Lista de obras -

A systematic review and meta-analysis of MDM2 polymorphisms in osteosarcoma susceptibility

artículo científico publicado en 2016

A systematic review and meta-analysis of MTHFR polymorphisms in methotrexate toxicity prediction in pediatric acute lymphoblastic leukemia.

artículo científico

Alpha2C-adrenoceptor Del322-325 polymorphism and risk of psychiatric disorders: significant association with opiate abuse and dependence

artículo científico publicado en 2016

Cell-free DNA as a biomarker in diffuse large B-cell lymphoma: A systematic review

artículo científico publicado en 2019

Chromosome instability in lymphocytes of children with coeliac disease.

artículo científico publicado en 2009

Confirmation of involvement of new variants at CDKN2A/B in pediatric acute lymphoblastic leukemia susceptibility in the Spanish population

artículo científico publicado en 2017

Detection of chromothripsis-like patterns with a custom array platform for chronic lymphocytic leukemia.

artículo científico publicado en 2015

Epigenetic activation of SOX11 in lymphoid neoplasms by histone modifications.

artículo científico publicado en 2011

Erratum to: Potential relationship between single nucleotide polymorphisms used in forensic genetics and diseases or other traits in European population.

artículo científico publicado en 2015

Genetic susceptibility in childhood acute lymphoblastic leukemia.

artículo científico publicado en 2017

Genetic variants in miRNA processing genes and pre-miRNAs are associated with the risk of chronic lymphocytic leukemia

artículo científico publicado en 2015

Homeobox NKX2-3 promotes marginal-zone lymphomagenesis by activating B-cell receptor signalling and shaping lymphocyte dynamics

artículo científico publicado en 2016

Intron 3 of the ARID5B gene: a hot spot for acute lymphoblastic leukemia susceptibility.

artículo científico publicado en 2013

Involvement of miRNA polymorphism in mucositis development in childhood acute lymphoblastic leukemia treatment

scientific article published on 01 December 2018

Lack of association of the CEP72 rs924607 TT genotype with vincristine-related peripheral neuropathy during the early phase of pediatric acute lymphoblastic leukemia treatment in a Spanish population

artículo científico publicado en 2015

Letter regarding Wang et al. entitled "Effects of murine double minute 2 polymorphisms on the risk and survival of osteosarcoma: a systematic review and meta-analysis".

artículo científico publicado en 2014

MTHFR polymorphisms in childhood acute lymphoblastic leukemia: influence on methotrexate therapy.

artículo científico publicado en 2017

Methylation of the nonhomologous end joining repair pathway genes does not explain the increase of translocations with aging.

artículo científico publicado en 2014

MiR-pharmacogenetics of methotrexate in childhood B-cell acute lymphoblastic leukemia

artículo científico publicado en 2016

Mir-pharmacogenetics of Vincristine and peripheral neurotoxicity in childhood B-cell acute lymphoblastic leukemia.

artículo científico publicado en 2017

Non-leukemic pediatric mixed phenotype acute leukemia/lymphoma: Genomic characterization and clinical outcome in a prospective trial for pediatric lymphoblastic lymphoma

artículo científico publicado en 2019

Noncoding RNA-related polymorphisms in pediatric acute lymphoblastic leukemia susceptibility.

artículo científico publicado en 2014

PNPLA3 rs738409 and Hepatotoxicity in Children With B-cell Acute Lymphoblastic Leukemia: A Validation Study in a Spanish Cohort.

artículo científico publicado en 2017

Pharmacoepigenetics in childhood acute lymphoblastic leukemia: involvement of miRNA polymorphisms in hepatotoxicity

scientific article published on 23 March 2018

Pharmacogenetics of childhood acute lymphoblastic leukemia.

artículo científico publicado en 2014

Polymorphisms in miRNA processing genes and their role in osteosarcoma risk.

artículo científico publicado en 2015

Polymorphisms of the SLCO1B1 gene predict methotrexate-related toxicity in childhood acute lymphoblastic leukemia.

artículo científico publicado en 2011

Potential relationship between single nucleotide polymorphisms used in forensic genetics and diseases or other traits in European population

artículo científico publicado en 2015

Re: novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations

artículo científico publicado en 2013

Research commentary regarding Savage et al. entitled "Genome-wide association study identifies two susceptibility loci for osteosarcoma".

artículo científico publicado en 2015

Role of miRNAs in treatment response and toxicity of childhood acute lymphoblastic leukemia.

artículo científico publicado en 2018

Role of rs10406069 in miR-5196 in hyperdiploid childhood acute lymphoblastic leukemia

artículo científico publicado en 2020

S-Adenosylmethionine increases circulating very-low density lipoprotein clearance in non-alcoholic fatty liver disease.

