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High Density SNP Association Study of a Major Autism Linkage Region on Chromosome 17.
Hum Mol Genet. 2007 Mar 21;

Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T, Yamrom B, Yamrom B, Yoon S, Krasnitz A, Kendall J, Leotta A, Pai D, Zhang R, Lee YH, Hicks J, Spence SJ, Lee AT, Puura K, Lehtimaki T, Ledbetter D, Gregersen PK, Bregman J, Sutcliffe JS, Jobanputra V, Chung W, Warburton D, King MC, Skuse D, Geschwind DH, Gilliam TC, Ye K, Wigler M.
Strong Association of De Novo Copy Number Mutations with Autism.
Science. 2007 Mar 15;

Hettinger JA, Liu X, Holden JJ.
The G22A Polymorphism of the ADA Gene and Susceptibility to Autism Spectrum Disorders.
J Autism Dev Disord. 2007 Mar 6; [Epub ahead of print]

Nishimura K, Nakamura K, Anitha A, Yamada K, Tsujii M, Iwayama Y, Hattori E, Toyota T, Takei N, Miyachi T, Iwata Y, Suzuki K, Matsuzaki H, Kawai M, Sekine Y, Tsuchiya K, Sugihara GI, Suda S, Ouchi Y, Sugiyama T, Yoshikawa T, Mori N.
Genetic analyses of the brain-derived neurotrophic factor (BDNF) gene in autism.
Biochem Biophys Res Commun. 2007 Mar 5;

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.
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Nat Genet. 2007 Mar;39(3):319-28. Epub 2007 Feb 18.

Nicholas B, Rudrasingham V, Nash S, Kirov G, Owen MJ, Wimpory DC.
Association of Per1 and Npas2 with autistic disorder: support for the clock genes/social timing hypothesis.
Mol Psychiatry. 2007 Jan 30;

Cheslack-Postava K, Fallin MD, Avramopoulos D, Connors SL, Zimmerman AW, Eberhart CG, Newschaffer CJ.
beta(2)-Adrenergic receptor gene variants and risk for autism in the AGRE cohort.
Mol Psychiatry. 2007 Jan 2;

Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA.
Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
Mol Psychiatry. 2006 Dec 19;

Harvey CG, Menon SD, Stachowiak B, Noor A, Proctor A, Mensah AK, Mnatzakanian GN, Alfred SE, Guo R, Scherer SW, Kennedy JL, Roberts W, Srivistava AK, Minassian BA, Vincent JB.
Sequence variants within exon 1 of MECP2 occur in females with mental retardation.
Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 14;

Muscarella LA, Guarnieri V, Sacco R, Militerni R, Bravaccio C, Trillo S, Schneider C, Melmed R, Elia M, Mascia ML, Rucci E, Piemontese MR, D'Agruma L, Persico AM.
HOXA1 gene variants influence head growth rates in humans.
Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 14.

Sakurai T, Ramoz N, Reichert JG, Corwin TE, Kryzak L, Smith CJ, Silverman JM, Hollander E, Buxbaum JD.
Association analysis of the NrCAM gene in autism and in subsets of families with severe obsessive-compulsive or self-stimulatory behaviors.
Psychiatr Genet. 2006 Dec;16(6):251-7.

Lee LC, Zachary AA, Leffell MS, Newschaffer CJ, Matteson KJ, Tyler JD, Zimmerman AW.
HLA-DR4 in Families With Autism.
Pediatr Neurol. 2006 Nov;35(5):303-7.

Campbell DB, Sutcliffe JS, Ebert PJ, Militerni R, Bravaccio C, Trillo S, Elia M, Schneider C, Melmed R, Sacco R, Persico AM, Levitt P.
A genetic variant that disrupts MET transcription is associated with autism.
Proc Natl Acad Sci U S A. 2006 Oct 19;.

Petek E, Schwarzbraun T, Noor A, Patel M, Nakabayashi K, Choufani S, Windpassinger C, Stamenkovic M, Robertson MM, Aschauer HN, Gurling HM, Kroisel PM, Wagner K, Scherer SW, Vincent JB.
Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome.
Mol Genet Genomics. 2006 Oct 17; .

Ramoz N, Cai G, Reichert JG, Corwin TE, Kryzak LA, Smith CJ, Silverman JM, Hollander E, Buxbaum JD
Family-based association study of TPH1 and TPH2 polymorphisms in autism.
Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 6;.

