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187
datasets available to search
ShareScore release 0.9.0
Dataset results
187 results for “Neurodevelopmental disorders”
Intelligence and Neurodevelopmental Disorders After Prenatal Exposure to General Anaesthesia
ClinicalTrials.gov study NCT06633406. IPD Sharing: NO. Countries: 1. Publications: 0.
The Contribution of Optical Mapping to the Characterization of Chromosomal Rearrangements in Patients With Neurodevelopmental Disorders
ClinicalTrials.gov study NCT07133789. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Sertraline vs. Placebo in the Treatment of Anxiety in Children and AdoLescents With NeurodevelopMental Disorders
ClinicalTrials.gov study NCT06081348. IPD Sharing: YES. Countries: 1. Publications: 0.
Natural History Study of GEMIN-5 Related Neurodevelopmental Disorder
ClinicalTrials.gov study NCT06776341. IPD Sharing: NO. Countries: 1. Publications: 0.
FOXP1 Syndrome: The Seaver Autism Center for Research and Treatment is Characterizing FOXP1-related Neurodevelopmental Disorders Using Genetic, Medical, and Neuropsychological Measures.
ClinicalTrials.gov study NCT03718923. IPD Sharing: NO. Countries: 1. Publications: 0.
Mental Health, Intellectual and Neurodevelopmental Disorder Detection With Artificial Intelligence Models
ClinicalTrials.gov study NCT06792175. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Brain Connectivity in Neurodevelopmental Disorders in Response to Treatment
ClinicalTrials.gov study NCT01364818. IPD Sharing: NO. Countries: 1. Publications: 0.
Transcriptomic Approach for the Identification and Prioritization of Genome Variants in Neurodevelopmental Disorders With Malformation
ClinicalTrials.gov study NCT06762678. IPD Sharing: UNDECIDED. Countries: 0. Publications: 0.
Assessment of the Pharmacokinetics of Circadin® in Children With Neurodevelopmental Disorders and Sleep Disturbances
ClinicalTrials.gov study NCT01903681. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Optical Genome Mapping for the Diagnosis of Neurodevelopmental Disorders
ClinicalTrials.gov study NCT06347562. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Study of Zatolmilast (BPN14770) in Participants With PPP2R5D Neurodevelopmental Disorder (Jordan's Syndrome [JS])
ClinicalTrials.gov study NCT06717438. IPD Sharing: NO. Countries: 1. Publications: 0.
Early Life Anemia and Children's Risk of Neurodevelopmental Disorders: National and Regional Register-based Studies
ClinicalTrials.gov study NCT06199362. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Gene expression in cord blood links genetic risk for neurodevelopmental disorders with maternal psychological distress and adverse childhood outcomes
GEO Series GSE114852. Homo sapiens. 149 samples. Type: Expression profiling by array.
Pathogenic variants in the splicing factor SF1 lead to a new neurodevelopmental disorder.
GEO Series GSE288121. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors
GEO Series GSE61492. Homo sapiens. 27 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
DNA methylation profile in animal models of neurodevelopmental disorders treated with TAK-418
GEO Series GSE165675. Mus musculus; Rattus norvegicus. 18 samples. Type: Methylation profiling by high throughput sequencing.
Variants in ZFX Cause an X-linked Neurodevelopmental Disorder with Recurrent Facial Gestalt
GEO Series GSE218688. Homo sapiens. 18 samples. Type: Expression profiling by high throughput sequencing.
Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes
GEO Series GSE140730. Homo sapiens. 130 samples. Type: Methylation profiling by high throughput sequencing.
Deficiency of the neurodevelopmental disorder-associated gene Cyfip2 alters retinal ganglion cell properties and visual acuity
GEO Series GSE176528. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Mutations of the histone linker H1-4 in neurodevelopmental disorders and functional characterization of neurons expressing C-terminus frameshift mutant H1.4
GEO Series GSE180609. Rattus norvegicus. 11 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.