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187
datasets available to search
ShareScore release 0.9.0
Dataset results
187 results for “Neurodevelopmental disorder”
Biallelic deleterious variants in SNAPIN, a retrograde dynein adaptor, cause a prenatal-onset neurodevelopmental disorder [1]
GEO Series GSE298991. Danio rerio. 4 samples. Type: Expression profiling by high throughput sequencing.
Spliceosome malfunction causes neurodevelopmental disorders with overlapping features
GEO Series GSE246137. Drosophila melanogaster; Homo sapiens. 39 samples. Type: Expression profiling by high throughput sequencing.
Homozygous deletion of the epigenetic regulator PHF20 in individuals with neurodevelopmental disorder
GEO Series GSE309878. Homo sapiens. 5 samples. Type: 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.
The ChAHP chromatin remodelling complex regulates neurodevelopmental disorder risk genes to scale the production of neocortical layers
GEO Series GSE262584. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Pro-cognitive restoration of PV interneuron plasticity in neurodevelopmental disorders
GEO Series GSE283741. Mus musculus. 9 samples. Type: Expression profiling by high throughput sequencing.
The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders [lnc-Nr2f1 overexpression]
GEO Series GSE125267. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
Genotype-phenotype-epiphenotype analysis to decipher severity, penetrance, pleiotropy and mechanisms in CHD8-related neurodevelopmental disorder
GEO Series GSE274977. Mus musculus. 6 samples. Type: Methylation profiling by high throughput sequencing.
Deep mutational scanning of CHD2 for variant interpretation in neurodevelopmental disorders
GEO Series GSE316550. Homo sapiens. 16 samples. Type: Methylation profiling by genome tiling array.
Bi-allelic SNAPC4 variants lead to altered global splicing and a neurodevelopmental disorder
GEO Series GSE211811. Homo sapiens. 22 samples. Type: Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing.
The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders [ChiRP]
GEO Series GSE115078. Mus musculus. 9 samples. Type: Other.
Deep mutational scanning of CHD2 for variant interpretation in neurodevelopmental disorders [RNA-seq]
GEO Series GSE316724. Homo sapiens. 16 samples. Type: Expression profiling by high throughput sequencing.
CRISPR activation for SCN2A-related neurodevelopmental disorders
GEO Series GSE193605. Mus musculus. 8 samples. Type: Expression profiling by high throughput sequencing.
Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder
GEO Series GSE248488. Danio rerio. 9 samples. Type: Expression profiling by high throughput sequencing.
The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders [RNA-seq]
GEO Series GSE115077. Mus musculus. 8 samples. Type: Expression profiling by high throughput sequencing.
Brain-specific deletion of histone variant H2A.z results in cortical neurogenesis defects and neurodevelopmental disorder
GEO Series GSE106679. Mus musculus. 4 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
The wide world of technological telerehabilitation for pediatric neurologic and neurodevelopmental disorders - A systematic review
<p>This record contains raw data related to the systematic review <span><span>The wide world of technological telerehabilitation for pediatric neurologic and neurodevelopmental disorders - A systematic review</span></span><span> </span></p> <p>In order to request the data you need to contact Dott.ssa Silvia Filogna at the following email: silvia.filogna@fsm.unipi.it</p>
Raw data - Mascheroni et al., (submittet) - Exploring DNA methylation in infants with neurodevelopmental disorders
<p>Raw data - Mascheroni et al., (submittet to journal) - Exploring DNA methylation in infants with neurodevelopmental disorders</p>
DATASET RELATED TO ARTICLE "MONOALLELIC AND BIALLELIC MUTATIONS IN RELN UNDERLIE A GRADED SERIES OF NEURODEVELOPMENTAL DISORDERS
<p>clinical data of a single RELN case patient followed at Fondazione Besta involved in the study at title</p>
De novo TLK1 and MDM1 mutations in a patient with a neurodevelopmental disorder and immunodeficiency
GEO Series GSE241032. Homo sapiens. 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.