Juan Luis
García Hernández
Investigador desde 2011
Hospital Universitario de Valladolid
Valladolid, EspañaPublicaciones en colaboración con investigadores/as de Hospital Universitario de Valladolid (11)
2023
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Adult T-cell leukemia/lymphoma in HTLV-1 non-endemic regions
Journal of Clinical Virology, Vol. 167
2016
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Chromothripsis is a recurrent genomic abnormality in high-risk myelodysplastic syndromes
PLoS ONE, Vol. 11, Núm. 10
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Genome-Wide DNA Copy Number Analysis of Acute Lymphoblastic Leukemia Identifies New Genetic Markers Associated with Clinical Outcome
PloS one, Vol. 11, Núm. 2, pp. e0148972
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The presence of genomic imbalances is associated with poor outcome in patients with burkitt lymphoma treated with dose-intensive chemotherapy including rituximab
British journal of haematology, Vol. 172, Núm. 3, pp. 428-438
2015
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MicroRNA-223 is a novel negative regulator of HSP90B1 in CLL
BMC Cancer, Vol. 15, Núm. 1
2014
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Genomic analysis of clonal eosinophils by CGH arrays reveals new genetic regions involved in chronic eosinophilia
European Journal of Haematology, Vol. 93, Núm. 5, pp. 422-428
2012
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Identification of a novel recurrent gain on 20q13 in chronic lymphocytic leukemia by array CGH and gene expression profiling
Annals of Oncology, Vol. 23, Núm. 8, pp. 2138-2146
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Incidence and clinical characteristics of myeloproliferative neoplasms displaying a PDGFRB rearrangement
European Journal of Haematology, Vol. 89, Núm. 1, pp. 37-41
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Molecular Characterization of Chronic Lymphocytic Leukemia Patients with a High Number of Losses in 13q14
PLoS ONE, Vol. 7, Núm. 11
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Response to imatinib mesylate in patients with hypereosinophilic syndrome
International Journal of Hematology, Vol. 96, Núm. 3, pp. 320-326
2004
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The value of flourescence in situ hybridization for the detection of 11q in multiple myeloma
Haematologica, Vol. 89, Núm. 10, pp. 1213-1218