Skip to Main Content

Author Details

Morten Mattingsdal
Faculty of Engineering and Science University of Agder Kristiansand Norway.
2003
48
29
PMIDPaper TitleJournal TitlePublished Year
36861025Estimating number of European eel (<i>Anguilla anguilla</i>) individuals using environmental DNA and haplotype count in small rivers.Ecol Evol2023
37627152A Breast Cancer Polygenic Risk Score Is Feasible for Risk Stratification in the Norwegian Population.Cancers (Basel)2023
35229385Combining population genomics with demographic analyses highlights habitat patchiness and larval dispersal as determinants of connectivity in coastal fish species.Mol Ecol2022
32064741Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.Addict Biol2021
34002043The genetic structure of Norway.Eur J Hum Genet2021
31733084Demographic history has shaped the strongly differentiated corkwing wrasse populations in Northern Europe.Mol Ecol2020
29665418A continuous genome assembly of the corkwing wrasse (Symphodus melops).Genomics2018
29930110Analysis of shared heritability in common disorders of the brain.Science2018
27869829Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.Nat Genet2017
26681495Genetic Markers of Human Evolution Are Enriched in Schizophrenia.Biol Psychiatry2016
24468824Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci.Mol Psychiatry2015
26540268Correction: Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate.PLoS Genet2015
26286434New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis.Int J Epidemiol2015
26222050Altered Brain Activation during Emotional Face Processing in Relation to Both Diagnosis and Polygenic Risk of Bipolar Disorder.PLoS One2015
25884492MicroRNAs enrichment in GWAS of complex human phenotypes.BMC Genomics2015
25978331Correction: Abundant Genetic Overlap between Blood Lipids and Immune-Mediated Diseases Indicates Shared Molecular Genetic Mechanisms.PLoS One2015
25392519Polygenic risk for schizophrenia associated with working memory-related prefrontal brain activation in patients with schizophrenia and healthy controls.Schizophr Bull2015
24399358The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data.Brain Imaging Behav2014
24961959Polygenic risk score and the psychosis continuum model.Acta Psychiatr Scand2014
24514567A genome-wide association study of anorexia nervosa.Mol Psychiatry2014
23274185Pathway analysis of genetic markers associated with a functional MRI faces paradigm implicates polymorphisms in calcium responsive pathways.Neuroimage2013
23933821Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.Nat Genet2013
23637625Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate.PLoS Genet2013
22384057Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders.PLoS One2012
23212060Up-regulation of NOTCH4 gene expression in bipolar disorder.Am J Psychiatry2012
22832956TCF4 sequence variants and mRNA levels are associated with neurodevelopmental characteristics in psychotic disorders.Transl Psychiatry2012
22828495Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach.Transl Psychiatry2012
22504417Identification of common variants associated with human hippocampal and intracranial volumes.Nat Genet2012
22444669Linkage-disequilibrium-based binning affects the interpretation of GWASs.Am J Hum Genet2012
22291603DNA methylation and gene expression changes in monozygotic twins discordant for psoriasis: identification of epigenetically dysregulated genes.PLoS Genet2012
22343285Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans.Proc Natl Acad Sci U S A2012
22417934Genome-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.Psychiatry Res2012
20554328Intron 12 in NTRK3 is associated with bipolar disorder.Psychiatry Res2011
21829632The genetic structure of the Swedish population.PLoS One2011
21972176Association analysis of ANK3 gene variants in nordic bipolar disorder and schizophrenia case-control samples.Am J Med Genet B Neuropsychiatr Genet2011
20080800Sex-dependent association of common variants of microcephaly genes with brain structure.Proc Natl Acad Sci U S A2010
20872766Association analysis of PALB2 and BRCA2 in bipolar disorder and schizophrenia in a scandinavian case-control sample.Am J Med Genet B Neuropsychiatr Genet2010
20451256A genome-wide association study of bipolar disorder in Norwegian individuals, followed by replication in Icelandic sample.J Affect Disord2010
20605701Catechol O-methyltransferase variants and cognitive performance in schizophrenia and bipolar disorder versus controls.Schizophr Res2010
20185149Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort.J Psychiatr Res2010
19301229Mutations in the melanocortin 4 receptor (MC4R) gene in obese patients in Norway.Exp Clin Endocrinol Diabetes2009
19208450Effects of intronic mutations in the LDLR gene on pre-mRNA splicing: Comparison of wet-lab and bioinformatics analyses.Mol Genet Metab2009
18415839Expression of genes in normal human monocytes in response to Aspergillus fumigatus.Med Mycol2008
18570182Genome-wide expression analysis of cells expressing gain of function mutant D374Y-PCSK9.J Cell Physiol2008
18342287SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome.Am J Hum Genet2008
17594340Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia.Eur J Neurol2007
16728973Are keratoacanthomas variants of squamous cell carcinomas? A comparison of chromosomal aberrations by comparative genomic hybridization.J Invest Dermatol2006
12824381ELM server: A new resource for investigating short functional sites in modular eukaryotic proteins.Nucleic Acids Res2003
  • 1 - 48 of 48

