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142
datasets available to search
ShareScore release 0.9.0
Dataset results
142 results for “Phenotypic syndrome”
Cardiovascular Phenotype Study in Patients With Obstructive Sleep Apnea Syndrome
ClinicalTrials.gov study NCT00764218. IPD Sharing: Not stated. Countries: 1. Publications: 11.
Whole Transcriptome Profiling and Metabolic Phenotyping in Children With ROHHAD Syndrome
ClinicalTrials.gov study NCT02602769. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Evaluation Genotypic, Phenotypic and Prognosis APECED Syndrome
ClinicalTrials.gov study NCT03751683. IPD Sharing: NO. Countries: 1. Publications: 1.
Biochemical and Phenotypical Aspects of Smith-Lemli-Opitz Syndrome and Related Disorders of Cholesterol Metabolism
ClinicalTrials.gov study NCT05047354. IPD Sharing: UNDECIDED. Countries: 1. Publications: 4.
Psychiatric Phenotype Characterization of Individuals With FOXP1 Syndrome
ClinicalTrials.gov study NCT06211673. IPD Sharing: NO. Countries: 1. Publications: 11.
Characterizing the Genotype and Phenotype in Adults With Bardet-Biedl Syndrome
ClinicalTrials.gov study NCT05400278. IPD Sharing: UNDECIDED. Countries: 1. Publications: 1.
Evaluation of Endocrine and Metabolic Parameters in the New Diagnostic Phenotypes of Polycystic Ovary Syndrome
ClinicalTrials.gov study NCT00784615. IPD Sharing: Not stated. Countries: 1. Publications: 37.
Clinical Evaluation of a Point of Care (POC) Assay to Identify Phenotypes in the Acute Respiratory Distress Syndrome
ClinicalTrials.gov study NCT04009330. IPD Sharing: YES. Countries: 2. Publications: 1.
Phenotype and Etiology of Pallister-Hall Syndrome
ClinicalTrials.gov study NCT00001404. IPD Sharing: Not stated. Countries: 2. Publications: 3.
Mutations and Phenotypes of Unclassifiable Inherited Bone Marrow Failure Syndromes
ClinicalTrials.gov study NCT05436587. IPD Sharing: NO. Countries: 1. Publications: 2.
Fragmentation and the context-dependence of dispersal syndromes: matrix harshness modifies resident-disperser phenotypic differences in microcosms
Open the record for dataset details and reuse information.
Highest Dose of Uproleselan in Combination With Fludarabine and Cytarabine for Patients With Acute Myeloid Leukemia, Myelodysplastic Syndrome, or Mixed Phenotype Acute Leukemia Relapsed or Refractory
ClinicalTrials.gov study NCT05146739. IPD Sharing: YES. Countries: 1. Publications: 0.
Fragile X Syndrome Patient–Derived Neurons Developing in the Mouse Brain Show FMR1-Dependent Phenotypes
GEO Series GSE202895. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
Clinical spectrum of multi-locus imprinting disturbances associated with maternal-effect variants range from overt Beckwith-Wiedemann syndrome to apparently healthy phenotype
GEO Series GSE133774. Homo sapiens. 10 samples. Type: Methylation profiling by array.
Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome
GEO Series GSE25542. Homo sapiens. 59 samples. Type: Expression profiling by array.
Patient-Specific and Genome-Edited Induced Pluripotent Stem Cell-Derived Cardiomyocytes Elucidate Single-Cell Phenotype of Brugada Syndrome
GEO Series GSE93530. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.
A deep phenotyping study in mouse and iPSC models to understand the role of oligodendroglia in optic neuropathy in Wolfram syndrome
GEO Series GSE264222. Homo sapiens. 24 samples. Type: Expression profiling by high throughput sequencing.
Deep phenotyping of Post-infectious Myalgic Encephalomyelitis/Chronic Fatigue Syndrome [PBMC RNA-Seq]
GEO Series GSE251872. Homo sapiens. 27 samples. Type: Expression profiling by high throughput sequencing.
A CRISPR-engineered Isogenic Model Reveals Altered Neuronal Phenotypes of the 22q11.2 A-B Syndromic Deletion
GEO Series GSE200225. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
EHMT1 gene truncation in HEK293 cells recapitulates Kleefstra Syndrome disease phenotype
GEO Series GSE157390. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
ScienceDex guides
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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.