Page 220 - ASHG 2012 Annual Meeting Program Guide

POSTER SESSIONS
209
POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
Psychiatric Genetics, Neurogenetics
and Neurodegeneration
2370
W Genetic association analysis between glycine
cleavage system and schizophrenia.
A. Yoshikawa,
F. Nishimura, H. Hibino, K. Kohda, M. Tochigi, Y. Kawamura,
T. Umekage, T. Sasaki, K. Kasai, C. Kakiuchi.
2371
T A gene search for a new spinocerebellar ataxia.
K. Ishikawa, N. Sato, Y. Hashimoto, M. Obayashi,
H. Matsuo, H. Mizusawa.
2372
F Combining genotype and gene expression data to
unravel the genetics of major depressive disorder.
S. Mostafavi, A. Battle, X. Zhu, S. Montgomery, J. B. Potash,
M. M. Weissman, C. Haudenschild, C. McCormick, K. B.
Beckman, R. Mei, A. Urban, D. Koller, D. F. Levinson.
2373
W Transcript profile analysis of interleukin-1
beta gene in immature and adult zebrafish brain after
seizure.
P. G. Barbalho, F. R. Pinto, R. Mangolin, C. V.
Maurer-Morelli.
2374
T An integrative analysis pinpoints the pathogenesis
of autism in the cerebellar vermis.
D.-A. Clevert,
S. Hochreiter.
2375
F Common genetic variants in the
GNB3, ARNTL
,
and
NPAS2
loci are associated with objectively
measured sleep traits in the elderly.
D. S. Evans,
N. Parimi, C. M. Nievergelt, K. L. Stone, T. Blackwell, S.
Redline, S. Ancoli-Israel, E. S. Orwoll, S. R. Cummings,
G. J. Tranah, Study of Osteoporotic Fractures and
Osteoporotic Fractures in Men Study Groups.
2376
W GWAS of alcohol abuse and dependence in the
CATIE schizophrenia sample.
V. F. Gonçalves, C. Zai, A.
Paterson, L. Sun, J. L. Kennedy, J. Knight.
2377
T Familial study of essential tremor at Columbia
University.
N. Hernandez, D. Tirri, L. Clark, E. Louis.
2378
F Significant linkage of familial essential tremor to
a novel locus on chromosome 5.
J. E. Hicks, I. Konidari,
J. R. Gilbert, W. K. Scott.
2379
W Autism and obesity: Is there any mechanistic
connection?
Z. Talebizadeh, M. Miralles.
2380
T Haplotypes in the expression quantitative
trait locus of interleukin-1 gene are associated with
schizophrenia.
M. Yoshida, K. Shiroiwa, K. Mouri, T.
Sasada, H. Ishiguro, T. Inada, T. Arinami, O. Shirakawa, A.
Hishimoto.
2381
F Selection of candidate genes from linkage
regions identified by the individual behavioral domains
of autism spectrum disorders.
A. Hare, J. Flax, Z.
Fermano, M. Azaro, A. Seto, S. Y. Cheong, S. Buyske, B.
Zimmerman-Bier, C. W. Bartlett, L. M. Brzustowicz.
2382
W Association of Neuregulin 1 polymorphisms
with a North Indian schizophrenia cohort.
P. Kukshal,
T. Bhatia, A. M. Bhagwat, R. E. Gur, R. C. Gur, S. N.
Despande, V. L. Nimgaonkar, B. K. Thelma.
2383
T Single nucleotide polymorphism fine mapping of
the
AVPR1A
and
OXTR
loci reveals an
OXTR
association
with a social memory endophenotype in probands
with autism and their family members.
A. Lori, I. Lee,
J. F. Cubells, E. B. Binder, T. Lehtimäki, K. Puura, K. N.
Conneely, L. J. Young, D. Skuse.
2384
F The effects of
ABCB1
polymorphisms and
expression in perinatal depression.
S. E. Parets, A. Lori,
M. N. To, D. J. Newport, Z. N. Stowe, J. F. Cubells, A. K.
Smith.
2385
W
HMNC1
and
COMT
gene polymorphism
associated with postpartum depression.
M. Romano-Silva, D. M. Miranda, P. Figueira,
H. Correa, A. Alvim-Soares.
2386
T Disrupted in schizophrenia 1 gene in autist
patients.
P. Sarda, J. Puechberty, M. Girard, A. Schneider,
S. Taviaux, G. Lefort, D. Genevieve, A. Baghdadli.
2387
F Phenotypic description of a child with a
10
q23.1 deletion involving only
NRG3
.
N. Sobreira, D.
Avramopoulos, A. Pulver, B. Menten, B. Loeys, D. Valle.
2388
W Determination of a rare variant and common
variants in COMT for their involvement in the etiology
of smoking dependence using Mid-South Tobacco
Case-Control study samples.
J. Yang, S. Wang, J. Z. Ma,
T. J. Payne, M. D. Li.
2389
T Copy number variations and agenesis of
the corpus callosum, narrowing the recurrent 8p
duplication interval.
S. Esmaeeli Nieh, L. Fernandez, S.
Sajan, E. Rider, P. Bukshpun, M. Wakahiro, J. T. Glessner,
H. Hakonarson, S. L. Christian, W. B. Dobyns, E. H. Sherr.
2390
F Serotonin transporter and receptor genes
significantly impact nicotine dependence through
genetic interactions in both European American and
African American smokers.
Z. Yang, C. Seneviratne, S.
Wang, J. Z. Ma, T. J. Payne, J. Wang, M. D. Li.
2391
W Genetic association of
FKBP5
and
CRHR1
with cortisol response to acute psychosocial stress in
healthy adults.
P. B. Mahon, P. P. Zandi, J. B. Potash,
G. Nestadt, G. S. Wand.
2392
T Associations of genetic polymorphisms in
GRIN2B
and
GABRG2
with epilepsy susceptibility.
C.
Chen, C. Hung, Y. Kao, H. Liou.
2393
F Interpreting the impact of mutations in
SCN1A
in the context of the most severe phenotypes amongst
the generalized epilepsies with febrile seizures plus.
M. Gonsales, P. Preto, M. A. Montenegro, M. M. Guerreiro,
I. Lopes-Cendes.