41
TITLE: The population genomics of archaeological transition in west Iberia: Investigation of ancient substructure using imputation and haplotype-based methods
AUTHORS: Martiniano, R; Cassidy, LM; Ó'Maoldúin, R; McLaughlin, R; Silva, NM; Manco, L; Fidalgo, D; Pereira, T; Coelho, MJ; Serra, M; Burger, J; Parreira, R; Moran, E; Valera, AC; Porfirio, E; Boaventura, R; Silva, AM ; Bradley, DG;
PUBLISHED: 2017, SOURCE: PLoS Genetics, VOLUME: 13, ISSUE: 7
INDEXED IN: Scopus CrossRef: 8 Handle
IN MY: ORCID
42
TITLE: Combined study of ADAMTS13 and complement genes in the diagnosis of thrombotic microangiopathies using next‐generation sequencing
AUTHORS: Teresa Fidalgo; Patrícia Martinho; Catarina S Pinto; Ana C Oliveira; Ramon Salvado; Nina Borràs; Margarida Coucelo; Licínio Manco; Tabita Maia; João J Mendes; Rafael Del Orbe Barreto; Irene Corrales; Francisco Vidal; Letícia L Ribeiro;
PUBLISHED: 2017, SOURCE: Research and Practice in Thrombosis and Haemostasis, VOLUME: 1, ISSUE: 1
INDEXED IN: CrossRef: 15
IN MY: ORCID
43
TITLE: Association of polymorphisms in 5-HTT (SLC6A4) and MAOA genes with measures of obesity in young adults of Portuguese origin  Full Text
AUTHORS: Dias, H; Muc, M; Padez, C ; Manco, L;
PUBLISHED: 2016, SOURCE: Archives of Physiology and Biochemistry in ARCHIVES OF PHYSIOLOGY AND BIOCHEMISTRY, VOLUME: 122, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef Handle
IN MY: ORCID
44
TITLE: Severe neonatal jaundice due to a de novo glucose-6-phosphate dehydrogenase deficient mutation
AUTHORS: Barreto, RD; Arrizabalaga, B; de la Hoz, AB; Aragues, P; Garcia Ruiz, JC; Arrieta, A; Adan, R; Manco, L; Macedo Ribeiro, S; Bento, C; Ribeiro, ML;
PUBLISHED: 2016, SOURCE: INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, VOLUME: 38, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
45
TITLE: Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study
AUTHORS: Manco, L; Bento, C; Victor, BL; Pereira, J; Relvas, L; Brito, RM; Seabra, C; Maia, TM; Ribeiro, ML;
PUBLISHED: 2016, SOURCE: Blood Cells, Molecules, and Diseases in BLOOD CELLS MOLECULES AND DISEASES, VOLUME: 60
INDEXED IN: Scopus WOS CrossRef Handle
IN MY: ORCID
46
TITLE: Congenital dyserythropoietic anemia associated to a GATA1 mutation aggravated by pyruvate kinase deficiency  Full Text
AUTHORS: Janet Pereira; Celeste Bento; Licinio Manco; Ataulfo Gonzalez; Jose Vagace; Maria Leticia Ribeiro;
PUBLISHED: 2016, SOURCE: ANNALS OF HEMATOLOGY, VOLUME: 95, ISSUE: 9
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
47
TITLE: Association study between near-MC4R variants and obesity-related variables in Portuguese young adults
AUTHORS: Manco, L; Muc, M; Padez, C ;
PUBLISHED: 2016, SOURCE: Gene Reports in GENE REPORTS, VOLUME: 5
INDEXED IN: Scopus WOS CrossRef Handle
IN MY: ORCID
48
TITLE: Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next-generation sequencing
AUTHORS: Barreto, RD; Arrizabalaga, B; De la Hoz, AB; Garcia Orad, A; Tejada, MI; Garcia Ruiz, JC; Fidalgo, T; Bento, C; Manco, L; Ribeiro, ML;
PUBLISHED: 2016, SOURCE: INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, VOLUME: 38, ISSUE: 6
INDEXED IN: WOS CrossRef: 35
IN MY: ORCID
49
TITLE: Triosephosphate isomerase gene promoter variation:-5G/A and-8G/A polymorphisms in clinical malaria groups in two African populations  Full Text
AUTHORS: Monica Guerra; Patricia Machado; Licinio Manco; Natercia Fernandes; Juliana Miranda; Ana Paula Arez;
PUBLISHED: 2015, SOURCE: INFECTION GENETICS AND EVOLUTION, VOLUME: 32
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
Page 5 of 7. Total results: 70.