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428
datasets available to search
ShareScore release 0.9.0
Dataset results
428 results for “Malformations”
Serial Inversions Induce Tissue-specific Architectural Stripes, Gene Misexpression and Congenital Malformations [Hi-C]
GEO Series GSE116791. Mus musculus. 3 samples. Type: Other.
Application of Array CGH technique for the clinical diagnosis of developmental delay and congenital malformations in Saudi Arabia [400k]
GEO Series GSE182081. Homo sapiens. 52 samples. Type: Genome variation profiling by genome tiling array.
Decreased endothelial cell retinoic acid signaling accelerates progression of single ventricle pulmonary arteriovenous malformations
GEO Series GSE312375. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Biallelic variant in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations through altered WNT signalling
GEO Series GSE190621. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.
Feasibility and efficacy of a social prediction training in virtual reality in children and young adults with cerebellar malformations
<p>Updated dataset including primary and secondary outcome measures assessed before the training (T0), after the training (T2), and at the follow-up session (T3)</p>
Family Study of Congenital Cardiovascular Malformations
ClinicalTrials.gov study NCT00005258. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Activation of Epidermal Growth Factor Receptor Pathway in Slow-Flow Vascular Malformations
GEO Series GSE130807. Homo sapiens. 11 samples. Type: Expression profiling by high throughput sequencing.
Induced Endothelial Cell Cycle Arrest Prevents Arterio-venous Malformations in Hereditary Hemorrhagic Telangiectasia
GEO Series GSE244923. Mus musculus. 4 samples. Type: Expression profiling by high throughput sequencing.
Discovery and Functional Characterization of Novel Non-Coding Variants in a Case of Late-Onset Familial Cerebral Cavernous Malformation [RNA-seq]
GEO Series GSE312998. Homo sapiens. 2 samples. Type: Expression profiling by high throughput sequencing.
Serial Inversions Induce Tissue-specific Architectural Stripes, Gene Misexpression and Congenital Malformations
GEO Series GSE116794. Mus musculus. 40 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Other; Expression profiling by high throughput sequencing.
Loss of Maenli lncRNA expression causes engrailed-1 dependent congenital limb malformations [ATAC-seq]
GEO Series GSE137330. Mus musculus. 4 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Loss of Maenli lncRNA expression causes engrailed-1 dependent congenital limb malformations [RNA-seq]
GEO Series GSE137329. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Loss of Maenli lncRNA expression causes engrailed-1 dependent congenital limb malformations [Derived Virtual 4C]
GEO Series GSE137334. Mus musculus. 3 samples. Type: Other.
Loss of Maenli lncRNA expression causes engrailed-1 dependent congenital limb malformations [ChIP-seq]
GEO Series GSE137331. Mus musculus. 39 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Expression data of miRNAs and lncRNAs from the lumbosacral spinal cord of fetal rats with anorectal malformations in embryonic day 19
GEO Series GSE190332. Rattus norvegicus. 12 samples. Type: Non-coding RNA profiling by high throughput sequencing.
MMRN2 mutation underlies a rare form of autosomal-dominant laryngeal malformation
GEO Series GSE143191. Mus musculus. 7 samples. Type: Expression profiling by high throughput sequencing.
Serial Inversions Induce Tissue-specific Architectural Stripes, Gene Misexpression and Congenital Malformations [ChIP-seq]
GEO Series GSE116790. Mus musculus. 7 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
A targeted vector for brain endothelial cell gene delivery and cerebrovascular malformation modelling II
GEO Series GSE268643. Mus musculus. 3 samples. Type: Expression profiling by high throughput sequencing.
Loss of Maenli lncRNA expression causes engrailed-1 dependent congenital limb malformations [DamID-seq]
GEO Series GSE137332. Mus musculus. 4 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
A targeted vector for brain endothelial cell gene delivery and cerebrovascular malformation modelling
GEO Series GSE247963. 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.