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102
datasets available to search
ShareScore release 0.9.0
Dataset results
102 results for “heart defects”
Maternal Biomarker Study for Single Ventricle Heart Defects
GEO Series GSE233362. Homo sapiens. 50 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Myocardial Reprogramming by HMGN1 Underlies Heart Defects in Trisomy 21
GEO Series GSE271447. Mus musculus; Homo sapiens. 84 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Single-nucleus RNA sequencing of OCTN2-defective engineered heart tissues and isogenic control
GEO Series GSE211650. Homo sapiens. 3 samples. Type: Expression profiling by high throughput sequencing.
Tet inactivation disrupts YY1 binding and long-range chromatin interactions to cause developmental defects in embryonic heart
GEO Series GSE121671. Mus musculus; Homo sapiens. 23 samples. Type: Methylation profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing; Other.
A CRISPR-Activation CROP-seq Screen Identifies HMGN1 as a Dosage Sensitive Regulator of Heart Defects in Down Syndrome (scRNA-Seq)
GEO Series GSE271444. Homo sapiens. 49 samples. Type: Expression profiling by high throughput sequencing.
Identification of Copy Number Variants in Patients with Hypoplastic Left Heart Syndrome and Other Congenital Heart Defects
GEO Series GSE66032. Homo sapiens. 70 samples. Type: Genome variation profiling by SNP array.
Neurodevelopmental and behavioral defects in congenital heart disease [methylation]
GEO Series GSE283525. Mus musculus. 11 samples. Type: Methylation profiling by genome tiling array.
Non-coding cause of congenital heart defects: Abnormal RNA splicing with multiple isoforms as a mechanism for heterotaxy
GEO Series GSE263414. Homo sapiens. 17 samples. Type: Expression profiling by high throughput sequencing.
Hand1 gene replacement with Hand2 reveals overlap in function with unique occurrence of omphalocele and heart defects [scRNA-seq]
GEO Series GSE299253. Mus musculus. 9 samples. Type: Expression profiling by high throughput sequencing.
Analysis of copy number variants on chromosome 21 in Down syndrome-associated congenital heart defects
GEO Series GSE93004. Homo sapiens. 526 samples. Type: Genome variation profiling by array.
Molecular Basis of Congenital Heart Defects
ClinicalTrials.gov study NCT00579358. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Neurodevelopmental Rehabilitation for Toddlers With Complex Heart Defects
ClinicalTrials.gov study NCT01239784. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Characterization and Support for Neurodevelopmental Disorders Associated with Congenital Heart Defects
ClinicalTrials.gov study NCT06442592. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Effect of Feeding With Nutrient Dense Formula in Malnourished Infants and Children With Congenital Heart Defects
ClinicalTrials.gov study NCT04795076. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Antenatal Investigation of Fetuses With Complex Congenital Heart Defects Using multiOMICS
ClinicalTrials.gov study NCT06705543. IPD Sharing: NO. Countries: 1. Publications: 0.
Optimizing Health Among Children With Congenital Heart Defects
ClinicalTrials.gov study NCT00974688. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Mind the Heart - Mental Health in Children and Adolescents With Congenital Heart Defects
ClinicalTrials.gov study NCT05709470. IPD Sharing: NO. Countries: 1. Publications: 0.
Cognitive and Speech Disorders in Children With Congenital Heart Defects
ClinicalTrials.gov study NCT06565299. IPD Sharing: NO. Countries: 1. Publications: 0.
Genetic and Nutritional Causes of Heart Birth Defects
ClinicalTrials.gov study NCT00368732. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Pediatric Exercise With Congenital Heart Defects (Kinderturnen Mit Angeborenem Herzfehler)
ClinicalTrials.gov study NCT00436098. IPD Sharing: Not stated. 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.