Page 84 - ASHG 2012 Annual Meeting Program Guide

INVITED AND PLATFORM SESSIONS
73
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INVITED AND PLATFORM SESSIONS
SESSION 11 – Genetics of Autism Spectrum Disorders
Hall D, Lower Level North, Moscone Center
Moderators
:
Fuki M. Hisama, Univ. of Washington; Dan
E. Arking, Johns Hopkins Sch. of Med.
7
/10:30
Genetic epidemiology of autism spectrum
disorder in a cohort of over 11,000 affected
sibships and half-sibships: Evidence of genetic and
maternal environmental effects.
N. Risch, T. J.
Hoffmann, M. Anderson, L. A. Croen, J. Grether, G.
Windham.
8
/10:45
Identifying inherited autism mutations using
whole exome sequencing.
T. W. Yu, M. H. Chahrour,
M. E. Coulter, S. Jiralerspong, K. Okamura-Ikeda, K.
Schmitz-Abe, G. H. Mochida, J. N. Partlow, R. S. Hill,
M. Al-Saffar, N. M. Mukaddes, A. Hashmi, S. Balkhy,
G. G. Gascon, O. Oner, S. Al-Saad, T. Ben-Omran, L.
Al-Gazali, V. Eapen, C. Stevens, S. Gabriel, K.
Markianos, H. Taniguchi, N. E. Braverman, E. M.
Morrow, C. A. Walsh.
9
/11:00
Identical by descent filtering in extended
families reveals novel autism genes detected by
exome sequencing.
H. N. Cukier, N. D. Dueker, S. H.
Slifer, J. M. Lee, P. L. Whitehead, E. Lalanne, N. Leyva,
I. Konidari, R. C. Gentry, W. F. Hulme, D. Van Booven,
D. J. Hedges, V. Mayo, S. S. Ramsook, B. A.
Barrionuevo, J. M. Jaworski, M. A. Schmidt, J. L.
Haines, M. L. Cuccaro, J. R. Gilbert, M. A. Pericak-
Vance.
10
/11:15
The discovery and validation of genes
recurrently disrupted in autism spectrum disorders.
B. J. O’Roak, L. Vives, A. Kumar, I. B. Stanaway, J.
Egertson, E. Turner, C. Lee, G. L. Carvil, I. G. Phelps,
D. R. O’Day, W. Fu, J. Hiatt, B. Martin, N. Krumm, B.
P. Coe, R. Levy, E. Borenstein, D. A. Nickerson, H. C.
Mefford, D. Doherty, J. M. Akey, R. Bernier, E. E.
Eichler, J. A. Shendure.
11
/11:30
Rare complete human knockouts:
Population distribution and significant role in
autism spectrum disorders.
E. T. Lim, M. J. Daly,
ARRA Autism Sequencing Consortium.
12
/11:45
Exome-based discovery of CNVs in
simplex autism families.
N. Krumm, B. Nelson, S.
Girirajan, M. Dennis, C. Baker, M. Malig, NHLBI Exome
Sequencing Project, A. Quinlan, D. A. Nickerson, E. E.
Eichler.
13
/12:00
Delta catenin (
CTNND2
):
Genetics and
function of a novel autism gene.
T . Turner, E. Oh, Y.
Liu, M. X. Sosa, S. Sanders, K. Sharma, D. Moreno-
De-Luca, T. Plona, K. Pike, D. Soppet, M. W. Smith,
M. State, S. W. Cheung, C. Lese Martin, R. Huganir, E.
Cook, N. Katsanis, A. Chakravarti.
14
/12:15
Novel hotspots of recurrent copy number
variation associated with autism spectrum disorder.
S. Girirajan, M. Y. Dennis, C. Baker, M. M. Malig, B. P.
Coe, C. D. Campbell, K. Mark, T. Vu, C. Alkan, Z.
Cheng, R. Bernier, E. E. Eichler.
15
/12:30
Cluster analysis defines subgroups of
phenotypic expression for autism spectrum
disorders.
O. J. Veatch, B. Yaspan, N. Schnetz-
Boutaud, M. A. Pericak-Vance, J. L. Haines.
Wednesday, November 7
10:30
AM
–12:45
PM
Concurrent Platform (abstract-driven)
Session A (11-19)