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Credit Name
Manco, Licínio
Full Name
Manco, Licínio Manuel Mendes
 
 
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Publications
(All)

Results 1-34 of 34 (Search time: 0.039 seconds).

Issue DateTitleAuthor(s)TypeAccess
12011Allele frequencies of 6 STR loci (TH01, TPOX, CSF1PO, D13S317, D16S539 and D7S820) in São Tomé e Príncipe (West Africa)Manco, Licínio ; Silva, Isabel ; Arede, Pedro ; Jesus Trovoada, M. ; Abade, Augusto ; Alvarez, Manuela articleopenAccess
22009Analysis of TPI gene promoter variation in three sub-Saharan Africa population samplesManco, Licínio ; Machado, Patrícia ; Lopes, Dinora ; Nogueira, Fátima ; Rosário, Virgílio E. Do ; Alonso, Pedro L. ; Varandas, Luís ; Trovoada, Maria De Jesus ; Amorim, António ; Arez, Ana Paula articleopenAccess
32013Análise haplotípica de mutações comuns no gene HFE associadas à Hemocromatose em PortugalToste, Sandra de Fátima Gomes masterThesisopenAccess
42010Anthropology and health: trends for the next decade: program - abstracts bookSantos, Ana Luísa ; Gama, Augusta ; Padez, Cristina ; Manco, Licínio ; Ferrão, Maria Miguel ; Marques, Vítor Rosado ; Matos, Vítor bookopenAccess
52017Association of 5-HTTLPR genotypes with antisocial behavior in response to childhood environment: A study in young adults of Portuguese originManco, Licínio ; Soares, Ana ; Wasterlain, Sofia N. articleembargoedAccess
62013Association of FTO Polymorphisms with Obesity and Obesity-Related Outcomes in Portuguese ChildrenAlbuquerque, David ; Nóbrega, Clévio ; Manco, Licínio articleopenAccess
72016Association of polymorphisms in 5-HTT (SLC6A4) and MAOA genes with measures of obesity in young adults of Portuguese originDias, Helena ; Muc, Magdalena ; Padez, Cristina ; Manco, Licínio articleopenAccess
82016Association study between near-MC4R variants and obesity-related variables in Portuguese young adultsManco, Licínio ; Muc, Magdalena ; Padez, Cristina articleopenAccess
92014Association study of common polymorphisms in MSRA, TFAP2B, MC4R, NRXN3, PPARGC1A, TMEM18, SEC16B, HOXB5 and OLFM4 genes with obesity-related traits among Portuguese childrenAlbuquerque, David ; Nóbrega, Clévio ; Rodríguez-López, Raquel ; Manco, Licínio articleopenAccess
102016Congenital dyserythropoietic anemia associated to a GATA1 mutation aggravated by pyruvate kinase deficiencyPereira, Janet ; Bento, Celeste ; Manco, Licinio ; Gonzalez, Ataulfo ; Vagace, Jose ; Ribeiro, Maria Letícia articleopenAccess
112015Current review of genetics of human obesity: from molecular mechanisms to an evolutionary perspectiveAlbuquerque, David ; Stice, Eric ; Rodríguez-López, Raquel ; Manco, Licíno ; Nóbrega, Clévio articleopenAccess
1228-Feb-2003A deficiência em piruvato-quinase (PK) na população portuguesa : estudos de genética molecular e populacionalManco, Licínio Manuel Mendes doctoralThesisembargoedAccess
132016Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next-generation sequencingDel Orbe Barreto, R. ; Arrizabalaga, B. ; De la Hoz, A. B. ; García-Orad, Á. ; Tejada, M. I. ; Garcia-Ruiz, J. C. ; Fidalgo, T. ; Bento, C. ; Manco, L. ; Ribeiro, M. L. articleopenAccess
141999Distribution of AMY2 polymorphism in S. Tomé and Príncipe (West Africa)Manco, L. ; Trovoada, M. ; Abade, A. ; Amorim, A. articleopenAccess
152013Distribution of the − 13910C>T polymorphism in the general population of Portugal and in subjects with gastrointestinal complaints associated with milk consumptionManco, Licínio ; Pires, Sara ; Lopes, Ana Isabel ; Figueiredo, Ima ; Albuquerque, David ; Alvarez, Manuela ; Rocha, Jorge ; Abade, Augusto articleopenAccess
162012Diversidade haplotípica associada a variantes no locus APOL1 que conferem resistência à doença do sono numa amostra populacional da Ilha do PríncipeTeixeira, Sérgio Amaro Antunes masterThesisopenAccess
172013Estudo de polimorfismos associados ao aumento da expressão de Hemoglobina Fetal (HbF)Pereira, Clara Inês Antunes masterThesisopenAccess
182015Estudo de variantes genéticas associadas a comportamentos agressivos numa amostra populacional portuguesaSoares, Ana Catarina de Almeida masterThesisopenAccess
