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Tatiana Amorim

Observed names: Amorim, Tatiana, T Amorim, Tatiana Regia Suzana Amorim Boa Sorte, Tatiana Régia Suzana Amorim Boa Sorte
ORCID: 0000-0002-0371-9104
Observed ORCID: 0000-0002-0371-9104
OpenAlex ID: A5041590878
Epidemiology of rare diseases in Brazil: protocol of the Brazilian Rare Diseases Network (RARAS-BRDN)
2022 · Têmis Maria Félix, Bibiana Mello de Oliveira, et al. · Orphanet Journal of Rare Diseases · 61
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Poor zinc and selenium status in phenylketonuric children and adolescents in Brazil
2008 · Junaura Rocha Barretto, Luciana Rodrigues Silva, et al. · Nutrition Research · 38
Dried blood spot testing for the antenatal screening of HTLV, HIV, syphilis, toxoplasmosis and hepatitis B and C: prevalence, accuracy and operational aspects
2014 · Ney Boa-Sorte, Antônio Purificação, et al. · The Brazilian Journal of Infectious Diseases · 32
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Hemoglobin A2 values in sickle cell disease patients quantified by high performance liquid chromatography and the influence of alpha thalassemia
2015 · Silvana Fahel da Fonseca, Tatiana Amorim, et al. · Revista Brasileira de Hematologia e Hemoterapia · 30
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Epidemiological characterization of rare diseases in Brazil: A retrospective study of the Brazilian Rare Diseases Network
2024 · Bibiana Mello de Oliveira, Filipe Andrade Bernardi, et al. · Orphanet Journal of Rare Diseases · 28
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Evaluation of plasma biomarkers of inflammation in patients with maple syrup urine disease
2018 · Giselli Scaini, Tássia Tonon, et al. · Journal of Inherited Metabolic Disease · 26
Pilot study of newborn screening for six lysosomal diseases in Brazil
2023 · Francyne Kubaski, Ines Sousa, et al. · Molecular Genetics and Metabolism · 20
Aspectos clínicos da fenilcetonúria em serviço de referência em triagem neonatal da Bahia
2005 · Tatiana Amorim, Sara P.P. Gatto, et al. · Revista Brasileira de Saúde Materno Infantil · 15
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Neonatal Screening for MPS Disorders in Latin America: A Survey of Pilot Initiatives
2020 · Francyne Kubaski, Inês Sousa, et al. · International Journal of Neonatal Screening · 14
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Maple syrup urine disease in Brazilian patients: variants and clinical phenotype heterogeneity
2020 · Ana Vitoria Barban Margutti, Wilson Araújo Silva, et al. · Orphanet Journal of Rare Diseases · 14
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Population medical genetics: translating science to the community
2019 · Roberto Giugliani, Fernanda Bender, et al. · Genetics and Molecular Biology · 14
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Mutation screening in the genes PAX-8, NKX2-5, TSH-R, HES-1 in cohort of 63 Brazilian children with thyroid dysgenesis
2018 · Taíse Lima de Oliveira Cerqueira, Yanne Rocha Ramos, et al. · Archives of Endocrinology and Metabolism · 14
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Aspectos clínicos e demográficos da fenilcetonúria no Estado da Bahia
2011 · Tatiana Amorim, Ney Boa-Sorte, et al. · Revista Paulista de Pediatria · 14
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Five-year performance analysis of a cystic fibrosis newborn screening program in northeastern Brazil
2022 · Carolina Godoy, Danielle C. Paixão, et al. · Jornal de Pediatria · 11
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Avaliação Do Programa De Triagem Neonatal Da Bahia Entre 2007 E 2009 – as Lições Da Doença Falciforme
2010 · Tatiana Amorim, Helena Pimentel, et al. · Gazeta Médica da Bahia · 11
The sickle cell trait and end stage renal disease in Salvador, Brazil
2018 · Dona J. Alladagbin, Paula N. Fernandes, et al. · PLoS ONE · 10
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Adherence to PKU guidelines among patients with phenylketonuria: A cross-sectional national multicenter survey-based study in Argentina, Brazil, and Mexico
2023 · Ana Chiesa, Norma Spécola, et al. · Molecular Genetics and Metabolism Reports · 9
The c.63A>G polymorphism in the NKX2.5 gene is associated with thyroid hypoplasia in children with thyroid dysgenesis
2015 · Taise Lima de Oliveira Cerqueira, Yanne Ramos, et al. · Archives of Endocrinology and Metabolism · 7
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Breastfeeding and the anthropometric profile of children with sickle cell anemia receiving follow-up in a newborn screening reference service
2015 · Zeni Drubi Nogueira, Ney Boa-Sorte, et al. · Revista Paulista de Pediatria (English Edition) · 6
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Metabolic Control and Body Composition of Children and Adolescents With Phenylketonuria
2021 · Zeni Drubi Nogueira, Ney Boa-Sorte, et al. · Revista Paulista de Pediatria · 5
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Aleitamento materno e perfil antropométrico de crianças com doença falciforme acompanhadas em serviço de referência em triagem neonatal
2015 · Zeni Drubi Nogueira, Ney Boa‐Sorte, et al. · Revista Paulista de Pediatria · 5
IRT/IRT as a newborn cystic fibrosis screening method: optimal cutoff points for a mixed population
2024 · Carolina Godoy, Pedro Paulo Brito, et al. · Cadernos de Saúde Pública · 3
Maple syrup urine disease diagnosis in Brazilian patients by massive parallel sequencing
2024 · Rafael Hencke Tresbach, Fernanda Sperb-Ludwig, et al. · Molecular Genetics and Metabolism · 1
FICHA A-GEN
2020 · Acosta, Angelina, Amorim, Tatiana, et al. · Figshare · 1
Erratum to: Serum Markers of Neurodegeneration in Maple Syrup Urine Disease
2016 · Giselli Scaini, Tássia Tonon, et al. · Molecular Neurobiology · 1
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Works count: 53
Citation count: 392
H-index: 13
I10-index: 16
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