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Author: Thomas Werge

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    • genetics: 76,501 (rank: 29 out of 32,586)
    • genomics: 4,587 (rank: 3,502 (tie) out of 37,100)
    • neuroscience: 194 (rank: 47,245 (tie) out of 56,873)

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Preprints

Genomic evaluation of circulating proteins for drug target characterisation and precision medicine

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Population genomics of the Viking world

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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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Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

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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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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

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A major role for common genetic variation in anxiety disorders

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

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Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

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Genome-wide association study identifies 48 common genetic variants associated with handedness

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

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Largest genome-wide association study for PTSD identifies genetic risk loci in European and African ancestries and implicates novel biological pathways

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Genome-wide association study implicates CHRNA2 in cannabis use disorder

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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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A genome-wide association study for shared risk across major psychiatric disorders in a nation-wide birth cohort implicates fetal neurodevelopment as a key mediator

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Genetic stratification of depression in UK Biobank suggests a subgroup linked to age of natural menopause

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Estimating Effect Sizes and Expected Replication Probabilities from GWAS Summary Statistics

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Mitochondrial DNA SNPs associated with Schizophrenia exhibit Highly Variable Inter-allelic Haplogroup Affiliation and Nuclear Genogeographic Affinity: Bi-Genomic Linkage Disequilibrium raises Major Concerns for Link to Disease

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Complex spatio-temporal distribution and genogeographic affinity of mitochondrial DNA haplogroups in 24,216 Danes

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Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores

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Low frequency and rare coding variation contributes to multiple sclerosis risk

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The iPSYCH2012 case-cohort sample: New directions for unravelling genetic and environmental architectures of severe mental disorders

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Genome-wide Association Study of Clinical Features in the Schizophrenia Psychiatric Genomics Consortium: Confirmation of Polygenic Effect on Negative Symptoms

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Elevated polygenic burden for autism is associated with differential DNA methylation at birth.

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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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Exploring contributors to variability in estimates of SNP-heritability and genetic correlations from the iPSYCH case-cohort and published meta-studies of major psychiatric disorders.

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The genetic structure of Norway

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Identification of risk variants and characterization of the polygenic architecture of disruptive behavior disorders in the context of ADHD

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Impute.me: an open source, non-profit tool for using data from DTC genetic testing to calculate and interpret polygenic risk scores.

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Meta-analysis of Scandinavian Schizophrenia Exomes

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AMPK signaling linked to the schizophrenia-associated 1q21.1 deletion is required for neuronal and sleep maintenance

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Analysis of genes within the schizophrenia-linked 22q11.2 deletion identifies interaction of night owl/LZTR1 and NF1 in GABAergic sleep control

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