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216
datasets available to search
ShareScore release 0.9.0
Dataset results
216 results for “intellectual disability”
Mutations in EBF3 disturb transcriptional profiles and cause intellectual disability, ataxia and facial dysmorphism
GEO Series GSE90682. Homo sapiens. 16 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing.
Targetted Microarray Testing for Intellectual Disability Provides Diagnoses and Identifies Novel Candidate Genes
GEO Series GSE39533. Homo sapiens. 334 samples. Type: Genome variation profiling by genome tiling array.
Haploinsufficiency of the intellectual disability-gene SETD5 disturbs developmental gene expression and cognition
GEO Series GSE119498. Mus musculus. 35 samples. Type: Expression profiling by high throughput sequencing.
Cortical versus hippocampal network dysfunction in a human brain assembloid model of epilepsy and intellectual disability
GEO Series GSE281622. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Comorbidities - microcephaly, facial dysmorphia and epilepsy - increase the risk of the pathogenic CNV finding in patients with intellectual disability and autism
GEO Series GSE132453. Homo sapiens. 112 samples. Type: Genome variation profiling by genome tiling array; Genome variation profiling by SNP array.
Aggression, cognitive and neurodevelopmental abnormalities associated with disruption of the intellectual disability and histone demethylase gene Kdm5c.
GEO Series GSE75866. Mus musculus. 6 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
A Point Mutation in the RNA Recognition Motif of CSTF2 Associated with Intellectual Disability in Humans Causes Defects in 3′ End Processing
GEO Series GSE152977. Mus musculus. 16 samples. Type: Other; Expression profiling by high throughput sequencing.
Intellectual disability associated with craniofacial dysmorphism due to POLR3B mutation and defect in spliceosomal machinery
GEO Series GSE184234. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
Reduction in nuclear speckles and transcriptome de-regulation in fibroblast of intellectually disabled patients with mutations at the FRAXE site
GEO Series GSE27953. Homo sapiens. 12 samples. Type: Expression profiling by array.
Effectiveness of Active Video Games in Children With Intellectual Disabilities
ClinicalTrials.gov study NCT04277130. IPD Sharing: NO. Countries: 0. Publications: 0.
Sleep in Children With Autism and Intellectual Disability
ClinicalTrials.gov study NCT06403969. IPD Sharing: NO. Countries: 0. Publications: 0.
Study of Mindfulness Course for Parents of Adults With Intellectual Disabilities
ClinicalTrials.gov study NCT04294082. IPD Sharing: NO. Countries: 0. Publications: 0.
The Feldenkrais Method for People With Intellectual Disability
ClinicalTrials.gov study NCT03203226. IPD Sharing: NO. Countries: 0. Publications: 0.
National Stigma Survey About Mental Illness, Intellectual Disability and Homelessness in Spain
ClinicalTrials.gov study NCT05174962. IPD Sharing: UNDECIDED. Countries: 0. Publications: 0.
Various Type of Genetic Events in Patients With Intellectual Disability
ClinicalTrials.gov study NCT02881333. IPD Sharing: NO. Countries: 0. Publications: 0.
Psychomotor Therapy Effects in Adaptive Behavior and Motor Proficiency in Intellectual Disability
ClinicalTrials.gov study NCT02746614. IPD Sharing: YES. Countries: 0. Publications: 0.
10 Intellectual Disability samples for clinically relevant CNV detection
GEO Series GSE46060. Homo sapiens. 10 samples. Type: Genome binding/occupancy profiling by SNP array; SNP genotyping by SNP array.
Variants in PUS7 cause intellectual disability with speech delay, microcephaly, short stature, and aggressive behavior
GEO Series GSE121177. Drosophila melanogaster. 16 samples. Type: Other.
Aggression, cognitive and neurodevelopmental abnormalities associated with disruption of the intellectual disability and histone demethylase gene Kdm5c
GEO Series GSE61036. Mus musculus. 38 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Biallelic variants in CSPG4 cause a novel neurodevelopmental disorder with intellectual disability, global developmental delay and facial anomalies
GEO Series GSE229401. Danio rerio. 4 samples. Type: Expression 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.