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TranscriptomicsTranscriptional regulation of neurodevelopmental and metabolic pathways by the psychiatric illness candidate gene NPAS3
The HEK293 cells were transiently transfected by pDEST40-SOX11 or control plasmid (pDEST40).Cells were collected at 24 hours post-transfection.Total RNA from alll samples was extracted.Biotinylated cRNA was prepared using the Illumina total Prep RNA application Kits.Hybridization, washing and scanni...
ORGANISM(S): Homo sapiens 
2011-10-18 | E-TABM-1082 | biostudies-arrayexpress
GenomicsAssociations between APOE status and cognitive ability across the lifecourse
The association between APOE genotype and cognitive function suggests a positive role for the e2 allele and a negative role for the e4 allele. Both alleles have relatively low frequencies in the general population, hence meta-analyses have been based on many small, heterogeneous studies. Here we rep...
EGAS00001001235 | EGA
UnknownGenetic architecture reconciles linkage and association studies of complex traits.
Not available
S-EPMC11835202 | biostudies-literature
Genomicsena-DATASET-IGMM-28-09-2016-11:49:17:763-561 - samples
Exome sequencing of isolate populations and Generation Scotland
EGAD00001002715 | EGA
GenomicsHomozygous loss-of-function variants in European cosmopolitan and isolate populations
Homozygous loss of function (HLOF) variants provide a valuable window on gene function in humans, as well as an inventory of the human genes that are not essential for survival and reproduction. All humans carry at least a few HLOF variants, but the exact number of inactivated genes that can be tole...
EGAS00001001606 | EGA
GenomicsQTL-DAC
Data Access Committee EGAC00001000063
EGAC00001000063 | EGA
UnknownGenome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.
Not available
S-EPMC8243879 | biostudies-literature
UnknownCommon schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Not available
S-EPMC5918692 | biostudies-literature
UnknownBiallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.
Not available
S-EPMC10932913 | biostudies-literature
UnknownIdentification of common genetic risk variants for autism spectrum disorder.
Not available
S-EPMC6454898 | biostudies-literature
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