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216
datasets available to search
ShareScore release 0.9.0
Dataset results
216 results for “intellectual disability”
YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction.
GEO Series GSE98478. Homo sapiens. 56 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Disruption of the intellectual disability-linked gene Hs6st2 in mice decreases heparan sulfate 6-O-sulfation in the brain and impairs memory
GEO Series GSE213745. Mus musculus. 15 samples. Type: Expression profiling by high throughput sequencing.
Recurrent disruption of HIP1 identified in patients with epilepsy, learning difficulties, intellectual disability, and neurobehavioral abnormalities
GEO Series GSE23834. Homo sapiens. 12 samples. Type: Genome variation profiling by genome tiling array.
TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome
GEO Series GSE245121. Homo sapiens; Mus musculus. 23 samples. Type: Expression profiling by high throughput sequencing.
YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction [RNA-seq]
GEO Series GSE98476. Homo sapiens. 18 samples. Type: Expression profiling by high throughput sequencing.
NONO mutations are a novel cause of syndromic intellectual disability and inhibitory synaptic defects
GEO Series GSE62575. Mus musculus. 14 samples. Type: Expression profiling by high throughput sequencing.
Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism and late-onset Alzheimer’s disease
GEO Series GSE201290. Mus musculus. 14 samples. Type: Expression profiling by high throughput sequencing.
De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway
GEO Series GSE189065. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.
The Psychiatric Risk Gene Transcription Factor 4 (TCF4) Regulates Neurodevelopmental Pathways Associated With Schizophrenia, Autism, and Intellectual Disability
GEO Series GSE96915. Homo sapiens. 4 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction [ChIP-seq]
GEO Series GSE98477. Homo sapiens. 38 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Complex Balanced Translocation Disrupting TCF4 and Altering TCF4 Isoform Expression Segregates as Mild Autosomal Dominant Intellectual Disability
GEO Series GSE77742. Homo sapiens. 3 samples. Type: Expression profiling by high throughput sequencing.
A non-coding mutation implicates HCFC1 in non-syndromic intellectual disability
GEO Series GSE39326. Homo sapiens. 11 samples. Type: Expression profiling by array.
Altered gene-regulatory function of KDM5C by a novel mutation associated with autism and intellectual disability
GEO Series GSE104319. Mus musculus. 4 samples. Type: Expression profiling by high throughput sequencing.
FASN-dependent metabolism links neurogenic stem/progenitor cell activity to intellectual disability
GEO Series GSE115851. Mus musculus. 4 samples. Type: Expression profiling by high throughput sequencing.
Distinct Pathogenic Genes Causing Intellectual Disability and Autism Exhibit a Common Neuronal Network Hyperactivity Phenotype
GEO Series GSE120061. Rattus norvegicus. 5 samples. Type: Expression profiling by high throughput sequencing.
De novo mutations in the genome organizer CTCF cause Intellectual Disability (RNA-Seq)
GEO Series GSE46831. Homo sapiens. 11 samples. Type: Expression profiling by high throughput sequencing.
The intellectual disability risk gene Kdm5b regulates long term memory consolidation in the hippocampus
GEO Series GSE240887. Mus musculus. 44 samples. Type: Expression profiling by high throughput sequencing.
Deficiency of intellectual disability-related gene Brpf1 attenuated hippocampal excitatory neurotransmission and impaired learning and memory behavior
GEO Series GSE174600. Mus musculus. 12 samples. Type: Expression profiling by high throughput sequencing.
Genome-Wide Copy Number Variation Analysis of Chinese Patients with Intellectual Disability
GEO Series GSE83414. Homo sapiens. 31 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
De novo mutations in the genome organizer CTCF cause Intellectual Disability (ChIP-Seq)
GEO Series GSE46832. Homo sapiens. 1 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.