Rodrigo Secolin, Ph.D.
Rodrigo Secolin, Ph.D.
Postdoc researcher, Department of Medical Genetics, University of Campinas - UNICAMP, Campinas, SP
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Cited by
Cited by
The genetic architecture of the human cerebral cortex
KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ...
Science 367 (6484), eaay6690, 2020
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
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
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), 2017
Genetic determinants of cortical structure (thickness, surface area and volumes) among disease free adults in the CHARGE Consortium
E Hofer, GV Roshchupkin, HHH Adams, MJ Knol, H Lin, S Li, H Zare, ...
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
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
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
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
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
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
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), 1-8, 2013
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
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
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
Haplotypes of susceptibility to chronic periodontitis in the Interleukin 8 gene do not influence protein level in the gingival crevicular fluid
SCT Corbi, G Anovazzi, LS Finoti, YJ Kim, MV Capela, R Secolin, ...
Archives of Oral Biology 57 (10), 1355-1361, 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
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
Normal ATXN3 allele but not CHIP polymorphisms modulates age at onset in Machado–Joseph disease
MC França Jr, VE Emmel, A D'Abreu, CV Maurer-Morelli, R Secolin, ...
Frontiers in neurology 3, 164, 2012
TSHR intronic polymorphisms (rs179247 and rs12885526) and their role in the susceptibility of the Brazilian population to Graves’ disease and Graves’ ophthalmopathy
NE Bufalo, RB Dos Santos, MA Marcello, RP Piai, R Secolin, ...
Journal of Endocrinological Investigation 38 (5), 555-561, 2015
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