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TITLE: Paternal half-sisters or unrelated-How can the X-chromosomal evidence be quantified when one female presents trisomy X?  Full Text
AUTHORS: Faustino, Marisa; Turchi, Chiara; Kling, Daniel; Gusmao, Leonor; Amorim, Antonio ; Pinto, Nadia ;
PUBLISHED: 2022, SOURCE: FORENSIC SCIENCE INTERNATIONAL GENETICS SUPPLEMENT SERIES, VOLUME: 8, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef Unpaywall
12
TITLE: Interplay between glycemia and the genetics of eNOS and ACE for the susceptibility to the onset and development of hypertension on the Portuguese population
AUTHORS: Aguiar, L; Ferreira, J; Matos, A; Mascarenhas, MR; Falcao, LM; Faustino, P; Bicho, M; Inacio, A;
PUBLISHED: 2021, SOURCE: GENE REPORTS, VOLUME: 22
INDEXED IN: Scopus WOS CrossRef: 1
IN MY: ORCID
13
TITLE: INTERPLAY BETWEEN GLYCEMIA AND THE GENETICS OF ENOS AND ACE GENES FOR THE SUSCEPTIBILITY TO THE ONSET AND DEVELOPMENT OF HYPERTENSION ON THE PORTUGUESE POPULATION  Full Text
AUTHORS: Aguiar, L; Ferreira, J; Matos, A; Mascarenhas, MR; Falcao, LM; Faustino, P; Bicho, M; Inacio, A;
PUBLISHED: 2021, SOURCE: 24th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 100, ISSUE: 4
INDEXED IN: WOS
IN MY: ORCID
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TITLE: MUTATIONAL SPECTRUM AND GEOGRAPHIC DISTRIBUTION OF ALPHA-THALASSEMIA IN AN ADULT MICROCYTIC AND/OR HYPOCHROMIC POPULATION LIVING IN PORTUGAL: RESULTS FROM THE FIRST NATIONAL HEALTH EXAMINATION SURVEY (INSEF 2015)
AUTHORS: Santos, D; Kislaya, I; Lopes, P; Matias Dias, C; Barreto, M; Faustino, P;
PUBLISHED: 2021, SOURCE: 24th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 100, ISSUE: 4
INDEXED IN: WOS Handle
IN MY: ORCID
15
TITLE: Differences in the genotype frequencies of genes related to blood pressure regulation - a comparative study between South-West Europe and Peri-equatorial Africa
AUTHORS: Aguiar, L; Semente, I; Ferreira, J; Carvalho, A; Silva, AP; Caroca, C; Caria, H; Damasceno, A; Laires, MJ; Sardinha, L; Monteiro, C; Mascarenhas, MR; Faustino, P; Inacio, A; Bicho, M;
PUBLISHED: 2021, SOURCE: AFRICAN HEALTH SCIENCES, VOLUME: 21, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef Handle
IN MY: ORCID
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TITLE: Biomarkers and genetic modulators of cerebral vasculopathy in sub-Saharan ancestry children with sickle cell anemia
AUTHORS: Silva, M; Vargas, S; Coelho, A; Ferreira, E; Mendonca, J; Vieira, L; Maia, R; Dias, A; Ferreira, T; Morais, A; Soares, IM; Lavinha, J; Silva, R; Kjollerstrom, P; Faustino, P;
PUBLISHED: 2020, SOURCE: BLOOD CELLS MOLECULES AND DISEASES, VOLUME: 83
INDEXED IN: Scopus WOS CrossRef: 8
IN MY: ORCID
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TITLE: Co-Inheritance of alpha-thalassemia and sickle cell disease in a cohort of Angolan pediatric patients  Full Text
AUTHORS: Santos, B; Delgadinho, M; Ferreira, J; Germano, I; Miranda, A; Arez, AP; Faustino, P; Brito, M;
PUBLISHED: 2020, SOURCE: MOLECULAR BIOLOGY REPORTS, VOLUME: 47, ISSUE: 7
INDEXED IN: Scopus WOS CrossRef: 10
IN MY: ORCID
18
TITLE: Prevalence of anemia in the Portuguese adult population: results from the first National Health Examination Survey (INSEF 2015)
AUTHORS: Samões, C; Kislaya, I; Sousa Uva, M; Gaio, V; Faustino, P; Nunes, B; Matias Dias, C; Barreto, M;
PUBLISHED: 2020, SOURCE: Journal of Public Health (Germany), VOLUME: 30, ISSUE: 4
INDEXED IN: Scopus CrossRef: 2
IN MY: ORCID
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TITLE: <i>VCAM1</i> modulation on endothelial cells - implications for vasculopathy in sickle cell anemia
AUTHORS: Silva, M; Vargas, S; Coelho, A; Lavinha, J; Faustino, P;
PUBLISHED: 2020, SOURCE: MEDICINE, VOLUME: 99, ISSUE: 9
INDEXED IN: WOS
IN MY: ORCID
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TITLE: Osteoporosis: Gene interaction between haptoglobin and HFE polymorphisms
AUTHORS: Aguiar, L; Ferreira, J; Laires, MJ; Mascarenhas, MR; Inácio, A; Faustino, P; Bicho, M;
PUBLISHED: 2020, SOURCE: MEDICINE, VOLUME: 99, ISSUE: 9
INDEXED IN: WOS
IN MY: ORCID
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