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UK10K_OBESITY_GS
Study
EGAS00001000242
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We performed whole-exome sequencing of 20 samples (10 actinic keratosis and 10 cutaneous squamous cell carcinoma) to investigate a potential relationship between DNA methylation-based subtypes and genetic mutation patterns (Rodriguez-Paredes et al., Nat Commun 2017)
Study
EGAS00001002670
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SHANK2 mutations associated with Autism Spectrum Disorder cause hyperconnectivity of human neurons
Study
EGAS00001003436
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TRACERx Renal 100
Study
EGAS00001002793
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Spatial multi-omic map of human myocardial infarction
Study
EGAS00001006330
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Single-nucleus transcriptomic profiling of aging Down Syndrome brains
Study
EGAS00001005691
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Circulating tumor cells Exome sequencing from breast cancer
Study
EGAS00001005228
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Immune and clinicopathological features predict HER2-positive breast cancer prognosis in the neoadjuvant NeoALTTO and CALGB 40601 trials
Study
EGAS00001007563
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NIDCD Otitis Media Genetic Susceptibility and Middle Ear Microbial Shifts
Study
phs001941
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Genome-Wide Association Study of Parkinson Disease: Genes and Environment
Study
phs000196