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1,336
datasets available to search
ShareScore release 0.9.0
Dataset results
1,336 results for “congenital”
Genome-wide analysis of differentially expressed miRNAs and their associated regulatory networks in lenses deficient for the congenital cataract-linked tudor domain containing protein TDRD7
GEO Series GSE157061. Mus musculus; synthetic construct. 6 samples. Type: Non-coding RNA profiling by array.
A mutation in the c-Fos gene associated with congenital generalized lipodystrophy
GEO Series GSE39825. Homo sapiens. 10 samples. Type: Expression profiling by array.
Human iPSC-derived heart organoids modeling the etiology of pregestational diabetes induced congenital heart defects
GEO Series GSE201343. Homo sapiens. 2 samples. Type: Expression profiling by high throughput sequencing.
Integrated multiomic characterization of congenital heart disease [ATAC-Seq]
GEO Series GSE203273. Homo sapiens. 24 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Genotypic and gene expression studies in Congenital Melanocytic Nevi: insight into initial step of tumoral melanogenesis
GEO Series GSE8525. Homo sapiens. 12 samples. Type: Expression profiling by array.
Comparative Analysis of Paraspinal Muscle Imbalance Between Idiopathic Scoliosis and Congenital Scoliosis from the Transcriptome Aspect
GEO Series GSE254300. Homo sapiens. 20 samples. Type: Expression profiling by high throughput sequencing.
Endothelial RNF20 Suppresses Endothelial-to-Mesenchymal Transition and Safeguards Physiological Angiocrine Signaling to Prevent Congenital Heart Disease [polyAbulkRNA_seq_Cd31_pos_EC_Rnf20_het]
GEO Series GSE246926. Mus musculus. 4 samples. Type: Expression profiling by high throughput sequencing.
Congenital iRHOM2 deficiency causes ADAM17 dysfunction and environmentally directed immunodysregulatory disease
GEO Series GSE184877. Homo sapiens. 47 samples. Type: Expression profiling by high throughput sequencing.
Microvascular preservation & cardiomyocyte hyperplasia underlie adaptive right ventricle development in congenital heart disease-pulmonary arterial hypertension
GEO Series GSE298749. Ovis aries. 12 samples. Type: Expression profiling by high throughput sequencing.
Genetic Abnormalities in Large to Giant Congenital Nevi: Beyond NRAS mutations
GEO Series GSE120597. Homo sapiens. 50 samples. Type: Expression profiling by high throughput sequencing; Other.
Elevated microRNA-187 causes cardiac endothelial dysplasia to promote congenital heart disease through inhibition of NIPBL [ATAC-seq Heart]
GEO Series GSE276222. Mus musculus. 4 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Epigenome-wide association study of the whole blood DNA in men with congenital hypopituitarism disease
GEO Series GSE107737. Homo sapiens. 24 samples. Type: Methylation profiling by array.
Integrated multiomic characterization of congenital heart disease
GEO Series GSE203275. Homo sapiens. 67 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
The molecular basis of analgesia in congenital insensitivity to pain associated with loss of Nav1.7 function
GEO Series GSE61373. Mus musculus. 18 samples. Type: Expression profiling by array.
Neurodevelopmental and behavioral defects in congenital heart disease [EMX-cre RNAseq]
GEO Series GSE283526. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Methylome analysis of congenital ectopic thyroids
GEO Series GSE17581. Homo sapiens. 6 samples. Type: Methylation profiling by genome tiling array.
Accelerated Epigenetic Aging and DNA Methylation Alterations in Berardinelli-Seip Congenital Lipodystrophy
GEO Series GSE214297. Homo sapiens. 16 samples. Type: Methylation profiling by high throughput sequencing.
Elevated microRNA-187 causes cardiac endothelial dysplasia to promote congenital heart disease through inhibition of NIPBL [Heart RNA-Seq]
GEO Series GSE275950. Mus. 4 samples. Type: Expression profiling by high throughput sequencing.
Elevated microRNA-187 causes cardiac endothelial dysplasia to promote congenital heart disease through inhibition of NIPBL [CUT&Tag]
GEO Series GSE275850. Homo sapiens. 5 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Single-cell Transcriptomic Profiling Unveils Cardiac Cell-type Specific Response to Maternal Hyperglycemia Underlying the Risk of Congenital Heart Defects
GEO Series GSE193746. Mus musculus. 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.