Tierney E, Bukelis I, Thompson RE, Ahmed K, Aneja A, Kratz L, Kelley RI
Abnormalities of cholesterol metabolism in autism spectrum disorders.
Am J Med Genet B Neuropsychiatr Genet. 2006 Jul 27;.

Zandi PP, Kalaydjian A, Avramopoulos D, Shao H, Fallin MD, Newschaffer CJ.
Rh and ABO maternal-fetal incompatibility and risk of autism.
Am J Med Genet B Neuropsychiatr Genet. 2006 Jul 19; [Epub ahead of print]

Baron CA, Liu SY, Hicks C, Gregg JP.
Utilization of Lymphoblastoid Cell Lines as a System for the Molecular Modeling of Autism.
J Autism Dev Disord. 2006 Jul 15; [Epub ahead of print]

Collins AL, Ma D, Whitehead PL, Martin ER, Wright HH, Abramson RK, Hussman JP, Haines JL, Cuccaro ML, Gilbert JR, Pericak-Vance MA.
Investigation of autism and GABA receptor subunit genes in multiple ethnic groups.
Neurogenetics. 2006 Jul;7(3):167-74. Epub 2006 Jun 13.

Walker SJ, Segal J, Aschner M.
Cultured lymphocytes from autistic children and non-autistic siblings up-regulate heat shock protein RNA in response to thimerosal challenge.
Neurotoxicology. 2006 Jun 16; [Epub ahead of print]

Spence SJ, Cantor RM, Chung L, Kim S, Geschwind DH, Alarcón M.
Stratification based on language-related endophenotypes in autism: Attempt to replicate reported linkage.
Am J Med Genet B Neuropsychiatr Genet. 2006 Jun 2; [Epub ahead of print]

Hu VW, Frank BC, Heine S, Lee NH, Quackenbush J
Gene expression profiling of lymphoblastoid cell lines from monozygotic twins discordant in severity of autism reveals differential regulation of neurologically relevant genes.
BMC Genomics. 2006 May 18;7(1):118.

Weiss LA, Kosova G, Delahanty RJ, Jiang L, Cook EH, Ober C, Sutcliffe JS
Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility.
Eur J Hum Genet. 2006 May 17;.

Ashley-Koch AE, Mei H, Jaworski J, Ma DQ, Ritchie MD, Menold MM, Delong GR, Abramson RK, Wright HH, Hussman JP, Cuccaro ML, Gilbert JR, Martin ER, Pericak-Vance MA.
An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder.
Ann Hum Genet. 2006 May;70(Pt 3):281-92.

Talebizadeh Z, Lam DY, Theodoro MF, Bittel DC, Lushington GH, Butler MG.
Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism.
J Med Genet. 2006 May;43(5):e21.

Ramoz N, Reichert JG, Corwin TE, Smith CJ, Silverman JM, Hollander E, Buxbaum JD.
Lack of Evidence for Association of the Serotonin Transporter Gene SLC6A4 with Autism.
Biol Psychiatry. 2006 Apr 6

Constantino JN, Lajonchere C, Lutz M, Gray T, Abbacchi A, McKenna K, Singh D, Todd RD
Autistic social impairment in the siblings of children with pervasive developmental disorders.
Am J Psychiatry. 2006 Feb;163(2):294-6.

Yonan AL, Palmer AA, Gilliam TC.
Hardy-Weinberg disequilibrium identified genotyping error of the serotonin transporter (SLC6A4) promoter polymorphism.
Psychiatr Genet. 2006 Feb;16(1):31-4.

Richler E, Reichert JG, Buxbaum JD, McInnes LA.
Autism and ultraconserved non-coding sequence on chromosome 7q.
Psychiatr Genet. 2006 Feb;16(1):19-23.

Baron CA, Tepper CG, Liu SY, Davis RR, Wang NJ, Schanen NC, Gregg JP
Genomic and Functional Profiling of Duplicated Chromosome 15 Cell Lines Reveal Regulatory Alterations in UBE3A-associated Ubiquitin-Proteasome Pathway Processes.
Hum Mol Genet. 2006 Jan 30.

