Author: Stefan Herms

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Preprints

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

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The genetic architecture of the human cerebral cortex

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Genomewide association study identifies 30 loci associated with bipolar disorder

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Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

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

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

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Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation

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Polygenic scores for major depressive disorder and depressive symptoms predict response to lithium in patients with bipolar disorder

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High genetic loading for schizophrenia predicts poor response to lithium in patients with bipolar disorder: A polygenic score and cross-trait genetic analysis

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

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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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Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

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Mapping the genetics of neuropsychological traits to the molecular network of the human brain using a data integrative approach

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Genetic factors influencing a neurobiological substrate for psychiatric disorders

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