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Evidence for multiple loci from a genome scan of autism kindreds.
Schellenberg GD, Dawson G, Sung YJ, Estes A, Munson J, Rosenthal E, Rothstein J, Flodman P, Smith M, Coon H, Leong L, Yu CE, Stodgell C, Rodier PM, Spence MA, Minshew N, McMahon WM, Wijsman EM. Schellenberg GD, et al. Among authors: smith m. Mol Psychiatry. 2006 Nov;11(11):1049-60, 979. doi: 10.1038/sj.mp.4001874. Epub 2006 Aug 1. Mol Psychiatry. 2006. PMID: 16880825 Free article.
Presence of large deletions in kindreds with autism.
Yu CE, Dawson G, Munson J, D'Souza I, Osterling J, Estes A, Leutenegger AL, Flodman P, Smith M, Raskind WH, Spence MA, McMahon W, Wijsman EM, Schellenberg GD. Yu CE, et al. Among authors: smith m. Am J Hum Genet. 2002 Jul;71(1):100-15. doi: 10.1086/341291. Epub 2002 Jun 7. Am J Hum Genet. 2002. PMID: 12058345 Free PMC article.
Autism and the serotonin transporter: the long and short of it.
Devlin B, Cook EH Jr, Coon H, Dawson G, Grigorenko EL, McMahon W, Minshew N, Pauls D, Smith M, Spence MA, Rodier PM, Stodgell C, Schellenberg GD; CPEA Genetics Network. Devlin B, et al. Among authors: smith m. Mol Psychiatry. 2005 Dec;10(12):1110-6. doi: 10.1038/sj.mp.4001724. Mol Psychiatry. 2005. PMID: 16103890 Clinical Trial.
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Autism Genome Project Consortium; Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, Marshall CR, Scherer SW, Vieland VJ, Bartlett C, Mangin LV, Goedken R, Segre A, Pericak-Vance MA, Cuccaro ML, Gilbert JR, Wright HH, Abramson RK, Betancur C, Bourgeron T, Gillberg C, Leboyer M, Buxbaum JD, Davis KL, Hollander E, Silverman JM, Hallmayer J, Lotspeich L, Sutcliffe JS, Haines JL, Folstein SE, Piven J, Wassink TH, Sheffield V, Geschwind DH, Bucan M, Brown WT, Cantor RM, Constantino JN, Gilliam TC, Herbert M, Lajonchere C, Ledbetter DH, Lese-Martin C, Miller J, Nelson S, Samango-Sprouse CA, Spence S, State M, Tanzi RE, Coon H, Dawson G, Devlin B, Estes A, Flodman P, Klei L, McMahon WM, Minshew N, Munson J, Korvatska E, Rodier PM, Schellenberg GD, Smith M, Spence MA, Stodgell C, Tepper PG, Wijsman EM, Yu CE, Rogé B, Mantoulan C, Wittemeyer K, Poustka A, Felder B, Klauck SM, Schuster C, Poustka F, Bölte S, Feineis-Matthews S, Herbrecht E, Schmötzer G, Tsiantis J, Papanikolaou K, Maestrini E, Bacchelli E, Blasi F, Carone S, Toma C, Van Engeland H, de Jonge M, Kemner C, Koop F, Langemei… See abstract for full author list ➔ Autism Genome Project Consortium, et al. Among authors: smith m. Nat Genet. 2007 Mar;39(3):319-28. doi: 10.1038/ng1985. Epub 2007 Feb 18. Nat Genet. 2007. PMID: 17322880 Free PMC article.
No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network.
Devlin B, Bennett P, Cook EH Jr, Dawson G, Gonen D, Grigorenko EL, McMahon W, Pauls D, Smith M, Spence MA, Schellenberg GD; Collaborative Programs of Excellence in Autism (CPEA) Genetics Network. Devlin B, et al. Among authors: smith m. Am J Med Genet. 2002 Aug 8;114(6):667-72. doi: 10.1002/ajmg.10603. Am J Med Genet. 2002. PMID: 12210285
Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network.
Devlin B, Bennett P, Dawson G, Figlewicz DA, Grigorenko EL, McMahon W, Minshew N, Pauls D, Smith M, Spence MA, Rodier PM, Stodgell C, Schellenberg GD; CPEA Genetics Network. Devlin B, et al. Among authors: smith m. Am J Med Genet B Neuropsychiatr Genet. 2004 Apr 1;126B(1):46-50. doi: 10.1002/ajmg.b.20125. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15048647
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