| 1 | AUTS1, AUTS10, AUTS11P, AUTS17, AUTS18, AUTS19, AUTS2, AUTS20, AUTS3, AUTS4, AUTS5, AUTS7, AUTS9, AUTSX1, AUTSX2, AUTSX3, SEMA5A
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| A genome-wide linkage and association scan reveals novel loci for autism.
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| Weiss LA, Arking DE; Gene Discovery Project of Johns Hopkins & the Autism Consortium, Daly MJ, Chakravarti A.
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| Nature 461(7265):802-8. 2009
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| 2 | AUTS1, AUTS10, AUTS17, AUTS18, AUTS19, AUTS2, AUTS20, AUTS3, AUTS4, AUTS5, AUTS6, AUTS7, AUTS9
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| Advances in autism genetics: on the threshold of a new neurobiology.
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| Abrahams BS, Geschwind DH.
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| Nat Rev Genet 9(5):341-55. 2008
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| 3 | AUTS9, MET
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| MET and autism susceptibility: family and case-control studies.
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| Sousa I, Clark TG, Toma C, Kobayashi K, Choma M, Holt R, Sykes NH, Lamb JA, Bailey AJ, Battaglia A, Maestrini E, Monaco AP.
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| Eur J Hum Genet ur J Hum Genet. 2008 Nov 12. [Epub ahead of print] 2008
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| 4 | AUTS9, MET
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| Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder.
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| Campbell DB, Li C, Sutcliffe JS, Persico AM, Levitt P.
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| Autism Res 1(3):159-68.
2008
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| 5 | DEL7Q31, SPCH1, AUTS9, FOXP2, WNT2
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| Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: Clinical report and review.
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| Lennon PA, Cooper ML, Peiffer DA, Gunderson KL, Patel A, Peters S, Cheung SW, Bacino CA.
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| Am J Med Genet A [Epub ahead of print] 2007
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| 6 | AUTS11P, AUTS19, AUTS5, AUTS7, AUTS9, NRXN1
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| Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
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| The 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, Roge B, Mantoulan C, Wittemeyer K, Poustka A, Felder B, Klauck SM, Schuster C, Poustka F, Bolte S, Feineis-Matthews S, Herbrecht E, Schmotzer 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, Langemeijer M, Hijimans C, Staal WG, Baird G, Bolton PF, Rutter ML, Weisblatt E, Green J, Aldred C, Wilkinson JA, Pickles A, Le Couteur A, Berney T, McConachie H, Bailey AJ, Francis K, Honeyman G, Hutchinson A, Parr JR, Wallace S, Monaco AP, Barnby G, Kobayashi K, Lamb JA, Sousa I, Sykes N, Cook EH, Guter SJ, Leventhal BL, Salt J, Lord C, Corsello C, Hus V, Weeks DE, Volkmar F, Tauber M, Fombonne E, Shih A.
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| Nat Genet 39(3):319-28. Epub 2007 Feb 18. 2007
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| 7 | AUTS9, AUTS5, AUTS10, AUTS7
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| Genetics of autism spectrum disorder.
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| Klauck SM.
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| Eur J Hum Genet 14(6):714-20. 2006
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| 8 | AUTS1, AUTS10, AUTS17, AUTS18, AUTS19, AUTS2, AUTS20, AUTS3, AUTS4, AUTS5, AUTS6, AUTS7, AUTS9
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| Searching for ways out of the autism maze: genetic, epigenetic and environmental clues.
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| Persico AM, Bourgeron T.
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| Trends Neurosci 29(7):349-58. Epub 2006 Jun 30. Review. 2006
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| 9 | AUTS9, MET
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| A genetic variant that disrupts MET transcription is associated with autism.
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| Campbell DB, Sutcliffe JS, Ebert PJ, Militerni R, Bravaccio C, Trillo S, Elia M, Schneider C, Melmed R, Sacco R, Persico AM, Levitt P.
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| Proc Natl Acad Sci U S A 103(45):16834-9. Epub 2006 Oct 19.
2006
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| 10 | AUTS4, AUTS9,
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| The genetics of autism.
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| Muhle R, Trentacoste SV, Rapin I.
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| Pediatrics 113(5):e472-86. Review. 2004
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| 11 | AUTS9, FOXP2
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| Defining the autism minimum candidate gene region on chromosome 7
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| Hutcheson HB, Bradford Y, Folstein SE, Gardiner MB, Santangelo SL, Sutcliffe JS, Haines JL.
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| Am J Med Genet 117B(1):90-6. 2003
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| 12 | AUTS9
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| Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.
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| [No authors listed]
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| Hum Mol Genet 10(9):973-82. 2001
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| 13 | AUTS9, CTTNBP2
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| Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31.
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| Cheung J, Petek E, Nakabayashi K, Tsui LC, Vincent JB, Scherer SW.
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| Genomics 78(1-2):7-11. 2001
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| 14 | AUTS9
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| Construction of a physical map of an autism susceptibility region in 7q32.3-q33.
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| Beyer KS, Klauck SM, Wiemann S, Poustka A.
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| Gene 272(1-2):85-91. 2001
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| 15 | AUTS9, AUTS5, AUTS17
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| A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.
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| International Molecular Genetic Study of Autism Consortium (IMGSAC).
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| Am J Hum Genet 69(3):570-81. Epub 2001 Jul 30. 2001
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| 16 | AUTS9
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| A genomic screen of autism: evidence for a multilocus etiology.
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| Risch N, et al.
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| Am J Hum Genet 65(2):493-507 1999
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| 17 | AUTS9
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| Genetic studies of autistic disorder and chromosome 7.
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| Ashley-Koch A, Wolpert CM, Menold MM, Zaeem L, Basu S, Donnelly SL, Ravan SA, Powell CM, Qumsiyeh MB, Aylsworth AS, Vance JM, Gilbert JR, Wright HH, Abramson RK, DeLong GR, Cuccaro ML, Pericak-Vance MA.
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| Genomics 61(3):227-36 1999
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| 18 | AUTS9, AUTS4
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| An autosomal genomic screen for autism.
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| Barrett S, Beck JC, Bernier R, Bisson E, Braun TA, Casavant TL, Childress D, Folstein SE, Garcia M, Gardiner MB, Gilman S, Haines JL, Hopkins K, Landa R, Meyer NH, Mullane JA, Nishimura DY, Palmer P, Piven J, Purdy J, Santangelo SL, Searby C, Sheffield V, Singleton J, Slager S, Struchen T.
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| Am J Med Genet 88(6):609-15 1999
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| 19 | AUTS9
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| A full genome screen for autism with evidence for linkage to a region on chromosome 7q.
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| International Molecular Genetic Study of Autism Consortium.
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| Hum Mol Genet 7 : 571-578. 1998
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