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Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.
Lionel AC, Tammimies K, Vaags AK, Rosenfeld JA, Ahn JW, Merico D, Noor A, Runke CK, Pillalamarri VK, Carter MT, Gazzellone MJ, Thiruvahindrapuram B, Fagerberg C, Laulund LW, Pellecchia G, Lamoureux S, Deshpande C, Clayton-Smith J, White AC, Leather S, Trounce J, Melanie Bedford H, Hatchwell E, Eis PS, Yuen RK, Walker S, Uddin M, Geraghty MT, Nikkel SM, Tomiak EM, Fernandez BA, Soreni N, Crosbie J, Arnold PD, Schachar RJ, Roberts W, Paterson AD, So J, Szatmari P, Chrysler C, Woodbury-Smith M, Brian Lowry R, Zwaigenbaum L, Mandyam D, Wei J, Macdonald JR, Howe JL, Nalpathamkalam T, Wang Z, Tolson D, Cobb DS, Wilks TM, Sorensen MJ, Bader PI, An Y, Wu BL, Musumeci SA, Romano C, Postorivo D, Nardone AM, Monica MD, Scarano G, Zoccante L, Novara F, Zuffardi O, Ciccone R, Antona V, Carella M, Zelante L, Cavalli P, Poggiani C, Cavallari U, Argiropoulos B, Chernos J, Brasch-Andersen C, Speevak M, Fichera M, Ogilvie CM, Shen Y, Hodge JC, Talkowski ME, Stavropoulos DJ, Marshall CR, Scherer SW. Lionel AC, et al. Among authors: szatmari p. Hum Mol Genet. 2014 May 15;23(10):2752-68. doi: 10.1093/hmg/ddt669. Epub 2013 Dec 30. Hum Mol Genet. 2014. PMID: 24381304 Free PMC article.
Genetics of autism: overview and new directions.
Szatmari P, Jones MB, Zwaigenbaum L, MacLean JE. Szatmari P, et al. J Autism Dev Disord. 1998 Oct;28(5):351-68. doi: 10.1023/a:1026096203946. J Autism Dev Disord. 1998. PMID: 9813773 Review.
Modifier effects in autism at the MAO-A and DBH loci.
Jones MB, Palmour RM, Zwaigenbaum L, Szatmari P. Jones MB, et al. Among authors: szatmari p. Am J Med Genet B Neuropsychiatr Genet. 2004 Apr 1;126B(1):58-65. doi: 10.1002/ajmg.b.20172. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15048649
Behavioral manifestations of autism in the first year of life.
Zwaigenbaum L, Bryson S, Rogers T, Roberts W, Brian J, Szatmari P. Zwaigenbaum L, et al. Among authors: szatmari p. Int J Dev Neurosci. 2005 Apr-May;23(2-3):143-52. doi: 10.1016/j.ijdevneu.2004.05.001. Int J Dev Neurosci. 2005. PMID: 15749241
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia.
Feuk L, Kalervo A, Lipsanen-Nyman M, Skaug J, Nakabayashi K, Finucane B, Hartung D, Innes M, Kerem B, Nowaczyk MJ, Rivlin J, Roberts W, Senman L, Summers A, Szatmari P, Wong V, Vincent JB, Zeesman S, Osborne LR, Cardy JO, Kere J, Scherer SW, Hannula-Jouppi K. Feuk L, et al. Among authors: szatmari p. Am J Hum Genet. 2006 Nov;79(5):965-72. doi: 10.1086/508902. Epub 2006 Sep 27. Am J Hum Genet. 2006. PMID: 17033973 Free PMC article.
A prospective case series of high-risk infants who developed autism.
Bryson SE, Zwaigenbaum L, Brian J, Roberts W, Szatmari P, Rombough V, McDermott C. Bryson SE, et al. Among authors: szatmari p. J Autism Dev Disord. 2007 Jan;37(1):12-24. doi: 10.1007/s10803-006-0328-2. Epub 2007 Jan 9. J Autism Dev Disord. 2007. PMID: 17211728
472 results