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1,336
datasets available to search
ShareScore release 0.9.0
Dataset results
1,336 results for “congenital”
Endothelial RNF20 Suppresses Endothelial-to-Mesenchymal Transition and Safeguards Physiological Angiocrine Signaling to Prevent Congenital Heart Disease
GEO Series GSE246904. Mus musculus. 2 samples. Type: Expression profiling by high throughput sequencing.
Disruption of Notch1 and Gata5 in mice leads to congenital aortic valve disease
GEO Series GSE285189. Mus musculus. 12 samples. Type: Expression profiling by high throughput sequencing.
The Genetic Architecture of Congenital Diarrhea and Enteropathy (CODE)
GEO Series GSE264461. Danio rerio. 4 samples. Type: Expression profiling by high throughput sequencing.
Copy number variations may contribute to congenital heart defect risk greatly by disrupting long noncoding RNAs
GEO Series GSE201076. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
Comparative DNA methylation and gene expression analysis identifies novel genes for structural congenital heart diseases
GEO Series GSE62629. Homo sapiens. 23 samples. Type: Methylation profiling by high throughput sequencing.
Molecular Signatures of cardiac defects in Down syndrome lymphoblastoid cell lines (congenital heart disease)
GEO Series GSE34457. Homo sapiens. 43 samples. Type: Expression profiling by array.
A multi-omics approach using a mouse model of cardiac malformations for prioritization of human congenital heart disease contributing genes
GEO Series GSE171239. Mus musculus. 7 samples. Type: Expression profiling by high throughput sequencing.
Epimutations as a novel cause of congenital disorders
GEO Series GSE89353. Homo sapiens. 620 samples. Type: Methylation profiling by genome tiling array.
Sex differences in metabolic adaptation in infants with cyanotic congenital heart disease
GEO Series GSE269353. Homo sapiens. 23 samples. Type: Expression profiling by high throughput sequencing.
Impaired signaling pathways on Berardinelli–Seip congenital lipodystrophy macrophages during Leishmania infantum infection
GEO Series GSE210555. Homo sapiens. 36 samples. Type: Expression profiling by high throughput sequencing.
Transcriptional profiling of organoid glomeruli isolated from human kidney organoids modelling congenital nephrotic syndrome
GEO Series GSE205647. Homo sapiens. 27 samples. Type: Expression profiling by high throughput sequencing.
A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
GEO Series GSE73263. Felis catus. 2 samples. Type: Expression profiling by high throughput sequencing.
Rabbit Model of Fetal Tracheal Occlusion for Congenital Diaphragmatic Hernia
GEO Series GSE84811. Oryctolagus cuniculus. 10 samples. Type: Expression profiling by high throughput sequencing.
Prenatal VEGF Nano-Delivery Reverses Congenital Diaphragmatic Hernia-Associated Pulmonary Abnormalities
GEO Series GSE267778. Mus musculus. 12 samples. Type: Expression profiling by high throughput sequencing.
A Congenital Anemia Dissociates the Pleiotropic Functions of Master Transcription Factor GATA1
GEO Series GSE133417. Homo sapiens; Mus musculus. 60 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Identification of new therapeutic candidates for Congenital Central Hypoventilation Syndrome
GEO Series GSE250244. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
The destiny of the resistance/susceptibility against GCRV has been congenitally destined by epigenetic mechanism in CIK cells [RNA-seq]
GEO Series GSE87408. Ctenopharyngodon idella. 3 samples. Type: Expression profiling by high throughput sequencing.
Maternal Vitamin C Deficiency and Genetic Risk Factors Contribute to Congenital Malformations through Dysregulation of DNA Methylation. [WGBS E8.5]
GEO Series GSE295921. Mus musculus. 18 samples. Type: Methylation profiling by high throughput sequencing.
Maternal Vitamin C Deficiency and Genetic Risk Factors Contribute to Congenital Malformations through Dysregulation of DNA Methylation. [RNA-Seq E8.5]
GEO Series GSE295923. Mus musculus. 29 samples. Type: Expression profiling by high throughput sequencing.
Maternal Vitamin C Deficiency and Genetic Risk Factors Contribute to Congenital Malformations through Dysregulation of DNA Methylation. [RNA-Seq E11.5]
GEO Series GSE295925. Mus musculus. 12 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.