Subclonal mutations in SETBP1 confer a poor prognosis in juvenile myelomonocytic leukemia

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SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations

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Somatic SETBP1 mutations in myeloid malignancies

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Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia

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Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia

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De novo mutations of SETBP1 cause Schinzel-Giedion syndrome

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ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

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SETBP1 overexpression is a novel leukemogenic mechanism that predicts adverse outcome in elderly patients with acute myeloid leukemia

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Genotype-phenotype correlation in cases of juvenile myelomonocytic leukemia with clonal RAS mutations

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