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Items: 43

1.

New avenues in molecular genetics for the diagnosis and application of therapeutics to the epilepsies.

Magalhães PHM, Moraes HT, Athie MCP, Secolin R, Lopes-Cendes I.

Epilepsy Behav. 2019 Aug 7:106428. doi: 10.1016/j.yebeh.2019.07.029. [Epub ahead of print] Review.

PMID:
31400936
2.

Association and interaction of genetic variants with occurrence of ischemic stroke among Brazilian patients.

Ferreira LE, Secolin R, Lopes-Cendes I, Cabral NL, França PHC.

Gene. 2019 May 5;695:84-91. doi: 10.1016/j.gene.2019.01.041. Epub 2019 Feb 8.

PMID:
30738964
3.

Dysregulation of NEUROG2 plays a key role in focal cortical dysplasia.

Avansini SH, Torres FR, Vieira AS, Dogini DB, Rogerio F, Coan AC, Morita ME, Guerreiro MM, Yasuda CL, Secolin R, Carvalho BS, Borges MG, Almeida VS, Araújo PAOR, Queiroz L, Cendes F, Lopes-Cendes I.

Ann Neurol. 2018 Mar;83(3):623-635. doi: 10.1002/ana.25187. Epub 2018 Mar 10.

4.

Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients.

McCormack M, Gui H, Ingason A, Speed D, Wright GEB, Zhang EJ, Secolin R, Yasuda C, Kwok M, Wolking S, Becker F, Rau S, Avbersek A, Heggeli K, Leu C, Depondt C, Sills GJ, Marson AG, Auce P, Brodie MJ, Francis B, Johnson MR, Koeleman BPC, Striano P, Coppola A, Zara F, Kunz WS, Sander JW, Lerche H, Klein KM, Weckhuysen S, Krenn M, Gudmundsson LJ, Stefánsson K, Krause R, Shear N, Ross CJD, Delanty N; EPIGEN Consortium;, Pirmohamed M, Carleton BC; Canadian Pharmacogenomics Network for Drug Safety;, Cendes F, Lopes-Cendes I, Liao WP, O'Brien TJ, Sisodiya SM; EpiPGX Consortium;, Cherny S, Kwan P, Baum L; International League Against Epilepsy Consortium on Complex Epilepsies;, Cavalleri GL.

Neurology. 2018 Jan 23;90(4):e332-e341. doi: 10.1212/WNL.0000000000004853. Epub 2017 Dec 29. Erratum in: Neurology. 2018 Oct 16;91(16):765.

5.

Is cerebral microbleed prevalence relevant as a biomarker in amnestic mild cognitive impairment and mild Alzheimer's disease?

Rabelo AG, Teixeira CV, Magalhães TN, Carletti-Cassani AFM, Amato Filho AC, Joaquim HP, Talib LL, Forlenza O, Ribeiro PA, Secolin R, Lopes-Cendes I, Cendes F, Balthazar ML.

Neuroradiol J. 2017 Oct;30(5):477-485. doi: 10.1177/1971400917720465. Epub 2017 Jul 17.

6.

Acute liver failure is associated with altered cerebral expression profiles of long non-coding RNAs.

Silva VR, Secolin R, Vemuganti R, Lopes-Cendes I, Hazell AS.

Neurosci Lett. 2017 Aug 24;656:58-64. doi: 10.1016/j.neulet.2017.06.038. Epub 2017 Jun 23.

PMID:
28648459
7.

Inducible Nitric Oxide Synthase Polymorphisms and Nitric Oxide Levels in Individuals with Chronic Periodontitis.

Scarel-Caminaga RM, Cera FF, Pigossi SC, Finoti LS, Kim YJ, Viana AC, Secolin R, Montenegro MF, Tanus-Santos JE, Orrico SRP, Cirelli JA.

Int J Mol Sci. 2017 Jun 15;18(6). pii: E1128. doi: 10.3390/ijms18061128.

8.

Association between interleukin-8 levels and chronic periodontal disease: A PRISMA-compliant systematic review and meta-analysis.

Finoti LS, Nepomuceno R, Pigossi SC, Corbi SC, Secolin R, Scarel-Caminaga RM.

Medicine (Baltimore). 2017 Jun;96(22):e6932. doi: 10.1097/MD.0000000000006932. Review.

9.

