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867 results

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Page 1
Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression.
Lintas C, Sacco R, Garbett K, Mirnics K, Militerni R, Bravaccio C, Curatolo P, Manzi B, Schneider C, Melmed R, Elia M, Pascucci T, Puglisi-Allegra S, Reichelt KL, Persico AM. Lintas C, et al. Among authors: elia m. Mol Psychiatry. 2009 Jul;14(7):705-18. doi: 10.1038/mp.2008.21. Epub 2008 Mar 4. Mol Psychiatry. 2009. PMID: 18317465
Two-loci ADA haplotypes in autistic disorder.
Lucarelli P, Saccucci P, Bottini N, De Luca D, Fiumara A, Elia M, Bottini N, Porfirio MC, Curatolo P. Lucarelli P, et al. Among authors: elia m. Am J Med Genet. 2002 Apr 1;108(4):339-40. doi: 10.1002/ajmg.10272. Am J Med Genet. 2002. PMID: 11920843 No abstract available.
Association study of autistic disorder and chromosome 16p.
Lucarelli P, Palminiello S, Saccucci P, Bottini N, De Luca D, Elia M, Fiumara A, Curatolo P. Lucarelli P, et al. Among authors: elia m. Am J Med Genet A. 2003 Jun 1;119A(2):242-6. doi: 10.1002/ajmg.a.10187. Am J Med Genet A. 2003. PMID: 12749074 No abstract available.
Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism.
Conciatori M, Stodgell CJ, Hyman SL, O'Bara M, Militerni R, Bravaccio C, Trillo S, Montecchi F, Schneider C, Melmed R, Elia M, Crawford L, Spence SJ, Muscarella L, Guarnieri V, D'Agruma L, Quattrone A, Zelante L, Rabinowitz D, Pascucci T, Puglisi-Allegra S, Reichelt KL, Rodier PM, Persico AM. Conciatori M, et al. Among authors: elia m. Biol Psychiatry. 2004 Feb 15;55(4):413-9. doi: 10.1016/j.biopsych.2003.10.005. Biol Psychiatry. 2004. PMID: 14960295
Enhanced APOE2 transmission rates in families with autistic probands.
Persico AM, D'Agruma L, Zelante L, Militerni R, Bravaccio C, Schneider C, Melmed R, Trillo S, Montecchi F, Elia M, Palermo M, Rabinowitz D, Pascucci T, Puglisi-Allegra S, Reichelt KL, Muscarella L, Guarnieri V, Melgari JM, Conciatori M, Keller F. Persico AM, et al. Among authors: elia m. Psychiatr Genet. 2004 Jun;14(2):73-82. doi: 10.1097/01.ypg.0000128768.37838.17. Psychiatr Genet. 2004. PMID: 15167692
Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions.
D'Amelio M, Ricci I, Sacco R, Liu X, D'Agruma L, Muscarella LA, Guarnieri V, Militerni R, Bravaccio C, Elia M, Schneider C, Melmed R, Trillo S, Pascucci T, Puglisi-Allegra S, Reichelt KL, Macciardi F, Holden JJ, Persico AM. D'Amelio M, et al. Among authors: elia m. Mol Psychiatry. 2005 Nov;10(11):1006-16. doi: 10.1038/sj.mp.4001714. Mol Psychiatry. 2005. PMID: 16027737
Association of a functional deficit of the BKCa channel, a synaptic regulator of neuronal excitability, with autism and mental retardation.
Laumonnier F, Roger S, Guérin P, Molinari F, M'rad R, Cahard D, Belhadj A, Halayem M, Persico AM, Elia M, Romano V, Holbert S, Andres C, Chaabouni H, Colleaux L, Constant J, Le Guennec JY, Briault S. Laumonnier F, et al. Among authors: elia m, m rad r. Am J Psychiatry. 2006 Sep;163(9):1622-9. doi: 10.1176/ajp.2006.163.9.1622. Am J Psychiatry. 2006. PMID: 16946189
A genetic variant that disrupts MET transcription is associated with autism.
Campbell DB, Sutcliffe JS, Ebert PJ, Militerni R, Bravaccio C, Trillo S, Elia M, Schneider C, Melmed R, Sacco R, Persico AM, Levitt P. Campbell DB, et al. Among authors: elia m. Proc Natl Acad Sci U S A. 2006 Nov 7;103(45):16834-9. doi: 10.1073/pnas.0605296103. Epub 2006 Oct 19. Proc Natl Acad Sci U S A. 2006. PMID: 17053076 Free PMC article.
HOXA1 gene variants influence head growth rates in humans.
Muscarella LA, Guarnieri V, Sacco R, Militerni R, Bravaccio C, Trillo S, Schneider C, Melmed R, Elia M, Mascia ML, Rucci E, Piemontese MR, D'Agruma L, Persico AM. Muscarella LA, et al. Among authors: elia m. Am J Med Genet B Neuropsychiatr Genet. 2007 Apr 5;144B(3):388-90. doi: 10.1002/ajmg.b.30469. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17171652
867 results