Vicente AM - Search Results

1

The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses.

Buxbaum JD, Bolshakova N, Brownfeld JM, Anney RJ, Bender P, Bernier R, Cook EH, Coon H, Cuccaro M, Freitag CM, Hallmayer J, Geschwind D, Klauck SM, Nurnberger JI, Oliveira G, Pinto D, Poustka F, Scherer SW, Shih A, Sutcliffe JS, Szatmari P, Vicente AM, Vieland V, Gallagher L. Buxbaum JD, et al. Among authors: vicente am. Mol Autism. 2014 May 20;5:34. doi: 10.1186/2040-2392-5-34. eCollection 2014. Mol Autism. 2014. PMID: 25392729 Free PMC article.

2

Partial tetrasomy of chromosome 3q and mosaicism in a child with autism.

Oliveira G, Matoso E, Vicente A, Ribeiro P, Marques C, Ataíde A, Miguel T, Saraiva J, Carreira I. Oliveira G, et al. J Autism Dev Disord. 2003 Apr;33(2):177-85. doi: 10.1023/a:1022943627660. J Autism Dev Disord. 2003. PMID: 12757357

3

Variants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autism.

Coutinho AM, Oliveira G, Morgadinho T, Fesel C, Macedo TR, Bento C, Marques C, Ataíde A, Miguel T, Borges L, Vicente AM. Coutinho AM, et al. Among authors: vicente am. Mol Psychiatry. 2004 Mar;9(3):264-71. doi: 10.1038/sj.mp.4001409. Mol Psychiatry. 2004. PMID: 15094787

4

Autoantibody repertoires to brain tissue in autism nuclear families.

Silva SC, Correia C, Fesel C, Barreto M, Coutinho AM, Marques C, Miguel TS, Ataide A, Bento C, Borges L, Oliveira G, Vicente AM. Silva SC, et al. Among authors: vicente am. J Neuroimmunol. 2004 Jul;152(1-2):176-82. doi: 10.1016/j.jneuroim.2004.03.015. J Neuroimmunol. 2004. PMID: 15223250

5

Mitochondrial dysfunction in autism spectrum disorders: a population-based study.

Oliveira G, Diogo L, Grazina M, Garcia P, Ataíde A, Marques C, Miguel T, Borges L, Vicente AM, Oliveira CR. Oliveira G, et al. Among authors: vicente am. Dev Med Child Neurol. 2005 Mar;47(3):185-9. doi: 10.1017/s0012162205000332. Dev Med Child Neurol. 2005. PMID: 15739723 Free article.

6

Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: no association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene.

Correia C, Coutinho AM, Diogo L, Grazina M, Marques C, Miguel T, Ataíde A, Almeida J, Borges L, Oliveira C, Oliveira G, Vicente AM. Correia C, et al. Among authors: vicente am. J Autism Dev Disord. 2006 Nov;36(8):1137-40. doi: 10.1007/s10803-006-0138-6. J Autism Dev Disord. 2006. PMID: 17151801

7

Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels.

Coutinho AM, Sousa I, Martins M, Correia C, Morgadinho T, Bento C, Marques C, Ataíde A, Miguel TS, Moore JH, Oliveira G, Vicente AM. Coutinho AM, et al. Among authors: vicente am. Hum Genet. 2007 Apr;121(2):243-56. doi: 10.1007/s00439-006-0301-3. Epub 2007 Jan 3. Hum Genet. 2007. PMID: 17203304 Free article.

8

Epidemiology of autism spectrum disorder in Portugal: prevalence, clinical characterization, and medical conditions.

Oliveira G, Ataíde A, Marques C, Miguel TS, Coutinho AM, Mota-Vieira L, Gonçalves E, Lopes NM, Rodrigues V, Carmona da Mota H, Vicente AM. Oliveira G, et al. Among authors: vicente am. Dev Med Child Neurol. 2007 Oct;49(10):726-33. doi: 10.1111/j.1469-8749.2007.00726.x. Dev Med Child Neurol. 2007. PMID: 17880640 Free article.

9

Genome-wide linkage analyses of quantitative and categorical autism subphenotypes.

Liu XQ, Paterson AD, Szatmari P; Autism Genome Project Consortium. Liu XQ, et al. Biol Psychiatry. 2008 Oct 1;64(7):561-70. doi: 10.1016/j.biopsych.2008.05.023. Epub 2008 Jul 16. Biol Psychiatry. 2008. PMID: 18632090 Free PMC article.

10

Association of the alpha4 integrin subunit gene (ITGA4) with autism.

Correia C, Coutinho AM, Almeida J, Lontro R, Lobo C, Miguel TS, Martins M, Gallagher L, Conroy J, Gill M, Oliveira G, Vicente AM. Correia C, et al. Among authors: vicente am. Am J Med Genet B Neuropsychiatr Genet. 2009 Dec 5;150B(8):1147-51. doi: 10.1002/ajmg.b.30940. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19259978

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