MicroRNA hsa-miR-134 is a circulating biomarker for mesial temporal lobe epilepsy.

Avansini SH, de Sousa Lima BP, Secolin R, Santos ML, Coan AC, Vieira AS, Torres FR, Carvalho BS, Alvim MK, Morita ME, Yasuda CL, Pimentel-Silva LR, Dogini DB, Rogerio F, Cendes F, Lopes-Cendes I.

PLoS One. 2017 Apr 6;12(4):e0173060. doi: 10.1371/journal.pone.0173060. eCollection 2017.

10.

A Prediction Algorithm for Drug Response in Patients with Mesial Temporal Lobe Epilepsy Based on Clinical and Genetic Information.

Silva-Alves MS, Secolin R, Carvalho BS, Yasuda CL, Bilevicius E, Alvim MK, Santos RO, Maurer-Morelli CV, Cendes F, Lopes-Cendes I.

PLoS One. 2017 Jan 4;12(1):e0169214. doi: 10.1371/journal.pone.0169214. eCollection 2017.

11.

Family-Based Genetic Association for Molar-Incisor Hypomineralization.

Jeremias F, Pierri RA, Souza JF, Fragelli CM, Restrepo M, Finoti LS, Bussaneli DG, Cordeiro RC, Secolin R, Maurer-Morelli CV, Scarel-Caminaga RM, Santos-Pinto L.

Caries Res. 2016;50(3):310-8. doi: 10.1159/000445726. Epub 2016 May 14.

PMID:
27179118
12.

A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population.

de Araujo TK, Secolin R, Félix TM, de Souza LT, Fontes MÍ, Monlleó IL, de Souza J, Fett-Conte AC, Ribeiro EM, Xavier AC, de Rezende AA, Simioni M, Ribeiro-dos-Santos ÂK, dos Santos SE, Gil-da-Silva-Lopes VL.

J Craniomaxillofac Surg. 2016 Jan;44(1):16-20. doi: 10.1016/j.jcms.2015.07.026. Epub 2015 Aug 13.

PMID:
26602496
13.

Neurocysticercotic Calcifications and Hippocampal Sclerosis: A Case-Control Study.

de Oliveira Taveira M, Morita ME, Yasuda CL, Coan AC, Secolin R, Luiz Cunha da Costa A, Cendes F.

PLoS One. 2015 Jul 1;10(7):e0131180. doi: 10.1371/journal.pone.0131180. eCollection 2015.

14.

p.Q192R SNP of PON1 seems not to be Associated with Carotid Atherosclerosis Risk Factors in an Asymptomatic and Normolipidemic Brazilian Population Sample.

Scherrer DZ, Zago VH, Vieira IC, Parra ES, Panzoldo NB, Alexandre F, Secolin R, Baracat J, Quintão EC, Faria EC.

Arq Bras Cardiol. 2015 Jul;105(1):45-52. doi: 10.5935/abc.20150053. Epub 2015 May 29. English, Portuguese.

15.

Lack of association between the prothrombin rs1799963 polymorphism and juvenile myoclonic epilepsy.

Born JP, Santos BP, Secolin R, Gameleira FT, Andrade TG, Machado LC, Gitaí LL, Gitaí DL.

Arq Neuropsiquiatr. 2015 Apr;73(4):289-92. doi: 10.1590/0004-282X20150010. Epub 2015 Apr 1.

16.

Polymorphisms of cell cycle control genes influence the development of sporadic medullary thyroid carcinoma.

Barbieri RB, Bufalo NE, Secolin R, Assumpção LV, Maciel RM, Cerutti JM, Ward LS.

Eur J Endocrinol. 2014 Dec;171(6):761-7. doi: 10.1530/EJE-14-0461.

PMID:
25565272
17.

TSHR intronic polymorphisms (rs179247 and rs12885526) and their role in the susceptibility of the Brazilian population to Graves' disease and Graves' ophthalmopathy.

Bufalo NE, Dos Santos RB, Marcello MA, Piai RP, Secolin R, Romaldini JH, Ward LS.

J Endocrinol Invest. 2015 May;38(5):555-61. doi: 10.1007/s40618-014-0228-9. Epub 2014 Dec 28.

PMID:
25543543
18.

Elevated micronucleus frequency in patients with type 2 diabetes, dyslipidemia and periodontitis.

