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Page 1
MLPA analysis in a cohort of patients with autism.
Peixoto S, Melo JB, Ferrão J, Pires LM, Lavoura N, Pinto M, Oliveira G, Carreira IM. Peixoto S, et al. Among authors: oliveira g. Mol Cytogenet. 2017 Feb 4;10:2. doi: 10.1186/s13039-017-0302-z. eCollection 2017. Mol Cytogenet. 2017. PMID: 28174603 Free PMC article.
Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders.
Correia CT, Conceição IC, Oliveira B, Coelho J, Sousa I, Sequeira AF, Almeida J, Café C, Duque F, Mouga S, Roberts W, Gao K, Lowe JK, Thiruvahindrapuram B, Walker S, Marshall CR, Pinto D, Nurnberger JI, Scherer SW, Geschwind DH, Oliveira G, Vicente AM. Correia CT, et al. Among authors: oliveira g, oliveira b. Mol Autism. 2014 Apr 10;5(1):28. doi: 10.1186/2040-2392-5-28. Mol Autism. 2014. PMID: 24720851 Free PMC article.
Genomic imbalances defining novel intellectual disability associated loci.
Lopes F, Torres F, Soares G, Barbosa M, Silva J, Duque F, Rocha M, Sá J, Oliveira G, Sá MJ, Temudo T, Sousa S, Marques C, Lopes S, Gomes C, Barros G, Jorge A, Rocha F, Martins C, Mesquita S, Loureiro S, Cardoso EM, Cálix MJ, Dias A, Martins C, Mota CR, Antunes D, Dupont J, Figueiredo S, Figueiroa S, Gama-de-Sousa S, Cruz S, Sampaio A, Eijk P, Weiss MM, Ylstra B, Rendeiro P, Tavares P, Reis-Lima M, Pinto-Basto J, Fortuna AM, Maciel P. Lopes F, et al. Among authors: oliveira g. Orphanet J Rare Dis. 2019 Jul 5;14(1):164. doi: 10.1186/s13023-019-1135-0. Orphanet J Rare Dis. 2019. PMID: 31277718 Free PMC article.
[Cerebral creatine deficiency syndromes].
Malheiro R, Diogo L, Garcia P, Fineza I, Oliveira G. Malheiro R, et al. Among authors: oliveira g. Acta Med Port. 2012 Nov-Dec;25(6):389-98. Epub 2013 Jan 28. Acta Med Port. 2012. PMID: 23534590 Free article. Portuguese.
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: oliveira g. 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.
[Autism and Early Neurodevelopmental Milestones].
Ferreira X, Oliveira G. Ferreira X, et al. Among authors: oliveira g. Acta Med Port. 2016 Mar;29(3):168-75. doi: 10.20344/amp.6790. Epub 2016 Mar 31. Acta Med Port. 2016. PMID: 27285092 Free article. Portuguese.
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: oliveira g. Mol Autism. 2014 May 20;5:34. doi: 10.1186/2040-2392-5-34. eCollection 2014. Mol Autism. 2014. PMID: 25392729 Free PMC article.
3,211 results