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| Rights | Preview | Issue Date | Title | Author(s) | Type |
| openAccess |  | 2015 | A low frequency of losses in 11q chromosome Is associated with better outcome and lower rate of genomic mutations in patients with chronic lymphocytic leukemia | Hernández, José Ángel; Hernández-Sánchez, María; Rodríguez-Vicente, Ana Eugenia; Benito, Rocío; Robledo, Cristina; Kohlmann, Alexander; González, Marcos  ; Espinet, Blanca; Hernández, Jesús M. | artículo |
| closedAccess |  | 2017 | A two-step approach for sequencing spliceosome-related genes as a complementary diagnostic assay in MDS patients with ringed sideroblasts | Janusz, Kamila; Rey, Mónica del; Abáigar, María ; Collado, Rosa; Ivars, David; Hernández-Sánchez, María; Valiente, Alberto; Robledo, Cristina; Benito, Rocío; Díez-Campelo, María; Ramos, Fernando; Kohlmann, Alexander; Cañizo, María Consuelo del; Hernández, Jesús M. | artículo |
| closedAccess |  | 2006 | Analysis of chromosomal imbalances in an elderly woman with a giant cell tumour | García, Juan L. ; Robledo, Cristina; Lumbreras, Eva ; Flores, Teresa; Ramos, Luis; Hernández, Jesús M. | artículo |
| openAccess |  | 2016 | Bone marrow fibrosis in myelodysplastic syndromes: a prospective evaluation including mutational analysis | Ramos, Fernando; Robledo, Cristina; Izquierdo-García, Francisco Miguel; Suárez-Vilela, Dimas; Benito, Rocío; Fuertes, Marta; Insunza, Andrés; Barragán, Eva; Rey, Mónica del; García-Ruiz de Morales, José María; Tormo, Mar; Salido, Eduardo; Zamora, Lurdes; Pedro, Carmen; Sánchez-del-Real, Javier; Díez-Campelo, María; Cañizo, María Consuelo del; Sanz, Guillermo F.; Hernández, Jesús M. | artículo |
| closedAccess |  | 2009 | Both expanded and uncultured mesenchymal stem cells from MDS patients are genomically abnormal, showing a specific genetic profile for the 5q− syndromeMesenchymal stem cells of 5q− syndrome | López-Villar, Olga; García, Juan L. ; Sánchez-Guijo, Fermín M.; Robledo, Cristina; Villarón, Eva M.; Díez-Campelo, María; Pérez-Simón, José A.; San Miguel, Jesús F. ; Cañizo, María Consuelo del | artículo |
| closedAccess |  | 2017 | Calreticulin mutations are exceedingly rare in patients with myelodysplastic syndromes with myelofibrosis | Montoro, Julia; Robledo, Cristina; Zamora, Lurdes; Valcárcel, David; Ramos, Fernando | artículo |
| closedAccess |  | 2004 | Chromosomal abnormalities are related to location and grade of osteoarthritis | Castellanos, Mariana V.; Hernández, Jesús M. ; Ramos, Luis; González, M. Belén; Gutiérrez, Norma Carmen; Leone, Paola E.; Lumbreras, Eva ; Robledo, Cristina; García, Juan L. | artículo |
| openAccess |  | 2016 | Chromothripsis is a recurrent genomic abnormality in high-risk myelodysplastic syndromes | Abáigar, María ; Robledo, Cristina; Benito, Rocío; Ramos, Fernando; Díez-Campelo, María; Hermosín, Lourdes; Sánchez-del-Real, Javier; Alonso, Jose M.; Cuello, Rebeca; Megido, Marta; Rodríguez, Juan-Nicolas; Martín-Núñez, Guillermo; Aguilar, Carlos; Vargas, Manuel; Martín, Ana-África; García, Juan L. ; Kohlmann, Alexander; Cañizo, María Consuelo del; Hernández, Jesús M. | artículo |
| closedAccess |  | 2013 | Clinical applications of BAC array-CGH to the study of diffuse large B-cell lymphomas | Robledo, Cristina; García, Juan L. ; Hernández, Jesús M. | capítulo de libro |
| closedAccess |  | 2012 | Expression of VAV1 in the tumour microenvironment of glioblastoma multiforme | García, Juan L. ; Couceiro, José R.; Gómez-Moreta, Juan A.; Santos-Briz, Ángel; Sauzeau, Vincent; Lumbreras, Eva ; Robledo, Cristina; Bustelo, Xosé R. ; Hernández, Jesús M. | artículo |
