Author: Manuel Mattheisen

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Preprints

Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

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

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Common risk variants identified in autism spectrum disorder

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Genomewide association study identifies 30 loci associated with bipolar disorder

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Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders.

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A Major Role for Common Genetic Variation in Anxiety Disorders

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Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology

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  • In psychiatry and clinical psychology: 20
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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

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Genetic Architecture of 11 Major Psychiatric Disorders at Biobehavioral, Functional Genomic, and Molecular Genetic Levels of Analysis

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  • In genetic and genomic medicine: 38
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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A genetic investigation of sex bias in the prevalence of attention deficit hyperactivity disorder

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Cell-type specific open chromatin profiling in human postmortem brain infers functional roles for non-coding schizophrenia loci

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Genome-wide Association Study of Anxiety and Stress-related Disorders in the iPSYCH Cohort

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Meta-analysis of problematic alcohol use in 435,563 individuals identifies 29 risk variants and yields insights into biology, pleiotropy and causality

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Examination of the Shared Genetic Basis of Anorexia Nervosa and Obsessive-Compulsive Disorder

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Genetic markers of ADHD-related variations in intracranial volume

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Cross-disorder GWAS meta-analysis for Attention Deficit/Hyperactivity Disorder, Autism Spectrum Disorder, Obsessive Compulsive Disorder, and Tourette Syndrome

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Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies

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The Anorexia Nervosa Genetics Initiative: Overview and Methods

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Genotype-phenotype association mining in bipolar disorder: market research meets complex genetics

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Identification of shared and differentiating genetic risk for autism spectrum disorder, attention deficit hyperactivity disorder and case subgroups.

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  • In psychiatry and clinical psychology: 228
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Predicting Eating Disorder and Anxiety Symptoms Using Anorexia Nervosa and Obsessive-Compulsive Disorder Polygenic Scores

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The genetic architecture of obsessive-compulsive disorder: alleles across the frequency spectrum contribute liability to OCD

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  • Site-wide: 115,680
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Polygenic heterogeneity across obsessive-compulsive disorder subgroups defined by a comorbid diagnosis

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