Serajee FJ, Zhong H, Mahbubul Huq AH.
Association of Reelin gene polymorphisms with autism.
Genomics. 2005 Nov 24; [Epub ahead of print]

Connors SL, Crowell DE, Eberhart CG, Copeland J, Newschaffer CJ, Spence SJ, Zimmerman AW.
beta2-Adrenergic Receptor Activation and Genetic Polymorphisms in Autism: Data from Dizygotic Twins.
J Child Neurol. 2005 Nov;20(11):876-84.

Ylisaukko-Oja T, Alarcón M, Cantor RM, Auranen M, Vanhala R, Kempas E, von Wendt L, Jarvela I, Geschwind DH, Peltonen L.
Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families.
Ann Neurol. 2005 Nov 15; [Epub ahead of print]

Sahoo T, Shaw CA, Young AS, Whitehouse NL, Schroer RJ, Stevenson RE, Beaudet AL.
Array-based comparative genomic hybridization analysis of recurrent chromosome 15q rearrangements.
Am J Med Genet A. 2005 Nov 11; [Epub ahead of print]

Hamilton SP, Woo JM, Carlson EJ, Ghanem N, Ekker M, Rubenstein JL. Analysis of four DLX homeobox genes in autistic probands.
BMC Genet. 2005 Nov 2;6(1):52 [Epub ahead of print]

Benayed R, Gharani N, Rossman I, Mancuso V, Lazar G, Kamdar S, Bruse SE, Tischfield S, Smith BJ, Zimmerman RA, DiCicco-Bloom E, Brzustowicz LM, and Millonig JH
Support for the Homeobox Transcription Factor Gene ENGRAILED 2 as an Autism Spectrum Disorder Susceptibility Locus
Am J Hum Genet. 2005 Nov 77(5):851-68.

Faham M, Zheng J, Moorhead M, Fakhrai-Rad H, Namsaraev E, Wong K, Wang Z, Chow SG, Lee L, Suyenaga K, Reichert J, Boudreau A, Eberle J, Bruckner C, Jain M, Karlin-Neumann G, Jones HB, Willis TD, Buxbaum JD, Davis RW.
Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays.
Proc Natl Acad Sci U S A. 2005 Oct 11;102(41):14717-22. Epub 2005 Oct 3.

Chen GK, Kono N, Geschwind DH, Cantor RM
Quantitative trait locus analysis of nonverbal communication in autism spectrum disorder.
Mol Psychiatry 2005 Sep 27

Talebizadeh Z, Bittel DC, Veatch OJ, Kibiryeva N, Butler MG.
Brief Report: Non-Random X Chromosome Inactivation in Females with Autism.
J Autism Dev Disord. 2005 Sep 16;:1-7

Ma DQ, Whitehead PL, Menold MM, Martin ER, Ashley-Koch AE, Mei H, Ritchie MD, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Hussman JP, Gilbert JR, Pericak-Vance MA.
Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism.
Am J Hum Genet. 2005 Sep;77(3):377-88. Epub 2005 Jul 15.

Prasad HC, Zhu CB, McCauley JL, Samuvel DJ, Ramamoorthy S, Shelton RC, Hewlett WA, Sutcliffe JS, Blakely RD.
Human serotonin transporter variants display altered sensitivity to protein kinase G and p38 mitogen-activated protein kinase.
Proc Natl Acad Sci U S A. 2005 Aug 9;102(32):11545-50. Epub 2005 Jul 29.

Philippi A, Roschmann E, Tores F, Lindenbaum P, Benajou A, Germain-Leclerc L, Marcaillou C, Fontaine K, Vanpeene M, Roy S, Maillard S, Decaulne V, Saraiva JP, Brooks P, Rousseau F, Hager J.
Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism.
Mol Psychiatry. 2005 Jul 19;

D'Amelio M, Ricci I, Sacco R, Liu X, D'Agruma L, Muscarella LA, Guarnieri V, Militerni R, Bravaccio C, Elia M, Schneider C, Melmed R, Trillo S, Pascucci T, Puglisi-Allegra S, Reichelt KL, Macciardi F, Holden JJ, Persico AM.
Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions.
Mol Psychiatry. 2005 Jul 19;

Sutcliffe JS, Delahanty RJ, Prasad HC, McCauley JL, Han Q, Jiang L, Li C, Folstein SE, Blakely RD.
Allelic Heterogeneity at the Serotonin Transporter Locus (SLC6A4) Confers Susceptibility to Autism and Rigid-Compulsive Behaviors.
Am J Hum Genet. 2005 Jul 1;77(2)

Molloy CA, Keddache M, Martin LJ
Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression.
Mol Psychiatry 2005 May 10;.