| openAccess |  | 2016 | Genome-wide DNA copy number analysis of acute lymphoblastic leukemia identifies new genetic markers associated with clinical outcome | Forero-Castro, Maribel; Robledo, Cristina; Benito, Rocío; Abáigar, María ; Martín, Ana-África; Arefi, Maryam; Fuster, José Luis; Heras, Natalia de las; Rodríguez, Juan-Nicolas; Quintero, Jonathan; Riesco, Susana; Hermosín, Lourdes; Fuente, Ignacio de la; Recio, Isabel; Ribera, Jordi; Labrador, Jorge; Alonso, Jose M.; Olivier, Carmen; Sierra, Magdalena; Megido, Marta; Corchete, Luis A.; Ciudad, Juana; García, Juan L. ; Ribera, Josep-Maria; Hernández, Jesús M. | artículo |
| closedAccess |  | 2014 | Genomic analysis of clonal eosinophils by CGH arrays reveals new genetic regions involved in chronic eosinophilia | Arefi, Maryam; Robledo, Cristina; Peñarrubia, María J.; García de Coca, Alfonso; Cordero, Miguel; Hernández, Jesús M. ; García, Juan L. | artículo |
| closedAccess |  | 2017 | Hyperdiploidy as a rare event that accompanies poor prognosis markers in CLL | González-Gascón y Marín, Isabel; Martín, Ana-África; Hernandez-Sánchez, Jesus M.; Robledo, Cristina; Hermosín, Lourdes; Heras, Natalia de las; Lacalle, Laura; Galende, Josefina; Arriba, Felipe de; Rodríguez-Vicente, Ana Eugenia; Hernández, José Ángel; Hernández, Jesús M. | artículo |
| closedAccess |  | 2012 | Identification of a novel recurrent gain on 20q13 in chronic lymphocytic leukemia by array CGH and gene expression profiling | Rodríguez-Vicente, Ana Eugenia; Robledo, Cristina; García, Juan L. ; Gutiérrez, Norma Carmen; Hernández, José Ángel; García de Coca, Alfonso; Risueño, A.; De Las Rivas, Javier ; Hernández, Jesús M. | artículo |
| closedAccess |  | 2012 | Imatinib therapy of chronic myeloid leukemia restores the expression levels of key genes for DNA damage and cell-cycle progression | Benito, Rocío; Lumbreras, Eva ; Gutiérrez, Norma Carmen; Robledo, Cristina; García, Juan L. ; Cañizo, María Consuelo del; Hernández, Jesús M. | artículo |
| openAccess |  | 2020 | Integrated genomic analysis of chromosomal alterations and mutations in B-cell acute lymphoblastic leukemia reveals distinct genetic profiles at relapse | Forero-Castro, Maribel; Montaño, Adrián; Robledo, Cristina; García de Coca, Alfonso; Fuster, José Luis; Heras, Natalia de las; Queizán, José-Antonio; Hernández-Sánchez, María; Corchete, Luis A.; Martín-Izquierdo, Marta; Ribera, Jordi; Ribera, Josep-Maria; Benito, Rocío; Hernández, Jesús M. | artículo |
| closedAccess |  | 2012 | Integration of global spectral karyotyping, CGH arrays, and expression arrays reveals important genes in the pathogenesis of glioblastoma multiforme | Leone, Paola E.; González, M. Belén; Gómez-Moreta, Juan A.; Lumbreras, Eva ; Robledo, Cristina; Santos-Briz, Ángel; Gutiérrez, Norma Carmen; Hernández, Jesús M. ; García, Juan L. | artículo |
| closedAccess |  | 2016 | MiRNA expression profile of chronic lymphocytic leukemia patients with 13q deletion | Hernández-Sánchez, María; Rodríguez-Vicente, Ana Eugenia; Hernández, José Ángel; Lumbreras, Eva ; Sarasquete, María Eugenia; Martín, Ana-África; Benito, Rocío; Vicente-Gutiérrez, Carlos; Robledo, Cristina; Heras, Natalia de las; Rodríguez, Juan-Nicolas; Alcoceba, Miguel; García de Coca, Alfonso; Aguilar, Carlos; González, Marcos ; Hernández, Jesús M. | artículo |
| openAccess |  | Sep-2011 | Molecular Characterization of the Region 7q22.1 in Splenic Marginal Zone Lymphomas | Robledo, Cristina; García, Juan L. ; Benito, Rocío; García García, Eva María; Hernández, Jesús M. | artículo |
| closedAccess |  | 2017 | Multidimensional assessment of patient condition and mutational analysis in peripheral blood, as tools to improve outcome prediction in myelodysplastic syndromes: A prospective study of the Spanish MDS group | Ramos, Fernando; Robledo, Cristina; Pereira, Arturo; Pedro, Carmen; Benito, Rocío; Paz, Raquel de; Rey, Mónica del; Insunza, Andrés; Tormo, Mar; Díez-Campelo, María; Xicoy, Blanca; Salido, Eduardo; Sánchez-del-Real, Javier; Arenillas, Leonor; Florensa, Lourdes; Luño, Elisa; Cañizo, María Consuelo del; Sanz, Guillermo F.; Hernández, Jesús M. | artículo |
