| The genetic architecture of the human cerebral cortex KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ... Science 367 (6484), eaay6690, 2020 | 732 | 2020 |
| Association between interleukin-8 levels and chronic periodontal disease: A PRISMA-compliant systematic review and meta-analysis LS Finoti, R Nepomuceno, SC Pigossi, SCT Corbi, R Secolin, ... Medicine 96 (22), e6932, 2017 | 164 | 2017 |
| Family-based genetic association for molar-incisor hypomineralization F Jeremias, RAG Pierri, JF Souza, CMB Fragelli, M Restrepo, LS Finoti, ... Caries research 50 (3), 310-318, 2016 | 148 | 2016 |
| Magnetic resonance imaging abnormalities in familial temporal lobe epilepsy with auditory auras E Kobayashi, NF Santos, FR Torres, R Secolin, LAC Sardinha, ... Archives of neurology 60 (11), 1546-1551, 2003 | 99 | 2003 |
| MicroRNA hsa-miR-134 is a circulating biomarker for mesial temporal lobe epilepsy SH Avansini, BP de Sousa Lima, R Secolin, ML Santos, AC Coan, ... PLoS One 12 (4), e0173060, 2017 | 62 | 2017 |
| A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population TK de Araujo, R Secolin, TM Félix, LT De Souza, MÍB Fontes, IL Monlleó, ... Journal of Cranio-Maxillofacial Surgery 44 (1), 16-20, 2016 | 61 | 2016 |
| Association of matrix metalloproteinase gene polymorphism with temporomandibular joint degeneration AC Planello, MIG Campos, CB Meloto, R Secolin, CM Rizatti‐Barbosa, ... European journal of oral sciences 119 (1), 1-6, 2011 | 61 | 2011 |
| Elevated micronucleus frequency in patients with type 2 diabetes, dyslipidemia and periodontitis SCT Corbi, AS Bastos, SRP Orrico, R Secolin, RA Dos Santos, ... Mutagenesis 29 (6), 433-439, 2014 | 60 | 2014 |
| Prospective neuroimaging study in hereditary spastic paraplegia with thin corpus callosum MC França Jr, A D'Abreu, CV Maurer‐Morelli, R Seccolin, S Appenzeller, ... Movement Disorders 22 (11), 1556-1562, 2007 | 54 | 2007 |
| Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function CO Dos Santos, S Zhou, R Secolin, X Wang, AF Cunha, DR Higgs, ... American journal of hematology 83 (2), 103-108, 2008 | 52 | 2008 |
| Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients M McCormack, H Gui, A Ingason, D Speed, GEB Wright, EJ Zhang, ... Neurology 90 (4), e332-e341, 2018 | 49 | 2018 |
| Genetic interaction of GSH metabolic pathway genes in cystic fibrosis FAL Marson, CS Bertuzzo, R Secolin, AF Ribeiro, JD Ribeiro BMC medical genetics 14, 1-8, 2013 | 44 | 2013 |
| Distribution of local ancestry and evidence of adaptation in admixed populations R Secolin, A Mas-Sandoval, LR Arauna, FR Torres, TK de Araujo, ... Scientific reports 9 (1), 13900, 2019 | 43 | 2019 |
| Genetic variability in COVID-19-related genes in the Brazilian population R Secolin, TK de Araujo, MC Gonsales, CS Rocha, M Naslavsky, ... Human genome variation 8 (1), 15, 2021 | 36 | 2021 |
| The Brazilian Initiative on Precision Medicine (BIPMed): fostering genomic data-sharing of underrepresented populations CS Rocha, R Secolin, MR Rodrigues, BS Carvalho, I Lopes-Cendes NPJ genomic medicine 5 (1), 42, 2020 | 35 | 2020 |
| A prediction algorithm for drug response in patients with mesial temporal lobe epilepsy based on clinical and genetic information MS Silva-Alves, R Secolin, BS Carvalho, CL Yasuda, E Bilevicius, ... PLoS One 12 (1), e0169214, 2017 | 35 | 2017 |
| Neurocysticercotic calcifications and hippocampal sclerosis: a case-control study M de Oliveira Taveira, ME Morita, CL Yasuda, AC Coan, R Secolin, ... PloS one 10 (7), e0131180, 2015 | 34 | 2015 |
| Genetic association study between Interleukin 10 gene and dental implant loss SC Pigossi, F Alvim-Pereira, CC Montes, LS Finoti, R Secolin, ... Archives of Oral Biology 57 (9), 1256-1263, 2012 | 33 | 2012 |
| A new candidate locus for bilateral perisylvian polymicrogyria mapped on chromosome Xq27 NF Santos, R Secolin, IL Brandão‐Almeida, MS Silva, FR Torres, ... American Journal of Medical Genetics Part A 146 (9), 1151-1157, 2008 | 31 | 2008 |
| TSHR intronic polymorphisms (rs179247 and rs12885526) and their role in the susceptibility of the Brazilian population to Graves’ disease and Graves … NE Bufalo, RB Dos Santos, MA Marcello, RP Piai, R Secolin, ... Journal of endocrinological investigation 38, 555-561, 2015 | 30 | 2015 |
Iscia Lopes-Cendes, M.D., Ph.D.University of Campinas - UNICAMP, Campinas, SP, BRAZILE-mail megerősítve itt: unicamp.br
