| 1 | AUTS2
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| Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus.
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| Beunders G, Voorhoeve E, Golzio C, Pardo LM, Rosenfeld JA, Talkowski ME, Simonic I, Lionel AC, Vergult S, Pyatt RE, van de Kamp J, Nieuwint A, Weiss MM, Rizzu P, Verwer LE, van Spaendonk RM, Shen Y, Wu BL, Yu T, Yu Y, Chiang C, Gusella JF, Lindgren AM, Morton CC, van Binsbergen E, Bulk S, van Rossem E, Vanakker O, Armstrong R, Park SM, Greenhalgh L, Maye U, Neill NJ, Abbott KM, Sell S, Ladda R, Farber DM, Bader PI, Cushing T, Drautz JM, Konczal L, Nash P, de Los Reyes E, Carter MT, Hopkins E, Marshall CR, Osborne LR, Gripp KW, Thrush DL, Hashimoto S, Gastier-Foster JM, Astbury C, Ylstra B, Meijers-Heijboer H, Posthuma D, Menten B, Mortier G, Scherer SW, Eichler EE, Girirajan S, Katsanis N, Groffen AJ, Sistermans EA.
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| Am J Hum Genet 92(2):210-20. doi: 10.1016/j.ajhg.2012.12.011. Epub 2013 Jan 17.
2013
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| 2 | AUTS2
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| Function and regulation of AUTS2, a gene implicated in autism and human evolution.
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| Oksenberg N, Stevison L, Wall JD, Ahituv N.
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| PLoS Genet 9(1):e1003221. doi: 10.1371/journal.pgen.1003221. Epub 2013 Jan 17.
2013
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| 3 | AUTS2, MRD26
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| Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus.
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| Beunders G, Voorhoeve E, Golzio C, Pardo LM, Rosenfeld JA, Talkowski ME, Simonic I, Lionel AC, Vergult S, Pyatt RE, van de Kamp J, Nieuwint A, Weiss MM, Rizzu P, Verwer LE, van Spaendonk RM, Shen Y, Wu BL, Yu T, Yu Y, Chiang C, Gusella JF, Lindgren AM, Morton CC, van Binsbergen E, Bulk S, van Rossem E, Vanakker O, Armstrong R, Park SM, Greenhalgh L, Maye U, Neill NJ, Abbott KM, Sell S, Ladda R, Farber DM, Bader PI, Cushing T, Drautz JM, Konczal L, Nash P, de Los Reyes E, Carter MT, Hopkins E, Marshall CR, Osborne LR, Gripp KW, Thrush DL, Hashimoto S, Gastier-Foster JM, Astbury C, Ylstra B, Meijers-Heijboer H, Posthuma D, Menten B, Mortier G, Scherer SW, Eichler EE, Girirajan S, Katsanis N, Groffen AJ, Sistermans EA.
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| Am J Hum Genet 92(2):210-20. doi: 10.1016/j.ajhg.2012.12.011. Epub 2013 Jan 17.
2013
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| 4 | AUTS2, PAX5
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| PAX5-AUTS2: a recurrent fusion gene in childhood B-cell precursor acute lymphoblastic leukemia.
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| Denk D, Nebral K, Bradtke J, Pass G, Möricke A, Attarbaschi A, Strehl S.
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| Leuk Res 36(8):e178-81. doi: 10.1016/j.leukres.2012.04.015. Epub 2012 May 12. Review.
2012
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| 5 | AUTS2
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| Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption.
