E. Arranz

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Hypermethylation of p15/ink4b/MTS2 gene is differentially implicated among non-Hodgkin’s lymphomas

J. Benítez, A. Osorio, B. Martínez-Delgado, 1998, Leukemia.

Chronic myeloid leukemia patients resistant to or intolerant of interferon alpha and subsequently treated with imatinib show reduced immunoglobulin levels and hypogammaglobulinemia.

E. Arranz, J. Steegmann, S. Osorio, 2003, Haematologica.

Fluorescence in situ hybridization improves the detection of 5q31 deletion in myelodysplastic syndromes without cytogenetic evidence of 5q-

L. Arenillas, S. Serrano, F. Solé, 2008, Haematologica.

Deletion of sequences flanking the t(9;22) breakpoint: a secondary genetic event associated with loss of cytogenetic response to interferon in a Philadelphia‐positive chronic myeloid leukaemia patient

E. Arranz, M. Renedo, A. Alegre, 2002, British journal of haematology.

Atypical IgM multiple myeloma with deletion of c‐MAF

E. Arranz, C. Burgaleta, A. Blasco, 2015, International journal of laboratory hematology.

Correlation between mutations in p53 gene and protein expression in human lymphomas

J. Benítez, B. Martínez-Delgado, C. Rivas, 1997, American journal of hematology.

Evaluation of CD7 and terminal deoxynucleotidyl transferase (TdT) expression in CD34+ myeloblasts from patients with myelodysplastic syndrome.

D. Subirá, P. Font, S. Castañón, 2006, Leukemia research.

N‐ras mutations: Incidence and clinical relevance in myelodysplastic syndrome and acute myelogenous leukemia

J. Benítez, M. Robledo, E. Arranz, 1995, American journal of hematology.

Incidence of homogeneously staining regions in non-Hodgkin lymphomas.

J. Benítez, C. Rivas, M. Robledo, 1996, Cancer genetics and cytogenetics.

Hypermethylation of a 5′ CpG island of p16 is a frequent event in non-Hodgkin’s lymphoma

J. Benítez, B. Martínez-Delgado, J. Fernández-Piqueras, 1997, Leukemia.

Cytogenetic and molecular studies of siblings with ataxia telangiectasia followed for 7 years.

J. Benítez, M. Robledo, E. Arranz, 1997, Cancer genetics and cytogenetics.

Detection of trisomy 8 using conventional cytogenetic techniques and interphase FISH analysis in 34 myeloid disorders: a comparative study.

J. Benítez, M. Robledo, E. Arranz, 1997, Cancer genetics and cytogenetics.

Clonal evolution in patients with chronic lymphocytic leukemia

E. Arranz, C. Burgaleta, A. Alegre, 2010, Leukemia & lymphoma.

Genetic instability of microsatellites in hematological neoplasms.

J. Benítez, C. Rivas, M. Robledo, 1995, Leukemia.

Frequent retinoic acid receptor alpha (Rar‐α) gene rearrangements and no point mutations of N‐Ras gene in fifteen cases of acute promyelocytic leukemia

M. Robledo, E. Arranz, A. Santón, 1994, American journal of hematology.

A Case of Myeloproliferative Neoplasm with BCR-FGFR1 Rearrangement: Favorable Outcome after Haploidentical Allogeneic Transplantation

E. Arranz, P. Villafuerte-Gutiérrez, P. Herrera, 2018, Case reports in hematology.

Identification of novel cytogenetic markers with prognostic significance in a series of 968 patients with primary myelodysplastic syndromes.

J. Cigudosa, F. Solé, M. Calasanz, 2005, Haematologica.

De novo erythroleukemia chromosome features include multiple rearrangements, with special involvement of chromosomes 11 and 19

J. Cigudosa, M. Urioste, J. Benítez, 2003, Genes, chromosomes & cancer.

Chromosomal changes pattern and gene amplification in T cell non-Hodgkin's lymphomas

M. Urioste, J. Benítez, B. Martínez-Delgado, 2001, Leukemia.

Comparison and cost analysis of three protocols for mobilization and apheresis of haematopoietic progenitor cells

E. Arranz, J. Lopéz, Francisco López-Castaño, 2019, Journal of clinical apheresis.

First-line treatment with rituximab-hyperCVAD alternating with rituximab-methotrexate-cytarabine and followed by consolidation with 90Y-ibritumomab-tiuxetan in patients with mantle cell lymphoma. Results of a multicenter, phase 2 pilot trial from the GELTAMO group

A. Salar, M. Terol, J. Sánchez, 2013, Haematologica.

A region of allelic imbalance in 1q31-32 in primary breast cancer coincides with a recombination hot spot.

D. Heine-Suñer, J. Benítez, A. Osorio, 1997, Cancer research.

Transforming and Tumorigenic Activity of JAK2 by Fusion to BCR: Molecular Mechanisms of Action of a Novel BCR-JAK2 Tyrosine-Kinase

J. Vizmanos, J. Bueren, E. Arranz, 2012, PloS one.

Linear and whorled nevoid hypermelanosis and Axenfeld-Rieger anomaly: a novel association.

E. Arranz, A. García‐Díez, D. De Argila, 2010, Acta dermato-venereologica.

Increased C-MYC oncogene copy number detected with combined modified comparative genomic hybridization and FISH analysis in a Richter syndrome case with complex karyotype.

J. Benítez, C. Rivas, E. Arranz, 1998, Cancer genetics and cytogenetics.

Identification by comparative genomic hybridization of genetic changes involved in tumoral progression of a T-cell non-Hodgkin lymphoma.

J. Benítez, A. Cebrián, A. Osorio, 2000, Cancer genetics and cytogenetics.

Trisomy 14 in a case of sideroblastic refractory anemia.

J. Benítez, E. Arranz, E. Prieto, 1994, Cancer genetics and cytogenetics.