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Genome wide association study on coronary heart disease in patients with familial hypercholesterolemia
Study
EGAS00001000734
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Next generation sequencing of sporadic schwannomatosis samples
Study
EGAS00001000767
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Systems biology of Colorectal Cancer
Study
EGAS00001000854
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Study on the proliferation history of colorectal adenomas
Study
EGAS00001000883
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Integrated genetic and epigenetic analysis defines novel molecular clusters in rhabdomyosarcoma
Study
EGAS00001000884
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Ischemic stroke in a Swedish case-control study.
Study
EGAS00001000936
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Genomic analyses of gynecologic carcinosarcomas reveal frequent mutations in chromatin remodeling genes
Study
EGAS00001000941
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Clinical and Molecular Investigation of Familial CEBPA-mutated Acute Myeloid Leukaemia
Study
EGAS00001000949
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BLUEPRINT ChIP-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000951
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BLUEPRINT RNA-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000953
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Genetic landscape of malignant peripheral nerve sheath tumors
Study
EGAS00001000974
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BLUEPRINT DNase accessibility of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000954
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Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X
Study
EGAS00001000957
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Genomic, transcriptomic and epigenomic profiling of GCTB
Study
EGAS00001003730
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Confirmation of a founder effect in a Northern European population (FRL) of a new beta-globin variant: HBB:c.23_26dup (codons 8/9 (+AGAA))
Study
EGAS00001000980
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Therapeutic Resistance to PI3K-alpha Inhibitors
Study
EGAS00001000991
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First genome-wide association study in an Australian Aboriginal population provides insights into genetic risk factors for Body Mass Index and Type 2 Diabetes
Study
EGAS00001001004
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MDS Sequencing Project_Cancer Cell
Study
EGAS00001001011
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Spatial heterogeneity in medulloblastoma
Study
EGAS00001001014
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Genome-wide prediction of human embryos
Study
EGAS00001001020
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Whole genome sequencing of ASD quartet families
Study
EGAS00001001023
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Exome Sequencing in Moebius Syndrome
Study
EGAS00001001250
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RB Loss in Resistant EGFR Mutant Lung Adenocarcinomas that Transform to Small Cell Lung Cancer
Study
EGAS00001001102
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Whole-exome and targeted sequencing of pediatric hyperdiploid B-cell precursor acute lymphoblastic leukemia
Study
EGAS00001001113
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Genome-wide association analysis on five isolated populations - Erasmus Rucphen Family (ERF) Study
Study
EGAS00001001134