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UnknownC9ORF72 repeat expansions in cases with previously identified pathogenic mutations.
Not available
S-EPMC3806926 | biostudies-literature
UnknownTranscriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder.
Not available
S-EPMC6443102 | biostudies-literature
UnknownNeuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders.
Not available
S-EPMC8233376 | biostudies-literature
UnknownWhole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy.
Not available
S-EPMC11330058 | biostudies-literature
UnknownIntegrative functional genomic analysis of human brain development and neuropsychiatric risks.
Not available
S-EPMC6413317 | biostudies-literature
UnknownCopy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells.
Not available
S-EPMC12089919 | biostudies-literature
UnknownDeciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing.
Not available
S-EPMC12032271 | biostudies-literature
UnknownMeta-analysis of individual-patient data from EVAR-1, DREAM, OVER and ACE trials comparing outcomes of endovascular or open repair for abdominal aortic aneurysm over 5 years.
Not available
S-EPMC5299468 | biostudies-literature
UnknownWhen the wild things are: Defining mammalian diel activity and plasticity.
Not available
S-EPMC11864191 | biostudies-literature
UnknownAnalysis of shared heritability in common disorders of the brain.
Not available
S-EPMC6097237 | biostudies-literature
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