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Genesis of Two Most Prevalent Variants Causing Combined Pituitary Hormone Deficiency in 21 Populations
Study
EGAS00001001165
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An integrative model of pathway convergence in genetically heterogeneous blast crisis chronic myeloid leukemia (CML)
Study
EGAS00001001751
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A reference map of potential determinants for the human serum metabolome
Study
EGAS00001004512
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Immune microenvironment and lineage tracing help deciphering Rosette-forming GlioNeuronal Tumors: a multi-omic analysis of 9 cases
Study
EGAS00001006502
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Genetic heritage of the Baphuthi highlights an over-ethnicised notion of 'Bushman' in the Maloti-Drakensberg, southern Africa
Study
EGAS00001007080
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IL7-receptor expression is frequent in T-cell acute lymphoblastic leukemia and predicts sensitivity to JAK-inhibition
Study
EGAS00001007144
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DNA Methylomic Profiling of Preeclampsia Across Pregnancy
Study
phs001937
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Analysis of Somatic Mutations in Pediatric AML FAB-M7 Subtype by Whole Transcriptome Sequencing
Study
phs000413
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Phenotype Risk Scores Identify Patients with Unrecognized Mendelian Disease Patterns
Study
phs001516
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VESPA: Vanderbilt Electronic Systems for Pharmacogenomic Assessment
Study
phs000991