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518
datasets available to search
ShareScore release 0.9.0
Dataset results
518 results for “Hereditary”
Evaluation of Pazopanib on Bleeding in Subjects With Hereditary Haemorrhagic Telangiectasia
ClinicalTrials.gov study NCT02204371. IPD Sharing: Not stated. Countries: 2. Publications: 0.
A Study With Lanadelumab in Persons With Hereditary Angioedema (HAE) in Poland
ClinicalTrials.gov study NCT05147181. IPD Sharing: YES. Countries: 1. Publications: 0.
Inhaled Granulocyte-Macrophage Colony Stimulating Factor (GM-CSF) in Hereditary Pulmonary Alveolar Proteinosis (PAP)
ClinicalTrials.gov study NCT01511068. IPD Sharing: Not stated. Countries: 1. Publications: 0.
A Survey of Lanadelumab in Participants With Hereditary Angioedema
ClinicalTrials.gov study NCT05397431. IPD Sharing: YES. Countries: 1. Publications: 0.
A Study to Explore Hereditary Angioedema (HAE) Symptoms and Treatment Patterns in Korean People
ClinicalTrials.gov study NCT06587464. IPD Sharing: YES. Countries: 1. Publications: 0.
Studies of Families With Hereditary Cataracts
ClinicalTrials.gov study NCT00001609. IPD Sharing: Not stated. Countries: 1. Publications: 3.
A Study About the Diagnosis and Management of Hereditary Angioedema (HAE) in Egypt
ClinicalTrials.gov study NCT07218393. IPD Sharing: YES. Countries: 1. Publications: 0.
Submucosal Bevacizumab for the Management of Recurrent Epistaxis in Patients With Hereditary Hemorrhagic Telangiectasia (HHT)
ClinicalTrials.gov study NCT01402531. IPD Sharing: Not stated. Countries: 1. Publications: 0.
A Study of Lanadelumab in Children With Hereditary Angioedema (HAE) in Multiple Countries
ClinicalTrials.gov study NCT07251933. IPD Sharing: YES. Countries: 0. Publications: 0.
Effect of Weight Loss on Cholesterol Metabolism in Hereditary Hypercholesterolemias and Overweight or Obesity.
ClinicalTrials.gov study NCT01995149. IPD Sharing: Not stated. Countries: 0. Publications: 1.
Prospective Psychometric Evaluation Study of a Patient-reported Outcomes (PRO) Instrument for Congenital Thrombotic Thrombocytopenic Purpura (cTTP, Upshaw-Schulman Syndrome [USS], Hereditary Thromboti
ClinicalTrials.gov study NCT03519672. IPD Sharing: YES. Countries: 2. Publications: 0.
Historical Case Record Survey of Visual Acuity Data From Patients With Leber's Hereditary Optic Neuropathy (LHON)
ClinicalTrials.gov study NCT02796274. IPD Sharing: Not stated. Countries: 7. Publications: 0.
Neurofilament light chain (NfL) as a biomarker of hereditary transthyretin-mediated amyloidosis
Open the record for dataset details and reuse information.
Data from: Measurement of systemic mitochondrial function in advanced primary open-angle glaucoma and Leber hereditary optic neuropathy
Open the record for dataset details and reuse information.
Data from: Combining GWAS and RNA-seq approaches for detection of the causal mutation for hereditary junctional epidermolysis bullosa in sheep
Open the record for dataset details and reuse information.
Non-coding variants alter Gata2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis
GEO Series GSE223274. Mus musculus. 12 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing.
miRNA expression profiling in hereditary breast tumors
GEO Series GSE44899. Rattus norvegicus; JC polyomavirus; Murid gammaherpesvirus 4; Betapolyomavirus hominis; Homo sapiens; Mus musculus; Human betaherpesvirus 5; Murid betaherpesvirus 1; Human immunodeficiency virus 1; Human alphaherpesvirus 1; human gammaherpesvirus 4; Betapolyomavirus macacae; Human gammaherpesvirus 8. 80 samples. Type: Non-coding RNA profiling by array.
CRISPR/Cas9-mediated gene correction in newborn rabbits with hereditary tyrosinemia type I [RNA-Seq]
GEO Series GSE142782. Oryctolagus cuniculus. 36 samples. Type: Expression profiling by high throughput sequencing.
Long Non-coding RNA expression profiles in Hereditary Haemorrhagic Telangiectasia
GEO Series GSE53515. Homo sapiens. 116 samples. Type: Expression profiling by array.
OXPHOS bioenergetic compensation does not explain disease penetrance in Leber hereditary optic neuropathy
GEO Series GSE144914. Homo sapiens. 9 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.