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56
datasets available to search
ShareScore release 0.9.0
Dataset results
56 results for “genotype-phenotype”
Genotype-phenotype Correlations in Children and Adults With CTNNB1 Mutation
ClinicalTrials.gov study NCT04812119. IPD Sharing: NO. Countries: 2. Publications: 0.
Genotype-Phenotype Correlations of Late Infantile Neuronal Ceroid Lipofuscinosis
ClinicalTrials.gov study NCT01035424. IPD Sharing: NO. Countries: 1. Publications: 0.
Genotype-phenotype Relationship Between Cryptogenic Cholestasis and Familial Intrahepatic Cholestasis
ClinicalTrials.gov study NCT06781242. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Neonatal Screening of Biotinidase Deficiency: Genotype-phenotype Correlation and Clinical Follow-up
ClinicalTrials.gov study NCT06723925. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Inherited Retinal Diseases: Natural History and Genotype-Phenotype Correlations
ClinicalTrials.gov study NCT07265895. IPD Sharing: NO. Countries: 1. Publications: 0.
Genotype-phenotype Correlation and Pathogenic Mechanism in Hereditary Ataxia
ClinicalTrials.gov study NCT05160870. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Genes and Phenotype (GAP) A National Resource for Genotype-Phenotype Studies of Immunological and Inflammatory Pathways
ClinicalTrials.gov study NCT01161056. IPD Sharing: Not stated. Countries: 1. Publications: 0.
A Genotype-Phenotype Urothelial Cancer Registry
ClinicalTrials.gov study NCT00902590. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Dystonia Genotype-Phenotype Correlation
ClinicalTrials.gov study NCT03428009. IPD Sharing: YES. Countries: 1. Publications: 0.
Establishing a Repository of Blood and DNA Samples From People With Sickle Cell Disease (Comprehensive Sickle Cell Centers Collaborative Genotype-Phenotype Database and Sample Repository)
ClinicalTrials.gov study NCT00528203. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Validating Cardiac MRI Biomarkers and Genotype-Phenotype Correlations for DMD
ClinicalTrials.gov study NCT02834650. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Limbal Stem Cell Deficiency of Genetic Origin: Genotype-phenotype Correlation
ClinicalTrials.gov study NCT02886611. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Detailed genotype-phenotype analysis of AOSD cohorts
GEO Series GSE244372. Homo sapiens. 37 samples. Type: Expression profiling by high throughput sequencing.
Genotype-phenotype Correlation of SLC26A4 in CI Patients With EVA
ClinicalTrials.gov study NCT04934605. IPD Sharing: UNDECIDED. Countries: 0. Publications: 0.
Study of the Natural History and Genotype-Phenotype Correlations of Hereditary Hemorrhagic Telangiectasia Patients
ClinicalTrials.gov study NCT00004649. IPD Sharing: Not stated. Countries: 0. Publications: 0.
dataset related to article "Italian cohort of Lafora disease: Clinical features, disease evolution, and genotype-phenotype correlations"
<p>dataset relateto to article at title</p>
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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.