Page 197 - ASHG 2013 Program Guide

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POSTER SESSIONS
W=W
ednesday authors will present; T=Thursday authors will present; F=Friday authors will pr
esent
1710
T Should we account for the random effect of
relatedness when using principal component analysis
in GWAS?
M. de Andrade, J. P. Soler.
1711
F Genome-wide association study of ventricular
fibrillation in the setting of acute myoca dial infarction.
R. Pazoki, J. S. S. G. de Jong, M. E. Adriaens, N.
Bruinsma, L. R. C. Dekker, L. Beekman, A. A. M. Wilde,
M. W. Tanck, C. R. Bezzina.
1712
W Genetic determinants of plasma levels of
vitamin D binding protein in U.S. black women.
E. A.
Ruiz-Narvaez, L. Rosenberg, S. A. Haddad, J. R. Palmer.
1713
T Bayesian polygenic risk prediction using
summary statistics.
B. J. Vilhjalmsson, J. Yang, S.
Lindstrom, A. Gusev, S. Ripke, N. Patsopoulos, R. Do,
E. Stahl, B. Pasaniuc, S. Pollack, N. Zaitlen, H.-H. Won,
S. Kathiresan, M. E. Goddard, N. Wray, P. L. De Jager,
M. Daly, P. M. Visscher, P. Kraft, N. Patterson, A. L. Price.
1714
F Genetic variations in telomere-maintaining
genes and adult-onset cancers.
S. Hwang, J. M.
Murabito, A. P. Reiner, A. Aviv, D. Levy.
1715
W Genetic analysis of
TOMM40
and
APOE
for the
onset of dementia in the Honolulu-Asia Aging Study.
M. W. Lutz, D. Goldgaber, D. K. Burns, A. M. Saunders,
L. R. White, A. D. Roses.
1716
T Molecular screening of
CFTR
gene mutations
in North Indian asthmatic children: A case-control
study.
P. Dixit, S. Awasthi, N. Maurya, S. Agarwal,
M. Srinivasan.
1717
F The association of
HLA-DQB1
alleles with
nonalcoholic fatty liver disease in Turkish population.
S. Katrinli, L. Doganay, Y. Colak, E. Senates, O. Ozturk,
C. Ulasoglu, N. Karatas, I. Tuncer.
1718
W Genetic susceptibility of
FCER2
gene
variants with asthma and its severity in North Indian
children: A case-control study.
N. Sharma, S. Awasthi,
S. R. Phadke.
1719
T Significant association of perilipin
polymorphisms with LDL-cholesterol level.
I. Naka,
R. Kimura, T. Inaoka, Y. Matsumura, J. Ohashi.
1720
F Genetic risk models: Model size and confidence
intervals of the risk estimates.
Y. Shan, D. T. Smelser,
G. Tromp, H. Kuivaniemi, D. E. Weeks.
1721
W Genetic risk score modeling in age-related
macular degeneration.
J. N. Cooke Bailey, J. D. Hoffman,
L. M. Olson, W. Cade, N. Schnetz-Boutaud, P. Mayo,
M. Allen, A. Agarwal, M. A. Brantley, W. K. Scott, M. A.
Pericak-Vance, J. L. Haines.
1722
T Genetic variation at the
CY2C19
gene
associated with metabolic syndrome susceptibility in
a South Portuguese population.
V. Gaio, A. Fernandes,
F. Mendonça, F. Horta Correia, A. Beleza, A. Gil, M.
Bourbon, A. Vicente, C. Dias, M. Barreto da Silva.
1699
F A genome-wide assay for regulatory functional
potential of sequence variants.
J. M. Peralta, J.
Blangero, L. J. Abraham, E. Moses.
1700
W DeepSAGE reveals genetic variants associated
with alternative polyadenylation and expression of
coding and non-coding transcripts.
D. V. Zhernakova,
E. de Klerk, H.-J. Westra, A. Mastrokolias, S. Amini, Y.
Ariyurek, R. Jansen, B. W. Penninx, J. J. Hottenga, G.
Willemsen, E. J. de Geus, D. I. Boomsma, J. H. Veldink,
L. H. van den Berg, C. Wijmenga, J. T. den Dunnen, G.-J.
B. van Ommen, P. A. C. ‘t Hoen, L. Franke.
1701
T The association of urinary interferon inducible
protein-10 levels with kidney allograft rejection.
S. Firasat, A. Raza, A. Abid, T. Aziz, M. Mubarak, S. A. A.
Naqvi, S. A. H. Rizvi, S. Khaliq, S. Q. Mehdi.
1702
F A general statistic framework for identifying
genetic variants of clinical significance
L. Ma, M. Xiong.
1703
W The n
5
1
problem in human genetics:
Identification of ra e disease mutations from single
genomes.
A. B. Wilfert, J. N. Constantino, D. F. Conrad.
1704
T Meta-analysis of twelve genome-wide
association studies identifies novel genetic loci
associated with mammographic density phenotypes.
S. Lindström, D. Thompson, A. D. Paterson, J. Li, G. L.
Gierach, J. Stone, J. A. Douglas, I. dos Santos Silva, J.
Benitez, C. Scott, P. A. Fasching, L. Baglietto, M. Southey,
G. Giles, M. Pollan, J. Figueroa, F. J. Couch, J. L. Hopper,
P. Hall, D. F. Easton, N. F. Boyd, C. M. Vachon, R. M.
Tamimi, Markers of Density (MODE) Consortium.
1705
F Significant ole of combined alleles of hormonal
receptors and hepatocanalicular transporter gene
in susceptibility to cholesterol gallstone disease.
A. Srivastava, A. Mishra, B. Mittal.
1706
W Bivariate heritability analyses of cardiac
conduction and repolarisation measures show a paucity
of shared genetic influences
J. Alghamdi, C. Hastie, C.
Schulz, C. Brown, L. Hocking, M. Luciano, D. Porteous, A.
Morris, B. Smith, A. Dominiczak, S. Padmanabhan.
1707
T A signal of polygenic inheritance from low
frequency variants in case-control genome-wide
association studies elucidates genetic architecture of
common diseases.
Y. Chan, E. T. Lim, N. Sandholm, A. J.
McKnight, S. Ripke, M. J. Daly, B. M. Neale, R. M. Salem,
J. N. Hirschhorn.
1708
F Identification of 6 novel type 2 diabetes
susceptibility loci using genome-wide association
studies imputed from a 1000 Genomes (June 2012)
reference panel.
I. Prokopenko, C. Ma, A. P. Morris,
H. Chen, S. M. Willems, Q. Qi, K. J. Gaulton, M. Li, C.
Ladenvall, N. Van Zuydam, J. S. Ried, D. Thuillier, Y. Lu,
G. Thorleifsson, C. Fuchsberger, R. Mägi, L. J. Scott, on
behalf of DIAGRAM
1
Consortium.
1709
W Predictive genetic modeling in identifying
metabolic syndrome development.
A. T. Kraja, M. A.
Province, I. B. Borecki.