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428
datasets available to search
ShareScore release 0.9.0
Dataset results
428 results for “Malformations”
Distinct Global Shifts in Genomic Binding Profiles of Limb Malformation Associated HOXD13 Mutations
GEO Series GSE44799. Gallus gallus. 13 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing.
Gene Expression Differences in Pediatric Lymphatic Cystic Malformations: Size Really Matters
GEO Series GSE98742. Homo sapiens. 18 samples. Type: Expression profiling by array.
Circulating Plasma miRNA Homologs in Mice and Humans Reflect Familial Cerebral Cavernous Malformation Disease [Human]
GEO Series GSE232008. Homo sapiens. 30 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Transcriptome-wide Profile of Cerebral Cavernous Malformations Patients Reveal Important Long noncoding RNA molecular signatures
GEO Series GSE137596. Homo sapiens. 14 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.
GEO Series GSE295926. Mus musculus. 67 samples. Type: Methylation profiling by high throughput sequencing; Expression profiling by high throughput sequencing.
Maternal Vitamin C Deficiency and Genetic Risk Factors Contribute to Congenital Malformations through Dysregulation of DNA Methylation. [WGBS E11.5]
GEO Series GSE295922. Mus musculus. 8 samples. Type: Methylation profiling by high throughput sequencing.
Global interpretation of novel alternative splicing events in human congenital pulmonary airway malformations
GEO Series GSE179404. Homo sapiens. 15 samples. Type: Expression profiling by high throughput sequencing.
KRAS-Dependent Metabolic Reprogramming of Endothelial Cells as a Therapeutic Vulnerability in Brain Arteriovenous Malformations
GEO Series GSE292538. Homo sapiens. 18 samples. Type: Expression profiling by high throughput sequencing.
Whole-genome methylation study of congenital lung malformations in children
GEO Series GSE174625. Homo sapiens. 29 samples. Type: Methylation profiling by genome tiling array.
The application of second-generation sequencing in congenital pulmonary airway malformations
GEO Series GSE190620. Homo sapiens. 9 samples. Type: Non-coding RNA profiling by high throughput sequencing.
microRNA analysis of infantile hemangioma, lymphatic malformation, and skin
GEO Series GSE69136. Homo sapiens. 24 samples. Type: Non-coding RNA profiling by array.
Knockout mice with pituitary malformations help identify human cases of hypopituitarism
GEO Series GSE246211. Mus musculus. 2 samples. Type: Expression profiling by high throughput sequencing.
Transcriptome Clarifies Mechanisms of Lesion Genesis Versus Progression in Models of Ccm3 Cerebral Cavernous Malformations [miRNA-seq]
GEO Series GSE134006. Mus musculus. 6 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Investigating the Etiology of Craniofacial and Cardiac Malformations in a Mouse Model of SF3B4-Related Syndromes
GEO Series GSE260990. Mus musculus. 6 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 [RNA-seq]
GEO Series GSE171237. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Gene expression profiling of endothelial-mesenchymal transition in cerebral arteriovenous malformation
GEO Series GSE262300. Mus musculus. 4 samples. Type: Expression profiling by high throughput sequencing.
Transient Pharmacological Inhibition of SUMOylation during Pregnancy Induces Craniofacial Malformations in Offspring Mice
GEO Series GSE288224. Mus musculus. 18 samples. Type: Expression profiling by high throughput sequencing.
Human iPSC-derived cerebral organoids reveal progenitor pathology in EML1-linked cortical malformation
GEO Series GSE195666. Homo sapiens. 2 samples. Type: Expression profiling by high throughput sequencing.
Quantitative trait loci (QTL) study identifies novel genomic regions associated to Chiari-Like Malformation in Griffon Bruxellois dogs
GEO Series GSE52221. Canis lupus familiaris. 80 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Mechanisms for the Generation of Two Quadruplications Associated with Split-Hand Malformation
GEO Series GSE75190. Homo sapiens. 6 samples. Type: Genome variation profiling by array.
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.