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.
412
datasets available to search
ShareScore release 0.7.1
Dataset results
412 results for “genetic risk”
Expression of long non-coding RNAs in autoimmunity and linkage to enhancer function and autoimmune disease risk genetic variants
GEO Series GSE92472. Homo sapiens. 15 samples. Type: Expression profiling by high throughput sequencing.
Increased Risk of Genetic and Epigenetic Instability in Human Embryonic Stem Cells Associated with Specific Culture Conditions
GEO Series GSE56851. Homo sapiens. 192 samples. Type: Expression profiling by array; Methylation profiling by genome tiling array; SNP genotyping by SNP array; Genome variation profiling by SNP array.
Genetic regulatory mechanisms of smooth muscle cells map to coronary artery disease risk loci
GEO Series GSE113348. Homo sapiens. 60 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Genetic risk of osteoarthritis operates during human skeletogenesis
GEO Series GSE214394. Homo sapiens. 22 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Integration of Alzheimer's disease genetics and myeloid genomics identifies disease risk regulatory elements and genes
GEO Series GSE164315. Homo sapiens. 7 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Genetic variability in response to Amyloid beta deposition influences Alzheimer's disease risk
GEO Series GSE137313. Mus musculus. 103 samples. Type: Expression profiling by high throughput sequencing.
Epigenomic partitioning of an polygenic risk score for asthma reveals distinct genetically driven disease pathways
GEO Series GSE245569. Homo sapiens. 23 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Non-coding genetic variants dominant in African American reveal prostate cancer risk
GEO Series GSE276748. Homo sapiens. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Genetic Endothelial Systems Biology of Sickle Stroke Risk
GEO Series GSE9877. Homo sapiens. 47 samples. Type: Expression profiling by array.
A human single cell atlas of the substantia nigra reveals novel cell specific pathways associated with the genetic risk of Parkinson’s disease and neuropsychiatric disorders
GEO Series GSE140231. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
Predictive computational obesity risk framework through integration of gene expression profiles and genetic risk score.
GEO Series GSE109597. Homo sapiens. 84 samples. Type: Expression profiling by array.
Expression data of small intestine crypts and villi from mice with nutritional and genetic risk factors for intestinal tumors
GEO Series GSE29538. Mus musculus. 47 samples. Type: Expression profiling by array.
The LHX2-OTX2 transcriptional regulatory module controls retinal pigmented epithelium differentiation and underlies genetic risk for age-related macular degeneration
GEO Series GSE178166. Homo sapiens. 13 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Genetic Counseling in Women at Risk for BRCA1 or BRCA2 Mutations
ClinicalTrials.gov study NCT00416754. IPD Sharing: NO. Countries: 0. Publications: 0.
Genetic Mechanisms and Additional Risk Factors Underlying Hip Dysplasia
ClinicalTrials.gov study NCT04563819. IPD Sharing: NO. Countries: 0. Publications: 0.
Prenatal Cell-free DNA Screening in Pregnancies With Diverse Genetic Risk Profiles Utilizing Targeted and Whole-exome Sequencing
ClinicalTrials.gov study NCT07106853. IPD Sharing: YES. Countries: 0. Publications: 0.
Disclosure of Genetic Risk for Salt Sensitivity
ClinicalTrials.gov study NCT03775720. IPD Sharing: NO. Countries: 0. Publications: 0.
Phase I Study of UCART123 in Patient With Adverse Genetic Risk Acute Myeloid Leukemia
ClinicalTrials.gov study NCT04106076. IPD Sharing: UNDECIDED. Countries: 0. Publications: 0.
Genetic and Environmental Risk Factors Related to Esophageal Cancer
ClinicalTrials.gov study NCT01035398. IPD Sharing: NO. Countries: 1. Publications: 0.
Genome-wide Association Study of Different Types of Diabetes and Construction of Genetic Risk Score
ClinicalTrials.gov study NCT06791330. IPD Sharing: Not stated. Countries: 0. Publications: 0.
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.