Recommended Authors

Sarah A Gagliano
Center for Statistical Genetics, University of Michigan ann arbor
Career Start Year 2014
Number of shared co-authors 10
Hilary C Martin
Wellcome Sanger Institute
Career Start Year 2010
Number of shared co-authors 13
Liping Hou
Harrison International Peace Hospital
Career Start Year 2009
Number of shared co-authors 90
Karol Estrada
Brandeis University
Career Start Year 2009
Number of shared co-authors 56
Elizabeth T Cirulli
Duke University
Career Start Year 2007
Number of shared co-authors 28
Hongsheng Gui
Behavioral Health Services
Career Start Year 2007
Number of shared co-authors 10
Shane McCarthy
Wellcome Sanger Institute
Career Start Year 2004
Number of shared co-authors 49
Anna C Need
Imperial College London
Career Start Year 2003
Number of shared co-authors 40
Xiangning Chen
Center for Precision Health, The University of Texas Health Science Center at Houston
Career Start Year 2003
Number of shared co-authors 43
Stephen J Newhouse
King's College London
Career Start Year 2003
Number of shared co-authors 51
Nirmala Akula
National Institutes of Health
Career Start Year 2002
Number of shared co-authors 92
Jessica M Maia
Institute for Genomic Medicine, Columbia University
Career Start Year 2001
Number of shared co-authors 13
Andrew D Skol
The University of Chicago
Career Start Year 2001
Number of shared co-authors 17
Ilja M Nolte
University of Groningen, University Medical Center Groningen
Career Start Year 2000
Number of shared co-authors 61
Charles Curtis
NIHR Maudsley Biomedical Research Centre, King's College London
Career Start Year 2000
Number of shared co-authors 70
Gon??alo R Abecasis
Regeneron Pharmaceuticals Inc.
Career Start Year 2000
Number of shared co-authors 118
Patrick M A Sleiman
The Center for Applied Genomics, Children's Hospital of Philadelphia
Career Start Year 1999
Number of shared co-authors 66
Hywel J Williams
Cardiff University
Career Start Year 1998
Number of shared co-authors 39
Mathieu Lemire
The Hospital for Sick Children
Career Start Year 1997
Number of shared co-authors 17
Unnur Thorsteinsdottir
University of Iceland
Career Start Year 1995
Number of shared co-authors 102
Simon Heath
Barcelona Institute of Science and Technology (BIST)
Career Start Year 1995
Number of shared co-authors 64
David J Cutler
Emory University School of Medicine
Career Start Year 1994
Number of shared co-authors 42
David Altshuler
Broad Institute of Harvard and Massachusetts Institute of Technology (MIT)
Career Start Year 1992
Number of shared co-authors 57
David A Hinds
23andMe Inc.
Career Start Year 1992
Number of shared co-authors 80
Panos Deloukas
William Harvey Research Institute, Queen Mary University of London
Career Start Year 1992
Number of shared co-authors 143
David B Goldstein
Institute for Genomic Medicine, Columbia University Irving Medical Center
Career Start Year 1992
Number of shared co-authors 75
Dimitrios Avramopoulos
Johns Hopkins School of Medicine
Career Start Year 1992
Number of shared co-authors 40
Gudmar Thorleifsson
deCODE genetics/Amgen Inc.
Career Start Year 1991
Number of shared co-authors 79
Andrew A Hicks
Institute for Biomedicine, Affiliated institute of the University of Lubeck
Career Start Year 1990
Number of shared co-authors 58
Pak C Sham
the University of Hong Kong
Career Start Year 1989
Number of shared co-authors 98

Collaborators

Ole A Andreassen
Oslo University Hospital & Institute of Clinical Medicine, University of Oslo
Co-authored papers 35
Srdjan Djurovic
Oslo University Hospital
Co-authored papers 29
Ingrid Melle
University of Oslo
Co-authored papers 23
Ingrid Agartz
Diakonhjemmet Hospital
Co-authored papers 20
Thomas Werge
Co-authored papers 12
Sven Cichon
University Hospital Basel and University of Basel
Co-authored papers 11
Marcella Rietschel
Central Institute of Mental Health, University of Mannheim
Co-authored papers 10
Anders M Dale
University of California San Diego
Co-authored papers 10
Vidar M Steen
University of Oslo, Oslo University Hospital
Co-authored papers 9
Manuel Mattheisen
Dalhousie University
Co-authored papers 9
Markus M N??then
Institute of Human Genetics, University Hospital Bonn
Co-authored papers 8
Thomas Espeseth
University of Oslo, Oslo New University College
Co-authored papers 8
Andrew A Brown
Co-authored papers 8
Pamela Sklar
Co-authored papers 8
Stephan Ripke
Massachusetts General Hospital and Harvard Medical School
Co-authored papers 8
Kenneth S Kendler
Virginia Commonwealth University
Co-authored papers 8
Patrick F Sullivan
University of North Carolina at Chapel Hill
Co-authored papers 7
Andrew J Schork
The Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH)
Co-authored papers 7
Phil H Lee
Center for Genomic Medicine, Massachusetts General Hospital
Co-authored papers 6
Michael C O'Donovan
Co-authored papers 6
Bertram M??ller-Myhsok
Max Planck Institute of Psychiatry
Co-authored papers 6
Francesco Bettella
Oslo University Hospital and University of Oslo
Co-authored papers 6
Stephanie Le Hellard
University of Bergen
Co-authored papers 6
Wesley K Thompson
The Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH)
Co-authored papers 6
Derek W Morris
Co-authored papers 6
Nelson B Freimer
Co-authored papers 6
Dorret I Boomsma
Co-authored papers 5
Nicholas J Schork
University of California San Diego
Co-authored papers 5
Sarah E Medland
Co-authored papers 5
Jordan W Smoller
Center for Genomic Medicine, Massachusetts General Hospital
Co-authored papers 5
Release 1.2