Author: Jaroslav Bendl

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Preprints

Integration of Alzheimer’s disease genetics and myeloid genomics reveals novel disease risk mechanisms

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  • Site-wide: 4,418
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Common genetic variation influencing human white matter microstructure

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  • In genetics: 547
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The three-dimensional landscape of chromatin accessibility in Alzheimer's disease

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  • In neuroscience: 2,745
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Common variants contribute to intrinsic human brain functional networks

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  • Site-wide: 26,979
  • In genetics: 1,186
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Transcriptional and epigenetic characterization of early striosomes identifies Foxf2 and Olig2 as factors required for development of striatal compartmentation and neuronal phenotypic differentiation

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  • In neuroscience: 5,184
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Population-level variation of enhancer expression identifies novel disease mechanisms in the human brain

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  • In neuroscience: 5,272
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Trans-ethnic eQTL meta-analysis of human brain reveals regulatory architecture and candidate causal variants for brain-related traits

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  • Site-wide: 42,080
  • In genetic and genomic medicine: 199
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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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  • Site-wide: 50,410
  • In psychiatry and clinical psychology: 192
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Sex differences in the human brain transcriptome of cases with schizophrenia

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From compartments to gene loops: Functions of the 3D genome in the human brain

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  • In genomics: 5,575
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Acetylated Chromatin Domains Link Chromosomal Organization to Cell- and Circuit-level Dysfunction in Schizophrenia and Bipolar Disorder

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  • In genomics: 5,845
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Genetics of the human microglia regulome refines Alzheimer's disease risk loci

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  • Site-wide: 126,095
  • In genetic and genomic medicine: 727
• Year to date:
  • Site-wide: 40,987
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