Page 186 - ASHG 2013 Program Guide

POSTER SESSIONS
  173
POSTER SESSIONS
W=W
ednesday authors will present; T=Thursday authors will present; F=Friday authors will pr
esent
1422
T Co-expression networks implicate human
mid-fetal deep cortical projection neurons in the
pathogenesis of autism.
A. J. Willsey, S. J. Sanders, M.
Li, S. Dong, A. T. Tebbenkamp, R. A. Muhle, S. K. Reilly, L.
Lin, S. Fertuzinhos, J. A. Miller, M. T. Murtha, C. Bichsel,
W. Niu, J. Cotney, A. G. Ercan-Sencicek, J. Gockley, W.
Han, X. He, L. Klei, J. Lei, L. Liu, C. Lu, X. Xu, E. S. Lein,
L. Wei, J. P. Noonan, K. Roeder, B. Devlin, N. Sestan, M.
W. State.
1423
F Genome-wide methylome and transcriptome
analyses reveal novel epigenetic regulation
patterns in schizophrenia and bipolar disorder.
C. Xu,
Y. Xiao, Y. Li, C. Camarillo, Y. Ping, J. Xu, T. Arana,
H. Zhao, P. Thompson, C. Xu, Z. Zhao, H. Chen, C. Mao,
Y. Zhang, B. Su, M. Escamilla, A. Ontiveros, H. Nicolini,
A. Jerez, X. Li.
1424
W Neuronal cellular models of 22q11.2 DS exhibit
disruptions to the miRNA regulatory pathway and may
increase the rate of schizophrenia in individuals with
22
q11.2 DS.
W. Manley, M. R. Ababon, M. P. Moreau,
P. G. Matteson, J. H. Millonig, L. M. Brzustowicz.
1425
T A case of monozygotic female triplets
diagnosed with autism: Comprehensive genomic
analyses.
Z. Talebizadeh, S. Soden, A. Gadashova.
1426
F Does presymptomatic testing changes age
at onset (PAON): A prospective study in Huntington
disease.
A. Durr, S. Tezenas du Montcel, M. F. Jutras,
C. Jauffret, S. Benaich, A. Herson, J. Feingold, M. Gargiulo.
1427
W Genome-wide expression changes in a higher
state of consciousness.
M. Ravnik-Glavac, S. Hrasovec,
J. Bon, J. Dreo, D. Glavac.
1428
T Differences in gene expression and DNA
methylation in drug-naïve first-episode psychosis
patients.
V. K. Ota, C. S. Noto, A. Gadelha, M. L. Santoro,
B. B. Ortiz, R. S. Stilhano, E. S. Gouvea, P. N. Silva,
C. G. Olmos, L. M. N. Spindola, E. H. S. Andrade, M. I.
Melaragno, M. A. C. Smith, S. W. Han, Q. Cordeiro, R. A.
Bressan, S. I. Belangero.
1429
F Investigating the role of the histidine
decarboxylase gene in Tourette syndrome etiology.
I. Karagiannidis, H. Potamianou, G. Heiman, L. Deng,
J. Xing, N. Sun, C. Nasello, P. Sandor, C. Barr, P. Paschou.
1430
W Identification of target genes for the
language-related FOXP2 and its isoform.
T. Ohta,
N. Niikawa, T. Oikawa.
Bioinformatics and Genomic
Technology
1431
W Reference-free quality assessment and
complexity estimation of next-generation sequencing
data.
S. Y. Anvar, L. Khachatryan, M. Vermaat, M. van
Galen, I. Pulyakhina, Y. Ariyurek, K. Kraaijeveld, P. A.
C. ‘t Hoen, J. T. den Dunnen, P. de Knijff, J. F. J. Laros.
1410
T Detailed audiological evaluation of a
patient with xeroderma pigmentosum with neural
degeneration.
D. Mercer, F. Tsien, A. Hurley.
1411
F Characterizing the aging human brain
transcriptome.
N. Pochet, D. Borges-Rivera, B. Haas,
S. Rajagopal, J. Xu, C. McCabe, O. Gevaert, G. Srivastava,
A. Regev, J. Schneider, D. Bennett, P. De Jager.
1412
W Mucolipidosis type IV: Progressive gliosis,
synaptic dysfunction and cognitive deficits in Mcoln1
knockout mouse.
Y. Grishchuk, S. Sri, W. Ma, N.
Rudinskiy, M. Cottle, K. Stember, E. Sapp, A. Muzikansky,
M. Difiglia, R. Betensky, B. Hyman, R. Kelleher, J. Cooper,
S. Slaugenhaupt.
1413
T Identifying novel candidate genes for
neurological diseases.
K. Summers.
1414
F The genetic architecture of schizophrenia: How
do CNVs and polygenic scores contribute to disease
risk?
S. E. Bergen, J. W. Smoller, J. Sebat, S. Purcell,
B. Neale, K. S. Kendler, ISC, Swedish Schizophrenia
Consortium, Psychiatric Genomics Consortium CNV and
Schizophrenia Groups.
1415
W Copy number variants implicated in autism
spectrum disorder among individuals of Hispanic
ethnicity.
N. Dueker, A. J. Griswold, H. N. Cukier, J.
Jaworski, Y. N. Park, S. Slifer, I. Konidari, P. L. Whitehead,
M. Schmidt, J. R. Gilbert, J. L. Haines, M. L. Cuccaro, E.
R. Martin, M. A. Pericak-Vance.
1416
T High resolution copy number variation analysis
in monozygotic twins discordant for schizophrenia and
delusional disorder.
F. Nishimura, A. Yoshikawa, T. Kato,
T. Sasaki, K. Kasai, C. Kakiuchi.
1417
F Characterization of age-related expression of
the interleukin-1beta gene in immature zebrafish brain
after pentylenetetrazole- evoked seizures.
P. Barbalho,
D. Nakata, C. Maurer-Morelli.
1418
W A corrective gene silencing by RNA interference
to control over-expressed
SNCA
.
M. Takahashi, M.
Suzuki, N. Fujikake, M. Murata, K. Wada, Y. Nagai, H.
Hohjoh.
1419
T Partitioning the heritability of Tourette syndrome
and obsessive compulsive disorder reveals differences
in genetic architecture.
L. Davis, on behalf of Tourette
Syndrome Association International Consortium for
Genetics (TSAICG).
1420
F Association of
DLG4
haplotype with
increased risk of schizophrenia.
S. Balan, K. Yamada,
E. Hattori, Y. Iwayama, T. Toyota, T. Ohnishi, M. Maekawa,
M. Toyoshima, Y. Iwata, K. Suzuki, M. Kikuchi,
T. Yoshikawa.
1421
W
MGluR
gene network alterations confer risk
for autism spectrum disorder in 22q11.2 deletion
syndrome.
T. L. Wenger, C. Kao, D. M. McDonald-
McGinn, A. Bailey, R. T. Schultz, B. S. Emanuel, B. E.
Morrow, E. H. Zackai, H. Hakonarson.