Dogini DB, Pascoal VD, Avansini SH, Vieira AS, Pereira TC, Lopes-Cendes I. The new world of RNAs. Genet Mol Biol. 2014 Mar;37(1 Suppl):285-93. Review. PubMed PMID: 24764762; PubMed Central PMCID: PMC3983583.
Dogini DB, Avansini SH, Vieira AS, Lopes-Cendes I. MicroRNA regulation and dysregulation in epilepsy. Front Cell Neurosci. 2013 Oct 4;7:172. doi: 10.3389/fncel.2013.00172. Review. PubMed PMID: 24109432; PubMed Central PMCID: PMC3790106.
Secolin R, Banzato CE, Mella LF, Santos ML, Dalgalarrondo P, Lopes-Cendes I. Refinement of chromosome 3p22.3 region and identification of a susceptibility gene for bipolar affective disorder. Am J Med Genet B Neuropsychiatr Genet. 2013 Mar;162B(2):163-8. doi: 10.1002/ajmg.b.32127. Epub 2012 Dec 31. PubMed PMID: 23280964.
Secolin R, Pascoal VD, Lopes-Cendes I, Pereira TC. Analysis of energetically biased transcripts of viruses and transposable elements. Genet Mol Biol. 2012 Dec;35(4):868-73. doi: 10.1590/S1415-47572012005000078. Epub 2012 Nov 13. PubMed PMID: 23271949; PubMed Central PMCID: PMC3526096.
Morita ME, Yasuda CL, Betting LE, Pacagnella D, Conz L, Barbosa PH, Maurer-Morelli CV, Costa AL, Kobayashi E, Lopes-Cendes I, Cendes F. MRI and EEG as long-term seizure outcome predictors in familial mesial temporal lobe epilepsy. Neurology. 2012 Dec 11;79(24):2349-54. doi: 10.1212/WNL.0b013e318278b63f. Epub 2012 Nov 28. PubMed PMID: 23197748.
França MC Jr, Emmel VE, D'Abreu A, Maurer-Morelli CV, Secolin R, Bonadia LC, da Silva MS, Nucci A, Jardim LB, Saraiva-Pereira ML, Marques W Jr, Paulson H, Lopes-Cendes I. Normal ATXN3 Allele but Not CHIP Polymorphisms Modulates Age at Onset in Machado-Joseph Disease. Front Neurol. 2012 Nov 19;3:164. doi: 10.3389/fneur.2012.00164. eCollection 2012. PubMed PMID: 23181052; PubMed Central PMCID: PMC3500826.
Maurer-Morelli CV, Secolin R, Morita ME, Domingues RR, Marchesini RB, Santos NF, Kobayashi E, Cendes F, Lopes-Cendes I. A Locus Identified on Chromosome18P11.31 is Associated with Hippocampal Abnormalities in a Family with Mesial Temporal Lobe Epilepsy. Front Neurol. 2012 Aug 10;3:124. eCollection 2012. PubMed PMID: 23015801; PubMed Central PMCID: PMC3449496.
Simioni M, Vieira TP, Sgardioli IC, Freitas EL, Rosenberg C, Maurer-Morelli CV, Lopes-Cendes I, Fett-Conte AC, Gil-da-Silva-Lopes VL. 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. Am J Med Genet A. 2012 Nov;158A(11):2905-10. doi: 10.1002/ajmg.a.35603. Epub 2012 Sep 18. PubMed PMID: 22991255.
Pedrazzoli M, Secolin R, Esteves LO, Pereira DS, Koike Bdel V, Louzada FM, Lopes-Cendes I, Tufik S. Interactions of polymorphisms in different clock genes associated with circadian phenotypes in humans. Genet Mol Biol. 2010 Oct;33(4):627-32. doi: 10.1590/S1415-47572010005000092. Epub 2010 Dec 1. PubMed PMID: 21637568; PubMed Central PMCID: PMC3036144.
Maurer-Morelli CV, de Vasconcellos JF, Reis-Pinto FC, Rocha Cde S, Domingues RR, Yasuda CL, Tedeschi H, De Oliveira E, Cendes F, Lopes-Cendes I. A comparison between different reference genes for expression studies in human hippocampal tissue. J Neurosci Methods. 2012 Jun 30;208(1):44-7. doi: 10.1016/j.jneumeth.2012.04.020. Epub 2012 May 3. PubMed PMID: 22575486.