Alarcón M, Yonan AL, Gilliam TC, Cantor RM, Geschwind DH.
Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs.
Mol Psychiatry. 2005 Apr 12; [Epub ahead of print]

Cantor RM, Kono N, Duvall JA, Alvarez-Retuerto A, Stone JL, Alarcón M, Nelson SF, Geschwind DH.
Replication of Autism Linkage: Fine-Mapping Peak at 17q21.
Am J Hum Genet. 2005 Apr 1;76(6) [Epub ahead of print]

Butler MG, Dasouki MJ, Zhou XP, Talebizadeh Z, Brown M, Takahashi TN, Miles JH, Wang CH, Stratton R, Pilarski R, Eng C.
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations.
J Med Genet. 2005 Apr;42(4):318-21.

Bartlett CW, Gharani N, Millonig JH, Brzustowicz LM.
Three autism candidate genes: a synthesis of human genetic analysis with other disciplines.
Int J Dev Neurosci. 2005 Apr-May;23(2-3):221-34.

Bartlett CW, Goedken R, Vieland VJ.
Effects of Updating Linkage Evidence across Subsets of Data: Reanalysis of the Autism Genetic Resource Exchange Data Set.
Am J Hum Genet. 2005 Feb 23;76(4)

Odell D, Maciulis A, Cutler A, Warren L, McMahon WM, Coon H, Stubbs G, Henley K, Torres A.
Confirmation of the association of the C4B null allelle in autism.
Hum Immunol. 2005 Feb;66(2):140-5.

McCauley JL, Li C, Jiang L, Olson LM, Crockett G, Gainer K, Folstein SE, Haines JL, Sutcliffe JS.
Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates.
BMC Med Genet. 2005 Jan 12;6(1):1

Talebizadeh Z, Bittel DC, Veatch OJ, Butler MG, Takahashi TN, Miles JH.
Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism?
J Autism Dev Disord. 2004 Dec;34(6):735-6.
PMID: 15679194

Rabionet R, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA.
Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes.
Neurosci Lett. 2004 Dec 6;372(3):209-14.

Skaar DA, Shao Y, Haines JL, Stenger JE, Jaworski J, Martin ER, Delong GR, Moore JH, McCauley JL, Sutcliffe JS, Ashley-Koch AE, Cuccaro ML, Folstein SE, Gilbert JR, Pericak-Vance MA.
Analysis of the RELN gene as a genetic risk factor for autism.
Mol Psychiatry. 2004 Nov 23

Junaid MA, Kowal D, Barua M, Pullarkat PS, Sklower Brooks S, Pullarkat RK.
Proteomic studies identified a single nucleotide polymorphism in glyoxalase I as autism susceptibility factor.
Am J Med Genet. 2004 Nov 15;131A(1):11-7.

Stone JL, Merriman B, Cantor RM, Yonan AL, Gilliam TC, Geschwind DH, Nelson SF.
Evidence for Sex-Specific Risk Alleles in Autism Spectrum Disorder.
Am J Hum Genet. 2004 Oct 5;75(6) [Epub ahead of print]

Jiang YH, Sahoo T, Michaelis RC, Bercovich D, Bressler J, Kashork CD, Liu Q, Shaffer LG, Schroer RJ, Stockton DW, Spielman RS, Stevenson RE, Beaudet AL.
A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A.
Am J Med Genet. 2004 Aug 30 [Epub ahead of print]

McCauley JL, Olson LM, Delahanty R, Amin T, Nurmi EL, Organ EL, Jacobs MM, Folstein SE, Haines JL, Sutcliffe JS.
A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism.
Am J Med Genet. 2004 Aug 24 [Epub ahead of print]

Vincent JB, Kolozsvari D, Roberts WS, Bolton PF, Gurling HM, Scherer SW.
Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands.
Am J Med Genet. 2004 Aug 15;129B(1):82-4.

Kolevzon A, Smith CJ, Schmeidler J, Buxbaum JD, Silverman JM.
Familial symptom domains in monozygotic siblings with autism.
Am J Med Genet. 2004 Aug 15;129B(1):76-81.

