Page 176 - ASHG 2013 Program Guide

POSTER SESSIONS
  163
POSTER SESSIONS
W=W
ednesday authors will present; T=Thursday authors will present; F=Friday authors will pr
esent
1192
F
TRPM8
variants that protect from migraine
make individuals less susceptible to cold pain.
M.
A. Kaunisto, E. J. Holmström, V. Anttila, M. Kallela, E.
Hämäläinen, A. Stubhaug, M. Wessman, C. S. Nielsen, E.
Kalso, A. Palotie.
1193
W The role of
CNTNAP2
in a developmental
language disorder and potential mechanisms.
N. Li,
S. L. Wolock, S. A. Petrill, J. F. Flax, A. S. Bassett, L. M.
Brzustowicz, C. W. Bartlett.
1194
T Association of language impairment with
language, reading, and ADHD candidate genes.
S.
Smith, J. Gayan, M. Rice.
1195
F Molecular delineation of the 1p36.3 locus and
candidate gene resequencing in 363 patients with
polymicrogyria.
S. Beijnsberger, G. L. Carvill, S. F.
Berkovic, I. E. Scheffer, W. B. Dobyns, H. C. Mefford.
1196
W Application of customized CGH-array for
mGluR genes in attention deficit/hyperactivity diso der.
R. Pellegrino, C. Kao, L. Vazquez, D. Hadley, A. Kini,
J. Glessner, H. Hakonarson.
1197
T
FOXG1
is implicated in abnormal brain
development in two unrelated cases with 14q
aberrations.
G. Macintyre, K. Schlade-Bartusiak, M. L.
Martínez-Fernández, M. L. Martinez-Frías, R. Arteaga,
P. O’Brien, M. A. Ferguson-Smith, D. W. Cox.
1198
F Uncovering obsessive-compulsive disorder
risk genes using a high-resolution genome-wide CNV
approach.
M. J. Gazzellone, S. M. Shaheen, B. Li, R. J.
Schachar, A. C. Lionel, B. Thiruvahindrapduram, M. Uddin,
K. D. Fitzgerald, C. R. Marshall, D. R. Rosenberg, N.
Soreni, G. L. Hanna, P. D. Arnold, S. W. Scherer.
1199
W Family structure is predictive of genetic
architecture in autism spectrum disorders.
K. Schmitz-
Abe, M. Chahrour, T. Yu, S. Hill, G. Sanchez-Schmitz, J.
Partlow, B. Barry, B. Mehta, S. Servattalab, A. Ngoc Lam,
C. Walsh, K. Markianos.
1200
T Susceptibility loci for pigmentation and
melanoma in relation to Parkinson’s disease.
J. Dong,
J. Gao, M. Nalls, X. Gao, X. Huang, J. Han, A. Singleton,
Intl. Parkinson’s Dis. Genomics Consortium, H. Chen.
1201
F Genetic risk factors in Utah pedigrees at
high risk for suicide.
H. Coon, R. Pimentel, K. R. Smith,
C. Huff, H. Hu, L. Jerominski, J. Hansen, M. Klein, W. B.
Callor, J. Byrd, A. Bakian, S. Crowell, W. M. McMahon,
E. McGlade, D. Yurgelun-Todd, P. Renshaw, T. Grey,
D. Gray.
1202
W Association study of BDNF with completed
suicide in the Japanese population.
A. Hishimoto,
W. Ratta-apha, K. Shiroiwa, I. Sora.
1203
T Rare and common variants near
CHRNB3-
CHRNA6
are associated with cocaine dependence.
B. Sadler, G. Haller, N. Saccone, L. Bierut, A. Goate,
Study of Addiction, Genetics and Environment (SAGE)
Collaborators.
Psychiatric Genetics, Neurogenetics
and Neurodegeneration
1181
W AutDB: A modular database for accelerating
ASD genetic research.
E. Larsen, U. Kuppuswamy,
S. Banerjee-Basu.
1182
T General financial risk factors for risk and
ambiguity associated respectively with dopamine D4
receptor (
DRD4
)
and serotonin transporter (5-HTTLPR).
R. P. Ebstein, M. Monakhov, S. H. Chew.
1183
F A molecular genetic study of amyotrophic
lateral sclerosis/parkinsonism-dementia complex in
Kii Peninsula of Japan.
H. Ishiura, Y. Fukuda, B. Ahsan,
J. Mitsui, Y. Kokubo, S. Kuzuhara, S. Yoshida, T. Kihira,
J. Yoshimura, K. Doi, K. Higasa, S. Morishita, A. Toyoda, A.
Fujiyama, R. Kuwano, K. Hara, M. Nishizawa, J. Goto, S. Tsuji.
1184
W HLA-DQB1*03:02 is associated with narcolepsy
in the Japanese population.
T. Miyagawa, H. Toyoda,
A. Hirataka, S. S. Khor, M. Yamasaki, Y. Honda, M. Honda,
K. Tokunaga.
1185
T Association between the dopamine D4 receptor
(
DRD4
)
and political ideology in a large Singapore Han
Chinese sample.
M. Monakhov, S. H. Chew, R. P. Ebstein.
1186
F An approach to complex disease modifier genes
and mouse-to-human translation: Transcriptome
analysis of mouse strains reveals Alzheimer disease
modifier gene
T. Morihara, N. Hayashi, H. Akatsu,
M. Silverman, M. Yokokoji, N. Kimura, M. Sato, K. Kamino,
Y. Yamagichi, T. Tsunoda, T. Tanaka, M. Takeda.
1187
W Expression of neurotransmitter receptors and
regulators genes in peripheral blood of a drug-naïve
first-episode psychosis sample befo e and after
antipsychotic treatment.
M. L. Santoro, V. K. Ota, C. S.
Noto, A. Gadelha, P. N. Silva, M. I. Melaragno, M. A. C.
Smith, Q. Cordeiro, R. A. Bressan, S. I. Belangero.
1188
T The cerebral glucose transporter
SLC45A1
is
mutated in individuals with non-syndromic intellectual
disability and epilepsy.
M. Srour, N. Shimokawa, F. F.
Hamdan, S. Dobrzeniecka, G. A. Rouleau, C. Poulin,
J. L. Michaud.
1189
F Adducin function is essential for sustained
changes in neuronal activity upon learning.
V. Vukojevic,
F. Peter, P. Demougin, N. Hadziselimovic, J.-F. de
Quervain, A. Papassotiropoulos, A. Stetak.
1190
W Influence of Alzheimer s disease genes on
cognitive decline: The Guangzhou Biobank Cohort
Study.
S. S. Cherny, H. S. Gui, L. Xu, P. C. Sham, C. Q.
Jiang, T. H. Lam, B. Liu, Y. L. Jin, T. Zhu, W. S. Zhang, G.
N. Thomas, K. K. Cheng.
1191
T Fine mapping and association analysis of
candidate genes for autism spectrum disorder and
language impairment in the NJLAGS sample.
A. Hare, A.
Seto, J. Flax, M. Azaro, S. Buyske, C. Bartlett, L. Brzustowicz.