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1,336
datasets available to search
ShareScore release 0.9.0
Dataset results
1,336 results for “congenital”
Plasma Metanephrines in Patients With Cyanotic and Acyanotic Congenital Heart Disease
ClinicalTrials.gov study NCT04891081. IPD Sharing: NO. Countries: 1. Publications: 0.
Gene expression profile of erythroblastic cells induced from congenital dyserythropoietic anemia (CDA) patient-derived induced pluripotent stem cells
GEO Series GSE102985. Homo sapiens. 2 samples. Type: Expression profiling by array.
Congenital hypothryrodism and male rat liver: control vs congenital hypothryoidism
GEO Series GSE32705. Rattus norvegicus. 4 samples. Type: Expression profiling by array.
Congenital heart disease associated bronchopulmonary dysplasia and its underlying mechanisms
GEO Series GSE201522. Rattus norvegicus. 10 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
GEO Series GSE87414. Ctenopharyngodon idella. 9 samples. Type: Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing; Methylation profiling by high throughput sequencing.
Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspring [case 1]
GEO Series GSE65451. Homo sapiens. 5 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
5-aza-2-deoxycytidine improves skeletal muscle function in a mouse model for recessive RYR1-related congenital myopathy
GEO Series GSE277979. Mus musculus. 45 samples. Type: Methylation profiling by array.
A tracheal aspirate-derived airway basal cell model reveals a proinflammatory epithelial defect in congenital diaphragmatic hernia (RNA-Seq)
GEO Series GSE211789. Homo sapiens. 24 samples. Type: Expression profiling by high throughput sequencing.
Comparative Genomic Hybridization: genomic control vs. Ullrich Congenital Muscular Dystrophy and Bethlem myopathy
GEO Series GSE20025. Homo sapiens. 8 samples. Type: Genome variation profiling by genome tiling array.
Impact of maternal compensation on developmental phenotypes in a zebrafish model of severe congenital muscular dystrophy
GEO Series GSE314061. Danio rerio. 21 samples. Type: Expression profiling by high throughput sequencing.
NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets
GEO Series GSE44902. Mus musculus. 10 samples. Type: Genome binding/occupancy profiling by genome tiling array.
Expression of candidate genes associated with congenital heart disease in adult human atrial and ventricular tissue
GEO Series GSE161016. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.
RNA-sequencing Analysis Reveals Utility and Limitations of iPSC-derived Cardiomyocytes from Congenital Heart Disease Patients
GEO Series GSE132401. Homo sapiens. 15 samples. Type: Expression profiling by high throughput sequencing.
Conjunctival mRNA and miRNA expression profiles in congenital aniridia are genotype and phenotype dependent
GEO Series GSE137997. Homo sapiens. 80 samples. Type: Non-coding RNA profiling by array; Expression profiling by array.
Developmental, cellular, and behavioral phenotypes in a mouse model of congenital hypoplasia of the dentate gyrus
GEO Series GSE157983. Mus musculus. 8 samples. Type: Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing.
Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspring.
GEO Series GSE65454. Homo sapiens. 10 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array; Genome variation profiling by genome tiling array.
Systems analysis of de novo mutations in congenital heart diseases identified a protein network in the hypoplastic left heart syndrome
GEO Series GSE197709. Homo sapiens. 10 samples. Type: Expression profiling by high throughput sequencing.
Elevated microRNA-187 causes cardiac endothelial dysplasia to promote congenital heart disease through inhibition of NIPBL [Endothelial cell RNA-seq]
GEO Series GSE275849. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
Screening for chromosomal aberrations by array CGH in 74 patients with congenital hypothyroidism
GEO Series GSE18152. Homo sapiens. 80 samples. Type: Genome variation profiling by genome tiling array.
Elevated microRNA-187 causes cardiac endothelial dysplasia to promote congenital heart disease through inhibition of NIPBL
GEO Series GSE275951. Homo sapiens. 4 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.