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Copy number signatures and mutational processes in ovarian carcinoma.
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.
Transcriptional risk scores link GWAS to eQTLs and predict complications in Crohn's disease.
MYB-QKI rearrangements in angiocentric glioma drive tumorigenicity through a tripartite mechanism.
Corrigendum: The genomic landscape of juvenile myelomonocytic leukemia.
COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis.
Cooperative loss of RAS feedback regulation drives myeloid leukemogenesis.
Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia.
Common variants at five new loci associated with early-onset inflammatory bowel disease.
Rearrangement of CRLF2 in B-progenitor- and Down syndrome-associated acute lymphoblastic leukemia.
