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Page 1
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.
Bucan M, Abrahams BS, Wang K, Glessner JT, Herman EI, Sonnenblick LI, Alvarez Retuerto AI, Imielinski M, Hadley D, Bradfield JP, Kim C, Gidaya NB, Lindquist I, Hutman T, Sigman M, Kustanovich V, Lajonchere CM, Singleton A, Kim J, Wassink TH, McMahon WM, Owley T, Sweeney JA, Coon H, Nurnberger JI, Li M, Cantor RM, Minshew NJ, Sutcliffe JS, Cook EH, Dawson G, Buxbaum JD, Grant SF, Schellenberg GD, Geschwind DH, Hakonarson H. Bucan M, et al. Among authors: coon h. PLoS Genet. 2009 Jun;5(6):e1000536. doi: 10.1371/journal.pgen.1000536. Epub 2009 Jun 26. PLoS Genet. 2009. PMID: 19557195 Free PMC article.
Autism, regression, and the broader autism phenotype.
Lainhart JE, Ozonoff S, Coon H, Krasny L, Dinh E, Nice J, McMahon W. Lainhart JE, et al. Among authors: coon h. Am J Med Genet. 2002 Dec 1;113(3):231-7. doi: 10.1002/ajmg.10615. Am J Med Genet. 2002. PMID: 12439889
Performance on Cambridge Neuropsychological Test Automated Battery subtests sensitive to frontal lobe function in people with autistic disorder: evidence from the Collaborative Programs of Excellence in Autism network.
Ozonoff S, Cook I, Coon H, Dawson G, Joseph RM, Klin A, McMahon WM, Minshew N, Munson JA, Pennington BF, Rogers SJ, Spence MA, Tager-Flusberg H, Volkmar FR, Wrathall D. Ozonoff S, et al. Among authors: coon h. J Autism Dev Disord. 2004 Apr;34(2):139-50. doi: 10.1023/b:jadd.0000022605.81989.cc. J Autism Dev Disord. 2004. PMID: 15162933
Confirmation of the association of the C4B null allelle in autism.
Odell D, Maciulis A, Cutler A, Warren L, McMahon WM, Coon H, Stubbs G, Henley K, Torres A. Odell D, et al. Among authors: coon h. Hum Immunol. 2005 Feb;66(2):140-5. doi: 10.1016/j.humimm.2004.11.002. Hum Immunol. 2005. PMID: 15694999
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: coon h. Mol Psychiatry. 2005 Dec;10(12):1110-6. doi: 10.1038/sj.mp.4001724. Mol Psychiatry. 2005. PMID: 16103890 Clinical Trial.
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: coon h. 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.
Head circumference and height in autism: a study by the Collaborative Program of Excellence in Autism.
Lainhart JE, Bigler ED, Bocian M, Coon H, Dinh E, Dawson G, Deutsch CK, Dunn M, Estes A, Tager-Flusberg H, Folstein S, Hepburn S, Hyman S, McMahon W, Minshew N, Munson J, Osann K, Ozonoff S, Rodier P, Rogers S, Sigman M, Spence MA, Stodgell CJ, Volkmar F. Lainhart JE, et al. Among authors: coon h. Am J Med Genet A. 2006 Nov 1;140(21):2257-74. doi: 10.1002/ajmg.a.31465. Am J Med Genet A. 2006. PMID: 17022081 Free PMC 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, Langemei… See abstract for full author list ➔ Autism Genome Project Consortium, et al. Among authors: coon h. Nat Genet. 2007 Mar;39(3):319-28. doi: 10.1038/ng1985. Epub 2007 Feb 18. Nat Genet. 2007. PMID: 17322880 Free PMC article.
Heterogeneous association between engrailed-2 and autism in the CPEA network.
Brune CW, Korvatska E, Allen-Brady K, Cook EH Jr, Dawson G, Devlin B, Estes A, Hennelly M, Hyman SL, McMahon WM, Munson J, Rodier PM, Schellenberg GD, Stodgell CJ, Coon H. Brune CW, et al. Among authors: coon h. Am J Med Genet B Neuropsychiatr Genet. 2008 Mar 5;147B(2):187-93. doi: 10.1002/ajmg.b.30585. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 17948868
A high-density SNP genome-wide linkage scan in a large autism extended pedigree.
Allen-Brady K, Miller J, Matsunami N, Stevens J, Block H, Farley M, Krasny L, Pingree C, Lainhart J, Leppert M, McMahon WM, Coon H. Allen-Brady K, et al. Among authors: coon h. Mol Psychiatry. 2009 Jun;14(6):590-600. doi: 10.1038/mp.2008.14. Epub 2008 Feb 19. Mol Psychiatry. 2009. PMID: 18283277
287 results