Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.
Loss of Tsc1 from striatal direct pathway neurons impairs endocannabinoid-LTD and enhances motor routine learning.
Genome-wide by environment interaction study of stressful life events and hospital-treated depression in the iPSYCH2012 sample.
Spatiotemporally heterogeneous coordination of cholinergic and neocortical activity.
S100B dysregulation during brain development affects synaptic SHANK protein networks via alteration of zinc homeostasis.
De novo variants in the PSMC3 proteasome AAA-ATPase subunit gene cause neurodevelopmental disorders associated with type I interferonopathies.
Wide spectrum of neuronal and network phenotypes in human stem cell-derived excitatory neurons with Rett syndrome-associated MECP2 mutations.
Saturated reconstruction of living brain tissue.
GATK-gCNV: A rare copy number variant discovery algorithm and its application to exome sequencing in the UK Biobank.
Spatiotemporally heterogeneous coordination of cholinergic and neocortical activity.
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