The phenotypic spectrum of congenital Zika syndrome M Del Campo, IML Feitosa, EM Ribeiro, DDG Horovitz, ALS Pessoa, ... American Journal of Medical Genetics Part A 173 (4), 841-857, 2017 | 234 | 2017 |
Erythema Nodosum Leprosum: Update and challenges on the treatment of a neglected condition PSS Costa, LR Fraga, TW Kowalski, ELR Daxbacher, L Schuler-Faccini, ... Acta tropica 183, 134-141, 2018 | 60 | 2018 |
Epidemiological surveillance of birth defects compatible with thalidomide embryopathy in Brazil FSL Vianna, JS Lopez-Camelo, JCL Leite, MTV Sanseverino, MG Dutra, ... Plos one 6 (7), e21735, 2011 | 54 | 2011 |
Teratogens: a public health issue–a Brazilian overview T Mazzu-Nascimento, DG Melo, GG Morbioli, E Carrilho, FSL Vianna, ... Genetics and Molecular Biology 40, 387-397, 2017 | 53 | 2017 |
Zika virus as a possible risk factor for autism spectrum disorder: neuroimmunological aspects P Vianna, JA Gomes, JA Boquett, LR Fraga, JB Schuch, FSL Vianna, ... Neuroimmunomodulation 25 (5-6), 320-327, 2019 | 45 | 2019 |
p53 signaling pathway polymorphisms associated to recurrent pregnancy loss LR Fraga, CG Dutra, JA Boquett, FSL Vianna, RO Gonçalves, ... Molecular biology reports 41, 1871-1877, 2014 | 43 | 2014 |
Recognition of the phenotype of thalidomide embryopathy in countries endemic for leprosy: new cases and review of the main dysmorphological findings FSL Vianna, L Schüler-Faccini, JCL Leite, SHC de Sousa, LMM da Costa, ... Clinical dysmorphology 22 (2), 59-63, 2013 | 42 | 2013 |
Thalidomide embryopathy: Follow‐up of cases born between 1959 and 2010 TW Kowalski, MTV Sanseverino, L Schuler‐Faccini, FSL Vianna Birth Defects Research Part A: Clinical and Molecular Teratology 103 (9 …, 2015 | 41 | 2015 |
Zika virus: A new human teratogen? Implications for women of reproductive age L Schuler‐Faccini, MTV Sanseverino, FSL Vianna, AA Da Silva, ... Clinical Pharmacology & Therapeutics 100 (1), 28-30, 2016 | 40 | 2016 |
Is intrauterine exposure to acetaminophen associated with emotional and hyperactivity problems during childhood? Findings from the 2004 Pelotas birth cohort L Tovo-Rodrigues, BC Schneider, T Martins-Silva, B Del-Ponte, ... Bmc Psychiatry 18, 1-11, 2018 | 39 | 2018 |
Music genetics research: Association with musicality of a polymorphism in the AVPR1A gene LM Mariath, AM Silva, TW Kowalski, GS Gattino, GA Araujo, ... Genetics and molecular biology 40, 421-429, 2017 | 31 | 2017 |
Leprosy in Southern Brazil: a twenty-year epidemiological profile AP Nazario, J Ferreira, L Schuler-Faccini, M Fiegenbaum, O Artigalás, ... Revista da Sociedade Brasileira de Medicina Tropical 50, 251-255, 2017 | 31 | 2017 |
Lack of association between thrombophilic gene variants and recurrent pregnancy loss CG Dutra, LR Fraga, AP Nácul, EP Passos, RO Gonçalves, OL Nunes, ... Human Fertility 17 (2), 99-105, 2014 | 31 | 2014 |
The impact of thalidomide use in birth defects in Brazil FSL Vianna, TW Kowalski, LR Fraga, MTV Sanseverino, ... European Journal of Medical Genetics 60 (1), 12-15, 2017 | 28 | 2017 |
Impact on pregnancies in south Brazil from the influenza A (H1N1) pandemic: cohort study AA Silva, TMS Ranieri, FD Torres, FSL Vianna, GR Paniz, ... PloS one 9 (2), e88624, 2014 | 27 | 2014 |
Pharmacoepidemiology and thalidomide embryopathy surveillance in Brazil FSL Vianna, MZ de Oliveira, MTV Sanseverino, EF Morelo, DLR Neto, ... Reproductive Toxicology 53, 63-67, 2015 | 24 | 2015 |
Angiogenesis and oxidative stress-related gene variants in recurrent pregnancy loss MF Fortis, LR Fraga, JA Boquett, TW Kowalski, CG Dutra, RO Gonçalves, ... Reproduction, Fertility and Development 30 (3), 498-506, 2018 | 19 | 2018 |
Polymorphisms in the endothelial nitric oxide synthase gene in thalidomide embryopathy FSL Vianna, LR Fraga, L Tovo-Rodrigues, A Tagliani-Ribeiro, F Biondi, ... Nitric Oxide 35, 89-92, 2013 | 18 | 2013 |
TP53 p.Arg337His germline mutation prevalence in Southern Brazil: Further evidence for mutation testing in young breast cancer patients EC Hahn, CM Bittar, FSL Vianna, CBO Netto, JV Biazús, R Cericatto, ... PLoS One 13 (12), e0209934, 2018 | 16 | 2018 |
Germline MLH1, MSH2 and MSH6 variants in Brazilian patients with colorectal cancer and clinical features suggestive of Lynch Syndrome NB Schneider, T Pastor, AE Paula, MI Achatz, ÂR Santos, FSL Vianna, ... Cancer medicine 7 (5), 2078-2088, 2018 | 15 | 2018 |