Browsing by author Marques, Herlander Subscribe author statistics Marques, Herlander

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

or enter first few letters:  

Showing results 1 to 18 of 18.
Issue DateTitleAuthor(s)TypeAccess
Jun-2019Clinical significance of metabolism-related biomarkers in non-Hodgkin lymphoma - MCT1 as potential target in diffuse large B cell lymphomaAfonso, Julieta Alexandra Pereira; Pinto, Tatiana; Sousa, Susana Patrícia Simões, et al.ArticleOpen access
Sep-2016A common variant within the HNF1B gene is associated with overall survival of multiple myeloma patients: results from the IMMEnSE consortium and meta-analysisRíos-Tamayo, Rafael; Lupiañez, Carmen Belén; Campa, Daniele, et al.ArticleOpen access
May-2012Comprehensive investigation of genetic variation in the 8q24 region and multiple myeloma risk in the IMMEnSE consortiumReis, R. M.; Campa, Danielr; Martino, Alessandro, et al.ArticleRestricted access (UMinho)
9-Dec-2015Corrigendum: Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patientsZiv, Elad; Dean, Eric; Hu, Donglei, et al.CorrigendumOpen access
Dec-2012Detection 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 prognosisMarques, Herlander; Catarino, Raquel; Domingues, Nelson, et al.ArticleOpen access
Apr-2014Genetic variants and multiple myeloma risk : IMMEnSE validation of the best reported associations : an extensive replication of the associations from the Candidate gene eraMartino, Alessandro; Campa, Daniele; Jurczyszyn, Artur, et al.ArticleRestricted access (UMinho)
2012Genetics and molecular epidemiology of multiple myeloma : the rationale for the IMMEnSE consortium (review)Martino, Alessandro; Sainz, Juan; Buda, Gabriele, et al.ArticleOpen access
2015Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patientsZiv, Elad; Dean, Eric; Hu, Donglei, et al.ArticleOpen access
2016Hotspot TERT promoter mutations are rare events in testicular germ cell tumorsCárcano, Flavio Mavignier; Vidal, Daniel Onofre; Lengert, André van Helvoort, et al.ArticleRestricted access (Author)
9-Feb-2017Identification of miRSNPs associated with the risk of multiple myelomaMacauda, Angelica; Calvetti, Diego; Maccari, Giuseppe, et al.ArticleOpen access
2012Impact of polymorphic variation at 7p15.3, 3p22.1 and 2p23.3 loci on risk of multiple myelomaReis, R. M.; Martino, Alessandro; Campa, Daniele, et al.Letter to the editorRestricted access (UMinho)
Nov-2018Inherited variation in the xenobiotic transporter pathway and survival of multiple myeloma patientsMacauda, Angelica; Castelli, Eleonora; Buda, Gabriele, et al.ArticleRestricted access (Author)
Oct-2016Methodology for single nucleotide polymorphism selection in promoter regions for clinical use. An example of its applicabilityMarques, Herlander; Freitas, J.; Medeiros, Rui, et al.ArticleOpen access
2013Polymorphisms 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 IMMEnSE consortiumMartino, Alessandro; Sainz, Juan; Reis, R. M., et al.ArticleRestricted access (UMinho)
Mar-2015Risk of multiple myeloma is associated with polymorphisms within telomerase genes and telomere lengthCampa, Daniele; Martino, Alessandro; Varkonyi, Judit, et al.ArticleOpen access
Feb-2012The rs5743836 polymorphism in TLR9 confers a population-based increased risk of non-Hodgkin lymphomaCarvalho, Agostinho; Cunha, Cristina; Almeida, A. J., et al.ArticleOpen access
2015Type 2 diabetes-related variants influence the risk of developing multiple myeloma: results from the IMMEnSE consortiumRíos, Rafael; Lupiañez, Carmen Belén; Campa, Daniele, et al.ArticleOpen access
24-Mar-2014Vírus herpes-γ e polimorfismos dos sistemas de processamento antigénico : importância na oncogénese e no prognóstico dos linfomas de células BMarques, HerlanderDoctoral thesisRestricted access (UMinho)