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Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
1,336
datasets available to search
ShareScore release 0.9.0
Dataset results
1,336 results for “congenital”
The thyroid hormone clearing type 3 deiodinase protects from cardiac congenital abnormalities
GEO Series GSE198416. Mus musculus. 8 samples. Type: Expression profiling by high throughput sequencing.
Congenital iRHOM2 deficiency causes ADAM17 dysfunction and environmentally directed immunodysregulatory disease [whole blood]
GEO Series GSE184876. Homo sapiens. 10 samples. Type: Expression profiling by high throughput sequencing.
Cardiovascular Mettl3 Deficiency Causes Congenital Cardiac Defects and Postnatal Lethality in Mice
GEO Series GSE288034. Mus musculus. 12 samples. Type: Other.
Molecular Alterations of Extracellular Matrix in the Brain of Newborns with Congenital Zika Syndrome
GEO Series GSE125554. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.
Oligogenic inheritance of congenital heart disease involving a NKX2-5 modifier [human]
GEO Series GSE131322. Homo sapiens. 9 samples. Type: Expression profiling by high throughput sequencing.
A multi-omics approach using a mouse model of cardiac malformations for prioritization of human congenital heart disease contributing genes [RNA-seq]
GEO Series GSE171237. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Metabolic stress and therapeutic response in heart failure associated with congenital heart disease
GEO Series GSE146341. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.
Mutation in LBX1/Lbx1 precludes transcription factor cooperativity and causes congenital hypoventilation in humans and mice [RNA-seq]
GEO Series GSE215415. Mus musculus. 12 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.
Endothelial RNF20 Suppresses Endothelial-to-Mesenchymal Transition and Safeguards Physiological Angiocrine Signaling to Prevent Congenital Heart Disease
GEO Series GSE246928. Mus musculus. 12 samples. Type: Expression profiling by high throughput sequencing.
Disrupted prenatal RNA processing and myogenesis in congenital myotonic dystrophy
GEO Series GSE97806. Mus musculus; Homo sapiens. 25 samples. Type: Expression profiling by high throughput sequencing.
Loss of Ahnak is associated with Congenital Anomalies of the Kidney and Urinary Tract
GEO Series GSE218925. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Neurodevelopmental and behavioral defects in congenital heart disease [methylation]
GEO Series GSE283525. Mus musculus. 11 samples. Type: Methylation profiling by genome tiling array.
Conjunctival mRNA and miRNA expression profiles in congenital aniridia are genotype and phenotype dependent (AKK mRNA)
GEO Series GSE137996. Homo sapiens. 40 samples. Type: Expression profiling by array.
An experimental loop design improves the detection of congenital chromosomal aberrations by array CGH
GEO Series GSE6538. Homo sapiens. 27 samples. Type: Genome variation profiling by genome tiling array.
Reduced representation bisulfite sequencing (RRBS) of the retina of crumbs 2a (crb2a m289/m289) zebrafish model of Leber congenital amaurosis and retinitis pigmentosa.
GEO Series GSE178842. Danio rerio. 6 samples. Type: Methylation profiling by high throughput sequencing.
Transcriptome (RNA-seq) analysis of the retina of crumbs 2a (crb2a m289/m289) zebrafish model of Leber congenital amaurosis and retinitis pigmentosa.
GEO Series GSE178709. Danio rerio. 11 samples. Type: Expression profiling by high throughput sequencing.
mRNA-seq read counts of peripheral blood mononuclear cells from congenital generalized lipodystrophy patients and their gender/aged-matched controls
GEO Series GSE159337. Homo sapiens. 14 samples. Type: Expression profiling by high throughput sequencing.
Gene therapy of dominant CRX-Leber congenital amaurosis using patient retinal organoids II
GEO Series GSE153099. Homo sapiens. 5 samples. Type: Expression profiling by high throughput sequencing.
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.
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.