192008Estudo populacional de 6 STRs (TH01, TPOX, CSF1PO, D7S820, D13S317 e D16S539) na região Centro de PortugalManco, Licínio ; Arede, Pedro ; Silva, Isabel ; Alvarez, Manuela ; Abade, Augusto articleopenAccess
202015Familial thrombotic risk based on the genetic background of Protein C Deficiency in a Portuguese StudyFidalgo, Teresa ; Martinho, Patrícia ; Salvado, Ramon ; Manco, Licínio ; Oliveira, Ana C. ; Pinto, Catarina S. ; Gonçalves, Elsa ; Marques, Dalila ; Sevivas, Teresa ; Martins, Natália ; Ribeiro, Maria Letícia articleopenAccess
212016Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular studyManco, Licínio ; Bento, Celeste ; Victor, Bruno L. ; Pereira, Janet ; Relvas, Luís ; Brito, Rui M. ; Seabra, Carlos ; Maia, Tabita M. ; Ribeiro, M. Letícia articleopenAccess
222015Influence of physical activity on the association between the FTO variant rs9939609 and adiposity in young adultsMuc, Magdalena ; Padez, Cristina ; Manco, Licínio articleopenAccess
23Jun-2015Intragenic haplotype analysis of common HFE mutations in the Portuguese populationToste, Sandra ; Relvas, Luís ; Pinto, Catarina ; Bento, Celeste ; Abade, Augusto ; Ribeiro, M Letícia ; Manco, Licínio articleembargoedAccess
242014Legado Genético do Cromossoma Y . Caracterização do haplogrupo J em amostras de origem portuguesa com foco na zona centroAlbuquerque, Joana Isabel Silva de masterThesisopenAccess
252006Molecular characterization of five Portuguese patients with pyrimidine 5’-nucleotidase deficient hemolytic anemia showing three new P5’N-I mutationsManco, Licínio ; Relvas, Luís ; Pinto, C. Silva ; Pereira, Janet ; Almeida, A. Bessa ; Ribeiro, M. Letícia articleopenAccess
262007Mutations and haplotype diversity in 70 Portuguese G6PD-deficient individuals: an overview on the origin and evolution of mutated allelesManco, Licínio ; Gonçalves, Paula ; Antunes, Patrícia ; Maduro, Filomena ; Abade, Augusto ; Ribeiro, M. Letícia articleopenAccess
272014Novel Variants in theMC4RandLEPRGenes among Severely Obese Children from the Iberian PopulationAlbuquerque, David ; Estévez, Manuela Núñez ; Víbora, Pilar Beato ; Giralt, Plácida Sánchez ; Balsera, Aránzazu Margallo ; Cortés, Pedro Gil ; López, Mercedes Jiménez ; Luego, Luis Miguel ; Gervasini, Guillermo ; Hernández, Sergio Barroso ; Arroyo-Díez, Javier ; Vacas, Manuel Arrobas ; Nóbrega, Clévio ; Manco, Licínio ; Rodríguez-López, Raquel articleopenAccess
282015Polymorphic variations influencing fetal hemoglobin levels: Association study in beta-thalassemia carriers and in normal individuals of Portuguese originPereira, Clara ; Relvas, Luís; Bento, Celeste; Abade, Augusto ; Ribeiro, M. Letícia; Manco, Licínio articleopenAccess
292016Severe neonatal jaundice due to ade novoglucose-6-phosphate dehydrogenase deficient mutationDel Orbe Barreto, R. ; Arrizabalaga, B. ; de la Hoz, A. B ; Aragües, P. ; Garcia-Ruiz, J. C. ; Arrieta, A. ; Adán, R. ; Manco, L. ; Macedo-Ribeiro, S. ; Bento, C. ; Ribeiro, M. L. articleopenAccess
3011-May-2015Study of genetic variants associated with obesity in Portuguese childrenAlbuquerque, David dos Santos doctoralThesisopenAccess
312013The lactase persistence -13910C>T polymorphism shows indication of association with abdominal obesity among Portuguese childrenAlbuquerque, David ; Nóbrega, Clévio ; Manco, Licínio articleopenAccess
322015Triosephosphate isomerase gene promoter variation: -5G/A and -8G/A polymorphisms in clinical malaria groups in two African populationsGuerra, Mónica ; Machado, Patrícia ; Manco, Licínio ; Fernandes, Natércia ; Miranda, Juliana ; Arez, Ana Paula articleopenAccess
332005Two new glucose-6-phosphate dehydrogenase mutations causing chronic hemolysisManco, Licínio ; Gonçalves, Paula ; Macedo-Ribeiro, Sandra ; Seabra, Carlos ; Melo, Paula ; Ribeiro, Maria Letícia articleopenAccess
342013Y -chromosome diversity in central Portugal reveals signatures of ancient maritime expansionsMartiniano, Rui ; Feitosa, Yara ; Abade, Augusto ; Manco, Licínio articleopenAccess