Concha Muñoz

Different distribution of <i>NOTCH1</i> mutations in chronic lymphocytic leukemia with isolated trisomy 12 or associated with other chromosomal alterations

Cristina López, Julio Delgado, Dolors Costa et al. · Genes Chromosomes and Cancer · 2012 · 58 citations

Identification and characterization of novel uroporphyrinogen decarboxylase gene mutations in a large series of porphyria cutanea tarda patients and relatives

Célia Bádenas, Jordi To‐Figueras, J. D. Phillips et al. · Clinical Genetics · 2009 · 38 citations

Do we need to do fluorescence in situ hybridization analysis in myelodysplastic syndromes as often as we do?

Dolors Costa, Sandra Valera, Ana Carrió et al. · Leukemia Research · 2010 · 32 citations

Hematological Malignancy, Medicine, Hematology +10

TERT and AURKA Gene Copy Number Gains Enhance the Detection of Acral Lentiginous Melanomas by Fluorescence in Situ Hybridization

Alba Díaz, Joan Anton Puig‐Butillé, Alexandra Valera et al. · Journal of Molecular Diagnostics · 2014 · 29 citations

High levels of global DNA methylation are an independent adverse prognostic factor in a series of 90 patients with de novo myelodysplastic syndrome

Xavier Calvo, Meritxell Nomdedéu, Alfons Navarro et al. · Leukemia Research · 2014 · 20 citations

Chromatin, Myelodysplastic Syndrome, Medicine +12