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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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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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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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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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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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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The DLX1and DLX2 genes and susceptibility to autism spectrum disorders von Liu, Xudong, 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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Understanding the impact of 1q21.1 copy number variant von Harvard, Chansonette, Strong, Emma, Mercier, Eloi, Colnaghi, Rita, Alcantara, Diana, Chow, Eva, Martell, Sally, Tyson, Christine, Hrynchak, Monica, McGillivray, Barbara, Hamilton, Sara, Marles, Sandra, Mhanni, Aziz, Dawson, Angelika J, Pavlidis, Paul, Qiao, Ying, Holden, Jeanette J, Lewis, Suzanne M E, O'Driscoll, Mark, Rajcan-Separovic, Evica

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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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Developmental Trajectories in Syndromes with Intellectual Disability, with a Focus on Wolf-Hirschhorn and Its Cognitive-Behavioral Profile von Fisch, Gene S, Carpenter, Nancy, Howard-Peebles, Patricia N, Holden, Jeanette J. A, Tarleton, Jack, Simensen, Richard, Battaglia, Agatino

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The course of cognitive-behavioral development in children with the FMR1 mutation, Williams-Beuren syndrome, and neurofibromatosis type 1: The effect of gender von Fisch, Gene S., Carpenter, Nancy, Howard-Peebles, Patricia N., Holden, Jeanette J.A., Tarleton, Jack, Simensen, Richard

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2p15–p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders von Liu, Xudong, Malenfant, Patrick, Reesor, Chelsea, Lee, Alana, Hudson, Melissa L, Harvard, Chansonette, Qiao, Ying, Persico, Antonio M, Cohen, Ira L, Chudley, Albert E, Forster-Gibson, Cynthia, Rajcan-Separovic, Evica, Lewis, ME Suzanne, Holden, Jeanette JA

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Studies of age-correlated features of cognitive-behavioral development in children and adolescents with genetic disorders von Fisch, Gene S., Carpenter, Nancy, Howard-Peebles, Patricia N., Holden, Jeanette J.A., Tarleton, Jack, Simensen, Richard, Nance, Walter

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Trends in Special Education Code Assignment for Autism: Implications for Prevalence Estimates von Ouellette-Kuntz, Helene, Coo, Helen, Lloyd, Jennifer E. V, Kasmara, Liza, Holden, Jeanette J. A, Lewis, Suzanne M. E

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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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Large-scale copy number variants (CNVs): distribution in normal subjects and FISH/real-time qPCR analysis von Qiao, Ying, Liu, Xudong, Harvard, Chansonette, Nolin, Sarah L, Brown, W Ted, Koochek, Maryam, Holden, Jeanette J A, Lewis, M E Suzanne, Rajcan-Separovic, Evica

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Addressing Health Disparities Through Promoting Equity for Individuals with Intellectual Disability von Ouellette-Kuntz, Hélène, Garcin, Nathalie, Lewis, M.E. Suzanne, Minnes, Patricia, Martin, Carol, Holden, Jeanette J.A.

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Association of MAOA, 5-HTT, and NET promoter polymorphisms with gene expression and protein activity in human placentas von Zhang, Huiping, Smith, Graeme N, Liu, Xudong, Holden, Jeanette J A

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