Author

Emília Vieira

Observed names: Emilia Vieira, Emília Vieira, Vieira, Emília

Institutions: University of Lisbon, National Centre for Scientific Research

Observed institutions: University of Lisbon, Universidade do Porto, Hospital de Santo António, Centro Hospitalar de Vila Nova de Gaia, National Institute of Health Dr. Ricardo Jorge, Centro Hospitalar do Porto, Unidade Local de Saúde de Santo António EPE, National Centre for Scientific Research, Instituto de Ciências Biomédicas Albel Salazar

OpenAlex ID: A5103608426

LAMA2gene mutation update: Toward a more comprehensive picture of the laminin-α2 variome and its related phenotypes

2018 · Jorge Oliveira, Angela Gruber, et al. · Human Mutation · 114

New variants, challenges and pitfalls in DMD genotyping: implications in diagnosis, prognosis and therapy

2014 · Rosário Santos, Ana Gonçalves, et al. · Journal of Human Genetics · 39

Analysis of the UDP-glucuronosyltransferase gene in Portuguese patients with a clinical diagnosis of Gilbert and Crigler–Najjar syndromes

2005 · Elísio Costa, Emília Vieira, et al. · Blood Cells Molecules and Diseases · 32

Impact of UGT1A1 gene variants on total bilirubin levels in Gilbert syndrome patients and in healthy subjects

2012 · Carina Rodrigues, Emília Vieira, et al. · Blood Cells Molecules and Diseases · 29

The Polymorphism c.-3279T>G in the Phenobarbital-Responsive Enhancer Module of the Bilirubin UDP-Glucuronosyltransferase Gene Is Associated with Gilbert Syndrome

2005 · Elísio Costa, Emília Vieira, et al. · Clinical Chemistry · 29

Oxidized low‐density lipoprotein and lipoprotein(a) levels in chronic kidney disease patients under hemodialysis: Influence of adiponectin and of a polymorphism in the apolipoprotein(a) gene

2012 · Sandra Ribeiro, Maria do Sameiro Faria, et al. · Hemodialysis International · 25

Adipokine Gene Single-Nucleotide Polymorphisms in Portuguese Obese Adolescents: Associations with Plasma Concentrations of Adiponectin, Resistin, IL-6, IL-1β, and TNF-α

2016 · Henrique Nascimento, Emília Vieira, et al. · Childhood Obesity · 24

Bilirubin Dependence on UGT1A1 Polymorphisms, Hemoglobin, Fasting Time and Body Mass Index

2011 · Carina Rodrigues, Elísio Costa, et al. · The American Journal of the Medical Sciences · 21

Glucose-6-phosphate dehydrogenase Aveiro: a de novo mutation associated with chronic nonspherocytic hemolytic anemia

2000 · Elı́sio Costa, José Manuel Cabeda, et al. · Blood · 16

Private dysferlin exon skipping mutation (c.5492G>A) with a founder effect reveals further alternative splicing involving exons 49–51

2010 · Rosário Santos, Jorge Oliveira, et al. · Journal of Human Genetics · 15

A New Case of (ta)8 Allele in the Ugt1a1 Gene Promoter in a Caucasian Girl With Gilbert’ Syndrome

2004 · Henrique Coelho, Elísio Costa, et al. · Pediatric Hematology and Oncology · 12

Novel ancestral Dysferlin splicing mutation which migrated from the Iberian peninsula to South America

2011 · Luis Vernengo, Jorge Oliveira, et al. · Neuromuscular Disorders · 10

Bilirubin Levels and Redox Status in a Young Healthy Population

2013 · Carina Rodrigues, Susana Rocha, et al. · Acta Haematologica · 7

TATA-Box polymorphism in the uridine diphosphate glucuronosyl transferase gene in Portuguese patients with clinical diagnosis of Gilbert Syndrome.

2002 · Elísio Costa, Emília Vieira, et al. · PubMed · 5

A novel CFTR-AQP7 protein complex regulates glycerol transport and motility of human sperm

2025 · João C Ribeiro, Raquel L Bernardino, et al. · Human Reproduction · 3

Identification of a novel deletion in UDP-glucuronosyltransferase gene in a patient with Crigler–Najjar syndrome type I

2009 · Elísio Costa, Emília Vieira, et al. · Blood Cells Molecules and Diseases · 3

[Glucose-6-phosphate dehydrogenase deficiency, neonatal hyperbilirubinemia and Gilbert syndrome].

2002 · Elísio Costa, Emilia Vieira, et al. · PubMed · 3

A Novel Missense Mutation in the Alphatropomyosin (tpm1) Gene in a Family Affected With Hypertrophic Cardiomyopathy

2016 · Vieira, Emília, Oliveira, Márcia E, et al. · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) · 2

Ethnobotanical and symbiotic insights into northwestern Angola’s useful legumes

2026 · Miguel Brilhante, Emília Vieira, et al. · Symbiosis

Intronic long interspersed nuclear element (LINE-1) insertion in the DMD gene as a cause of Becker muscular dystrophy

2015 · Ana Gonçalves, Teresa Coelho, et al. · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

Distribution of limb girdle muscular dystrophy subtypes among Portuguese patients

2012 · Emília Vieira · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

BETA-SARCOGLICANOPATIA- uma distrofia muscular das cinturas com diferentes prognósticos

2012 · A. C. O. Dias, Ricardo Taipa, et al. · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

Complexo distrofina-gllcoproteínas - a propósito de um doente com distrofia de Becker

2012 · Cecília Monteiro, Ricardo Taipa, et al. · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

O Papel da neuropatologia no diagnóstico das distrofias das cinturas autossómicas recessivas

2012 · Cecília Monteiro, Ricardo Taipa, et al. · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

Nova abordagem no diagnóstico diferencial de doentes Portugueses com LGMD2A (ou Calpainopatia)

2012 · Márcia E. Oliveira, Nuno Maia, et al. · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

Works count: 40

Citation count: 389

H-index: 11

I10-index: 12