Thomas Werge

发表

Roadmap for a precision-medicine initiative in the Nordic region

Søren Brunak, Andres Metspalu, Eivind Hovig, 2019, Nature Genetics.

Serotonin transporter: Evolution and impact of polymorphic transcriptional regulation

Line Olsen, Karen Søeby, Thomas Werge, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Gene-Based Analysis of Regionally Enriched Cortical Genes in GWAS Data Sets of Cognitive Traits and Psychiatric Disorders

Ole A. Andreassen, Vidar M. Steen, Manuel Mattheisen, 2012, PloS one.

Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, American journal of human genetics.

Combinations of SNPs Related to Signal Transduction in Bipolar Disorder

Lars Vedel Kessing, Ole A. Andreassen, Henrik Dam, 2011, PloS one.

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

Jakob Grove, Esben Agerbo, Robert Plomin, 2018, Nature Genetics.

Association analysis of schizophrenia on 18 genes involved in neuronal migration: MDGA1 as a new susceptibility gene

Ole A. Andreassen, Vidar M. Steen, Erik G. Jönsson, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

Jakob Grove, Stephan Ripke, Preben Bo Mortensen, 2015, Nature Genetics.

Discovery of the first genome-wide significant risk loci for ADHD

Jakob Grove, Esben Agerbo, Anders D. Børglum, 2017, bioRxiv.

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1

Thomas Meitinger, Michael Inouye, Martin Dichgans, 2010, Nature Genetics.

Antipsychotic-Like Effect of the Muscarinic Acetylcholine Receptor Agonist BuTAC in Non-Human Primates

Anders Fink-Jensen, Christian C. Felder, Thomas Werge, 2015, PloS one.

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

Wei Cheng, Jianxin Shi, Elvira Bramon, 2016, Nature Genetics.

Use of Living Columns to Select Specific Phage Antibodies

Thomas Werge, Antonino Cattaneo, T. Werge, 1993, Bio/Technology.

Common risk variants identified in autism spectrum disorder

Jakob Grove, Esben Agerbo, Anders D. Børglum, 2017, bioRxiv.

An Empirical Bayes Mixture Model for Effect Size Distributions in Genome-Wide Association Studies

Anders M. Dale, Wesley K. Thompson, Ole A. Andreassen, 2015, PLoS genetics.

Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

Qi Xu, Peng Wang, Dengtang Liu, 2011, Nature Genetics.

Correlation between Genetic and Geographic Structure in Europe

Christian Gieger, Jaume Bertranpetit, Michael Krawczak, 2008, Current Biology.

Brain Expressed microRNAs Implicated in Schizophrenia Etiology

Ole A. Andreassen, Ingrid Agartz, Line Olsen, 2007, PloS one.

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

Jianxin Shi, Susmita Datta, Aribert Rothenberger, 2013, Nature Genetics.

Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder

Jakob Grove, Esben Agerbo, Andres Metspalu, 2017, bioRxiv.

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

Yadav Sapkota, Thomas Meitinger, Andres Metspalu, 2017, Nature Communications.

DCLK1 Variants Are Associated across Schizophrenia and Attention Deficit/Hyperactivity Disorder

Ole A. Andreassen, Vidar M. Steen, Manuel Mattheisen, 2012, PloS one.

Association study of PDE4B gene variants in scandinavian schizophrenia and bipolar disorder multicenter case–control samples

Ingrid Agartz, Mona K. Otnæss, Henrik Dam, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Disruption of the neurexin 1 gene is associated with schizophrenia.

Elvira Bramon, Chiara Sabatti, Kari Stefansson, 2009, Human molecular genetics.

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

Dan M Roden, Kari Stefansson, Gudmar Thorleifsson, 2011, Nature Genetics.

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Jakob Grove, Anders D. Børglum, Aysu Okbay, 2016, Nature Genetics.

Genome-wide association study identifies five new schizophrenia loci

Anders D. Børglum, Peter Donnelly, Jianxin Shi, 2011, Nature Genetics.

Genome‐wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness

Stephan Ripke, Andrew McQuillin, Hugh Gurling, 2016, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Evidence for a possible association of neurotrophin receptor (NTRK-3) gene polymorphisms with hippocampal function and schizophrenia

Ole A. Andreassen, Joseph H. Callicott, Erik G. Jönsson, 2009, Neurobiology of Disease.

Two methylenetetrahydrofolate reductase gene (MTHFR) polymorphisms, schizophrenia and bipolar disorder: An association study

Ingrid Agartz, Kristina Larsson, Thomas Werge, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, Nature Neuroscience.

Redox dysregulation in the pathophysiology of schizophrenia and bipolar disorder: insights from animal models.

Thomas Werge, A. Ingason, T. Werge, 2013, Antioxidants & redox signaling.

Association between a disrupted-in-schizophrenia 1 (DISC1) single nucleotide polymorphism and schizophrenia in a combined Scandinavian case–control sample

Ole A. Andreassen, Erik G. Jönsson, Per Lundmark, 2008, Schizophrenia Research.

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Jakob Grove, Anders D. Børglum, Aysu Okbay, 2016 .

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

Anders M. Dale, Elvira Bramon, Ole A. Andreassen, 2011, Biological Psychiatry.