Author: Marie Baekvad-Hansen

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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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ASD and ADHD have a similar burden of rare protein-truncating variants

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Genome-wide association study implicates CHRNA2 in cannabis use disorder

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Genome-wide association study of over 40,000 bipolar disorder cases provides novel biological insights

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

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

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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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Polygenic prediction of school performance in children with and without psychiatric disorders

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The iPSYCH2015 Case-Cohort sample: updated directions for unravelling genetic and environmental architectures of severe mental disorders

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