Secolin R, Banzato CE, Oliveira MC, Bittar MF, Santos ML, Dalgalarrondo P, Lopes-Cendes I. Family-based association study for bipolar affective disorder. Psychiatr Genet. 2010 Jun;20(3):126-9. doi: 10.1097/YPG.0b013e32833a2050. PubMed PMID: 20414141.
Secolin R, Maurer-Morelli C, Cendes F, Lopes-Cendes I. Segregation analysis in mesial temporal lobe epilepsy with hippocampal atrophy. Epilepsia. 2010 Feb;51 Suppl 1:47-50. doi: 10.1111/j.1528-1167.2009.02445.x. PubMed PMID: 20331715.
Dogini DB, Ribeiro PA, Rocha C, Pereira TC, Lopes-Cendes I. MicroRNA expression profile in murine central nervous system development. J Mol Neurosci. 2008 Jul;35(3):331-7. doi: 10.1007/s12031-008-9068-4. Epub 2008 May 2. PubMed PMID: 18452032.
Tsuneda SS, Torres FR, Montenegro MA, Guerreiro MM, Cendes F, Lopes-Cendes I. A new missense mutation found in the FLNA gene in a family with bilateral periventricular nodular heterotopia (BPNH) alters the splicing process. J Mol Neurosci. 2008 Jun;35(2):195-200. doi: 10.1007/s12031-008-9050-1. Epub 2008 Apr 22. PubMed PMID: 18427995.
Santos NF, Secolin R, Brandão-Almeida IL, Silva MS, Torres FR, Tsuneda SS, Guimarães CA, Hage SR, Cendes F, Guerreiro MM, Lopes-Cendes I. A new candidate locus for bilateral perisylvian polymicrogyria mapped on chromosome Xq27. Am J Med Genet A. 2008 May 1;146A(9):1151-7. doi: 10.1002/ajmg.a.32270. PubMed PMID: 18384144.
Secolin R, Rocha CS, Torres FR, Santos ML, Maurer-Morelli CV, Santos NF, Lopes-Cendes I. LINKGEN: a new algorithm to process data in genetic linkage studies. Genomics. 2008 Jun;91(6):544-7. doi: 10.1016/j.ygeno.2008.02.001. Epub 2008 Apr 2. PubMed PMID: 18378114.
França MC Jr, D'Abreu A, Maurer-Morelli CV, Seccolin R, Appenzeller S, Alessio A, Damasceno BP, Nucci A, Cendes F, Lopes-Cendes I. Prospective neuroimaging study in hereditary spastic paraplegia with thin corpus callosum. Mov Disord. 2007 Aug 15;22(11):1556-62. PubMed PMID: 17516453.
Maurer-Morelli CV, Marchesini RB, Secolin R, Santos NF, Kobayashi E, Cendes F, Lopes-Cendes I. Linkage study of voltage-gated potassium channels in familial mesial temporal lobe epilepsy. Arq Neuropsiquiatr. 2007 Mar;65(1):20-3. PubMed PMID: 17420821.
Maurer-Morelli CV, Secolin R, Marchesini RB, Santos NF, Kobayashi E, Cendes F, Lopes-Cendes I. THE SCN2A gene is not a likely candidate for familial mesialtemporal lobe epilepsy. Epilepsy Res. 2006 Oct;71(2-3):233-6. Epub 2006 Aug 17. PubMed PMID: 16914293.
Torres FR, Montenegro MA, Marques-De-Faria AP, Guerreiro MM, Cendes F, Lopes-Cendes I. Mutation screening in a cohort of patients with lissencephaly and subcortical band heterotopia. Neurology. 2004 Mar 9;62(5):799-802. PubMed PMID: 15007136.
Santos NF, Sousa SC, Kobayashi E, Torres FR, Sardinha JA, Cendes F, Lopes-Cendes I. Clinical and genetic heterogeneity in familial temporal lobe epilepsy. Epilepsia. 2002;43 Suppl 5:136. PubMed PMID: 12121308.