69 A Unique Cognitive Profile of ASD Evident in Siblings, Parents, and Grandparents of Individuals with ASD
M. Losh L. Bush K. Nayar M. Lee G. E. Martin M. Winston S. Crawford J. Sideris D. Achorn S. Lapham C. Persico J. Ferrie D. Figlio

70 AUT-Priori: A Web-Based Tool for Autism Gene Prioritization
A. J. Griswold D. Van Booven E. R. Martin M. L. Cuccaro J. P. Hussman M. A. Pericak-Vance

71 Clinical and Neurophysiological Phenotype of Phelan Mcdermid Syndrome: Communication Disorder or Autism?
L. Ponson M. Gomot R. Blanc C. Barthelemy S. Roux A. Munnich N. Hernandez E. Houy-Durand S. Romana V. Malan F. Bonnet-Brilhault

72 Cord-Blood Based Methylome-Wide Association Study of the Social and Communication Disorders Checklist
A. T. Massrali H. Brunel S. Baron-Cohen V. Warrier

73 Distinct Sources of Genetic Risk for Autism from Social and Non-Social Domains
V. Warrier N. The 23andMe Research Team N. iPSYCH-BROAD ASD Group T. Bourgeron S. Baron-Cohen

74 Epigenetic Alterations in Childhood Reflect Prenatal Exposure to Maternal Infection
M. Brucato S. Andrews Y. Qian G. C. Windham D. Schendel L. Schieve C. J. Newschaffer A. P. Feinberg L. A. Croen M. D. Fallin C. Ladd-Acosta

75 Evidence for Widespread Associations between Broadly Expressed Genes in Blood Leukocytes and Neural Systems Response to Speech in Autism
M. V. Lombardo T. Pramparo V. Gazestani L. Eyler K. Pierce E. Courchesne

76 FMR1 mRNA in Blood As a Predictor of Intellectual Functioning and Autism Severity in Fragile X Syndrome: Is There a Difference between Sexes?
E. K. Baker M. Arpone S. Aliaga L. Bretherton M. Bui C. Kraan A. Alliende V. Faundes L. Santa Maria C. Rogers M. Field D. Amor D. E. Godler

77 Genetic Investigation of Insistence on Sameness in Autism
M. L. Cuccaro S. Luzi E. R. Martin A. J. Griswold D. Dykxhoorn H. N. Cukier M. A. Pericak-Vance

78 Genetic, Molecular, and Phentoypic Characterization of the Autism-Associated FOXP1 Syndrome
J. Buxbaum S. De Rubeis M. P. Trelles R. Lozano A. Kolevzon E. Drapeau P. M. Siper A. R. Durkin D. Di Marino Y. Frank

79 High-Resolution View of Genetic Architecture Underlying Autism
E. Larsen W. Pereanu S. Banerjee-Basu

80 Identification of Autism Spectrum Disorder with Salivary RNA
S. D. Hicks M. Chroneos K. Wagner C. Tierney-Aves F. A. Middleton

81 Inherited and Multiple De Novo Mutations in Autism Risk Genes Suggests a Multifactorial Model
H. Guo T. Wang H. Wu M. Long B. P. Coe R. Bernier E. E. Eichler K. Xia

82 Linkage Analysis and Fine-Mapping in Autism Pedigrees Confirms and Refines Regions on Chromosomes 7 and 12
E. R. Martin S. Luzi L. Gomez P. Whitehead J. Jaworski A. J. Griswold M. L. Cuccaro M. A. Pericak-Vance

83 microRNAs and Gene-Environment Interactions in Autism: Prenatal Maternal Stress and the SERT Gene
D. Q. Beversdorf A. Shah J. Noel-MacDonnell P. Hecht B. J. Ferguson Z. Talebizadeh

84 Modifiers of Severity in Autism Spectrum Disorder
S. P. Smieszek R. Igo J. Haines

85 Monogenic Disorders Associated with ASD in a Large Portuguese Sample
F. Duque J. Rosmaninho-Salgado C. Café S. Mouga D. Sousa A. Oliveira S. Ferreira P. Maciel I. Carreira A. M. Vicente G. Oliveira

86 Patient and Provider Factors Influence Completion Rates of Genetic Testing for Autism Spectrum Disorders
N. Abreu M. Chiujdea N. Huntington S. J. Spence

87 Protecting DNA: Shortened Telomere Length Is Associated with Autism Spectrum Disorder
B. B. Braden C. R. Lewis K. Agrawal S. Ringenbach M. Huentelman

Quantification of Genetic Risk of ASD for a Planned Child Based on the Genomes of Its Parents (Withdrawn)
S. S. Bittker

89 Rare Copy Number Variation As Predictors for Treatment Response to Social Skills Training in Children with Autism Spectrum Disorder
K. Tammimies I. Rabkina D. Li S. Stamouli M. Becker S. Berggren U. Jonsson N. Choque Olsson S. Bolte

90 SPARK (Simons Foundation Powering Autism Research for Knowledge): A US Cohort of 50,000 Families to Accelerate Autism Research
P. Feliciano L. Grosvenor A. Daniels W. K. Chung L. A. Green Snyder H. Zaydens

91 The Australian Autism Biobank: A National Initiative to Accelerate ASD Discovery Research
G. A. Alvares C. Dissanayake V. Eapen H. Heussler F. J. Rose A. J. Whitehouse

92 The Autism Speaks Mssng Whole Genome Sequencing Resource
S. Walker R. K. Yuen D. Merico M. Bookman J. Howe B. Thiruvahindrapuram R. V. Patel J. Whitney N. Deflaux J. Bingham Z. Wang G. Pellecchia J. A. Buchanan C. Marshall N. Hoang S. L. Pereira T. Paton W. Van Etten M. Szego L. J. Strug B. Fernandez L. Zwaigenbaum B. M. Knoppers E. Anagnostou P. Szatmari W. Roberts R. H. Ring D. Glazer T. W. Frazier S. W. Scherer

93 The Clinical Relevance of Intragenic NRXN1 Deletions
N. Cosemans L. Vandenhove S. Shen J. Fitzgerald L. Gallagher H. Peeters

94 To Test or NOT to Test? Fragile X Premutation Analysis in Minors- Ethical and Medical Dilemmas and Considerations
L. V. Gabis A. Raas-Rothschild

95 Translating the Complex ASD Genetic Architecture into Clinical Phenotype Using an Integrative System Biology Approach
M. Asif H. Martiniano C. Rasga A. R. Marques J. Santos G. Oliveira F. M. Couto A. M. Vicente