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Lack of replication of previous autism spectrum disorder GWAS hits in European populations.
Torrico B, Chiocchetti AG, Bacchelli E, Trabetti E, Hervás A, Franke B, Buitelaar JK, Rommelse N, Yousaf A, Duketis E, Freitag CM, Caballero-Andaluz R, Martinez-Mir A, Scholl FG, Ribasés M; ITAN; Battaglia A, Malerba G, Delorme R, Benabou M, Maestrini E, Bourgeron T, Cormand B, Toma C. Torrico B, et al. Among authors: maestrini e. Autism Res. 2017 Feb;10(2):202-211. doi: 10.1002/aur.1662. Epub 2016 Jul 15. Autism Res. 2017. PMID: 27417655
Mutation analysis of the coding sequence of the MECP2 gene in infantile autism.
Beyer KS, Blasi F, Bacchelli E, Klauck SM, Maestrini E, Poustka A; International Molecular Genetic Study of Autism Consortium (IMGSAC). Beyer KS, et al. Among authors: maestrini e. Hum Genet. 2002 Oct;111(4-5):305-9. doi: 10.1007/s00439-002-0786-3. Epub 2002 Aug 14. Hum Genet. 2002. PMID: 12384770
Autism spectrum disorders: molecular genetic advances.
Bacchelli E, Maestrini E. Bacchelli E, et al. Among authors: maestrini e. Am J Med Genet C Semin Med Genet. 2006 Feb 15;142C(1):13-23. doi: 10.1002/ajmg.c.30078. Am J Med Genet C Semin Med Genet. 2006. PMID: 16419096 Review.
Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection.
Blasi F, Bacchelli E, Pesaresi G, Carone S, Bailey AJ, Maestrini E; International Molecular Genetic Study of Autism Consortium (IMGSAC). Blasi F, et al. Among authors: maestrini e. Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 5;141B(3):220-1. doi: 10.1002/ajmg.b.30287. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16508939
Analysis of X chromosome inactivation in autism spectrum disorders.
Gong X, Bacchelli E, Blasi F, Toma C, Betancur C, Chaste P, Delorme R, Durand CM, Fauchereau F, Botros HG, Leboyer M, Mouren-Simeoni MC, Nygren G, Anckarsäter H, Rastam M, Gillberg IC, Gillberg C, Moreno-De-Luca D, Carone S, Nummela I, Rossi M, Battaglia A; International Molecular Genetic Study of Autism Consortium (IMGSAC); Jarvela I, Maestrini E, Bourgeron T. Gong X, et al. Among authors: maestrini e. Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):830-5. doi: 10.1002/ajmg.b.30688. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18361425 Free PMC article.
MET and autism susceptibility: family and case-control studies.
Sousa I, Clark TG, Toma C, Kobayashi K, Choma M, Holt R, Sykes NH, Lamb JA, Bailey AJ, Battaglia A, Maestrini E, Monaco AP; International Molecular Genetic Study of Autism Consortium (IMGSAC). Sousa I, et al. Among authors: maestrini e. Eur J Hum Genet. 2009 Jun;17(6):749-58. doi: 10.1038/ejhg.2008.215. Epub 2008 Nov 12. Eur J Hum Genet. 2009. PMID: 19002214 Free PMC article.
Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection.
Sykes NH, Toma C, Wilson N, Volpi EV, Sousa I, Pagnamenta AT, Tancredi R, Battaglia A, Maestrini E, Bailey AJ, Monaco AP; International Molecular Genetic Study of Autism Consortium (IMGSAC). Sykes NH, et al. Among authors: maestrini e. Eur J Hum Genet. 2009 Oct;17(10):1347-53. doi: 10.1038/ejhg.2009.47. Epub 2009 Apr 22. Eur J Hum Genet. 2009. PMID: 19384346 Free PMC article.
81 results