Corbi SC, Bastos AS, Orrico SR, Secolin R, Dos Santos RA, Takahashi CS, Scarel-Caminaga RM.

Mutagenesis. 2014 Nov;29(6):433-9. doi: 10.1093/mutage/geu043. Epub 2014 Sep 18.

PMID:
25239120
19.

SLC23A2-05 (rs4987219) and KRAS-LCS6 (rs61764370) polymorphisms in patients with squamous cell carcinoma of the head and neck.

Santiago MB, DE Lima Marson FA, Secolin R, Ribeiro JD, Lima CS, Bertuzzo CS.

Oncol Lett. 2014 Jun;7(6):1803-1811. Epub 2014 Apr 3.

20.

PER2 rs2304672, CLOCK rs1801260, and PER3 rs57875989 polymorphisms are not associated with juvenile myoclonic epilepsy.

Santos B, Marques T, Malta M, Gameleira F, Secolin R, Andrade T, Gitaí L, Gitaí D.

Epilepsy Behav. 2014 Jul;36:82-5. doi: 10.1016/j.yebeh.2014.04.024. Epub 2014 Jun 2.

21.

Study of candidate genes for dyslexia in Brazilian individuals.

Svidnicki MC, Salgado CA, Lima RF, Ciasca SM, Secolin R, Pomilio MC, Junqueira PA, Pinto MS, Pereira MM, Sartorato EL.

Genet Mol Res. 2013 Nov 7;12(4):5356-64. doi: 10.4238/2013.November.7.10.

22.

Clinical outcomes of periodontal therapy are not influenced by the ATC/TTC haplotype in the IL8 gene.

Corbi SC, Finoti LS, Anovazzi G, Tanaka MH, Kim YJ, Secolin R, Marcaccini AM, Gerlach RF, Orrico SR, Cirelli JA, Scarel-Caminaga RM.

J Periodontal Res. 2014 Aug;49(4):489-98. doi: 10.1111/jre.12128. Epub 2013 Aug 29.

PMID:
24033189
23.

Genetic interaction of GSH metabolic pathway genes in cystic fibrosis.

de Lima Marson FA, Bertuzzo CS, Secolin R, Ribeiro AF, Ribeiro JD.

BMC Med Genet. 2013 Jun 10;14:60. doi: 10.1186/1471-2350-14-60.

24.

Association between IL8 haplotypes and pathogen levels in chronic periodontitis.

Finoti LS, Corbi SC, Anovazzi G, Teixeira SR, Steffens JP, Secolin R, Kim YJ, Orrico SR, Cirelli JA, Mayer MP, Scarel-Caminaga RM.

Eur J Clin Microbiol Infect Dis. 2013 Oct;32(10):1333-40. doi: 10.1007/s10096-013-1884-y. Epub 2013 May 10.

PMID:
23660697
25.

Refinement of chromosome 3p22.3 region and identification of a susceptibility gene for bipolar affective disorder.

Secolin R, Banzato CE, Mella LF, Santos ML, Dalgalarrondo P, Lopes-Cendes I.

Am J Med Genet B Neuropsychiatr Genet. 2013 Mar;162B(2):163-8. doi: 10.1002/ajmg.b.32127. Epub 2012 Dec 31.

PMID:
23280964
26.

Analysis of energetically biased transcripts of viruses and transposable elements.

Secolin R, Pascoal VD, Lopes-Cendes I, Pereira TC.

Genet Mol Biol. 2012 Dec;35(4):868-73. doi: 10.1590/S1415-47572012005000078. Epub 2012 Nov 13.

27.

Preliminary Analysis of the Nonsynonymous Polymorphism rs17563 in BMP4 Gene in Brazilian Population Suggests Protection for Nonsyndromic Cleft Lip and Palate.

Araújo TK, Simioni M, Félix TM, de Souza LT, Fontes MÍ, Monlleó IL, Souza J, Fett-Conte AC, Secolin R, Lopes-Cendes I, Maurer-Morelli CV, Gil-da-Silva-Lopes VL.

Plast Surg Int. 2012;2012:247104. doi: 10.1155/2012/247104. Epub 2012 Nov 27.

28.

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.

Front Neurol. 2012 Nov 19;3:164. doi: 10.3389/fneur.2012.00164. eCollection 2012.

29.

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.

