Find research datasets worth reusing
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”
Clinical and Molecular Characteristics of Congenital Glioblastoma Multiforme
GEO Series GSE32374. Homo sapiens. 21 samples. Type: Expression profiling by array.
Global misregulation of genes largely uncoupled to DNA methylome epimutations characterizes a congenital overgrowth syndrome
GEO Series GSE93775. Bos indicus x Bos taurus. 8 samples. Type: Methylation profiling by high throughput sequencing.
Expression data from Congenital disorders of Glycosylation type-1 patients (CDG-I)
GEO Series GSE8440. Homo sapiens. 36 samples. Type: Expression profiling by array.
Genomic DNA methylation profile in peripheral blood of children with Congenital biliary dilatation
GEO Series GSE275555. Homo sapiens. 61 samples. Type: Methylation profiling by genome tiling array.
Oligogenic inheritance of congenital heart disease involving a NKX2-5 modifier
GEO Series GSE131323. Homo sapiens; Mus musculus. 17 samples. Type: Expression profiling by high throughput sequencing.
Next-Generation Sequencing Revealed L-Carnitine Rescues Congenital Myopathy in Transgenic Zebrafish with Tropomyosin 3 Novel Mutation
GEO Series GSE149261. Danio rerio. 10 samples. Type: Expression profiling by high throughput sequencing.
Mutation in LBX1/Lbx1 precludes transcription factor cooperativity and causes congenital hypoventilation in humans and mice
GEO Series GSE214975. Mus musculus. 6 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Novel molecular and phenotypic insights into congenital lung malformations
GEO Series GSE100442. Homo sapiens. 24 samples. Type: Expression profiling by array.
Maternal Serum tRNA-derived Fragments (tRFs) as Potential Candidates for Diagnosis of Fetal Congenital Heart Disease
GEO Series GSE221349. Homo sapiens. 12 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Gene Expression of Kidney from HSRA-S (congenital solitary kidney) and HSRA-C (two-kidney) using Rat Gene 1.1 ST Array [RaGene-1_1-st]
GEO Series GSE62092. Rattus norvegicus. 8 samples. Type: Expression profiling by array.
Transcriptional Atlas of Cardiogenesis Maps Congenital Heart Disease Interactome
GEO Series GSE51483. Mus musculus. 45 samples. Type: Expression profiling by array.
Maternal plasma micro-RNAs in fetal congenital diaphragmatic hernia: A potential non-invasive tool for prenatal diagnosis and risk stratification
GEO Series GSE309606. Homo sapiens. 28 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Human induced pluripotent stem cells reveal early developmental molecular correlates with a probable Leber congenital amaurosis type I
GEO Series GSE43946. Homo sapiens. 34 samples. Type: Expression profiling by array.
Thyroidal transcriptomic profiles of pathoadaptive responses to congenital hypothyroidism in XB130 knockout mic
GEO Series GSE197052. Mus musculus. 24 samples. Type: Expression profiling by array.
Modelling erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) for diagnosis and molecular dissection.
GEO Series GSE125175. Homo sapiens. 32 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
A tracheal aspirate-derived airway basal cell model reveals a proinflammatory epithelial defect in congenital diaphragmatic hernia
GEO Series GSE211790. Homo sapiens. 32 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Placental gene expression data from human fetuses with isolated spina bifida and fetuses with no congenital anomalies
GEO Series GSE252552. Homo sapiens. 33 samples. Type: Expression profiling by array.
Array CGH in congenital heart disease
GEO Series GSE7527. Homo sapiens. 119 samples. Type: Genome variation profiling by genome tiling array.
Loss of Runx3 in osteoblasts provokes severe congenital osteopenia
GEO Series GSE57195. Mus musculus. 4 samples. Type: Expression profiling by array.
RNaseT2 deficient mice reveal the interferon-driven brain phenotype of congenital CMV infection and type I interferonopathies
GEO Series GSE180138. Mus musculus. 64 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.