Ramón
García Sanz
Profesor Titular de Universidad
Víctor
Moreno Aguado
Víctor Moreno Aguado-rekin lankidetzan egindako argitalpenak (12)
2021
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Common gene variants within 3′-untranslated regions as modulators of multiple myeloma risk and survival
International Journal of Cancer, Vol. 148, Núm. 8, pp. 1887-1894
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Genetically determined telomere length and multiple myeloma risk and outcome
Blood Cancer Journal, Vol. 11, Núm. 4
2019
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Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma
Leukemia
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Genetic polymorphisms in genes of class switch recombination and multiple myeloma risk and survival: an IMMEnSE study
Leukemia and Lymphoma, Vol. 60, Núm. 7, pp. 1803-1811
2017
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Identification of miRSNPs associated with the risk of multiple myeloma
International Journal of Cancer, Vol. 140, Núm. 3, pp. 526-534
2015
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Risk of multiple myeloma is associated with polymorphisms within telomerase genes and telomere length
International Journal of Cancer, Vol. 136, Núm. 5, pp. E351-E358
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Type 2 diabetes-related variantsinfluence the risk of developing multiple myeloma: Results from the IMMEnSE consortium
Endocrine-Related Cancer, Vol. 22, Núm. 4, pp. 545-559
2014
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Genetic variants and multiple myeloma risk: IMMEnSE validation of the best reported associations - An extensive replication of the associations from the candidate gene era
Cancer Epidemiology Biomarkers and Prevention, Vol. 23, Núm. 4, pp. 670-674
2013
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Polymorphisms in regulators of xenobiotic transport and metabolism genes PXR and CAR do not affect multiple myeloma risk: A case-control study in the context of the IMMEnSE consortium
Journal of Human Genetics, Vol. 58, Núm. 3, pp. 155-159
2012
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Comprehensive investigation of genetic variation in the 8q24 region and multiple myeloma risk in the IMMEnSE consortium
British Journal of Haematology, Vol. 157, Núm. 3, pp. 331-338
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Genetics and molecular epidemiology of multiple myeloma: The rationale for the IMMEnSE consortium (review)
International Journal of Oncology, Vol. 40, Núm. 3, pp. 625-638
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Impact of polymorphic variation at 7p15.3, 3p22.1 and 2p23.3 loci on risk of multiple myeloma
British Journal of Haematology