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Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1.
Palmieri L, Papaleo V, Porcelli V, Scarcia P, Gaita L, Sacco R, Hager J, Rousseau F, Curatolo P, Manzi B, Militerni R, Bravaccio C, Trillo S, Schneider C, Melmed R, Elia M, Lenti C, Saccani M, Pascucci T, Puglisi-Allegra S, Reichelt KL, Persico AM. Palmieri L, et al. Among authors: schneider c. Mol Psychiatry. 2010 Jan;15(1):38-52. doi: 10.1038/mp.2008.63. Epub 2008 Jul 8. Mol Psychiatry. 2010. PMID: 18607376
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: schneider c. Mol Psychiatry. 2009 Jul;14(7):705-18. doi: 10.1038/mp.2008.21. Epub 2008 Mar 4. Mol Psychiatry. 2009. PMID: 18317465
Clinical, morphological, and biochemical correlates of head circumference in autism.
Sacco R, Militerni R, Frolli A, Bravaccio C, Gritti A, Elia M, Curatolo P, Manzi B, Trillo S, Lenti C, Saccani M, Schneider C, Melmed R, Reichelt KL, Pascucci T, Puglisi-Allegra S, Persico AM. Sacco R, et al. Among authors: schneider c. Biol Psychiatry. 2007 Nov 1;62(9):1038-47. doi: 10.1016/j.biopsych.2007.04.039. Epub 2007 Jul 20. Biol Psychiatry. 2007. PMID: 17644070
Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.
Persico AM, D'Agruma L, Maiorano N, Totaro A, Militerni R, Bravaccio C, Wassink TH, Schneider C, Melmed R, Trillo S, Montecchi F, Palermo M, Pascucci T, Puglisi-Allegra S, Reichelt KL, Conciatori M, Marino R, Quattrocchi CC, Baldi A, Zelante L, Gasparini P, Keller F; Collaborative Linkage Study of Autism. Persico AM, et al. Among authors: schneider c. Mol Psychiatry. 2001 Mar;6(2):150-9. doi: 10.1038/sj.mp.4000850. Mol Psychiatry. 2001. PMID: 11317216
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: schneider c. Mol Psychiatry. 2005 Nov;10(11):1006-16. doi: 10.1038/sj.mp.4001714. Mol Psychiatry. 2005. PMID: 16027737
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: schneider c. Biol Psychiatry. 2004 Feb 15;55(4):413-9. doi: 10.1016/j.biopsych.2003.10.005. Biol Psychiatry. 2004. PMID: 14960295
Candidate gene study of HOXB1 in autism spectrum disorder.
Muscarella LA, Guarnieri V, Sacco R, Curatolo P, Manzi B, Alessandrelli R, Giana G, Militerni R, Bravaccio C, Lenti C, Saccani M, Schneider C, Melmed R, D'Agruma L, Persico AM. Muscarella LA, et al. Among authors: schneider c. Mol Autism. 2010 May 25;1(1):9. doi: 10.1186/2040-2392-1-9. Mol Autism. 2010. PMID: 20678259 Free PMC article.
Family-based association study of ITGB3 in autism spectrum disorder and its endophenotypes.
Napolioni V, Lombardi F, Sacco R, Curatolo P, Manzi B, Alessandrelli R, Militerni R, Bravaccio C, Lenti C, Saccani M, Schneider C, Melmed R, Pascucci T, Puglisi-Allegra S, Reichelt KL, Rousseau F, Lewin P, Persico AM. Napolioni V, et al. Among authors: schneider c. Eur J Hum Genet. 2011 Mar;19(3):353-9. doi: 10.1038/ejhg.2010.180. Epub 2010 Nov 24. Eur J Hum Genet. 2011. PMID: 21102624 Free PMC article.
3,715 results