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76 results for “Association studies in genetics”

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geo24/100

Genome-wide association studies identify novel genetic loci for epigenetic age acceleration among survivors of childhood cancer [Metadata_SJLIFE2_502]

GEO Series GSE197675. Homo sapiens. 502 samples. Type: Methylation profiling by genome tiling array.

openGEO-OpenMar 2022View details →
geo24/100

PTSD or resilient - Genetic and Epigenetic association studies in police officers

GEO Series GSE99755. Homo sapiens. 67 samples. Type: Methylation profiling by genome tiling array.

openGEO-OpenJan 2018View details →
geo24/100

Genetic Association study of Autism in Saudi Females using SNP array

GEO Series GSE221098. Homo sapiens. 73 samples. Type: Genome variation profiling by SNP array.

openGEO-OpenDec 2022View details →
geo24/100

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.

openGEO-OpenJan 2023View details →
geo24/100

Genome-wide association studies identify novel genetic loci for epigenetic age acceleration among survivors of childhood cancer [Metadata_SJLIFE_controls_282]

GEO Series GSE197676. Homo sapiens. 282 samples. Type: Methylation profiling by genome tiling array.

openGEO-OpenMar 2022View details →
geo24/100

Deciphering the genetic regulation of peripheral blood transcriptome in pigs through allele-specific expression analysis and expression genome-wide association study

GEO Series GSE97374. Sus scrofa. 243 samples. Type: Expression profiling by array.

openGEO-OpenFeb 2018View details →
geo24/100

A study of genetic variants associated with skin traits in the Vietnamese population

GEO Series GSE248483. Homo sapiens. 96 samples. Type: SNP genotyping by SNP array.

openGEO-OpenNov 2023View details →
geo24/100

Multi-omics co-localization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus [RNA-Seq]

GEO Series GSE172367. Homo sapiens. 190 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJun 2021View details →
zenodo24/100

Figure 4 from: Al-Musawi ZJMA, Al-Juhaishi AMR (2024) Association study between D2 receptor A-241G, rs1799978 genetic variation and olanzapine efficacy in Iraqi schizophrenic patients. Pharmacia 71: 1-6. https://doi.org/10.3897/pharmacia.71.e111984

Figure 4 The PANSS score of schizophrenic and healthy volunteers.

opencc-by-4.0Jan 2024View details →
zenodo24/100

Figure 2 from: Al-Musawi ZJMA, Al-Juhaishi AMR (2024) Association study between D2 receptor A-241G, rs1799978 genetic variation and olanzapine efficacy in Iraqi schizophrenic patients. Pharmacia 71: 1-6. https://doi.org/10.3897/pharmacia.71.e111984

Figure 2 The Prevalence of D2 receptor alleles A-241G (rs1799978) among volunteers.

opencc-by-4.0Jan 2024View details →
zenodo24/100

Figure 1 from: Al-Musawi ZJMA, Al-Juhaishi AMR (2024) Association study between D2 receptor A-241G, rs1799978 genetic variation and olanzapine efficacy in Iraqi schizophrenic patients. Pharmacia 71: 1-6. https://doi.org/10.3897/pharmacia.71.e111984

Figure 1 Genotyping of D2 receptor genes A-241G (rs1799978).

opencc-by-4.0Jan 2024View details →
ClinicalTrials.gov24/100

The BRAVE Study- The Identification of Genetic Variants Associated With Bicuspid Aortic Valve Using a Combination of Case-control and Family-based Approaches.

ClinicalTrials.gov study NCT04514445. IPD Sharing: NO. Countries: 1. Publications: 0.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov24/100

Genetic Variants Replication Study Associated With Dependence on Sulfonylurea in Participants With Type 2 Diabetes

ClinicalTrials.gov study NCT04123587. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov24/100

Research for Genetic Factors Involved in Congenital Dislocation of Hip: Genome-wide Association Study in Grand West France

ClinicalTrials.gov study NCT02900482. IPD Sharing: NO. Countries: 1. Publications: 0.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov24/100

Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants

ClinicalTrials.gov study NCT05589714. IPD Sharing: YES. Countries: 14. Publications: 0.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov24/100

A Prospective Observational Cohort to Study the Genetics of Obstructive Sleep Apnea and Associated Co-Morbidities

ClinicalTrials.gov study NCT01857427. IPD Sharing: NO. Countries: 1. Publications: 0.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov24/100

Genetic Studies of Strabismus, Nystagmus, and Associated Disorders

ClinicalTrials.gov study NCT04770519. IPD Sharing: YES. Countries: 1. Publications: 0.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov24/100

Identification of Genetic Polymorphism Related to Acute Kidney Injury After Liver Transplantation Through Genome-wide Association Study (GWAS) in Korean Population

ClinicalTrials.gov study NCT03344380. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov24/100

Study to Estimate How Common it is to Have Genetic Variants Associated With NAFLD

ClinicalTrials.gov study NCT04494360. IPD Sharing: YES. Countries: 1. Publications: 0.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov24/100

A Genetic Substudy Associated With the Avastin (Bevacizumab) Study MO19390 in Patients With Advanced or Recurrent Non-Squamous Cell Lung Cancer.

ClinicalTrials.gov study NCT00642824. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →

ScienceDex guides

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record