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187
datasets available to search
ShareScore release 0.9.0
Dataset results
187 results for “Neurodevelopmental disorders”
Rare germline heterozygous missense variants of the BRCA1-Associated Protein 1 gene, BAP1, heterozygous missense variants cause a syndromic neurodevelopmental disorder
GEO Series GSE190394. Homo sapiens. 10 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Nr2f1 shapes mitochondria in the mouse brain unraveling novel insights into the neurodevelopmental disorder BBSOAS
GEO Series GSE228566. Mus musculus. 3 samples. Type: Expression profiling by high throughput sequencing.
Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders [RNA-seq]
GEO Series GSE227014. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
Personalized genome sequencing coupled with iPSC technology identifies GTDC1 as a gene involved in Neurodevelopmental Disorders
GEO Series GSE87568. Homo sapiens. 20 samples. Type: Expression profiling by array.
Loss of ER and nuclear envelope-associated neutral sphingomyelinase SMPD4 causes a severe neurodevelopmental disorder with microcephaly and congenital arthrogryposis
GEO Series GSE133264. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Anxiety Disorders in Children - Association With Neurodevelopmental Delay/Disorder
ClinicalTrials.gov study NCT00553085. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Exercise Intervention for Sleep in Neurodevelopmental Disorders
ClinicalTrials.gov study NCT04416789. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN)
ClinicalTrials.gov study NCT07329257. IPD Sharing: NO. Countries: 1. Publications: 0.
Characterization and Support of Neurodevelopmental Disorders Associated With Congenital Cardiac malfoRmations - Neonatal
ClinicalTrials.gov study NCT06690151. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Safety, Usability, and Effectiveness of a Gait Exoskeleton for Children and Adolescents With Neurodevelopmental Disorders.
ClinicalTrials.gov study NCT07159360. IPD Sharing: Not stated. Countries: 2. Publications: 0.
TAP-GRIN: Interventional Study on Patients With GRIN-related Neurodevelopmental Disorders
ClinicalTrials.gov study NCT07377032. IPD Sharing: NO. Countries: 3. Publications: 0.
Characterization and Support for Neurodevelopmental Disorders Associated with Congenital Heart Defects
ClinicalTrials.gov study NCT06442592. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Neurodevelopmental Disorder Diagnosis During Adulthood
ClinicalTrials.gov study NCT06691048. IPD Sharing: NO. Countries: 1. Publications: 0.
Feasibility and Efficiency of Screening for Neurodevelopmental Disorders by an Advanced Practice Nurse in Children With Congenital Heart Disease
ClinicalTrials.gov study NCT06431269. IPD Sharing: Not stated. Countries: 1. Publications: 0.
NEOnatal Multiexposure to Medical Devices Plasticizers: Endocrine Disruption MIXture Effects and Neurodevelopmental Disorders
ClinicalTrials.gov study NCT06726824. IPD Sharing: NO. Countries: 1. Publications: 0.
Patterns of Neurodevelopmental Disorders
ClinicalTrials.gov study NCT06213090. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Cognitive Benefit of Intensive Rehabilitation Using Rhythmic Music Training in Children With Complex Neurodevelopmental Disorder
ClinicalTrials.gov study NCT07303049. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Personalized Antisense Oligonucleotide for a Single Participant With MAPK8IP3 Neurodevelopmental Disorder With or Without Variable Brain Abnormalities (NEDBA)
ClinicalTrials.gov study NCT07197294. IPD Sharing: Not stated. Countries: 1. Publications: 0.
MYT1L Syndrome: a Rare Paediatric Genetic Syndrome Responsible for a Neurodevelopmental Disorder
ClinicalTrials.gov study NCT07008612. IPD Sharing: YES. Countries: 1. Publications: 0.
Transgenerational Metabolic-Immune Biomarkers of Neurological and Neurodevelopmental Disorders
ClinicalTrials.gov study NCT04322734. IPD Sharing: YES. Countries: 1. Publications: 0.
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.