Secolin R - Search Results

1

Genetic variability in COVID-19-related genes in the Brazilian population.

Secolin R, de Araujo TK, Gonsales MC, Rocha CS, Naslavsky M, Marco L, Bicalho MAC, Vazquez VL, Zatz M, Silva WA, Lopes-Cendes I. Secolin R, et al. Hum Genome Var. 2021 Apr 2;8:15. doi: 10.1038/s41439-021-00146-w. eCollection 2021. Hum Genome Var. 2021. PMID: 33824725 Free PMC article.

2

THE SCN2A gene is not a likely candidate for familial mesial temporal lobe epilepsy.

Maurer-Morelli CV, Secolin R, Marchesini RB, Santos NF, Kobayashi E, Cendes F, Lopes-Cendes I. Maurer-Morelli CV, et al. Among authors: secolin r. Epilepsy Res. 2006 Oct;71(2-3):233-6. doi: 10.1016/j.eplepsyres.2006.06.016. Epub 2006 Aug 17. Epilepsy Res. 2006. PMID: 16914293

3

Linkage study of voltage-gated potassium channels in familial mesial temporal lobe epilepsy.

Maurer-Morelli CV, Marchesini RB, Secolin R, Santos NF, Kobayashi E, Cendes F, Lopes-Cendes I. Maurer-Morelli CV, et al. Among authors: secolin r. Arq Neuropsiquiatr. 2007 Mar;65(1):20-3. doi: 10.1590/s0004-282x2007000100006. Arq Neuropsiquiatr. 2007. PMID: 17420821 Free article.

4

LINKGEN: a new algorithm to process data in genetic linkage studies.

Secolin R, Rocha CS, Torres FR, Santos ML, Maurer-Morelli CV, Santos NF, Lopes-Cendes I. Secolin R, et al. Genomics. 2008 Jun;91(6):544-7. doi: 10.1016/j.ygeno.2008.02.001. Epub 2008 Apr 2. Genomics. 2008. PMID: 18378114 Free article.

5

A new candidate locus for bilateral perisylvian polymicrogyria mapped on chromosome Xq27.

Santos NF, Secolin R, Brandão-Almeida IL, Silva MS, Torres FR, Tsuneda SS, Guimarães CA, Hage SR, Cendes F, Guerreiro MM, Lopes-Cendes I. Santos NF, et al. Among authors: secolin r. Am J Med Genet A. 2008 May 1;146A(9):1151-7. doi: 10.1002/ajmg.a.32270. Am J Med Genet A. 2008. PMID: 18384144

6

Segregation analysis in mesial temporal lobe epilepsy with hippocampal atrophy.

Secolin R, Maurer-Morelli C, Cendes F, Lopes-Cendes I. Secolin R, et al. Epilepsia. 2010 Feb;51 Suppl 1:47-50. doi: 10.1111/j.1528-1167.2009.02445.x. Epilepsia. 2010. PMID: 20331715 Free article. No abstract available.

7

Family-based association study for bipolar affective disorder.

Secolin R, Banzato CE, Oliveira MC, Bittar MF, Santos ML, Dalgalarrondo P, Lopes-Cendes I. Secolin R, et al. Psychiatr Genet. 2010 Jun;20(3):126-9. doi: 10.1097/YPG.0b013e32833a2050. Psychiatr Genet. 2010. PMID: 20414141

8

Interactions of polymorphisms in different clock genes associated with circadian phenotypes in humans.

Pedrazzoli M, Secolin R, Esteves LO, Pereira DS, Koike Bdel V, Louzada FM, Lopes-Cendes I, Tufik S. Pedrazzoli M, et al. Among authors: secolin r. Genet Mol Biol. 2010 Oct;33(4):627-32. doi: 10.1590/S1415-47572010005000092. Epub 2010 Dec 1. Genet Mol Biol. 2010. PMID: 21637568 Free PMC article.

9

A Locus Identified on Chromosome18P11.31 is Associated with Hippocampal Abnormalities in a Family with Mesial Temporal Lobe Epilepsy.

Maurer-Morelli CV, Secolin R, Morita ME, Domingues RR, Marchesini RB, Santos NF, Kobayashi E, Cendes F, Lopes-Cendes I. Maurer-Morelli CV, et al. Among authors: secolin r. Front Neurol. 2012 Aug 10;3:124. doi: 10.3389/fneur.2012.00124. eCollection 2012. Front Neurol. 2012. PMID: 23015801 Free PMC article.

10

Normal ATXN3 Allele but Not CHIP Polymorphisms Modulates Age at Onset in Machado-Joseph Disease.

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. França MC Jr, et al. Among authors: secolin r. Front Neurol. 2012 Nov 19;3:164. doi: 10.3389/fneur.2012.00164. eCollection 2012. Front Neurol. 2012. PMID: 23181052 Free PMC article.

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