Licínio Manuel Mendes Manco
AuthID: R-000-94T
11
TITLE: ANALYSIS OF R1B-M269 SUBHAPLOGROUS IN THE CENTRAL REGION OF PORTUGAL Full Text
AUTHORS: Nunes, Fabio; Manco, Licinio;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
AUTHORS: Nunes, Fabio; Manco, Licinio;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
INDEXED IN: 
WOS
WOS12
TITLE: DROPLET DIGITAL PCR FOR EPIGENETIC AGE ESTIMATION USING DNA METHYLATION IN ELOVL2 AND PDE4C GENES Full Text
AUTHORS: Dias, Helena Correia; Manco, Licinio;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
AUTHORS: Dias, Helena Correia; Manco, Licinio;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
INDEXED IN: WOS
WOS13
TITLE: MOLECULAR CHARACTERIZATION OF CONGENITAL ERYTHROCYTOSIS AND IDIOPATHIC ERYTHROCYTOSIS ANALYSED BY NEXT-GENERATION SEQUENCING Full Text
AUTHORS: Frias, Raquel; Pereira, Janet; Relvas, Luis; Cunha, Elizabete; Manco, Licinio; Maia, Tabita Magalhaes; Bento, Celeste;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
AUTHORS: Frias, Raquel; Pereira, Janet; Relvas, Luis; Cunha, Elizabete; Manco, Licinio; Maia, Tabita Magalhaes; Bento, Celeste;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
INDEXED IN: WOS
WOS14
TITLE: Differential sex-association between <i>PCSK1</i> polymorphisms and obesity risk in Portuguese children Full Text
AUTHORS: Manco, Licinio; Albuquerque, David; Aranda, Beatriz; Rodrigues, Daniela; Machado Rodrigues, Aristides M. ; Padez, Cristina ;
PUBLISHED: 2023, SOURCE: AMERICAN JOURNAL OF HUMAN BIOLOGY, VOLUME: 36, ISSUE: 5
AUTHORS: Manco, Licinio; Albuquerque, David; Aranda, Beatriz; Rodrigues, Daniela; Machado Rodrigues, Aristides M. ; Padez, Cristina ;
PUBLISHED: 2023, SOURCE: AMERICAN JOURNAL OF HUMAN BIOLOGY, VOLUME: 36, ISSUE: 5
15
TITLE: DNA methylation analysis of ELOVL2 gene using droplet digital PCR for age estimation purposes
AUTHORS: Manco, Licinio; Dias, Helena Correia;
PUBLISHED: 2022, SOURCE: FORENSIC SCIENCE INTERNATIONAL, VOLUME: 333
AUTHORS: Manco, Licinio; Dias, Helena Correia;
PUBLISHED: 2022, SOURCE: FORENSIC SCIENCE INTERNATIONAL, VOLUME: 333
16
TITLE: Vigorous physical activity: A potential ally in adolescent obesity management
AUTHORS: Videira Silva, A; Manco, L; Sardinha, LB; Fonseca, H;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF SPORT SCIENCE, VOLUME: 23, ISSUE: 4
AUTHORS: Videira Silva, A; Manco, L; Sardinha, LB; Fonseca, H;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF SPORT SCIENCE, VOLUME: 23, ISSUE: 4
17
TITLE: Association study of KLF1 gene variations with HbF and HbA2 levels in beta-thalassemia carriers of Portuguese origin
AUTHORS: Manco, Licinio; Bento, Celeste; Relvas, Luis; Maia, Tabita; Leticia Ribeiro, M.;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 30, ISSUE: SUPPL 1
AUTHORS: Manco, Licinio; Bento, Celeste; Relvas, Luis; Maia, Tabita; Leticia Ribeiro, M.;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 30, ISSUE: SUPPL 1
INDEXED IN: WOS
WOS18
TITLE: Hb F Levels in beta-Thalassemia Carriers and Normal Individuals: Known and Unknown Quantitative Trait Loci in the beta-Globin Gene Cluster Full Text
AUTHORS: Manco, Licinio; Santos, Raquel; Rocha, Catarina; Relvas, Luis; Bento, Celeste; Maia, Tabita; Gomes, Veronica; Amorim, Antonio ; Prata, Maria J. ;
PUBLISHED: 2022, SOURCE: HEMOGLOBIN, VOLUME: 46, ISSUE: 3
AUTHORS: Manco, Licinio; Santos, Raquel; Rocha, Catarina; Relvas, Luis; Bento, Celeste; Maia, Tabita; Gomes, Veronica; Amorim, Antonio ; Prata, Maria J. ;
PUBLISHED: 2022, SOURCE: HEMOGLOBIN, VOLUME: 46, ISSUE: 3
19
TITLE: Novel homozygous nonsense mutation in the P5 ' N-1 coding gene as an alternative cause for hereditary anemia with basophilic stippling
AUTHORS: Kirschner, Martin; Heinen, Inga Rebecca; Koschmieder, Steffen; Manco, Licinio; Bento, Celeste; Eggermann, Thomas; Kurth, Ingo; Jost, Edgar; Bruemmendorf, Tim H.; Fuchs, Roland;
PUBLISHED: 2022, SOURCE: CLINICAL CASE REPORTS, VOLUME: 10, ISSUE: 3
AUTHORS: Kirschner, Martin; Heinen, Inga Rebecca; Koschmieder, Steffen; Manco, Licinio; Bento, Celeste; Eggermann, Thomas; Kurth, Ingo; Jost, Edgar; Bruemmendorf, Tim H.; Fuchs, Roland;
PUBLISHED: 2022, SOURCE: CLINICAL CASE REPORTS, VOLUME: 10, ISSUE: 3
20
TITLE: Molecular Heterogeneity of Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency in the Portuguese Population Full Text
AUTHORS: Manco, Licinio; Bento, Celeste; Relvas, Luis; Maia, Tabita; Ribeiro, Maria Leticia;
PUBLISHED: 2022, SOURCE: ACTA MEDICA PORTUGUESA, VOLUME: 36, ISSUE: 2
AUTHORS: Manco, Licinio; Bento, Celeste; Relvas, Luis; Maia, Tabita; Ribeiro, Maria Leticia;
PUBLISHED: 2022, SOURCE: ACTA MEDICA PORTUGUESA, VOLUME: 36, ISSUE: 2
INDEXED IN: 
Scopus WOS
Scopus WOS