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| Schumann G, Coin LJ, Lourdusamy A, Charoen P, Berger KH, Stacey D, Desrivières S, Aliev FA, Khan AA, Amin N, Aulchenko YS, Bakalkin G, Bakker SJ, Balkau B, Beulens JW, Bilbao A, de Boer RA, Beury D, Bots ML, Breetvelt EJ, Cauchi S, Cavalcanti-Proença C, Chambers JC, Clarke TK, Dahmen N, de Geus EJ, Dick D, Ducci F, Easton A, Edenberg HJ, Esko T, Fernández-Medarde A, Foroud T, Freimer NB, Girault JA, Grobbee DE, Guarrera S, Gudbjartsson DF, Hartikainen AL, Heath AC, Hesselbrock V, Hofman A, Hottenga JJ, Isohanni MK, Kaprio J, Khaw KT, Kuehnel B, Laitinen J, Lobbens S, Luan J, Mangino M, Maroteaux M, Matullo G, McCarthy MI, Mueller C, Navis G, Numans ME, Núñez A, Nyholt DR, Onland-Moret CN, Oostra BA, O'Reilly PF, Palkovits M, Penninx BW, Polidoro S, Pouta A, Prokopenko I, Ricceri F, Santos E, Smit JH, Soranzo N, Song K, Sovio U, Stumvoll M, Surakk I, Thorgeirsson TE, Thorsteinsdottir U, Troakes C, Tyrfingsson T, Tönjes A, Uiterwaal CS, Uitterlinden AG, van der Harst P, van der Schouw YT, Staehlin O, Vogelzangs N, Vollenweider P, Waeber G, Wareham NJ, Waterworth DM, Whitfield JB, Wichmann EH, Willemsen G, Witteman JC, Yuan X, Zhai G, Zhao JH, Zhang W, Martin NG, Metspalu A, Doering A, Scott J, Spector TD, Loos RJ, Boomsma DI, Mooser V, Peltonen L, Stefansson K, van Duijn CM, Vineis P, Sommer WH, Kooner JS, Spanagel R, Heberlein UA, Jarvelin MR, Elliott P.
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| Proc Natl Acad Sci U S A 108(17):7119-24. Epub 2011 Apr 6. Erratum in: Proc Natl Acad Sci U S A. 2011 May 31;108(22):9316. Esk, Tõnu [corrected to Esko, 2011
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| 6 | AUTS2
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| A de novo balanced translocation breakpoint truncating the autism susceptibility candidate 2 (AUTS2) gene in a patient with autism.
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| Huang XL, Zou YS, Maher TA, Newton S, Milunsky JM.
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| Am J Med Genet A 152A(8):2112-4. No abstract available. PMID: 20635338 2010
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| 7 | AUTS2, TBR1
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| Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex.
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| Bedogni F, Hodge RD, Elsen GE, Nelson BR, Daza RA, Beyer RP, Bammler TK, Rubenstein JL, Hevner RF.
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| Proc Natl Acad Sci U S A 107(29):13129-34. Epub 2010 Jul 6.PMID: 20615956 2010
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| 8 | 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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| 9 | 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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| 10 | AUTS2, PIBF1, KLF5, LYZL4
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| Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation.
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| Kalscheuer VM, Fitzpatrick D, Tommerup N, Bugge M, Niebuhr E, Neumann LM, Tzschach A, Shoichet SA, Menzel C, Erdogan F, Arkesteijn G, Ropers HH, Ullmann R.
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| Hum Genet 121(3-4):501-9. Epub 2007 Jan 9. 2007
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| 11 | DUP7Q11, AUTS2
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| Autism, language delay and mental retardation in a patient with 7q11 duplication.
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| Depienne C, Heron D, Betancur C, Benyahia B, Trouillard O, Bouteiller D, Verloes A, Leguern E, Leboyer M, Brice A.
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| J Med Genet [Epub ahead of print] 2007
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| 12 | 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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| 13 | AUTS2, LAMB1, NRCAM
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| Mutation screening and association analysis of six candidate genes for autism on chromosome 7q.
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| Bonora E, Lamb JA, Barnby G, Sykes N, Moberly T, Beyer KS, Klauck SM, Poustka F, Bacchelli E, Blasi F, Maestrini E, Battaglia A, Haracopos D, Pedersen L, Isager T, Eriksen G, Viskum B, Sorensen EU, Brondum-Nielsen K, Cotterill R, Engeland H, Jonge M, Kemner C, Steggehuis K, Scherpenisse M, Rutter M, Bolton PF, Parr JR, Poustka A, Bailey AJ, Monaco AP; International Molecular Genetic Study of Austism Consortium.
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| Eur J Hum Genet 13(2):198-207. 2005
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| 14 | AUTS2
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| Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins.
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| Sultana R, Yu C, Yu J, Munson J, Chen D, Hua W, Estes A, Cortes F, de la Barra F, Yu D, Haider S, Trask B, Green E, Raskind W, Disteche C, Wijsman E, Dawson G, Storm D, Schellenberg G, Villacres E.
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| Genomics 80(2):129. 2002
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| 15 | ATN1, AUTS2, WWP2, MAGI1, WWP1
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| Atrophin-1, the DRPLA gene product, interacts with two families of WW domain-containing proteins.
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| Wood JD, Yuan J, Margolis RL, Colomer V, Duan K, Kushi J, Kaminsky Z, Kleiderlein JJ, Sharp AH, Ross CA.
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| Mol Cell Neurosci 11(3):149-60. 1998
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