| Sarcomatoid renal cell carcinoma has a distinct molecular pathogenesis, driver mutation profile, and transcriptional landscape Z Wang, TB Kim, B Peng, J Karam, C Creighton, A Joon, F Kawakami, ... Clinical Cancer Research 23 (21), 6686-6696, 2017 | 83 | 2017 |
| 45, X/46, XY mosaicism: report on 14 patients from a Brazilian hospital. A retrospective study RFM Rosa, WFB D'Ecclesiis, RP Dibbi, RCM Rosa, P Trevisan, ... Sao Paulo medical journal 132, 332-338, 2014 | 49 | 2014 |
| Congenital heart disease and chromossomopathies detected by the karyotype P Trevisan, RFM Rosa, DB Koshiyama, TD Zen, GA Paskulin, PRG Zen Revista Paulista de Pediatria 32, 262-271, 2014 | 36* | 2014 |
| Chromosomal abnormalities in patients with congenital heart disease P Trevisan, TD Zen, RFM Rosa, JN Silva, DB Koshiyama, GA Paskulin, ... Arquivos brasileiros de cardiologia 101, 2013 | 27 | 2013 |
| Evaluation of genotoxic effects of benzene and its derivatives in workers of gas stations P Trevisan, JN Da Silva, AP Da Silva, RFM Rosa, GA Paskulin, ... Environmental monitoring and assessment 186, 2195-2204, 2014 | 25 | 2014 |
| Evaluation of genotoxic effects of benzene and its derivatives in workers of gas stations P Trevisan, JN Da Silva, AP Da Silva, RFM Rosa, GA Paskulin, ... Environmental monitoring and assessment 186, 2195-2204, 2014 | 25 | 2014 |
| Congenital heart disease and chromossomopathies detected by the karyotype P Trevisan, RFM Rosa, DB Koshiyama, TD Zen, GA Paskulin, PRG Zen Revista Paulista de Pediatria 32, 262-271, 2014 | 24 | 2014 |
| Gestational and family risk factors for carriers of congenital heart defects in southern Brazil TD Zen, RFM Rosa, PRG Zen, P Trevisan, AP da Silva, CP Ricachinevsky, ... Pediatrics International 53 (4), 551-557, 2011 | 24 | 2011 |
| Gómez-López-Hernández syndrome in a child born to consanguineous parents: new evidence for an autosomal-recessive pattern of inheritance? VF de Mattos, C Graziadio, RFM Rosa, R Lenhardt, RPM Alves, ... Pediatric Neurology 50 (6), 612-615, 2014 | 18 | 2014 |
| Clinical and cytogenetic features of a Brazilian sample of patients with phenotype of oculo-auriculo-vertebral spectrum: a cross-sectional study AP Silva, RFM Rosa, P Trevisan, JC Dorneles, CS Mesquita, VF Mattos, ... Sao Paulo Medical Journal 133, 191-198, 2014 | 17 | 2014 |
| Frequency and clinical significance of chromosome 7 and 10 aneuploidies, amplification of the EGFR gene, deletion of PTEN and TP53 genes, and 1p/19q … DB Koshiyama, P Trevisan, C Graziadio, RFM Rosa, B Cunegatto, ... Journal of Neuro-Oncology 135, 465-472, 2017 | 14 | 2017 |
| Trisomy 18 and neural tube defects RFM Rosa, P Trevisan, RCM Rosa, MB Lorenzen, PRG Zen, CA Oliveira, ... Pediatric Neurology 49 (3), 203-204, 2013 | 12 | 2013 |
| Síndrome de deleção 22q11 e cardiopatias congênitas complexas RFM Rosa, P Trevisan, DB Koshiyama, CB Pilla, PRG Zen, ... Revista da Associação Médica Brasileira 57, 62-65, 2011 | 9 | 2011 |
| 22q11. 2 deletion syndrome and complex congenital heart defects RFM Rosa, P Trevisan, DB Koshiyama, CB Pilla, PRG Zen, ... Revista Da Associação Médica Brasileira (English Edition) 57 (1), 62-65, 2011 | 9 | 2011 |
| Ensino de ciências para surdos através de software educacional PFF Trevisan Universidade do Estado do Amazonas, 2008 | 9 | 2008 |
| Microarray-based comparative genomic hybridization, multiplex ligation-dependent probe amplification, and high-resolution karyotype for differential diagnosis … AB Glaeser, BL Diniz, D Deconte, AS Santos, RFM Rosa, PRG Zen Journal of Pediatric Genetics 9 (03), 149-157, 2020 | 7 | 2020 |
| Clinical and molecular characterization of adult glioblastomas in Southern Brazil P Trevisan, C Graziadio, DBK Rodrigues, RFM Rosa, FP Soares, ... Journal of Neuropathology & Experimental Neurology 78 (4), 297-304, 2019 | 7 | 2019 |
| Anormalidades cromossômicas entre pacientes com cardiopatia congênita P Trevisan, TD Zen, RFM Rosa, JN Silva, DB Koshiyama, GA Paskulin, ... Arquivos Brasileiros de Cardiologia 101, 2013 | 6 | 2013 |
| Ensino de Ciências para Surdos através de Software educacional. 2008 PFF TREVISAN Dissertação (Mestrado em Ensino de Ciências)-Universidade do Estado do …, 2008 | 6 | 2008 |
| Report of a patient with fragile X syndrome unexpectedly identified by karyotype analysis MA Floriani, MRV Boas, RFM Rosa, P Trevisan, LE Dorfman, R Rosa, ... Jornal Brasileiro de Patologia e Medicina Laboratorial 53, 108-109, 2017 | 5 | 2017 |
