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.
990
datasets available to search
ShareScore release 0.9.0
Dataset results
990 results for “coronary artery disease”
Whole Blood Cell Gene Expression Profiling in Patients with Coronary Artery Disease from the PREDICT Trial
GEO Series GSE20681. Homo sapiens. 198 samples. Type: Expression profiling by array.
Galectin-3 binding protein (Gal-3BP), coronary artery disease and cardiovascular mortality – insights from the LURIC study
GEO Series GSE97244. Homo sapiens. 4 samples. Type: Expression profiling by array.
LncRNA expression profiling for 6 human monocytes samples from Coronary Artery Disease patients and non Coronary Artery Disease patients
GEO Series GSE69587. Homo sapiens. 6 samples. Type: Non-coding RNA profiling by array.
FOXO3a functions as a transcriptional and co-transcriptional splicing regulator in vascular endothelial cell lines in coronary artery disease
GEO Series GSE225605. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Alternations in gut microbiota and host transcriptome of patients with coronary artery disease [16S_rRNA]
GEO Series GSE242047. Homo sapiens. 52 samples. Type: Expression profiling by high throughput sequencing.
Integrative vascular endothelial cell genomics identify AIDA as a coronary artery disease candidate gene (Hi-C)
GEO Series GSE126199. Homo sapiens. 4 samples. Type: Other.
LncRNA Expression Profile and Identification of Novel LncRNA Biomarkers for Diagnosing Coronary Artery Disease
GEO Series GSE113079. Homo sapiens. 141 samples. Type: Non-coding RNA profiling by array.
DNA methylation patterns from peripheral blood separate coronary artery disease patients with and without heart failure.
GEO Series GSE134766. Homo sapiens. 20 samples. Type: Methylation profiling by high throughput sequencing.
Cell-specific chromatin landscape in human coronary artery resolves regulatory mechanisms of disease risk
GEO Series GSE175621. Homo sapiens. 44 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
An integrative multiomic network model links the canonical lipid metabolism pathway to glucose regulation in coronary artery disease
GEO Series GSE157223. Mus musculus. 12 samples. Type: Expression profiling by high throughput sequencing.
Quantitative trait loci mapped for TCF21 binding, chromatin accessibility and chromosomal looping in coronary artery smooth muscle cells reveal molecular mechanisms of coronary disease loci (ChIP-Seq)
GEO Series GSE141751. Homo sapiens. 1 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Differences in monocyte miRNA profiles between patients with coronary artery disease and healthy controls
GEO Series GSE105449. Homo sapiens. 105 samples. Type: Non-coding RNA profiling by array.
Whole Blood Cell Gene Expression Profiling in Patients with Coronary Artery Disease from the Cathgen Registry
GEO Series GSE20680. Homo sapiens. 195 samples. Type: Expression profiling by array.
Plasma-derived exosomal circular RNA hsa_circ_0005540 as a novel diagnostic biomarker for coronary artery disease
GEO Series GSE152498. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Quantitative trait loci mapped for TCF21 binding, chromatin accessibility and chromosomal looping in coronary artery smooth muscle cells reveal molecular mechanisms of coronary disease loci [array]
GEO Series GSE150403. Homo sapiens. 15 samples. Type: SNP genotyping by SNP array; Genome variation profiling by SNP array.
Integrative vascular endothelial cell genomics identify AIDA as a coronary artery disease candidate gene (ChIPseq)
GEO Series GSE126197. Homo sapiens. 12 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
High-content CRISPR screens link coronary artery disease genes to endothelial cell programs [Pilot scRNA-seq]
GEO Series GSE212396. Homo sapiens. 15 samples. Type: Expression profiling by high throughput sequencing.
Colocalization of GWAS and molecular QTL signals in human vascular smooth muscle cells predict candidate causal genes for coronary artery disease and vascular disorders
GEO Series GSE193817. Homo sapiens. 284 samples. Type: Expression profiling by high throughput sequencing.
High-content CRISPR screens link coronary artery disease genes to endothelial cell programs [RNAseq]
GEO Series GSE210522. Homo sapiens. 52 samples. Type: Expression profiling by high throughput sequencing.
Integrative analysis of liver-specific noncoding regulatory variants associated with the risk of coronary artery disease
GEO Series GSE157306. Homo sapiens. 10 samples. Type: Genome binding/occupancy 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.