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Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 67,594 bioRxiv papers from 298,298 authors.

Author: Manuel Mattheisen

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  • All-time downloads: 46,749 (rank: 315 out of 298,225)
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    • genetics: 40,556 (rank: 85 out of 29,790)
    • genomics: 6,193 (rank: 2,000 out of 34,003)

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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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Genomewide association study identifies 30 loci associated with bipolar disorder

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Common risk variants identified in autism spectrum 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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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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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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

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

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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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The Anorexia Nervosa Genetics Initiative: Overview and Methods

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

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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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    • In genetics: 2,438 out of 3,799
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