Eduardo Vieira Neto, MD, PhD

  • Postdoctoral Associate

Vieira Neto graduated from State University of Rio de Janeiro, Brazil. He received training in medical genetics at Federal University of Rio de Janeiro (UFRJ). In his Master of Sciences at UFRJ, he acquired skills in newborn screening by ESI-MS/MS. He obtained his PhD degree at the same institution in 2018. His Doctoral Thesis was: Phenylketonuria in Rio de Janeiro - mutational profile and outcomes of early treatment. He was trained in biochemical and molecular genetics at Dr. Jacinto Magalhães Medical Genetics Center, University of Porto, Portugal. His main publications investigated the mutation profile of PKU in Rio de Janeiro, and the high discordance rate between genotype and phenotype in PKU patients. In his present postdoctoral research project at Dr. Vockley lab, University of Pittsburgh, he is investigating the effect of mutations in the mitochondrial trifunctional protein (TFP) subunits on mitochondrial bioenergetics and lipid composition.

Professional and Scientific Society Memberships

  • Brazilian Society of Newborn Screening and Inborn Errors of Metabolism, 1999-Present
  • Brazilian Society of Medical Genetics and Genomics, 2013-Present

Education & Training

  • MD, College of Medical Sciences of the State University of Rio de Janeiro, Brazil, 1980
  • Internship in Preventive Medicine, State of Rio de Janeiro Secretary of Health, Brazil 1980
  • Fellowship in Microbiology, Instituto Oswaldo Cruz, Brazil, 1981-1985
  • Fellowship in Medical Genetics, Federal University of Rio de Janeiro, Brazil, 2004-2005
  • MS, Clinical Laboratory Medicine, College of Medicine of the Federal University of Rio de Janeiro, Brazil, 2006-2008
  • PhD, Inborn Errors of Metabolism, Medical Genetics, Joint with College of Medicine of the Federal University of Rio de Janeiro, Brazil and University of Porto, Portugal, 2013-2018

Selected Publications

Malta DC, Bernal RTI, Vieira Neto E, Curci KA, Pasinato MTM, Lisboa RM, Cachapuz RF, Coelho KSC, Santos FPD, Freitas MIF. Noncommunicable diseases, risk factors, and protective factors in adults with and without health Insurance. Cien Saude Colet. 2020 Aug;25(8):2973-83.

Vieira Neto E, Cardoso CBMA, Carvalho EC, Fonseca A. Second trimester serum markers in antenatal screening of Down's syndrome and neural tube defects: medians from a group of Brazilian pregnant women. J Bras Patol. 1996;32(4):179-87.

Vieira Neto E, Loureiro IG, Carvalho EC, Fonseca A. Second trimester maternal serum inhibin-A: a new biochemical marker of Down's syndrome. J Bras Patol. 1999;35(4):217-23.

Vieira Neto E, Carvalho EC, Fonseca A. Adaptation of alpha-fetoprotein and intact human chorionic gonadotropin fluoroimmunometric assays to dried blood spots. Clin Chim Acta. 2005;360(1-2):151-9. Epub 2005/07/05. doi: 10.1016/j.cccn.2005.04.023. PMID: 15993391.

Vieira Neto E, Fonseca AA, Almeida RF, Figueiredo MP, Porto MA, Ribeiro MG. Analysis of acylcarnitine profiles in umbilical cord blood and during the early neonatal period by electrospray ionization tandem mass spectrometry. Braz J Med Biol Res. 2012;45(6):546-56. Epub 2012/04/11. doi: 10.1590/s0100-879x2012007500056. PMID: 22488223.

Vieira EN, Maia HSF, Monteiro CB, Carvalho LM, Tonon T, Vanz AP, Schwartz IVD, Ribeiro MG. Quality of life and adherence to treatment in early-treated Brazilian phenylketonuria pediatric patients. Braz J Med Biol Res. 2017;51(2):e6709. doi: 10.1590/1414-431X20176709. PMID: 29267500.

Malta DC, Bernal RTI, Vieira Neto E, Curci KA, Pasinato MTM, Lisboa RM, Cachapuz RF, Coelho KSC. Trends in risk and protective factors for non-communicable diseases in the population with health insurance in Brazil from 2008 to 2015. Rev Bras Epidemiol. 2018;21(suppl 1):e180020. doi: 10.1590/1980-549720180020.supl.1. PMID: 30517471.

Vieira Neto E, Laranjeira F, Quelhas D, Ribeiro I, Seabra A, Mineiro N, Carvalho LM, Lacerda L, Ribeiro MG. Mutation analysis of the PAH gene in phenylketonuria patients from Rio de Janeiro, Southeast Brazil. Mol Genet Genomic Med. 2018. doi: 10.1002/mgg3.408. PMID: 29749107.

Vieira Neto E, Maia Filho HS, Monteiro CB, Carvalho LM, da Cruz TS, de Barros BV, Ribeiro MG. Behavioral and emotional problems in early-treated Brazilian children and adolescents with phenylketonuria. Med Sci Monit. 2018;24:7759-69. doi: 10.12659/MSM.909146. PMID: 30375370.

Vieira Neto E, Laranjeira F, Quelhas D, Ribeiro I, Seabra A, Mineiro N, Carvalho LM, Lacerda L, Ribeiro MG. Genotype-phenotype correlations and BH4 estimated responsiveness in patients with phenylketonuria from Rio de Janeiro, Southeast Brazil. Mol Genet Genomic Med. 2019;7(5):e610. doi: 10.1002/mgg3.610. PMID: 30829006.

Bösch F, Landolt MA, Baumgartner MR, Zeltner N, Kölker S, Gleich F, Burlina A, Cazzorla C, Packman W, Schwartz IVD, Vieira Neto E, Ribeiro MG, Martinelli D, Olivieri G, Huemer M. Health-related quality of life in paediatric patients with intoxication-type inborn errors of metabolism: Analysis of an international data set. J Inherit Metab Dis. 2020 Aug.

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Academic and Research Interests

  • Mitochondrial Metabolism
  • Fatty Acid Oxidation Disorders
  • Mitochondrail Bioenergetics
  • Mitochondrial Tri-functional Protein Deficiency
  • Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency 
  • Mitochondrial Phospholipids

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