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Luísa Mota‐Vieira

Observed names: L. Mota-Vieira, L. Mota‐Vieira, Louisa Mota-Vieira, Luisa MOTA VIEIRA, Luisa Mota Vieira, Luisa Mota-Vieira, Luisa Mota‐Vieira, Luís Vieira, Luísa Mota Vieira, Luísa Mota-Vieira, Vieira, Luisa, Vieira, Luísa Mota
Observed institutions: University of Lisbon, Inserm, Unidade Local de Saúde de São José, Hospital do Divino Espírito Santo, Institut Cochin, National Institute of Health Dr. Ricardo Jorge, Instituto Gulbenkian de Ciência, Universidade Nova de Lisboa
ORCID: 0000-0003-1451-6705
Observed ORCID: 0000-0003-1451-6705
OpenAlex ID: A5038903900
Epidemiology of autism spectrum disorder in Portugal: prevalence, clinical characterization, and medical conditions
2007 · Guiomar Oliveira, Assunção Ataíde, et al. · Developmental Medicine & Child Neurology · 167
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Clinical and Genetic Spectrum of Bartter Syndrome Type 3
2017 · Elsa Seys, Olga Andrini, et al. · Journal of the American Society of Nephrology · 118
Molecular and Clinical Characteristics in 46 Families Affected with Peutz–Jeghers Syndrome
2007 · Hamid Mehenni, Nicoletta Resta, et al. · Digestive Diseases and Sciences · 83
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Diagnosis of Human Leptospirosis in a Clinical Setting: Real-Time PCR High Resolution Melting Analysis for Detection of Leptospira at the Onset of Disease
2018 · Lisa M. Esteves, Sara M. Bulhões, et al. · Scientific Reports · 82
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Low frequency of CD4+CD25+ Treg in SLE patients: a heritable trait associated with CTLA4 and TGFβ gene variants
2009 · Marta Barreto, Ricardo C Ferreira, et al. · BMC Immunology · 82
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MECP2 coding sequence and 3′UTR variation in 172 unrelated autistic patients
2007 · Ana M. Coutinho, Guiomar Oliveira, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 65
Oxidative stress and mitochondrial dysfunction play a role in myelodysplastic syndrome development, diagnosis, and prognosis: A pilot study
2015 · A. C. Gonçalves, E. Cortesão, et al. · Free Radical Research · 53
A New PAX8 Mutation Causing Congenital Hypothyroidism in Three Generations of a Family Is Associated with Abnormalities in the Urogenital Tract
2013 · Ana Carvalho, Pia Hermanns, et al. · Thyroid · 48
International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation
2010 · Ana Peixoto, Catarina Santos, et al. · Breast Cancer Research and Treatment · 38
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Human Leptospirosis: Seroreactivity and Genetic Susceptibility in the Population of São Miguel Island (Azores, Portugal)
2014 · Lisa M. Esteves, Sara M. Bulhões, et al. · PLoS ONE · 35
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Oxidative stress levels are correlated with P15 and P16 gene promoter methylation in myelodysplastic syndrome patients
2015 · Ana Cristina Gonçalves, Emília Cortesão, et al. · Clinical and Experimental Medicine · 31
The Y-chromosomal Heritage of the Azores Islands Population
2005 · P. R. Pacheco, C. C. Branco, et al. · Annals of Human Genetics · 31
Massive dissemination of a SARS-CoV-2 Spike Y839 variant in Portugal
2020 · Vítor Borges, Joana Isidro, et al. · Emerging Microbes & Infections · 28
Unraveling the genetic background of individuals with a clinical familial hypercholesterolemia phenotype
2023 · Ana Margarida Medeiros, Ana Catarina Alves, et al. · Journal of Lipid Research · 27
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Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy
2007 · Elodie Chabrol, Isabelle Gourfinkel-An, et al. · Epilepsy Research · 27
Evaluation of reference-based two-color methods for measurement of gene expression ratios using spotted cDNA microarrays
2006 · Bernardo R Peixoto, Ricardo ZN Vêncio, et al. · BMC Genomics · 27
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Failure to Find α-Synuclein Gene Dosage Changes in 190 Patients With Familial Parkinson Disease
2005 · Suzana Gispert, Claudia Trenkwalder, et al. · Archives of Neurology · 25
Transcriptional and translational mechanisms of cytochrome b5 reductase isoenzyme generation in humans
2001 · Alena LEROUX, Luisa MOTA VIEIRA, et al. · Biochemical Journal · 24
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DNA Methylation Is Correlated with Oxidative Stress in Myelodysplastic Syndrome—Relevance as Complementary Prognostic Biomarkers
2021 · Ana Cristina Gonçalves, Raquel Alves, et al. · Cancers · 22
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A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
2018 · Zoe Argyropoulou, Lu Liu, et al. · BMC Dermatology · 22
Disease Knowledge and Attitudes toward Predictive Testing and Prenatal Diagnosis in Families with Machado-Joseph Disease from the Azores Islands (Portugal)
2001 · M. Lima, T. Kay, et al. · Public Health Genomics · 22
Yoga in primary health care: A quasi-experimental study to access the effects on quality of life and psychological distress
2018 · Sara B. Ponte, Carolina Lino, et al. · Complementary Therapies in Clinical Practice · 21
Genetic variants involved in oxidative stress, base excision repair, DNA methylation, and folate metabolism pathways influence myeloid neoplasias susceptibility and prognosis
2016 · Ana Cristina Gonçalves, Raquel Alves, et al. · Molecular Carcinogenesis · 20
First isolation of human Leptospira strains, Azores, Portugal
2010 · Ana T. Gonçalves, Clara Paiva, et al. · International Journal of Infectious Diseases · 19
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Epidemiology and genetic variability of respiratory syncytial virus in Portugal, 2014–2018
2019 · Emma Sáez-López, Paula Cristóvão, et al. · Journal of Clinical Virology · 18
Works count: 86
Citation count: 1,491
H-index: 21
I10-index: 40
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