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Genome-wide SNP data of Fulani populations from the Sahel belt
Study
EGAS50000000451
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Association studies using the Metabochip array - Samples analysed by the WTCCC (1958 British Birth Cohort (58BC), Hypertension cohort (HT), Type 2 Diabetes Cohort (T2D) and Coronary Artery Disease (CAD) cohort)
Study
EGAS00000000115
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Deregulation of FOXF1/FENDRR from t(14;16)(q32;q24) defines a subtype of high risk lineage ambiguous leukemia
Study
EGAS50000001255
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Whole-genome sequencing of two probands with hereditary spastic paraplegia reveals novel splice-donor region mutation and known pathogenic mutation in SPG11
Study
EGAS00001001849
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Recurrent somatic JAK-STAT mutations within a novel RUNX1-mutated pedigree
Study
EGAS00001001862
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Comparison of EGF and PDGF driven glioblastomas.
Study
EGAS00001001900
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Novel regional age-associated DNA methylation changes within human common disease-associated loci
Study
EGAS00001001910
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Understanding_the_development_of_resident_memory_T_cells__Trm__in_the_human_small_intestine_using_integrative_multiomic_approaches__Adult_RNA
Study
EGAS00001008257
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DNA methylation and the adverse metabolic outcomes of adiposity
Study
EGAS00001001922
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InsPIRE islets
Study
EGAS00001003997