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412
datasets available to search
ShareScore release 0.7.1
Dataset results
412 results for “genetic risk”
Serotonin-1A receptor, a psychiatric disease risk factor, modulates offspring immunity via sex-dependent genetic nurture
GEO Series GSE217086. Mus musculus. 4 samples. Type: Expression profiling by high throughput sequencing.
Activity-Dependent Transcriptional Program in NGN2+ Neurons Enriched for Genetic Risk for Brain-Related Disorders
GEO Series GSE203082. Homo sapiens. 66 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Genome-wide discovery of multiple sclerosis genetic risk variant allelic regulatory activity
GEO Series GSE293036. Homo sapiens. 19 samples. Type: Expression profiling by high throughput sequencing; Other.
Integrated single-cell chromatin and transcriptomic analyses of human scalp reveal etiological insights into genetic risk for hair and skin disease [scATAC-Seq]
GEO Series GSE212448. Homo sapiens. 13 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Convergent coexpression of autism associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies
GEO Series GSE222259. Homo sapiens. 30 samples. Type: Expression profiling by high throughput sequencing.
Glucocorticoids Unmask Silent Non-Coding Genetic Risk Variants for Common Diseases [ChIP-seq]
GEO Series GSE185928. Homo sapiens. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Integrative Epigenome-Wide Analysis Shows That DNA Methylation May Mediate Genetic Risk In Inflammatory Bowel Disease [Expression profiling]
GEO Series GSE86434. Homo sapiens. 251 samples. Type: Expression profiling by array.
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.
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.
Non-coding genetic variation in GATA3 increases acute lymphoblastic leukemia risk through local and global changes in chromatin conformation
GEO Series GSE145997. Homo sapiens. 74 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other.
Discovering human diabetes-risk gene function with genetics and physiological assays
GEO Series GSE116369. Homo sapiens. 8 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.
Coronary artery disease genes SMAD3 and TCF21 promote opposing interactive genetic programs that regulate smooth muscle cell differentiation and disease risk [RNA-seq]
GEO Series GSE115318. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Nutrigenomic profiling identifies ZIP10 (SLC39A10) as a regulator of erythroid zinc homeostasis with genetic associations to anemia risk
GEO Series GSE310594. Mus musculus. 12 samples. Type: Expression profiling by high throughput sequencing.
Deficiency of Autism Risk Factor Ash1l in Prefrontal Cortex Induces Genetic Aberrations, Synaptic Imbalance and Severe Seizures
GEO Series GSE181819. Mus musculus. 4 samples. Type: Expression profiling by high throughput sequencing.
Building a schizophrenia genetic network: Transcription Factor 4 regulates genes involved in neuronal development and schizophrenia risk
GEO Series GSE112704. Homo sapiens. 5 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Glucocorticoids Unmask Silent Non-Coding Genetic Risk Variants for Common Diseases [HiChIP]
GEO Series GSE189453. Homo sapiens. 2 samples. Type: Other.
Functional Validation of Common Idiopathic Pulmonary Fibrosis Genetic Risk Variants [mRNA sequencing]
GEO Series GSE175457. Homo sapiens. 422 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.