Serajee FJ, Nabi R, Zhong H, Huq M.
Polymorphisms in xenobiotic metabolism genes and autism.
J Child Neurol. 2004 Jun;19(6):413-7.

Persico AM, D'Agruma L, Zelante L, Militerni R, Bravaccio C, Schneider C, Melmed R, Trillo S, Montecchi F, Elia M, Palermo M, Rabinowitz D, Pascucci T, Puglisi-Allegra S, Reichelt KL, Muscarella L, Guarnieri V, Melgari JM, Conciatori M, Keller F.
Enhanced APOE2 transmission rates in families with autistic probands.
Psychiatr Genet. 2004 Jun;14(2):73-82.

McCauley JL, Olson LM, Dowd M, Amin T, Steele A, Blakely RD, Folstein SE, Haines JL, Sutcliffe JS.
Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism.
Am J Med Genet. 2004 May 15;127B(1):104-12.

Ramoz N, Reichert JG, Smith CJ, Silverman JM, Bespalova IN, Davis KL, Buxbaum JD.
Linkage and Association of the Mitochondrial Aspartate/Glutamate Carrier SLC25A12 Gene With Autism.
Am J Psychiatry. 2004 Apr;161(4):662-9.

Gharani N, Benayed R, Mancuso V, Brzustowicz LM, Millonig JH.
Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder.
Mol Psychiatry. 2004 Mar 16 :1-11 [Epub ahead of print]

Conciatori M, Stodgell CJ, Hyman SL, O'Bara M, Militerni R, Bravaccio C, Trillo S, Montecchi F, Schneider C, Melmed R, Elia M, Crawford L, Spence SJ, Muscarella L, Guarnieri V, D'Agruma L, Quattrone A, Zelante L, Rabinowitz D, Pascucci T, Puglisi-Allegra S, Reichelt KL, Rodier PM, Persico AM.
Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism.
Biol Psychiatry. 2004 Feb 15;55(4):413-9.

Nabi R, Serajee FJ, Chugani DC, Zhong H, Huq AH.
Association of tryptophan 2,3 dioxygenase gene polymorphism with autism.
Am J Med Genet. 2004 Feb 15;125B(1):63-8.

Raiford KL, Shao Y, Allen IC, Martin ER, Menold MM, Wright HH, Abramson RK, Worley G, DeLong GR, Vance JM, Cuccaro ML, Gilbert JR, Pericak-Vance MA.
No association between the APOE gene and autism.
Am J Med Genet. 2004 Feb 15;125B(1):57-60.

Vincent JB, Thevarkunnel S, Kolozsvari D, Paterson AD, Roberts W, Scherer SW.
Association and transmission analysis of the FMR1 IVS10 + 14C-T variant in autism.
Am J Med Genet. 2004 Feb 15;125B(1):54-6.

Buxbaum JD, Silverman J, Keddache M, Smith CJ, Hollander E, Ramoz N, Reichert JG.
Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: Evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19.
Mol Psychiatry. 2004 Feb;9(2):144-150.

Serajee FJ, Nabi R, Zhong H, Mahbubul Huq AH.
Association of INPP1, PIK3CG, and TSC2 gene variants with autistic disorder: implications for phosphatidylinositol signalling in autism.
J Med Genet. 2003 Nov;40(11):e119.

Yonan AL, Palmer AA, Smith KC, Feldman I, Lee HK, Yonan JM, Fischer SG, Pavlidis P, Gilliam TC.
Bioinformatic analysis of autism positional candidate genes using biological databases and computational gene network prediction.
Genes Brain Behav. 2003 Oct;2(5):303-20.

Yonan AL, Alarcón M, Cheng R, Magnusson PK, Spence SJ, Palmer AA, Grunn A, Juo SH, Terwilliger JD, Liu J, Cantor RM, Geschwind DH, Gilliam TC.
A genomewide screen of 345 families for autism-susceptibility loci. Am J Hum Genet. 2003 Oct;73(4):886-97. Epub 2003 Sep 17.

Nabi R, Zhong H, Serajee FJ, Huq AH.
No association between single nucleotide polymorphisms in DLX6 and Piccolo genes at 7q21-q22 and autism.
Am J Med Genet 2003 May 15;119B(1):98-101.

