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428
datasets available to search
ShareScore release 0.9.0
Dataset results
428 results for “Malformations”
Combinatorial effects on gene expression at the Lbx1/Fgf8 locus resolve Split-Hand/Foot Malformation type 3 [Capture Hi-C, Virtual4C]
GEO Series GSE223450. Mus musculus. 20 samples. Type: Other.
Impaired neurovascular remodeling mediated by Apelin signaling and Cdc42 activity in endothelial Rbpj deficient brain arteriovenous malformation [RNA-seq]
GEO Series GSE223531. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Q241R mutation of Braf gene causes neurological abnormalities in a mouse model of cardio-facio-cutaneous syndrome independent of developmental malformations
GEO Series GSE235033. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Somatic Gain of KRAS Function in the Endothelium is Sufficient to Cause Vascular Malformations that Require MEK but not PI3K Signaling
GEO Series GSE150426. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
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.
KRIT1 heterozygous mutations are sufficient to induce a pathological phenotype in patient-derived iPSC models of Cerebral Cavernous Malformation
GEO Series GSE291768. Homo sapiens. 18 samples. Type: Expression profiling by high throughput sequencing.
Comprehensive Transcriptome Analysis of Cerebral Cavernous Malformation Across Multiple Species and Genotypes
GEO Series GSE123968. Homo sapiens; Caenorhabditis elegans; Mus musculus. 32 samples. Type: Expression profiling by high throughput sequencing.
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development
GEO Series GSE218022. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Induced Endothelial Cell Cycle Arrest Prevents Arterio-venous Malformations in Hereditary Hemorrhagic Telangiectasia (Bulk RNA-Seq)
GEO Series GSE245197. Mus musculus. 9 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.
Hopeful monsters: Unintended sequencing of famously malformed mite mitochondrial tRNAs reveals widespread expression and processing of sense-antisense pairs
GEO Series GSE162913. Tetranychus urticae. 6 samples. Type: Non-coding RNA 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.
PRDM1 DNA-binding zinc finger domain is required for normal limb development and is disrupted in Split Hand/Foot Malformation
GEO Series GSE217486. Danio rerio. 10 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
High-throughput differentiation of human blood vessel organoids reveals overlapping and distinct functions of the cerebral cavernous malformation proteins
GEO Series GSE276497. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.
Modeling the Blood-Brain Barrier Formation and Cerebral Cavernous Malformations in human PSCs- and primary tissue-derived organoids
GEO Series GSE263669. Homo sapiens. 1 samples. Type: Other.
Thrombospondin1 replacement prevents cerebral cavernos malformations
GEO Series GSE85657. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Developmental Venous Anomalies are a Genetic Primer for Cerebral Cavernous Malformations
GEO Series GSE195732. Homo sapiens. 25 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Circulating Plasma miRNA Homologs in Mice and Humans Reflect Familial Cerebral Cavernous Malformation Disease[Mouse]
GEO Series GSE232009. Mus musculus. 41 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Transcriptomic signatures of individual cell types in cerebral cavernous malformation
GEO Series GSE233210. Homo sapiens. 29 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.