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A Targeted Resequencing Study Allows the Detection of a Common Polymorphism At Mirna-223 Binding Site in 3′Untranslated Region Which Deregulates HSP90B1 Expression in Chronic Lymphocytic Leukemia

Blood, 2012-11, Vol.120 (21), p.1776-1776

2012

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Molecular Characterization of Chronic Lymphocytic Leukemia Patients with a High Number of Losses in 13q14

Blood, 2012-11, Vol.120 (21), p.2871-2871

2012

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Epigenetic Silencing of BCL2, ETS1, IL27RA and DICER1 in Low-Risk MDS Patients

Blood, 2012-11, Vol.120 (21), p.1704-1704

2012

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Transcriptome Analysis Reveals Molecular Profiles Associated with Evolving Steps of Monoclonal Gammopathies

Blood, 2012-11, Vol.120 (21), p.2914-2914

2012

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SNP-Based Mapping Arrays Reveal High Genomic Complexity in Monoclonal Gammopathies: From the MGUS to Myeloma Status

Blood, 2011-11, Vol.118 (21), p.295-295

2011

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Mutations in the Toll-like receptor/MYD88 pathway in young (≤50 years) CLL patients

Clinical lymphoma, myeloma and leukemia, 2015-06, Vol.15, p.S203-S203

2015

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Analysis of Spanish Experience During Imiglucerase Shortage

Blood, 2010-11, Vol.116 (21), p.4725-4725

2010

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Secondary myeloid neoplasias: an emerging group of diseases

Revista brasileira de hematologia e hemoterapia, 2011-01, Vol.33 (6), p.403-404

Hernández-Rivas, Jesús M

2011

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Clinical Impact of Copy Number Variation Revealed By Next Generation Sequencing in Acute Myeloid Leukemia

Blood, 2021-11, Vol.138 (Supplement 1), p.4463-4463

2021

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Machine Learning Improves Risk Stratification in Myelofibrosis: An Analysis of the Spanish Registry of Myelofibrosis

Blood, 2022-11, Vol.140 (Supplement 1), p.826-827

2022

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Does RAD21 Co-Mutation Have a Role in DNMT3A Mutated AML? Results of Harmony Alliance AML Database

Blood, 2021-11, Vol.138 (Supplement 1), p.608-608

2021

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Impact of Gender on Molecular AML Subclasses - a Harmony Alliance Study

Blood, 2021-11, Vol.138 (Supplement 1), p.3438-3438

2021

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Different Prognostic Impact of Recurrent Gene Mutations in IGHV-Mutated and IGHV-Unmutated Chronic Lymphocytic Leukemia: A Retrospective, Multi-Center Cohort Study By Eric, the European Research Initiative on CLL, in Harmony

BLOOD, 2021, Vol.138 (Supplement 1), p.2617-2617

2021

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ALL-154: t(1;19)(q23;p13) TCF3-PBX1 May Not Be an Intermediate-Risk Subtype in Adult B-Cell Precursor Acute Lymphoblastic Leukemia Patients Treated With MRD-Oriented Protocols from the PETHEMA Group

Clinical lymphoma, myeloma and leukemia, 2021-09, Vol.21, p.S270-S271

2021

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Poster: ALL-154: t(1;19)(q23;p13) TCF3-PBX1 May Not Be an Intermediate-Risk Subtype in Adult B-Cell Precursor Acute Lymphoblastic Leukemia Patients Treated With MRD-Oriented Protocols from the PETHEMA Group

Clinical lymphoma, myeloma and leukemia, 2021-09, Vol.21, p.S207-S207

2021

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Vascular target organ damage in patients with Philadelphia negative myeloproliferative syndrome: A propensity score analysis

Medicina clínica (English ed.), 2022-06, Vol.158 (11), p.503-508

2022

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Correlation of myelodysplastic syndromes with i(17)(q10) and TP 53 and SETBP 1 mutations

