Connection

GUILLERMO GARCIA-MANERO to Chromosomes, Human, Pair 17

This is a "connection" page, showing publications GUILLERMO GARCIA-MANERO has written about Chromosomes, Human, Pair 17.
  1. Myeloid neoplasms with isolated isochromosome 17q demonstrate a high frequency of mutations in SETBP1, SRSF2, ASXL1 and NRAS. Oncotarget. 2016 Mar 22; 7(12):14251-8.
    View in: PubMed
    Score: 0.111
  2. Prognostic implications of chromosome 17 abnormalities in the context of monosomal karyotype in patients with acute myeloid leukemia and complex cytogenetics. Clin Lymphoma Myeloma Leuk. 2014 Apr; 14(2):163-71.
    View in: PubMed
    Score: 0.095
  3. Myeloid neoplasms with isolated isochromosome 17q represent a clinicopathologic entity associated with myelodysplastic/myeloproliferative features, a high risk of leukemic transformation, and wild-type TP53. Cancer. 2012 Jun 01; 118(11):2879-88.
    View in: PubMed
    Score: 0.082
  4. Chromosomal abnormalities in chronic lymphocytic leukemia. N Engl J Med. 2001 Apr 19; 344(16):1254.
    View in: PubMed
    Score: 0.039
  5. Whole-arm translocation of der(5;17)(p10;q10) with concurrent TP53 mutations in acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS): A unique molecular-cytogenetic subgroup. Cancer Genet. 2016 05; 209(5):205-14.
    View in: PubMed
    Score: 0.028
Connection Strength

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Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.