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Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene.
Wassink TH, Piven J, Vieland VJ, Jenkins L, Frantz R, Bartlett CW, Goedken R, Childress D, Spence MA, Smith M, Sheffield VC. Wassink TH, et al. Among authors: spence ma. Am J Med Genet B Neuropsychiatr Genet. 2005 Jul 5;136B(1):36-44. doi: 10.1002/ajmg.b.30180. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15892143 Free article.
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, L… See abstract for full author list ➔ Autism Genome Project Consortium, et al. Among authors: spence ma, spence s. 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: spence ma. Am J Med Genet. 2002 Aug 8;114(6):667-72. doi: 10.1002/ajmg.10603. Am J Med Genet. 2002. PMID: 12210285 Free article.
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: spence ma. 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 Free article.
Nuclear and mitochondrial genome defects in autisms.
Smith M, Spence MA, Flodman P. Smith M, et al. Among authors: spence ma. Ann N Y Acad Sci. 2009 Jan;1151:102-32. doi: 10.1111/j.1749-6632.2008.03571.x. Ann N Y Acad Sci. 2009. PMID: 19154520 Free article. Review.
Affecteds-only linkage methods are not a panacea.
Greenberg DA, Hodge SE, Vieland VJ, Spence MA. Greenberg DA, et al. Among authors: spence ma. Am J Hum Genet. 1996 Apr;58(4):892-5. Am J Hum Genet. 1996. PMID: 8644756 Free PMC article. No abstract available.
215 results