International Meeting for Autism Research (London, May 15-17, 2008): Human Genetics Posters 1
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Human Genetics Posters 1

Thursday, May 15, 2008: 8:30 AM-1:00 PM
Champagne Terrace/Bordeaux (Novotel London West)
11:30 AM
105.01
17 The DLX1and DLX2 Genes and Susceptibility to Autism Spectrum Disorders
X. Liu, N. Novosedlik, M. Hudson, A. Wang, I. L. Cohen, A. Chudley, C. Forster-Gibson, S. M. Lewis and J. J. Holden
10:30 AM
105.02
18 Yield of Standard Genetic Testing in a Large Autism Diagnostic Clinic
P. Manning-Courtney and J. Ruschman
11:30 AM
105.03
19 BIOCHEMICAL AND GENETIC STUDIES OF THE MITOCHONDRIAL ASPARTATE/GLUTAMATE CARRIER AGC1
L. Palmieri, V. Papaleo, V. Porcelli, P. Scarcia, R. Sacco, J. Hager, F. Rousseau and A. M. Persico
11:30 AM
105.04
20 REELIN GENE EXPRESSION AND EPIGENETIC STATUS IN TEMPORAL CORTEX OF AUTISTIC BRAINS
C. Lintas, K. Garbett, K. Mirnics and A. M. Persico
10:30 AM
105.05
21 A genome-wide association study of autism
X. Q. Liu, A. P. Thompson, D. Pinto, J. Skaug, L. Zwaigenbaum, W. Roberts, S. W. Scherer, P. Szatmari and A. D. Paterson
10:30 AM
105.06
22 COGNITIVE AND BEHAVIORAL CHARACTERIZATION OF THE POTOCKI-LUPSKI SYNDROME
D. E. Treadwell-Deering, M. P. Powell, J. R. Lupski and L. Potocki
10:30 AM
105.07
23 Descriptive Analysis of 252 Twin Sets Recruited Through a National Online ASD Registry and Research Database
K. Law, A. R. Marvin, C. Anderson, C. Cohen and P. Law
11:30 AM
105.08
24 Human Cerebellar Malformations and Autism Share Susceptibility Loci
K. A. Aldinger, I. D. Krantz, W. B. Dobyns and K. J. Millen
10:30 AM
105.09
25 Replication and Association Analysis of a 1p13-q12 Locus for Nonverbal Communication Deficits in Autism Spectrum Disorder
J. L. Yoon, M. Alarcon, D. Geschwind and R. M. Cantor
10:30 AM
105.10
26 Detecting Cognitive Endophenotypes for Autism Using a General Population Twin Family Sample
R. A. Hoekstra, M. Bartels, G. F. Estourgie-van Burk, S. Baron-Cohen and D. I. Boomsma
10:30 AM
105.11
27 The relationship between molecular subtype and autism symptom severity in Angelman Syndrome
S. U. Peters, L. M. Bird, R. Barbieri-Welge, W. H. Tan, R. J. Hundley, S. Skinner, A. Bauer-Carlin, T. Sahoo and C. A. Bacino
10:30 AM
105.12
28 Differences in Clinical Presentation of Trisomy 21 with and without Autism
C. A. Molloy, D. S. Murray, H. Castillo, F. J. Hickey, B. Patterson and A. Kinsman
11:30 AM
105.13
29 CADHERIN-11 as a possible candidate gene for autism
A. C. Crepel, H. Peeters, J. R. Vermeesch, J. Steyaert, D. Walleghem and K. Devriendt
11:30 AM
105.14
30 Association of MET with Autism Spectrum Disorder and Co-Occurring Gastrointestinal Symptoms
D. B. Campbell, T. M. Buie, H. S. Winter, M. Bauman, J. S. Sutcliffe, J. M. Perrin and P. Levitt
10:30 AM
105.15
31 GENOMIC COPY NUMBER AND PHENOTYPIC VARIABILITY OF THE AUTISM SPECTRUM DISORDERS
Y. Qiao, X. Liu, M. Koochek, N. Riendeau, P. Malenfant, C. Harvard, J. M. Hildebrand, J. J. Holden, E. Rajcan-Separovic and S. M. Lewis
10:30 AM
105.16
32 Rate of Chromosomal Anomalies in an Iranian Autism Sample
A. Tolouei, R. Sasanfar, S. Haddad, M. Houshmand, M. Rostami and S. L. Santangelo
11:30 AM
105.17
33 Expression and methylation of the serotonin transporter gene in lymphoblastoïde cell lines from autistic patients carrying different genotypes for 5–HTTLPR
P. Vourc'h, R. Tabagh, S. Védrine, C. Barthelemy, C. Moraine and C. R. Andres
11:30 AM
105.18
34 The Association of a MET Promoter Variant with Autism is Dependent on Disease Classification
P. B. Jackson, L. Boccuto, C. Skinner, J. S. Collins, R. E. Stevenson, G. Neri, F. Gurrieri and C. E. Schwartz
10:30 AM
105.19
35 Social behavior and autism traits in a sex chromosomal disorder: Klinefelter (47XXY) syndrome
S. Van Rijn, H. Swaab, A. Aleman and R. S. Kahn
11:30 AM
105.20
36 NLGN4X GENE OVEREXPRESSION IS ASSOCIATED WITH AUTISM AND PROFOUND MENTAL RETARDATION
H. Daoud, F. Bonnet-Brilhault, S. Védrine, P. Vourc'h, R. Tabagh, C. R. Andres, C. Barthelemy, P. Guérin, F. Laumonnier and S. Briault
11:30 AM
105.21
37 ASSOCIATION STUDY OF BRAIN-DERIVED NEUROTROPHIC FACTOR (BDNF) AND NEURAL CELL ADHESION MOLECULE (NRCAM) POLYMORPHISMS WITH FRENCH AUTISTIC PATIENTS
F. Zaidi, P. Gorwood, B. Golse, L. Robel and N. Ramoz
11:30 AM
105.22
38 Analysis of functional serotonin transporter polymorphisms in a German sample of patients with autism
S. M. Klauck, B. Felder, M. Urrutia Villavicencio, A. Benner, F. Poustka and A. Poustka
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