List of works - Morten Mattingsdal

A continuous genome assembly of the corkwing wrasse (Symphodus melops).

scientific article published on 14 April 2018

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

A genome-wide association study of anorexia nervosa

scientific article

A genome-wide association study of bipolar disorder in Norwegian individuals, followed by replication in Icelandic sample

scientific article published on 07 May 2010

Abundant genetic overlap between blood lipids and immune-mediated diseases indicates shared molecular genetic mechanisms

scientific article published on 8 April 2015

Altered Brain Activation during Emotional Face Processing in Relation to Both Diagnosis and Polygenic Risk of Bipolar Disorder

scientific article

Analysis of shared heritability in common disorders of the brain

scientific article published on 21 June 2018

Are keratoacanthomas variants of squamous cell carcinomas? A comparison of chromosomal aberrations by comparative genomic hybridization

scientific article published on 25 May 2006

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

article

Association analysis of PALB2 and BRCA2 in bipolar disorder and schizophrenia in a scandinavian case-control sample

article

Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans

scientific article published on 16 February 2012

Catechol O-methyltransferase variants and cognitive performance in schizophrenia and bipolar disorder versus controls

scientific article published on June 2010

Combining population genomics with demographic analyses highlights habitat patchiness and larval dispersal as determinants of connectivity in coastal fish species

scientific article published on 01 March 2022

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

scientific article

Correction: Abundant Genetic Overlap between Blood Lipids and Immune-Mediated Diseases Indicates Shared Molecular Genetic Mechanisms

scientific article published on 15 May 2015

Correction: Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate

scientific article published on 5 November 2015

DNA methylation and gene expression changes in monozygotic twins discordant for psoriasis: identification of epigenetically dysregulated genes

scientific article

Demographic history has shaped the strongly differentiated corkwing wrasse populations in Northern Europe

scientific article published on 04 December 2019

ELM server: A new resource for investigating short functional sites in modular eukaryotic proteins

scientific article

Effects of intronic mutations in the LDLR gene on pre-mRNA splicing: Comparison of wet-lab and bioinformatics analyses

scientific article

Expression of genes in normal human monocytes in response to Aspergillus fumigatus.

scientific article

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

scientific journal article

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

scientific article

Genetic Markers of Human Evolution Are Enriched in Schizophrenia

scientific article

Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci

scientific article

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

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 Study Reveals First Locus for Anorexia Nervosa and Metabolic Correlations

scholarly article

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

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

Genome-wide expression analysis of cells expressing gain of function mutant D374Y-PCSK9.

scientific article

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

scientific article published on 8 August 2017

Identification of common variants associated with human hippocampal and intracranial volumes

scientific article published on 15 April 2012

Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate

scientific article

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

scientific article

Intron 12 in NTRK3 is associated with bipolar disorder.

scientific article

Linkage-disequilibrium-based binning affects the interpretation of GWASs

scientific article published on 22 March 2012

MicroRNAs enrichment in GWAS of complex human phenotypes

scientific article

Mutations in the melanocortin 4 receptor (MC4R) gene in obese patients in Norway.

scientific article published on 19 March 2009

New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis

scientific article

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

Polygenic risk for schizophrenia associated with working memory-related prefrontal brain activation in patients with schizophrenia and healthy controls

scientific article

Polygenic risk score and the psychosis continuum model

scientific article published on 25 June 2014

SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome

scientific article published on 13 March 2008

Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia

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

scientific article

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

scientific article published on 16 February 2020

TCF4 sequence variants and mRNA levels are associated with neurodevelopmental characteristics in psychotic disorders

scientific article

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

scientific article

The genetic structure of the Swedish population

scientific article published in 2011

Up-regulation of NOTCH4 gene expression in bipolar disorder

scientific article published in December 2012

List of works by Morten Mattingsdal

A continuous genome assembly of the corkwing wrasse (Symphodus melops).

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

A genome-wide association study of anorexia nervosa

A genome-wide association study of bipolar disorder in Norwegian individuals, followed by replication in Icelandic sample

Abundant genetic overlap between blood lipids and immune-mediated diseases indicates shared molecular genetic mechanisms

Altered Brain Activation during Emotional Face Processing in Relation to Both Diagnosis and Polygenic Risk of Bipolar Disorder

Analysis of shared heritability in common disorders of the brain

Are keratoacanthomas variants of squamous cell carcinomas? A comparison of chromosomal aberrations by comparative genomic hybridization

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

Association analysis of PALB2 and BRCA2 in bipolar disorder and schizophrenia in a scandinavian case-control sample

Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans

Catechol O-methyltransferase variants and cognitive performance in schizophrenia and bipolar disorder versus controls

Combining population genomics with demographic analyses highlights habitat patchiness and larval dispersal as determinants of connectivity in coastal fish species

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

Correction: Abundant Genetic Overlap between Blood Lipids and Immune-Mediated Diseases Indicates Shared Molecular Genetic Mechanisms

Correction: Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate

DNA methylation and gene expression changes in monozygotic twins discordant for psoriasis: identification of epigenetically dysregulated genes

Demographic history has shaped the strongly differentiated corkwing wrasse populations in Northern Europe

ELM server: A new resource for investigating short functional sites in modular eukaryotic proteins

Effects of intronic mutations in the LDLR gene on pre-mRNA splicing: Comparison of wet-lab and bioinformatics analyses

Expression of genes in normal human monocytes in response to Aspergillus fumigatus.

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

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

Genetic Markers of Human Evolution Are Enriched in Schizophrenia

Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci

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

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

Genome-Wide Association Study Reveals First Locus for Anorexia Nervosa and Metabolic Correlations

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

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

Genome-wide expression analysis of cells expressing gain of function mutant D374Y-PCSK9.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

Identification of common variants associated with human hippocampal and intracranial volumes

Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate

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

Intron 12 in NTRK3 is associated with bipolar disorder.

Linkage-disequilibrium-based binning affects the interpretation of GWASs

MicroRNAs enrichment in GWAS of complex human phenotypes

Mutations in the melanocortin 4 receptor (MC4R) gene in obese patients in Norway.

New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis

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

Polygenic risk for schizophrenia associated with working memory-related prefrontal brain activation in patients with schizophrenia and healthy controls

Polygenic risk score and the psychosis continuum model

SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome

Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia

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

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

TCF4 sequence variants and mRNA levels are associated with neurodevelopmental characteristics in psychotic disorders

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

The genetic structure of the Swedish population

Up-regulation of NOTCH4 gene expression in bipolar disorder