Serajee FJ, Zhong H, Nabi R, Huq AH.
The metabotropic glutamate receptor 8 gene at 7q31: partial duplication and possible association with autism.
J Med Genet 2003 Apr;40(4):e42.

Cisternas FA, Vincent JB, Scherer SW, Ray PN.
Cloning and characterization of human CADPS and CADPS2, new members of the Ca(2+)-dependent activator for secretion protein family.
Genomics 2003 Mar;81(3):279-91.

Weiss LA, Escayg A, Kearney JA, Trudeau M, MacDonald BT, Mori M, Reichert J, Buxbaum JD, Meisler MH.
Sodium channels SCN1A, SCN2A and SCN3A in familial autism.
Mol Psychiatry 2003 Feb;8(2):186-94.

Zhong H, Serajee FJ, Nabi R, Huq AH.
No association between the EN2 gene and autistic disorder.
J Med Genet 2003 Jan;40(1):e4.

Vincent JB, Petek E, Thevarkunnel S, Kolozsvari D, Cheung J, Patel M, Scherer SW.
The RAY1/ST7 tumor-suppressor locus on chromosome 7q31 represents a complex multi-transcript system.
Genomics 2002 Sep;80(3):283-94.

Yamagata T, Aradhya S, Mori M, Inoue K, Momoi MY, Nelson DL.
The human secretin gene: fine structure in 11p15.5 and sequence variation in patients with autism.
Genomics 2002 Aug;80(2):185-94.

Torres AR, Maciulis A, Stubbs EG, Cutler A, Odell D.
The transmission disequilibrium test suggests that HLA-DR4 and DR13 are linked to autism spectrum disorder.
Hum Immunol 2002 Apr;63(4):311-6.

Fatemi SH.
The role of Reelin in pathology of autism.
Mol Psychiatry 2002;7(9):919-20.

Zhang H, Liu X, Zhang C, Mundo E, Macciardi F, Grayson DR, Guidotti AR, Holden JJ.
Reelin gene alleles and susceptibility to autism spectrum disorders.
Mol Psychiatry 2002;7(9):1012-7.

Fatemi SH, Stary JM, Egan EA.
Reduced blood levels of reelin as a vulnerability factor in pathophysiology of autistic disorder.
Cell Mol Neurobiol. 2002 Apr;22(2):139-52

Buxbaum JD, Silverman JM, Smith CJ, Greenberg DA, Kilifarski M, Reichert J, Cook EH Jr, Fang Y, Song CY, Vitale R.
Association between a GABRB3 polymorphism and autism.
Mol Psychiatry 2002;7(3):311-6.

Silverman JM, Smith CJ, Schmeidler J, Hollander E, Lawlor BA, Fitzgerald M, Buxbaum JD, Delaney K, Galvin P; Autism Genetic Research Exchange Consortium.
Symptom domains in autism and related conditions: evidence for familiality.
Am J Med Genet 2002 Jan 8;114(1):64-73

Alarcón M, Cantor RM, Liu J, Gilliam TC, Geschwind DH; Autism Genetic Research Exchange Consortium.
Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families.
Am J Hum Genet 2002 Jan;70(1):60-71

Greenberg DA, Hodge SE, Sowinski J, Nicoll D.
Excess of twins among affected sibling pairs with autism: implications for the etiology of autism.
Am J Hum Genet 2001 Nov;69(5):1062-7

Cheung J, Petek E, Nakabayashi K, Tsui LC, Vincent JB, Scherer SW
Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31.
Genomics. 2001 Nov; 78(1-2):7-11.

Geschwind DH, Sowinski J, Lord C, Iversen P, Shestack J, Jones P, Ducat L, Spence SJ; AGRE Steering Committee.
The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions.
Am J Hum Genet. 2001 Aug;69(2):463-6.

Liu J, Nyholt DR, Magnussen P, Parano E, Pavone P, Geschwind D, Lord C, Iversen P, Hoh J, Ott J, Gilliam TC; Autism Genetic Resource Exchange Consortium.
A genomewide screen for autism susceptibility loci.
Am J Hum Genet. 2001 Aug;69(2):327-40. Epub 2001 Jul 10.

Buxbaum JD, Silverman JM, Smith CJ, Kilifarski M, Reichert J, Hollander E, Lawlor BA, Fitzgerald M, Greenberg DA, Davis KL.
Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity.
Am J Hum Genet 2001 Jun;68(6):1514-20.

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