Dopamine receptor D4 gene variation predicts preschoolers' developing theory of mind von Lackner, Christine, Sabbagh, Mark A., Hallinan, Elizabeth, Liu, Xudong, Holden, Jeanette J.A.

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Length of uninterrupted CGG repeats determines instability in the FMR1 gene von Reiss, Allan L, Thibodeau, Stephen N, Richards, C. Sue, Eichler, Evan E, Holden, Jeanette J.A, Popovich, Bradley W, Nelson, David L, Ward, Patricia A, Snow, Karen

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Association of GTF2i in the Williams-Beuren Syndrome Critical Region with Autism Spectrum Disorders von Malenfant, Patrick, Liu, Xudong, Hudson, Melissa L., Qiao, Ying, Hrynchak, Monica, Riendeau, Noémie, Hildebrand, M. Jeannette, Cohen, Ira L., Chudley, Albert E., Forster-Gibson, Cynthia, Mickelson, Elizabeth C. R., Rajcan-Separovic, Evica, Lewis, M. E. Suzanne, Holden, Jeanette J. A.

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Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox von Fu, Ying-Hui, Kuhl, Derek P.A., Pizzuti, Antonio, Pieretti, Maura, Sutcliffe, James S., Richards, Stephen, Verkert, Annemieke J.M.H., Holden, Jeanette J.A., Fenwick, Raymond G., Warren, Stephen T., Oostra, Ben A., Nelson, David L., Caskey, C.Thomas

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Age at Diagnosis of Autism Spectrum Disorders in Four Regions of Canada von Ouellette-Kuntz, Hélène M.J., Coo, Helen, Lam, Miu, Yu, C.T., Breitenbach, Marlene M., Hennessey, Paula E., Holden, Jeanette J.A., Brown, Hilary K., Noonan, Andrea L., Gauthier, Robert B., Crews, Lori R.

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The obsessive-compulsive trait of Incompleteness in parents of children with autism spectrum disorders von Kloosterman, Patricia H, Summerfeldt, Laura J, Parker, James D.A, Holden, Jeanette J.A

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Face-brain asymmetry in autism spectrum disorders von Hammond, P, Forster-Gibson, C, Chudley, A E, Allanson, J E, Hutton, T J, Farrell, S A, McKenzie, J, Holden, J J A, Lewis, M E S

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Population- and Family-Based Studies Associate the MTHFR Gene with Idiopathic Autism in Simplex Families von Liu, Xudong, Solehdin, Fatima, Cohen, Ira L., Gonzalez, Maripaz G., Jenkins, Edmund C., Lewis, M. E. Suzanne, Holden, Jeanette J. A.

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Development and Initial Validation of a Parent Report Measure of the Behavioral Development of Infants at Risk for Autism Spectrum Disorders von Feldman, Maurice A., Ward, Rebecca A., Savona, Danielle, Regehr, Kaleigh, Parker, Kevin, Hudson, Melissa, Penning, Henderika, Holden, Jeanette J. A.

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Trends in Autism Prevalence: Diagnostic Substitution Revisited von Coo, Helen, Ouellette-Kuntz, Hélène, Lloyd, Jennifer E. V., Kasmara, Liza, Holden, Jeanette J. A., Lewis, M. E. Suzanne

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A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families von Hettinger, Joe A., Liu, Xudong, Schwartz, Charles E., Michaelis, Ron C., Holden, Jeanette J.A.

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Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1 von Rajcan-Separovic, E, Harvard, C, Liu, X, McGillivray, B, Hall, J G, Qiao, Y, Hurlburt, J, Hildebrand, J, Mickelson, E C R, Holden, J J A, Lewis, M E S

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Haplotype Study of Intermediate-Length Alleles at the Fragile X (FMR1) Gene: ATL1, FMRb, and Microsatellite Haplotypes Differ from Those Found in Common-Size FMR1 Alleles von CURLIS, YVETTE, ZHANG, CUILING, HOLDEN, JEANETTE J. A., KIRKBY, KEN, LOESCH, DANUTA, MITCHELL, R. JOHN

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Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability von Qiao, Y, Tyson, C, Hrynchak, M, Lopez-Rangel, E, Hildebrand, J, Martell, S, Fawcett, C, Kasmara, L, Calli, K, Harvard, C, Liu, X, Holden, JJA, Lewis, SME, Rajcan-Separovic, E

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Autism severity is associated with child and maternal MAOA genotypes von Cohen, IL, Liu, X, Lewis, MES, Chudley, A, Forster-Gibson, C, Gonzalez, M, Jenkins, EC, Brown, WT, Holden, JJA

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Differential impact of the FMR1 gene on visual processing in fragile X syndrome von Kogan, Cary S., Boutet, Isabelle, Cornish, Kim, Zangenehpour, Shahin, Mullen, Kathy T., Holden, Jeanette J. A., Der Kaloustian, Vazken M., Andermann, Eva, Chaudhuri, Avi

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Brief Report: Telephone Administration of the Autism Diagnostic Interview—Revised: Reliability and Suitability for Use in Research von Ward-King, Jessica, Cohen, Ira L., Penning, Henderika, Holden, Jeanette J. A.

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DRD2 and PPP1R1B (DARPP-32) polymorphisms independently confer increased risk for autism spectrum disorders and additively predict affected status in male-only affected sib-pair fa... von Hettinger, Joe A, Liu, Xudong, Hudson, Melissa L, Lee, Alana, Cohen, Ira L, Michaelis, Ron C, Schwartz, Charles E, Lewis, Suzanne M E, Holden, Jeanette J A

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The DLX1and DLX2 genes and susceptibility to autism spectrum disorders von XUDONG LIU, NOVOSEDLIK, Natalia, WANG, Ami, HUDSON, Melissa L, COHEN, Ira L, CHUDLEY, Albert E, FORSTER-GIBSON, Cynthia J, LEWIS, Suzanne M. E, HOLDEN, Jeanette J. A

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Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions von D'AMELIO, M, RICCI, I, SCHNEIDER, C, MELMED, R, TRILLO, S, PASCUCCI, T, PUGLISI-ALLEGRA, S, REICHELT, K.-L, MACCIARDI, F, HOLDEN, J. J. A, PERSICO, A. M, SACCO, R, LIU, X, D'AGRUMA, L, MUSCARELLA, L. A, GUARNIERI, V, MILITERNI, R, BRAVACCIO, C, ELIA, M

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