Vicente AM - Search Results

1

How personalised medicine will transform healthcare by 2030: the ICPerMed vision.

Vicente AM, Ballensiefen W, Jönsson JI. Vicente AM, et al. J Transl Med. 2020 Apr 28;18(1):180. doi: 10.1186/s12967-020-02316-w. J Transl Med. 2020. PMID: 32345312 Free PMC article.

2

Identification of biological mechanisms underlying a multidimensional ASD phenotype using machine learning.

Asif M, Martiniano HFMC, Marques AR, Santos JX, Vilela J, Rasga C, Oliveira G, Couto FM, Vicente AM. Asif M, et al. Among authors: vicente am. Transl Psychiatry. 2020 Jan 28;10(1):43. doi: 10.1038/s41398-020-0721-1. Transl Psychiatry. 2020. PMID: 32066720 Free PMC article.

3

The role of rare compound heterozygous events in autism spectrum disorder.

Lin BD, Colas F, Nijman IJ, Medic J, Brands W, Parr JR, van Eijk KR, Klauck SM, Chiocchetti AG, Freitag CM, Maestrini E, Bacchelli E, Coon H, Vicente A, Oliveira G, Pagnamenta AT, Gallagher L, Ennis S, Anney R, Bourgeron T, Luykx JJ, Vorstman J. Lin BD, et al. Transl Psychiatry. 2020 Jun 22;10(1):204. doi: 10.1038/s41398-020-00866-7. Transl Psychiatry. 2020. PMID: 32572023 Free PMC article.

4

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

5

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

6

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.

7

MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients.

Coutinho AM, Oliveira G, Katz C, Feng J, Yan J, Yang C, Marques C, Ataíde A, Miguel TS, Borges L, Almeida J, Correia C, Currais A, Bento C, Mota-Vieira L, Temudo T, Santos M, Maciel P, Sommer SS, Vicente AM. Coutinho AM, et al. Among authors: vicente am. Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 5;144B(4):475-83. doi: 10.1002/ajmg.b.30490. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17427193 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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