Page 170 - ASHG 2013 Program Guide

POSTER SESSIONS
  157
POSTER SESSIONS
W=W
ednesday authors will present; T=Thursday authors will present; F=Friday authors will pr
esent
1052
F Association analysis of candidate gene
polymorphisms in asthma, rhinitis and chronic
bronchitis: Preliminary results from the GEIRD study.
C. Bombieri, F. Belpinati, A. Baldan, A. R. Lo Presti, G.
Malerba, S. Accordini, L. Calciano, M. Ferrari, l. Perbellini,
P. F. Pignatti, R. De Marco.
1053
W Extending the population spectrum for
nonsyndromic orofacial clefting: Recruitment and genetic
analyses in an Arabian population from Yemen.
K. U.
Ludwig, K. Aldurai, A. C. Boehmer, B. Lippke, N. Daratsianos,
M. M. Noethen, A. Jaeger, M. Knapp, E. Mangold.
1054
T Further evidence suggesting a role for variation
in
ARHGAP29
in nonsyndromic cleft lip/palate.
L. Maili,
A. Letra, J. B. Mulliken, S. Slifer, S. H. Blanton, J. T. Hecht.
1055
F Association of
GABRG2
rs211307 polymorphism
with susceptibility to epilepsy in Asians: A multicentre
case control study and meta-analysis.
B. S. Haerian, L.
Baum, P. Kwan, S. S. Cherney, H. J. Tan, A. A. Raymond,
Z. Mohamed.
1056
W Myosin light chain kinase gene associates with
asthma in Spanish and Latino populations.
M. Acosta-
Herrera, M. Pino-Yanes, A. Corrales, A. Barreto-Luis, J.
Cumplido, E. Perez-Rodriguez, P. Campo, C. Eng, J. C.
Robaina, I. Machin, I. Quintela, J. Villar, M. Blanca, A.
Carracedo, T. Carrillo, J. G. Garcia, E. G. Burchard, S. F.
Ma, C. Flores.
1057
T
APOE
e2 homozygous individuals are
underrepresented among elderly Brazilian population.
M. S. Naslavsky, M. L. Lebrao, Y. A. O. Duarte, E. Amaro,
Jr., T. A. B. Mendes, A. S. Rodrigues, G. Bandeira, D.
Schlesinger, L. T. Grinberg, C. K. Suemoto, R. E. P. Leite,
R. E. L. Ferretti, C. A. Pasqualucci, J. M. Farfel, R. Nitrini,
W. Jacob Filho, M. Zatz.
1058
F GWAS-nominated variants in homogeneous
asthma sub-phenotypes.
E. Lavoie-Charland, J.-C.
Bérubé, M. Laviolette, L.-P. Boulet, Y. Bossé.
1059
W Genetic profiles of lipid-associated
polymorphisms for lipid-related traits for addressing
constitution-based discrepancy in Koreans.
S. Cha, S.
K. Chung, H. Yu, A. Y. Park, J. Y. Kim.
1060
T Pleiotropic effects of three SLE-associated
functional variants within
IFIH1
linked to several
autoimmune diseases.
J. E. Molineros, S. K. Nath.
1061
F Are genes previously associated with
schizophrenia also predictive of dimension-specifi
psychotic experiences in adolescence?
D. Sieradzka, R.
A. Power, F. Dudbridge, E. L. Meaburn, R. Plomin, A. Ronald.
1062
W Association of
GALNT10
genetic variants with
adiposity in African Americans.
M. E. Stromberg, J. M.
Hester, P. Mudgal, J. Li, P. J. Hicks, B. I. Freedman, D. W.
Bowden, M. C. Y. Ng.
1063
T Investigation of the rs2157719 SNP in the
CDKN2B-AS1
gene in a primary open-angle glaucoma
Brazilian population.
H. F. Nunes, J. P. C. Vasconcellos, V.
P. Costa, N. I. T. Zanchin, M. B. Melo.
1041
W Genetics of the sphingolipid metabolism in
hypertension.
M. Fenger, A. Linneberg, J. Jeppesen.
1042
T Characterization of gene expression biomarker
signatures for use as an Alopecia Areata Disease
Activity Index (ALADIN).
J. E. Cerise, A. Jabbari,
J. C. Chen, M. Duvic, M. Hordinsky, D. Norris, V. Price,
J. Mackay-Wiggan, R. Clynes, A. M. Christiano.
1043
F Psoriasis susceptibility genes in patient with
severe compared with mild phenotype.
P. Nikamo,
M. Ståhle.
1044
W Validating trans-eQTLs using evidence of
cis-mediation: a genome-wide analysis among
1,800
South Asians.
B. Pierce, L. Tong, R. Rahaman,
L. Chen, M. Kibriya, M. Argos, J. Farzana, R. Shantanu,
R. Paul-Brutus, R. Zaman, M. Rahman, J. Baron,
H. Ahsan.
1045
T Transcriptome analysis of CD4
1
lymphocytes in
asthmatics with or without depression.
J. He, T. Wang,
Z. Liang, X. Xiong, Y. Yang, Y. Ji.
1046
F Genetic variation in the ER stress response
network in the mouse.
C. Y. Chow, D. D. Riccardi, X.
Wang, M. F. Wolfner, A. G. Clark.
1047
W Global metabolite profiling and the risk of
osteoporotic fractures: A systems biology approach
by integrating genomics and tissue-specific gene
expression profiling, p oteomics and metabolomics
in postmenopausal Caucasian women.
Y.-H. Hsu,
S. Reppe, C.-L. Chi, D. Karasik, J. Brain, D. P. Kiel, K.
Gautvik.
1048
T Integrating genome-wide association data with
a protein-protein interaction network to define ch onic
obstructive pulmonary disease gene modules.
M.-L.
N. McDonald, M. Cho, M. Matthiesen, B. Harshfield, T. H.
Beaty, C. P. Hersh, C. Lange, E. K. Silverman, on behalf of
COPDGene Investigators.
1049
F Hypothesis independent pathway analysis
identifies biologic pathways influencing susceptibilit
to glaucoma.
J. L. Wiggs, J. N. Cooke Bailey, L. R.
Pasquale, S. J. Loomis, J. H. Kang, B. Yaspan, M.
Brilliant, W. Christen, J. H. Fingert, D. Gaasterland, T.
Gaasterland, R. K. Lee, P. R. Lichter, Y. Liu, S. E. Moroi,
L. M. Olson, J. E. Richards, J. S. Schuman, W. K. Scott,
K. Singh, A. Sit, D. Vollrath, G. Wollstein, D. J. Zack,
K. Zhang, R. R. Alllingham, M. A. Pericak-Vance, R. N.
Weinreb, M. A. Hauser, J. L. Haines, NEIGHBORHOOD
Consortium.
1050
W Gene expression profile of synovial flui
following meniscal injury: Osteoarthritis markers
found.
D. D. Vance, L. Wang, E. Rampersaud, T.
Guettouche, B. P. Lesniak, J. M. Vance, M. A. Pericak-
Vance, L. D. Kaplan.
1051
T Genetic association study of adaptor protein
complex 4 with cerebral palsy in Han Chinese
population.
Q. Xing, H. Wang, T. Li, M. Chen, Q. Shang,
D. Zhu, L. Wang, Q. Li, L. He, C. Zhu.