-
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants
Study
EGAS00001006058
-
Aging and genome-wide patterns of DNA methylation in an African rainforest hunter-gathering population
Study
EGAS00001002226
-
MYO5B mutations in Pheochromocytoma/Paraganglioma promote cancer progression
Study
EGAS00001003991
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Mult-omics Palbociclib Resistance Study in HR+/HER2– Metastatic Breast Cancer
Dataset
EGAD00001008314
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Clonal selection after gene therapy in sickle cell disease
Dataset
EGAD00001010914
-
Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, define pre-malignant neurofibromatosis type 1-associated atypical neurofibromas
Study
phs001993
-
Study of Controlled Human Malaria Infections to Evaluate Protection After Intravenous or Intramuscular Administration of PfSPZ Vaccine in Malaria-Naive Adults
Study
phs002423
-
Discovery and Characterization of Genetic Risk Loci in Sjogren's Syndrome
Study
phs002723
-
Genetic Aberrations and Subclonal Structure Impact Chronic Lymphocytic Leukemia
Study
phs000922
-
PCGP Ph-like ALL
Study
EGAS00001000654