2014 International Meeting for Autism Research: Genetics

11:30 AM

45 Association Between GABA(A) Receptor Subunit Polymorphisms and Autism Spectrum Disorder (ASD) in an Argentinean Sample
C. V. Sesarini, L. Costa, N. Granana, M. Naymark, A. R. Cajal, M. Garcia Coto, R. Pallia and P. F. Argibay

11:30 AM

173.046

46 Exploring the Nature of Quantitative Autistic Traits: A Factor Mixture Modeling Approach
R. Grove, A. J. Baillie, C. Allison, S. Baron-Cohen and R. A. Hoekstra

11:30 AM

173.047

47 The Genetic Basis of Autism Spectrum Disorders: Identification and Analysis of Rare Structural Variants in a Family Based Study
N. Brison, W. De La Marche, V. De Wolf, H. Olivié, J. Steyaert, I. Noens, J. Vermeesch, K. Devriendt and H. Peeters

11:30 AM

173.048

48 Analysis of Differential Methylation in Autism Spectrum Disease Using a Novel Probe-Based Algorithm
T. R. Magalhaes, S. Ennis, J. Conroy, R. Regan and J. Casey

11:30 AM

173.049

49 Assessment of Sources of Methylation Variation and Their Relationship to Autism Spectrum
M. D. Fallin, S. V. Andrews, B. K. Lee, C. J. Newschaffer, G. C. Windham, L. A. Schieve, L. A. Croen, A. P. Feinberg and C. Ladd-Acosta

11:30 AM

173.050

50 AutDB: A Modular Database for Accelerating Autism Genetic Research
E. Larsen, U. Kuppuswamy and S. B. Basu

11:30 AM

173.051

51 Blood-Brain DNA Methylation Concordance in Autism Spectrum Disorders
S. V. Andrews, L. A. Croen, L. A. Schieve, K. D. Hansen, B. K. Lee, C. J. Newschaffer, A. P. Feinberg, C. Ladd-Acosta and M. D. Fallin

11:30 AM

173.052

52 Common Polygenic Variations in Autism
J. Carayol, B. Génin, C. Amiet, F. Liebaert, R. Thiébaut, B. Abrahams and T. W. Frazier

11:30 AM

173.053

53 Common Polymorphisms in GABRB3 Are Associated with Asperger Syndrome and Related Endophenotypes
V. Warrier, S. Baron-Cohen and B. Chakrabarti

11:30 AM

173.054

54 Concordance in Symptom Severity and Face Processing Among Twins with and without Autism
E. E. Neuhaus, S. J. Webb, R. Bernier, A. Kresse and S. Faja

11:30 AM

173.055

55 Cross-Disorder CNV Interactome
R. Corominas, G. N. Lin, X. Yang, D. E. Hill, M. Vidal and L. M. Iakoucheva

11:30 AM

173.056

56 Defining the Clinical Phenotype of Recurrent Copy Number Variation at Chromosome 1q21.1
R. Bernier, B. Reilly, E. Hanson, R. P. Goin-Kochel, L. Green-Snyder, J. Tjernagel, J. Gerdts, A. Stevens, W. A. Faucett, E. H. Sherr, C. L. Martin, D. H. Ledbetter, J. E. Spiro and W. Chung

11:30 AM

173.057

57 Differentially Expressed Small Non-Coding RNA in the Temporal Cortex of the Autism Brain
B. P. Ander, N. Barger, B. Stamova, F. R. Sharp and C. M. Schumann

11:30 AM

173.058

58 Early Intervention in Autism: Wide-Locus GWAS Leading to Novel Treatment Options
K. M. Wittkowski, B. Bigio, V. Sonakya, M. K. Tonn, F. Shic, M. Ascano, C. Nasca and G. Gold-Von Simson

11:30 AM

173.060

60 Examining the Overlap of Autism Spectrum Disorder and 22Q11 Deletion Syndrome Using Standardized Clinical Assessments
N. Evans, S. Fernandez-Carriba, E. L. Smearman, K. Rockers, K. Coleman, J. F. Cubells and O. Ousley

11:30 AM

173.061

61 Heterogeneity in 5-Httlpr Genotype-Phenotype Effects
E. H. Cook, E. Kistner-Griffin, S. Jacob, F. Najjar, S. J. Guter, N. J. Cox and J. S. Sutcliffe

11:30 AM

173.062

62 Maternally Acting Gene Alleles (MAGAs) in Autism: A Meta-Analysis of Two GWAS Study Results
W. G. Johnson, E. Stenroos and S. Buyske

2014 International Meeting for Autism Research

May 14 - 17, 2014

Genetics

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