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Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients.Significance of glycolytic metabolism-related protein expression in colorectal cancer, lymph node and hepatic metastasis.The rs5743836 polymorphism in TLR9 confers a population-based increased risk of non-Hodgkin lymphomaA common variant within the HNF1B gene is associated with overall survival of multiple myeloma patients: results from the IMMEnSE consortium and meta-analysis.Indeterminate cell histiocytosis in association with acute myeloid leukemia.Genetics and molecular epidemiology of multiple myeloma: the rationale for the IMMEnSE consortium (review).Identification of miRSNPs associated with the risk of multiple myeloma.Hotspot TERT promoter mutations are rare events in testicular germ cell tumors.Type 2 diabetes-related variants influence the risk of developing multiple myeloma: results from the IMMEnSE consortium.Detection of the Epstein-Barr virus in blood and bone marrow mononuclear cells of patients with aggressive B-cell non-Hodgkin's lymphoma is not associated with prognosis.[Economic analysis of rituximab in combination with cyclophosphamide, vincristine and prednisolone in the treatment of patients with advanced follicular lymphoma in Portugal].Comprehensive investigation of genetic variation in the 8q24 region and multiple myeloma risk in the IMMEnSE consortium.Risk of multiple myeloma is associated with polymorphisms within telomerase genes and telomere length.Corrigendum: Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients.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.FcgammaRIIa polymorphism and clinical response to rituximab in non-Hodgkin lymphoma patients.Association of adult mastocytosis with M541L in the transmembrane domain of KIT.Absence of microsatellite instability and BRAF (V600E) mutation in testicular germ cell tumors.Genetic Variants and Multiple Myeloma Risk: IMMEnSE Validation of the Best Reported Associations--An Extensive Replication of the Associations from the Candidate Gene EraErratum: Polymorphisms in xenobiotic transporters ABCB1, ABCG2, ABCC2, ABCC1, ABCC3 and multiple myeloma risk: a case—control study in the context of the International Multiple Myeloma rESEarch (IMMEnSE) consortiumImpact of polymorphic variation at 7p15.3, 3p22.1 and 2p23.3 loci on risk of multiple myelomaPolymorphisms in xenobiotic transporters ABCB1, ABCG2, ABCC2, ABCC1, ABCC3 and multiple myeloma risk: a case–control study in the context of the International Multiple Myeloma rESEarch (IMMEnSE) consortiumThe mediator role of unmet needs on quality of life in myeloma patients
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