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412
datasets available to search
ShareScore release 0.7.1
Dataset results
412 results for “genetic risk”
Genetic Polymorphisms Associated With Cigarette Smoking and Risk of Graves' Disease
ClinicalTrials.gov study NCT00505011. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Bacterial and Host Genetic Risk Factors in Acute Pyelonephritis
ClinicalTrials.gov study NCT01137929. IPD Sharing: Not stated. Countries: 0. Publications: 0.
GENErating Behavior Change, An Integrative Health Coaching and Genetic Risk Testing Pilot
ClinicalTrials.gov study NCT01766271. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Fullscale_Intervention Study: Genetic Risk Communication in Coronary Heart Disease and Wearables
ClinicalTrials.gov study NCT05789966. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Interaction of Potassium and Genetic Risk Variants on Diabetes Risk
ClinicalTrials.gov study NCT03367455. IPD Sharing: NO. Countries: 0. Publications: 0.
Prevention of Recurrence and Metastasis in Genetically High-Risk Melanomas
ClinicalTrials.gov study NCT04285749. IPD Sharing: NO. Countries: 0. Publications: 0.
Massively parallel analysis of genotype-dependent enhancer activity among atopic dermatitis genetic risk variants
GEO Series GSE300756. Homo sapiens. 6 samples. Type: Genome binding/occupancy 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
GEO Series GSE115319. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Third-party reanalysis.
Lymphocyte DNA methylation mediates genetic risk at shared immune mediated disease loci
GEO Series GSE137634. Homo sapiens. 436 samples. Type: Methylation profiling by genome tiling array; Expression profiling by array; Third-party reanalysis.
Functional Validation of Common Idiopathic Pulmonary Fibrosis Genetic Risk Variants
GEO Series GSE175459. Homo sapiens. 969 samples. Type: Expression profiling by high throughput sequencing; Methylation profiling by genome tiling array.
DNA methylation in lung cells is a key modulator of asthma endotypes and genetic risk
GEO Series GSE85568. Homo sapiens. 200 samples. Type: Expression profiling by high throughput sequencing; Methylation profiling by array.
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
GEO Series GSE6754. Homo sapiens. 6971 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Genetic variants affecting RNA stability influence complex traits and disease risk II
GEO Series GSE298114. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
The Heritage (HEalth, RIsk factors, exercise Training And GEnetics) family study
GEO Series GSE47874. Homo sapiens. 52 samples. Type: Expression profiling by array.
Determinants of excess genetic risk of acute myocardial infarction – a matched case-control study
GEO Series GSE34198. Homo sapiens. 97 samples. Type: Expression profiling by array.
Genetic variants that impact alternative polyadenylation in cancer represent candidate causal risk loci [RNA-seq]
GEO Series GSE241699. Homo sapiens. 154 samples. Type: Expression profiling by high throughput sequencing.
Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions
GEO Series GSE255142. Homo sapiens. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Combining high-risk ADRD mutations across genetically distinct mice
GEO Series GSE293440. Mus musculus. 290 samples. Type: Expression profiling by high throughput sequencing.
Genetic Control of tRNA-Derived Fragments Contributes to Cancer Risk
GEO Series GSE304444. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Summary statistics for "Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke"
<p>Summary statistics of the GWA studies presented in <a href="https://doi.org/10.1101/718221">https://doi.org/10.1101/718221</a></p> <p>These are the summary statistics of all imputed SNPs, minus those that showed big differences in allele frequency between different populations (see manuscript for details).</p> <p>Header description:</p> <p>"rs_id" = the rs-id for the variant</p> <p>"chromosome" = the chromosome of the variant</p> <p>"base_pair_location" = the location in bases, according to human reference genome hg19</p> <p>"effect_allele" = the allele that is tested for association with the phenotype</p> <p>"other_allele" = the other allele</p> <p>"effect_allele_frequency" = the allele frequency of the effect allele (not necessarily the minor allele frequency)</p> <p>"IMPUTE2_info" = the imputation quality score as computed by IMPUTE2</p> <p>"beta" = the beta-coefficient from BOLT-LMM</p> <p>"standard_error" = the standard error of beta</p> <p>"p-value" = the p-value for association from BOLT-LMM</p> <p>To convert beta and standard error to odds ratios, you need to know the fraction of cases of the respective GWAS. These can be found in the supplementary material of the manuscript. Use the following formula with the case fraction μ: log OR = β / (μ * (1 - μ)). See the manuscript for more explanation.</p>
ScienceDex guides
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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.