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142
datasets available to search
ShareScore release 0.9.0
Dataset results
142 results for “Phenotypic syndrome”
Generation of a novel iPSC-based model to explore the molecular and functional phenotype of a rare genetic immunodeficiency, the ICF syndrome type 2.
GEO Series GSE262957. Homo sapiens. 5 samples. Type: Methylation profiling by genome tiling array.
Episignatures stratifying ADNP syndrome show modest correlation with phenotype [RNA-seq]
GEO Series GSE152421. Homo sapiens. 36 samples. Type: Expression profiling by high throughput sequencing.
Genome-wide transcription profiling of 22q11.2 deletion syndrome reveals functional pathways related to phenotypic expression of psychosis and autism spectrum disorder
GEO Series GSE59216. Homo sapiens. 112 samples. Type: Expression profiling by array.
A novel GATA2 enhancer single nucleotide mutation results in the MonoMAC syndrome phenotype in two second cousins
GEO Series GSE227436. Homo sapiens. 10 samples. Type: Expression profiling by high throughput sequencing.
Patients with a Kabuki syndrome phenotype demonstrate DNA methylation abnormalities.
GEO Series GSE116300. Homo sapiens. 44 samples. Type: Methylation profiling by genome tiling array.
A Marfan syndrome gene expression phenotype in cultured skin fibroblasts
GEO Series GSE8759. Homo sapiens. 101 samples. Type: Expression profiling by array.
A mouse mutation that dysregulates neighboring Galnt17 and Auts2 genes is associated with phenotypes related to the human AUTS2 syndrome
GEO Series GSE132684. Mus musculus. 24 samples. Type: Expression profiling by high throughput sequencing.
Increased Endothelial Sclerostin Caused by Elevated DSCAM Mediates Multiple Trisomy 21 (Down Syndrome) Phenotypes
GEO Series GSE253244. Homo sapiens. 20 samples. Type: Expression profiling by high throughput sequencing.
Sex-Dependent Sensory Phenotypes and Related Transcriptomic Expression Profiles Are Differentially Affected by Angelman Syndrome
GEO Series GSE130883. Mus musculus. 12 samples. Type: Expression profiling by high throughput sequencing.
Fragile X Syndrome Patient-Derived Neurons Developing in the Mouse Brain Show FMR1-Dependent Phenotypes
GEO Series GSE202894. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.
Deep phenotyping of Post-infectious Myalgic Encephalomyelitis/Chronic Fatigue Syndrome [RNA-Seq]
GEO Series GSE245661. Homo sapiens. 25 samples. Type: Expression profiling by high throughput sequencing.
Deep phenotyping of Post-infectious Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
GEO Series GSE251792. Homo sapiens. 136 samples. Type: Expression profiling by high throughput sequencing; Protein profiling by protein array.
Deep phenotyping of Post-infectious Myalgic Encephalomyelitis/Chronic Fatigue Syndrome [Protein]
GEO Series GSE251790. Homo sapiens. 42 samples. Type: Protein profiling by protein array.
BubR1 allelic effects drive phenotypic heterogeneity in MVA progeria syndrome [3 month old RNA-seq]
GEO Series GSE134781. Mus musculus. 9 samples. Type: Expression profiling by high throughput sequencing.
A murine model lacking Lyst recapitulates Chediak-Higashi syndrome with an earlier-onset neurodegenerative phenotype
GEO Series GSE266142. Mus musculus. 24 samples. Type: Expression profiling by high throughput sequencing.
A MYT1L Syndrome mouse model recapitulates patient phenotypes and reveals altered brain development due to disrupted neuronal maturation [ATAC-Seq]
GEO Series GSE173588. Mus musculus. 29 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Self-regulating gene therapy ameliorates phenotypes and overcomes gene dosage sensitivity in a mouse model of Rett syndrome
GEO Series GSE291883. Homo sapiens. 18 samples. Type: Expression profiling by high throughput sequencing.
A phenotypic rescue approach identifies lineage regionalization defects in a mouse model of DiGeorge syndrome.
GEO Series GSE206737. Mus musculus. 8 samples. Type: Expression profiling by high throughput sequencing.
Variability vs. phenotype: Multimodal analysis of Dravet syndrome brain organoids powered by deep learning
GEO Series GSE256142. Homo sapiens. 18 samples. Type: Expression profiling by high throughput sequencing.
A MYT1L Syndrome mouse model recapitulates patient phenotypes and reveals altered brain development due to disrupted neuronal maturation [RNA-Seq]
GEO Series GSE173926. Mus musculus. 28 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.