International Meeting for Autism Research (London, May 15-17, 2008): Human Genetics Posters 2

Human Genetics Posters 2

Friday, May 16, 2008: 8:30 AM-1:00 PM
Champagne Terrace/Bordeaux (Novotel London West)
10:30 AM
11:30 AM
35 Genes Analysed for Association with Autism and DBH Level
L. E. Cochrane, J. Conroy, K. Tansey, M. Gill, R. Anney and L. Gallagher
11:30 AM
36 IMMUNO PROFILE IN FRAGILE X AND AUTISM
F. Tassone, P. Ashwood, R. Hagerman and D. Nguyen
11:30 AM
37 A new candidate gene for autism suggested by the co-occurrence of a deletion and a mutation in a child with autism
J. A. S. Vorstman, E. Van Daalen, G. R. Jalali, W. G. Staal, B. van der Zwaag, P. Burbach, R. Ophoff, R. S. Kahn, B. S. Emanuel and H. Engeland
10:30 AM
39 ASSOCIATION OF COPY NUMBER VARIANTS IN THE ASMT GENE WITH AUTISM
G. Cai, A. Nakamine, J. G. Reichert, J. M. Silverman, C. Betancur and J. D. Buxbaum
11:30 AM
40 Developmental regression and GABA receptor genes in multiple racial-ethnic groups
M. L. Cuccaro, D. Ma, E. R. Martin, J. R. Gilbert, J. Jaworski, R. K. Abramson, H. H. Wright and M. A. Pericak-Vance
11:30 AM
41 A submicroscopic 5q11.2 deletion in a child with autism, mild mental retardation and mild facial dysmorphism
H. Peeters, A. C. Crepel, K. Devriendt, P. De Cock, J. R. Vermeesch and J. P. Fryns
11:30 AM
42 Autism sibling pair discordant for 22q11 microdeletion
S. Guter, J. Salt and E. H. Cook
11:30 AM
44 Serotonin Related Genes in Autism
J. Haines, B. M. Anderson, N. Schnetz-Boutaud, M. L. Summar, J. Bartlett, M. L. Cuccaro, J. R. Gilbert and M. A. Pericak-Vance
11:30 AM
45 Rare Mutation Burden of the Contactin Pathway in Autism Spectrum Disorders
B. J. O'Roak, B. Bakkaloglu, A. Louvi, C. Mason, A. R. Gupta, N. R. Davis, T. M. Morgan, M. T. Murtha, A. G. Ercan-Sencicek and M. W. State
10:30 AM
46 Genomic Imprinting of the X-Linked Gene Transketolase-like 1 in Mouse and Human
A. M. I. Nesbitt, M. J. O'Neill and J. J. LoTurco
11:30 AM
47 Peripheral Blood Gene Expression Profiling of Autism Spectrum Disorders
C. D. Collins, S. W. Kong, M. Galdzicki, D. Stephan, H. Peters, S. J. Brewster, I. A. Holm, R. J. Hundley, E. M. Hanson, L. A. Rappaport, L. M. Kunkel and I. S. Kohane
11:30 AM
48 The STX1A, CYLN2, and GTF2i genes in autism-associated 7q11.2 microduplication syndrome as candidate genes for Autism Spectrum Disorders
P. Malenfant, X. Liu, M. Hudson, Y. Qiao, J. M. Hildebrand, I. L. Cohen, A. Chudley, C. Forster-Gibson, S. M. Lewis, E. Rajcan-Separovic and J. J. A. Holden
10:30 AM
49 Analysis of Copy Number Variation within GABRA4
H. N. Cukier, M. Y. Rayner, D. Ma, H. H. Wright, R. K. Abramson, J. P. Hussman, J. Haines, M. L. Cuccaro, D. L. Hedges, J. R. Gilbert and M. A. Pericak-Vance
10:30 AM
50 Chromosome 17q21.31 Microdeletion in a Patient with Autism
D. Moreno De Luca, A. Gennetier, F. Devillard, V. Ginchat, B. Assouline, C. Gillberg, M. Leboyer and C. Betancur
10:30 AM
51 Autism open biological resource of Fondation Autisme
M. Ferguson, C. Stranieri and S. Briault
11:30 AM
54 Network oriented variant analysis of the serotonin transporter regulome
N. G. Campbell, E. Crawford, R. Game, R. D. Blakely and J. S. Sutcliffe
10:30 AM
55 HLA-DR4 as a Risk Allele for Autism, Acting in Mothers of Probands During Pregnancy
W. G. Johnson, S. Buyske, A. E. Mars, M. Sreenath, E. S. Stenroos, R. Stein and G. Lambert
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