11
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
INDEXED IN: WOS
12
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
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
13
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
INDEXED IN: Scopus WOS CrossRef: 14
IN MY: ORCID
14
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
INDEXED IN: WOS CrossRef: 2
IN MY: ORCID
15
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
INDEXED IN: WOS
16
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
INDEXED IN: WOS CrossRef
IN MY: ORCID
17
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
INDEXED IN: WOS CrossRef
IN MY: ORCID
18
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
INDEXED IN: Scopus WOS
19
TITLE: Challenges and (Un)Certainties for DNAm Age Estimation in Future
AUTHORS: Helena Correia Dias; Eugénia Cunha; Francisco Corte Real; Licínio Manco;
PUBLISHED: 2022, SOURCE: Forensic Sciences, VOLUME: 2, ISSUE: 3
INDEXED IN: CrossRef: 4
IN MY: ORCID
20
TITLE: Heterogeneidade Molecular da Deficiência em Glicose-6-Fosfato Desidrogenase (G6PD) na População Portuguesa
AUTHORS: Licínio Manco; Celeste Bento; Luís Relvas; Tabita Maia; Maria Letícia Ribeiro;
PUBLISHED: 2022, SOURCE: Acta Médica Portuguesa
INDEXED IN: CrossRef
IN MY: ORCID
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