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187
datasets available to search
ShareScore release 0.9.0
Dataset results
187 results for “Neurodevelopmental disorders”
Placenta and fetal brain share a neurodevelopmental disorder DNA methylation profile in a mouse model of prenatal PCB exposure [WGBS]
GEO Series GSE171016. Mus musculus. 88 samples. Type: Methylation profiling by high throughput sequencing.
Spliceosome malfunction causes neurodevelopmental disorders with overlapping features (fly)
GEO Series GSE246136. Drosophila melanogaster. 15 samples. Type: Expression profiling by high throughput sequencing.
SETBP1 variants outside the degron disrupt DNA-binding, transcription and neuronal differentiation capacity to cause a heterogeneous neurodevelopmental disorder [induced neurons]
GEO Series GSE301239. Homo sapiens. 51 samples. Type: Expression profiling by high throughput sequencing.
Placenta and fetal brain share a neurodevelopmental disorder DNA methylation profile in a mouse model of prenatal PCB exposure
GEO Series GSE180979. Mus musculus. 176 samples. Type: Methylation profiling by high throughput sequencing; Expression profiling by high throughput sequencing.
Modeling neurodevelopmental disorder-associated human AGO1 mutations in C. elegans Argonaute alg-1. [ribosome profiling]
GEO Series GSE252063. Caenorhabditis elegans. 18 samples. Type: Other.
Histone modification profile in animal models of neurodevelopmental disorders treated with TAK-418
GEO Series GSE165655. Mus musculus; Rattus norvegicus. 74 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
The imbalance of excitatory/inhibitory neuron differentiation in neurodevelopmental disorders with an NR2F1 point mutation
GEO Series GSE132965. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Role of miR-146a in neural stem cell differentiation and neural lineage determination: relevance for neurodevelopmental disorders
GEO Series GSE100670. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors [ChIP-Seq]
GEO Series GSE61487. Homo sapiens. 5 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Novel variants in the splicing factor gene SF3B1 are associated with neurodevelopmental disorders
GEO Series GSE287369. Homo sapiens. 15 samples. Type: Expression profiling by high throughput sequencing.
SETBP1 variants outside the degron disrupt DNA-binding, transcription and neuronal differentiation capacity to cause a heterogeneous neurodevelopmental disorder [fibroblast]
GEO Series GSE301238. Homo sapiens. 69 samples. Type: Expression profiling by high throughput sequencing.
Transcriptional analysis of T cells derived from individuals with neurodevelopmental disorder carrying de novo heterozygous PSMC5 variants.
GEO Series GSE306813. Homo sapiens. 10 samples. Type: Expression profiling by array.
The ChAHP chromatin remodelling complex regulates a network of neurodevelopmental disorder risk genes to scale the production of neocortical layers (cut&run-seq)
GEO Series GSE255599. Mus musculus. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Dissecting 16p11.2 hemi-deletion to study sex-specific striatal phenotypes of neurodevelopmental disorders
GEO Series GSE224750. Mus musculus. 58 samples. Type: Expression profiling by high throughput sequencing; Other.
Spliceosome malfunction causes neurodevelopmental disorders with overlapping features (human)
GEO Series GSE246135. Homo sapiens. 24 samples. Type: Expression profiling by high throughput sequencing.
Epigenome analysis of control and neurodevelopmental disorder lymphoblastoid cell lines
GEO Series GSE34099. Homo sapiens. 65 samples. Type: Methylation profiling by array.
CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors [RNA-Seq]
GEO Series GSE61491. Homo sapiens. 22 samples. Type: Expression profiling by high throughput sequencing.
A Convergent Mechanism of High Risk Factors ADNP and POGZ in Neurodevelopmental Disorders
GEO Series GSE188865. Mus musculus. 8 samples. Type: Expression profiling by high throughput sequencing.
Deciphering the role of CAPZA2 in neurodevelopmental disorders: Insights from mouse models
GEO Series GSE295653. Mus musculus. 2 samples. Type: Expression profiling by high throughput sequencing.
Transcriptional analysis of T cells derived from individuals with neurodevelopmental disorder carrying de novo heterozygous PSMD11 variants
GEO Series GSE262901. Homo sapiens. 5 samples. Type: Other.
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.