4 July 2013

Fast and efficient QTL mapper for thousands of molecular phenotypes.

scientific article published on 26 December 2015

Gene expression changes with age in skin, adipose tissue, blood and brain

scientific article

Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort

scientific journal article

Gene-gene and gene-environment interactions detected by transcriptome sequence analysis in twins

scientific article

Genetic interactions affecting human gene expression identified by variance association mapping

scientific article

Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach.

scientific article

Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma

scientific article published on 11 January 2016

Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis

scientific article

Genome-wide association study identifies genetic loci associated with body mass index and high density lipoprotein-cholesterol levels during psychopharmacological treatment - a cross-sectional naturalistic study

scientific article

Identification of common variants associated with human hippocampal and intracranial volumes

scientific article published on 15 April 2012

Influence of genetic variants on gene expression in human pancreatic islets – implications for type 2 diabetes

article

Local genetic effects on gene expression across 44 human tissues

article

Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans

scientific article published on 29 May 2015

Pathway analysis of genetic markers associated with a functional MRI faces paradigm implicates polymorphisms in calcium responsive pathways

scientific article published on 27 December 2012

Pathway-based factor analysis of gene expression data produces highly heritable phenotypes that associate with age.

scientific article

Predicting causal variants affecting expression by using whole-genome sequencing and RNA-seq from multiple human tissues

scientific article

Quantifying the degree of sharing of genetic and non-genetic causes of gene expression variability across four tissues

article

Quantifying the regulatory effect size of cis-acting genetic variation using allelic fold change.

scientific article published on 11 October 2017

Sex-dependent association of common variants of microcephaly genes with brain structure

scientific article

The impact of sex on gene expression across human tissues

scientific article

Time-dependent genetic effects on gene expression implicate aging processes

scientific article

ZNF804A and cortical thickness in schizophrenia and bipolar disorder

scientific article published on 4 April 2013

veqtl-mapper: variance association mapping for molecular phenotypes

scientific article published on 25 April 2017

List of works by Andrew A Brown

A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

A complete tool set for molecular QTL discovery and analysis

Age-dependent changes in mean and variance of gene expression across tissues in a twin cohort

Age-dependent changes in mean and variance of gene expression across tissues in a twin cohort

Association analysis of ANK3 gene variants in nordic bipolar disorder and schizophrenia case-control samples

Associations between variants near a monoaminergic pathways gene (PHOX2B) and amygdala reactivity: a genome-wide functional imaging study

CACNA1C risk variant and amygdala activity in bipolar disorder, schizophrenia and healthy controls

Candidate gene analysis of the human natural killer-1 carbohydrate pathway and perineuronal nets in schizophrenia: B3GAT2 is associated with disease risk and cortical surface area

Cell type-specific genetic regulation of gene expression across human tissues

Common genetic variants influence human subcortical brain structures

Common sequence variants in the major histocompatibility complex region associate with cerebral ventricular size in schizophrenia

Cross-tissue eQTL enrichment of associations in schizophrenia

Effect of DISC1 SNPs on brain structure in healthy controls and patients with a history of psychosis

Estimating the causal tissues for complex traits and diseases

Evaluation of PAX3 genetic variants and nevus number.

Fast and efficient QTL mapper for thousands of molecular phenotypes.

Gene expression changes with age in skin, adipose tissue, blood and brain

Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort

Gene-gene and gene-environment interactions detected by transcriptome sequence analysis in twins

Genetic interactions affecting human gene expression identified by variance association mapping

Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach.

Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma

Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis

Genome-wide association study identifies genetic loci associated with body mass index and high density lipoprotein-cholesterol levels during psychopharmacological treatment - a cross-sectional naturalistic study

Identification of common variants associated with human hippocampal and intracranial volumes

Influence of genetic variants on gene expression in human pancreatic islets – implications for type 2 diabetes

Local genetic effects on gene expression across 44 human tissues

Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans

Pathway analysis of genetic markers associated with a functional MRI faces paradigm implicates polymorphisms in calcium responsive pathways

Pathway-based factor analysis of gene expression data produces highly heritable phenotypes that associate with age.

Predicting causal variants affecting expression by using whole-genome sequencing and RNA-seq from multiple human tissues

Quantifying the degree of sharing of genetic and non-genetic causes of gene expression variability across four tissues

Quantifying the regulatory effect size of cis-acting genetic variation using allelic fold change.

Sex-dependent association of common variants of microcephaly genes with brain structure

The impact of sex on gene expression across human tissues

Time-dependent genetic effects on gene expression implicate aging processes

ZNF804A and cortical thickness in schizophrenia and bipolar disorder

veqtl-mapper: variance association mapping for molecular phenotypes