Front Neurol. 2012 Aug 10;3:124. eCollection 2012.

30.

Haplotypes of susceptibility to chronic periodontitis in the Interleukin 8 gene do not influence protein level in the gingival crevicular fluid.

Corbi SC, Anovazzi G, Finoti LS, Kim YJ, Capela MV, Secolin R, Marcaccini AM, Gerlach RF, Orrico SR, Cirelli JA, Scarel-Caminaga RM.

Arch Oral Biol. 2012 Oct;57(10):1355-61. doi: 10.1016/j.archoralbio.2012.07.003. Epub 2012 Aug 9.

PMID:
22877792
31.

The periodized resistance training promotes similar changes in lipid profile in middle-aged men and women.

Augusto Libardi C, Bonganha V, Soares Conceição M, Vergínia De Souza G, Fernandes Bernardes C, Secolin R, Aparecida Madruga V, Traina Chacon-Mikahil MP.

J Sports Med Phys Fitness. 2012 Jun;52(3):286-92.

PMID:
22648467
32.

Genetic association study between Interleukin 10 gene and dental implant loss.

Pigossi SC, Alvim-Pereira F, Montes CC, Finoti LS, Secolin R, Trevilatto PC, Scarel-Caminaga RM.

Arch Oral Biol. 2012 Sep;57(9):1256-63. doi: 10.1016/j.archoralbio.2012.02.020. Epub 2012 Mar 16.

33.

Evidence that polymorphisms in detoxification genes modulate the susceptibility for sporadic medullary thyroid carcinoma.

Barbieri RB, Bufalo NE, Secolin R, Silva AC, Assumpção LV, Maciel RM, Cerutti JM, Ward LS.

Eur J Endocrinol. 2012 Feb;166(2):241-5. doi: 10.1530/EJE-11-0843. Epub 2011 Nov 2.

PMID:
22048975
34.

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.

Genet Mol Biol. 2010 Oct;33(4):627-32. doi: 10.1590/S1415-47572010005000092. Epub 2010 Dec 1.

35.

Association of matrix metalloproteinase gene polymorphism with temporomandibular joint degeneration.

Planello AC, Campos MI, Meloto CB, Secolin R, Rizatti-Barbosa CM, Line SR, de Souza AP.

Eur J Oral Sci. 2011 Feb;119(1):1-6. doi: 10.1111/j.1600-0722.2010.00803.x.

PMID:
21244504
36.

Family-based association study for bipolar affective disorder.

Secolin R, Banzato CE, Oliveira MC, Bittar MF, Santos ML, Dalgalarrondo P, Lopes-Cendes I.

Psychiatr Genet. 2010 Jun;20(3):126-9. doi: 10.1097/YPG.0b013e32833a2050.

PMID:
20414141
37.

Segregation analysis in mesial temporal lobe epilepsy with hippocampal atrophy.

Secolin R, Maurer-Morelli C, Cendes F, Lopes-Cendes I.

Epilepsia. 2010 Feb;51 Suppl 1:47-50. doi: 10.1111/j.1528-1167.2009.02445.x. No abstract available.

38.

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.

Am J Med Genet A. 2008 May 1;146A(9):1151-7. doi: 10.1002/ajmg.a.32270.

PMID:
18384144
39.

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.

Genomics. 2008 Jun;91(6):544-7. doi: 10.1016/j.ygeno.2008.02.001. Epub 2008 Apr 2.

40.

Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function.

dos Santos CO, Zhou S, Secolin R, Wang X, Cunha AF, Higgs DR, Kwiatkowski JL, Thein SL, Gallagher PG, Costa FF, Weiss MJ.

Am J Hematol. 2008 Feb;83(2):103-8.

41.

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.

Arq Neuropsiquiatr. 2007 Mar;65(1):20-3.

42.

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.

Epilepsy Res. 2006 Oct;71(2-3):233-6. Epub 2006 Aug 17.

PMID:
16914293
43.

Magnetic resonance imaging abnormalities in familial temporal lobe epilepsy with auditory auras.

Kobayashi E, Santos NF, Torres FR, Secolin R, Sardinha LA, Lopez-Cendes I, Cendes F.

Arch Neurol. 2003 Nov;60(11):1546-51. Erratum in: Arch Neurol. 2004 Feb;61(2):199.

PMID:
14623726

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