| A novel deletion involving the connexin-30 gene, del (GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing … FJ Del Castillo, M Rodriguez-Ballesteros, A Alvarez, T Hutchin, ... Journal of medical genetics 42 (7), 588-594, 2005 | 374 | 2005 |
| Guidelines for the tetra-primer ARMS–PCR technique development RFV Medrano, CA De Oliveira Molecular biotechnology 56, 599-608, 2014 | 266 | 2014 |
| Early cytotoxic and genotoxic effects of atrazine on Wistar rat liver: A morphological, immunohistochemical, biochemical, and molecular study FD Campos-Pereira, CA Oliveira, AA Pigoso, E Silva-Zacarin, R Barbieri, ... Ecotoxicology and Environmental Safety, 2012 | 111 | 2012 |
| Epidemiological study of HPV in oral mucosa through PCR W Tristão, RMP Ribeiro, CA Oliveira, JC Betiol, JSR Bettini Brazilian journal of otorhinolaryngology 78, 66-70, 2012 | 59 | 2012 |
| Deafness resulting from mutations in the GJB2 (connexin 26) gene in Brazilian patients CA Oliveira, AT Maciel‐Guerra, EL Sartorato Clinical genetics 61 (5), 354-358, 2002 | 58 | 2002 |
| Determination of the frequency of the 35delG allele in Brazilian neonates EL Sartorato, E Gottardi, CA De Oliveira, LA Magna, ... Clinical Genetics 58 (4), 339-340, 2000 | 58 | 2000 |
| Newborn hearing screening and genetic testing in 8974 Brazilian neonates K de AB Nivoloni, SM da Silva-Costa, MCA Pomílio, T Pereira, KC Lopes, ... International journal of pediatric otorhinolaryngology 74 (8), 926-929, 2010 | 44 | 2010 |
| Molecular genetics of non-syndromic deafness VB Piatto, ECT Nascimento, F Alexandrino, CA Oliveira, ACP Lopes, ... Revista Brasileira de Otorrinolaringologia 71, 216-223, 2005 | 42 | 2005 |
| Molecular genetics study of deafness in Brazil: 8‐year experience CA de Oliveira, F Alexandrino, TV Christiani, CE Steiner, JLR Cunha, ... American Journal of Medical Genetics Part A 143 (14), 1574-1579, 2007 | 38 | 2007 |
| Frequency of the 35delG Mutation in the GJB2 Gene in Samples of European, Asian, and African Brazilians CA Oliveira, F Alexandrino, K Abe-Sandes, WA Silva Human biology 76, 2, 2004 | 38 | 2004 |
| Immune response mediated by Th1/IL-17/caspase-9 promotes evolution of periodontal disease MEL Sommer, RA Dalia, AVB Nogueira, JA Cirelli, MAR Vinolo, JL Fachi, ... Archives of Oral Biology 97, 77-84, 2019 | 35 | 2019 |
| Allelic frequencies of the 35delG mutation of the GJB2 gene in different Brazilian regions CA Oliveira, CJ Pimpinati, F Alexandrino, LA Magna, AT Maciel-Guerra, ... Genetic testing 11 (1), 1-3, 2007 | 32 | 2007 |
| Evolution of periodontal disease: immune response and RANK/RANKL/OPG system F Gibertoni, MEL Sommer, MAM Esquisatto, MEC Amaral, CA Oliveira, ... Brazilian Dental Journal 28 (6), 679-687, 2017 | 31 | 2017 |
| Screening for mutations in the GJB3 gene in Brazilian patients with nonsyndromic deafness F Alexandrino, CA Oliveira, FC Reis, AT Maciel-Guerra, EL Sartorato Journal of Applied Genetics 45 (2), 249-254, 2004 | 28 | 2004 |
| Genotoxic effect and rat hepatocyte death occurred after oxidative stress induction and antioxidant gene downregulation caused by long term fluoride exposure FD Campos-Pereira, L Lopes-Aguiar, FL Renosto, GAS Nogueira, ... Chemico-biological interactions 264, 25-33, 2017 | 25 | 2017 |
| Castration methods do not affect weight gain and have diverse impacts on the welfare of water buffalo males LT Martins, MC Gonçalves, KCS Tavares, S Gaudêncio, PCS Neto, ... Livestock Science 140 (1-3), 171-176, 2011 | 24 | 2011 |
| Perspectivas para triagem da deficiência auditiva genética: rastreamento da mutação 35delG em neonatos VB Piatto, CA Oliveira, F Alexandrino, CJ Pimpinati, EL Sartorato Jornal de Pediatria 81, 139-142, 2005 | 22 | 2005 |
| Single Nucleotide Polymorphisms of the GJB2 and GJB6 Genes Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss ANAP GRILLO, FM DE OLIVEIRA, GQ DE CARVALHO, RFV MEDRANO, ... BioMed Research International 2015, 8, 2015 | 21 | 2015 |
| Connexin mutations in Brazilian patients with skin disorders with or without hearing loss F Alexandrino, CA de Oliveira, RF Magalhaes, MEB Florence, ... American Journal of Medical Genetics Part A 149 (4), 681-684, 2009 | 19 | 2009 |
| Prospects for genetic hearing loss screening: 35delG mutation tracking in a newborn population VB Piatto, CA Oliveira, F Alexandrino, CJ Pimpinati, EL Sartorato Jornal de Pediatria 81, 139-142, 2005 | 19 | 2005 |
