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TranscriptomicsA comprehensive view of the transcriptome during development of the mouse cerebral cortex
The complexity of the mature adult brain is a result of both developmental processes and experience-dependent circuit formation. One way to look at the process of brain development is to examine gene expression changes, and previous studies have used microarrays to address this in a global manner. H...
ORGANISM(S): Mus musculus 
2013-02-10 | E-GEOD-39866 | biostudies-arrayexpress
UnknownUnderstanding monogenic Parkinson's disease at a global scale.
Not available
S-EPMC10962747 | biostudies-literature
TranscriptomicsAbundant Quantitative Trait Loci for CpG Methylation and Expression Across Human Brain Tissues
A fundamental challenge in the post-genome era is to understand and annotate the consequences of genetic variation, particularly within the context of human tissues. We describe a set of integrated experiments designed to investigate the effects of common genetic variability on DNA methylation, mRNA...
ORGANISM(S): Homo sapiens 
2010-04-20 | E-GEOD-15745 | biostudies-arrayexpress
UnknownDecreased SNCA expression in whole-blood RNA analysis of Parkinson's disease adjusting for neutrophils.
Not available
S-EPMC12521519 | biostudies-literature
UnknownThe Neurodegenerative Disease Knowledge Portal: Propelling Discovery Through the Sharing of Neurodegenerative Disease Genomic Resources.
Not available
S-EPMC11160810 | biostudies-literature
UnknownClinical-genetic model predicts incident impulse control disorders in Parkinson's disease.
Not available
S-EPMC5098340 | biostudies-literature
UnknownAccelerating Medicines Partnership: Parkinson's Disease. Genetic Resource.
Not available
S-EPMC8453903 | biostudies-literature
UnknownThe Parkinson's phenome-traits associated with Parkinson's disease in a broadly phenotyped cohort.
Not available
S-EPMC6437217 | biostudies-literature
UnknownCharacterizing a complex CT-rich haplotype in intron 4 of SNCA using large-scale targeted amplicon long-read sequencing.
Not available
S-EPMC11282088 | biostudies-literature
GenomicsGenome-Wide Association Study of Amyotrophic Lateral Sclerosis in Finland

The genetic etiology of amyotrophic lateral sclerosis (ALS) is not well understood. Finland has one of the highest incidence of ALS in the world, making it an ideal population for study. To identify genetic risk factors for this fatal neurodegenerative disease, we undertook a genome-wide associ...

phs000344.v1.p1 | EGA
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