British journal of haematology, 2015-10, Vol.171 (1), p.137-141

2015

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A Targeted Resequencing Study Allows the Detection of a Common Polymorphism At Mirna-223 Binding Site in 3′Untranslated Region Which Deregulates HSP90B1 Expression in Chronic Lymphocytic Leukemia

Molecular Characterization of Chronic Lymphocytic Leukemia Patients with a High Number of Losses in 13q14

Prognostic Value of Complex Karyotype and Monosomal Karyotype in Patients with Adult Acute Lymphoblastic Leukemia Treated with Risk-Adapted Protocols

Epigenetic Silencing of BCL2, ETS1, IL27RA and DICER1 in Low-Risk MDS Patients

Transcriptome Analysis Reveals Molecular Profiles Associated with Evolving Steps of Monoclonal Gammopathies

SNP-Based Mapping Arrays Reveal High Genomic Complexity in Monoclonal Gammopathies: From the MGUS to Myeloma Status

Is Azacitidine (AZA) Really Effective in High Risk MDS Patients with Chromosome 7 Abnormalities (Abn 7)? Results of a Retrospective Study From the GFM and GESMD Registries

Mutations in the Toll-like receptor/MYD88 pathway in young (≤50 years) CLL patients

Analysis of Spanish Experience During Imiglucerase Shortage

Evaluation of Lenalidomide (LEN) Vs Placebo in Non-Transfusion Dependent Low Risk Del(5q) MDS Patients. Final Results of Sintra-REV Phase III International Multicenter Clinical Trial

Secondary myeloid neoplasias: an emerging group of diseases

Clinical Impact of Copy Number Variation Revealed By Next Generation Sequencing in Acute Myeloid Leukemia

Machine Learning Improves Risk Stratification in Myelofibrosis: An Analysis of the Spanish Registry of Myelofibrosis

Sequential Study By RNA-Seq Shows a Reduction in Inflammation and a Cell Cycle Activation in T-Lymphocytes from Myelodysplastic Syndrome with Del(5q) after Lenalidomide Treatment in Patients Included in the “Sintra-REV” Clinical Trial

Does RAD21 Co-Mutation Have a Role in DNMT3A Mutated AML? Results of Harmony Alliance AML Database

Impact of Gender on Molecular AML Subclasses - a Harmony Alliance Study

Different Prognostic Impact of Recurrent Gene Mutations in IGHV-Mutated and IGHV-Unmutated Chronic Lymphocytic Leukemia: A Retrospective, Multi-Center Cohort Study By Eric, the European Research Initiative on CLL, in Harmony

Heterogeneous Landscape of RUNX1 Related Disorder: Four Families with Inherited Thrombocytopenias and Novel Genetic Variants in RUNX1 Associated to Relevant Clinical Complications

ALL-154: t(1;19)(q23;p13) TCF3-PBX1 May Not Be an Intermediate-Risk Subtype in Adult B-Cell Precursor Acute Lymphoblastic Leukemia Patients Treated With MRD-Oriented Protocols from the PETHEMA Group

Poster: ALL-154: t(1;19)(q23;p13) TCF3-PBX1 May Not Be an Intermediate-Risk Subtype in Adult B-Cell Precursor Acute Lymphoblastic Leukemia Patients Treated With MRD-Oriented Protocols from the PETHEMA Group

Vascular target organ damage in patients with Philadelphia negative myeloproliferative syndrome: A propensity score analysis

Correlation of myelodysplastic syndromes with i(17)(q10) and TP 53 and SETBP 1 mutations

Results of the “Evaluation of NGS in AML-Diagnostics (ELAN)” Study – an Inter-Laboratory Comparison Performed in 10 European Laboratories

Mutations in TLR/MYD88pathway identify a subset of young chronic lymphocytic leukemia patients with favorable outcome

Risk of Central Nervous System (CNS) Involvement in Patients with Mantle Cell Lymphoma (MCL): Analysis of Clinico-Biological Factors in a Series of 283 Cases

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