Claudia Vianna Maurer-Morelli
Claudia Vianna Maurer-Morelli
Assistant Professor, Department of Medical Genetics and Medical Genomics, School of Medical Sciences
Verified email at
Cited by
Cited by
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
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: official journal of the Movement Disorder Society 22 (11 …, 2007
Investigation of genetic factors underlying typical orofacial clefts: mutational screening and copy number variation
M Simioni, TK Araujo, IL Monlleo, CV Maurer-Morelli, ...
Journal of human genetics 60 (1), 17-25, 2015
MRI and EEG as long-term seizure outcome predictors in familial mesial temporal lobe epilepsy
ME Morita, CL Yasuda, LE Betting, D Pacagnella, L Conz, PH Barbosa, ...
Neurology 79 (24), 2349-2354, 2012
Indomethacin treatment prior to pentylenetetrazole-induced seizures downregulates the expression of il1b and cox2 and decreases seizure-like behavior in zebrafish larvae
PG Barbalho, I Lopes-Cendes, CV Maurer-Morelli
BMC neuroscience 17 (1), 1-9, 2016
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
Preliminary analysis of the nonsynonymous polymorphism rs17563 in BMP4 gene in Brazilian population suggests protection for nonsyndromic cleft lip and palate
TK Araújo, M Simioni, TM Félix, LT de Souza, MÍB Fontes, IL Monlleó, ...
Plastic surgery international 2012, 2012
Downregulation of 14q32 microRNAs in primary human desmoplastic medulloblastoma
DR Lucon, C Rocha, R Craveiro, D Dillo, IA Cardinalli, DP Cavalcanti, ...
Frontiers in Oncology 3, 254, 2013
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
Insertional translocation of 15q25‐q26 into 11p13 and duplication at 8p23. 1 characterized by high resolution arrays in a boy with congenital malformations and aniridia
M Simioni, TP Vieira, IC Sgardioli, ÉL Freitas, C Rosenberg, ...
American Journal of Medical Genetics Part A 158 (11), 2905-2910, 2012
Mutations in PYCR1 gene in three families with autosomal recessive cutis laxa, type 2.
DZ Scherrer, MB Baptista, AH Matos, CV Maurer-Morelli, CE Steiner
European journal of medical genetics 56 (6), 336-339, 2013
A comparison between different reference genes for expression studies in human hippocampal tissue
CV Maurer-Morelli, JF de Vasconcellos, FC Reis-Pinto, CS Rocha, ...
Journal of neuroscience methods 208 (1), 44-47, 2012
Fluoro-Jade, but not Fluoro-Jade B, stains non-degenerating cells in brain and retina of embryonic and neonatal rats
AMAP Fernandes, CV Maurer-Morelli, CBL Campos, MLS Mello, ...
Brain research 1029 (1), 24-33, 2004
Incorporation of silver nanoparticles on Ti7. 5Mo alloy surface containing TiO2 nanotubes arrays for promoting antibacterial coating–in vitro and in vivo study
APRA Claro, RT Konatu, AL do Amaral Escada, MC de Souza Nunes, ...
Applied Surface Science 455, 780-788, 2018
Cyclooxygenase-1 as a potential therapeutic target for seizure suppression: evidences from zebrafish pentylenetetrazole-seizure model
PG Barbalho, BS Carvalho, I Lopes-Cendes, CV Maurer-Morelli
Frontiers in neurology 7, 200, 2016
A locus identified on chromosome18p11. 31 is associated with hippocampal abnormalities in a family with mesial temporal lobe epilepsy
CV Maurer-Morelli, R Secolin, ME Morita, RR Domingues, RB Marchesini, ...
Frontiers in neurology 3, 124, 2012
Exploring the mechanisms of graphene oxide behavioral and morphological changes in zebrafish
CV Clemente Z, Silva GH, de Souza Nunes MC, Martinez DST, Maurer-Morelli CV ...
Environ Sci Pollut Res Int. 26, 30508-30523, 2019
THE SCN2A gene is not a likely candidate for familial mesial temporal lobe epilepsy
CV Maurer-Morelli, R Secolin, RB Marchesini, NF Santos, E Kobayashi, ...
Epilepsy research 71 (2-3), 233-236, 2006
LINKGEN: a new algorithm to process data in genetic linkage studies
R Secolin, CS Rocha, FR Torres, ML Santos, CV Maurer-Morelli, ...
Genomics 91 (6), 544-547, 2008
Linkage study of voltage-gated potassium channels in familial mesial temporal lobe epilepsy
CV Maurer-Morelli, RB Marchesini, R Secolin, NF Santos, E Kobayashi, ...
Arquivos de neuro-psiquiatria 65, 20-23, 2007
The system can't perform the operation now. Try again later.
Articles 1–20