artículo científico publicado en 2014

The miR-1206 microRNA variant is associated with methotrexate-induced oral mucositis in pediatric acute lymphoblastic leukemia.

artículo científico publicado en 2017

Variants in the 14q32 miRNA cluster are associated with osteosarcoma risk in the Spanish population

artículo científico publicado en 2018

Vincristine pharmacokinetics pathway and neurotoxicity during early phases of treatment in pediatric acute lymphoblastic leukemia.

artículo científico publicado en 2016

Lista de obras de

A systematic review and meta-analysis of MDM2 polymorphisms in osteosarcoma susceptibility

A systematic review and meta-analysis of MTHFR polymorphisms in methotrexate toxicity prediction in pediatric acute lymphoblastic leukemia.

Alpha2C-adrenoceptor Del322-325 polymorphism and risk of psychiatric disorders: significant association with opiate abuse and dependence

Cell-free DNA as a biomarker in diffuse large B-cell lymphoma: A systematic review

Chromosome instability in lymphocytes of children with coeliac disease.

Confirmation of involvement of new variants at CDKN2A/B in pediatric acute lymphoblastic leukemia susceptibility in the Spanish population

Detection of chromothripsis-like patterns with a custom array platform for chronic lymphocytic leukemia.

Epigenetic activation of SOX11 in lymphoid neoplasms by histone modifications.

Erratum to: Potential relationship between single nucleotide polymorphisms used in forensic genetics and diseases or other traits in European population.

Genetic susceptibility in childhood acute lymphoblastic leukemia.

Genetic variants in miRNA processing genes and pre-miRNAs are associated with the risk of chronic lymphocytic leukemia

Homeobox NKX2-3 promotes marginal-zone lymphomagenesis by activating B-cell receptor signalling and shaping lymphocyte dynamics

Intron 3 of the ARID5B gene: a hot spot for acute lymphoblastic leukemia susceptibility.

Involvement of miRNA polymorphism in mucositis development in childhood acute lymphoblastic leukemia treatment

Lack of association of the CEP72 rs924607 TT genotype with vincristine-related peripheral neuropathy during the early phase of pediatric acute lymphoblastic leukemia treatment in a Spanish population

Letter regarding Wang et al. entitled "Effects of murine double minute 2 polymorphisms on the risk and survival of osteosarcoma: a systematic review and meta-analysis".

MTHFR polymorphisms in childhood acute lymphoblastic leukemia: influence on methotrexate therapy.

Methylation of the nonhomologous end joining repair pathway genes does not explain the increase of translocations with aging.

MiR-pharmacogenetics of methotrexate in childhood B-cell acute lymphoblastic leukemia

Mir-pharmacogenetics of Vincristine and peripheral neurotoxicity in childhood B-cell acute lymphoblastic leukemia.

Non-leukemic pediatric mixed phenotype acute leukemia/lymphoma: Genomic characterization and clinical outcome in a prospective trial for pediatric lymphoblastic lymphoma

Noncoding RNA-related polymorphisms in pediatric acute lymphoblastic leukemia susceptibility.

PNPLA3 rs738409 and Hepatotoxicity in Children With B-cell Acute Lymphoblastic Leukemia: A Validation Study in a Spanish Cohort.

Pharmacoepigenetics in childhood acute lymphoblastic leukemia: involvement of miRNA polymorphisms in hepatotoxicity

Pharmacogenetics of childhood acute lymphoblastic leukemia.

Polymorphisms in miRNA processing genes and their role in osteosarcoma risk.

Polymorphisms of the SLCO1B1 gene predict methotrexate-related toxicity in childhood acute lymphoblastic leukemia.

Potential relationship between single nucleotide polymorphisms used in forensic genetics and diseases or other traits in European population

Re: novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations

Research commentary regarding Savage et al. entitled "Genome-wide association study identifies two susceptibility loci for osteosarcoma".

Role of miRNAs in treatment response and toxicity of childhood acute lymphoblastic leukemia.

Role of rs10406069 in miR-5196 in hyperdiploid childhood acute lymphoblastic leukemia

S-Adenosylmethionine increases circulating very-low density lipoprotein clearance in non-alcoholic fatty liver disease.

The miR-1206 microRNA variant is associated with methotrexate-induced oral mucositis in pediatric acute lymphoblastic leukemia.

Variants in the 14q32 miRNA cluster are associated with osteosarcoma risk in the Spanish population

Vincristine pharmacokinetics pathway and neurotoxicity during early phases of treatment in pediatric acute lymphoblastic leukemia.