Page 185 - ASHG 2012 Annual Meeting Program Guide

174
POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
Wang, S. Shete.
1579
F Bayesian-optimized linkage disequilibrium
improves gene-based association tests.
H. Huang, S.
Zahid, P. Chanda, D. E. Arking, J. S. Bader.
1580
W Statistical models and inference methods
for the in vivo DNA methylation process.
A. Q. Fu, D.
P. Genereux, R. Stoeger, A. F. Burden, C. D. Laird, M.
Stephens.
1581
T A comparison of statistical methods for the
analysis of methylome data.
M. LeBlanc, B. Kulle.
1582
F Designing GWAS arrays for efficient imputation-
based coverage.
Y. Zhan, Y. Lu, T. Webster, J. Schmidt.
1583
W Does a higher BMI directly influence levels of
physical activity in children? Mendelian randomization
using genotypic scores.
R. C. Richmond, G. Davey
Smith, D. M. Evans, B. St. Pourcain, J. P. Kemp, A. R.
Ness, S. M. Ring, K. Tilling, N. J. Timpson.
Cardiovascular Genetics
1584
T Role of
GATA5
,
FBN1
and
TGFBR2
mutation in
patients with bicuspid aortic valve.
N. Abdulkareem, J.
A. Aragon-Martin, G. Arno, V. Ramachandran, A. Child, M.
Jahangiri.
1585
T Re-sequencing of 3699 individuals reveals novel
low-frequency missense polymorphism in
SCN10A
associated with PR interval that alters channel
activation.
J. Brody, V. S. Macri, D. E. Arking, X. Yin, C.
Liu, A. C. Morrison, A. Alonso, J. C. Bis, S. R. Heckbert,
T. Lumley, C. Sitlani, L. A. Cupples, S. Pulit, C. Newton-
Cheh, C. J. O’Donnell, E. J. Benjamin, D. Muzny, R. Gibbs,
R. Jackson, J. W. Magnani, S. S. Rich, B. M. Psaty, E.
Boerwinkle, P. T. Ellinor, N. Sotoodehnia, Cohorts for Heart
and Aging Research in Genetic Epidemiology, NHLBI
Exome Sequencing Project.
1586
T A functional SNP at
APLN
gene confers a risk
to arterial stiffness in Chinese women.
Y. C. Liao, S. W.
Huang, Y. S. Wang, K. C. Chen, S. H. H. Juo.
1587
T Impact of inflammatory gene polymorphisms on
left ventricular dysfunction in coronary artery disease
patients.
A. Mishra, A. Srivastava, T. Mittal, N. Garg, B.
Mittal.
1588
T Identification of a new chromosomal locus for a
mutation causing left ventricular non-compaction with
ventricular tachycardia cardiopathology.
E. Muhammad,
A. Levitas, V. Sheffield, R. Parvari.
1589
T Sequencing candidate genes associated with
conotruncal heart defects.
K. Osoegawa, M. Ladner, K.
Schultz, C. Parodi, N. Mohammed, D. Noonan, G. Shaw,
E. Trachtenberg, E. Lammer.
cross-study analyses.
C. M. Hamilton, W. Huggins,
H. Pan, D. B. Hancock, J. G. Pratt, J. A. Hammond, T.
Hendershot, D. R. Maiese, K. A. Tryka, K. Sher, K. Conway,
M. Scott, W. R. Harlan, J. Haines, L. C. Strader, H. A.
Junkins, E. M. Ramos.
1567
F Comparison of genome-wide association
studies for smoking behavior between self-reported
and biomarker measures.
A. I. Stiby, N. Timpson, M.
Hickman, D. Evans, J. Kemp, G. Davey Smith, S. Ring, B.
St. Pourcain, J. Henderson, J. Macleod.
1568
W Design of sequencing studies in family
samples, with application to the study of substance
use disorders.
S. Feng, S. Vrieze, B. Tarrier, J. Bragg-
Gresham, X. Zhan, C. Sidore, M. McGue, W. Iacono, G.
Abecasis.
1569
T Family-based designs for sequencing studies.
D. Thomas.
1570
F From a large-scale discovery study to a
replication study.
C. Kuo, D. Zaykin.
1571
W Optimal sample selection for large-scale
next-generation sequencing experiments.
G. W.
Beecham, R. Rajbhandary, E. R. Martin, L. S. Wang, K.
Lunetta, R. Mayeux, J. L. Haines, L. Farrer, M. Pericak-
Vance, G. Schellenberg, Alzheimer’s Disease Genetics
Consortium.
1572
T Meta-analysis of
ITGAM
coding variant,
rs1143679 (R77H) in systemic lupus erythematosus
cases and controls.
X. Kim-Howard, V. Pradhan, K. H.
Chua, A. Maiti, K. Ghosh, S. Nath.
1573
F Understanding missing data in a large STR
dataset of over 100,000 Brazilian individuals genotyped
with PowerPlex 16 kit.
V. R. C. Aguiar, R. V. Rohlfs, K. E.
Lohmueller, A. M. Castro, F. S. V. Malta, A. C. S. Ferreira, I.
D. Louro, R. Nielsen.
1574
W Population based study of permanent teeth
agenesis in Japanese schoolchildren.
J. Machida, T.
Nishiyama, M. Kamamoto, S. Yamaguchi, M. Kimura,
A. Shibata, K. Yamamoto, S. Makino, H. Miyachi, K.
Shimozato, Y. Tokita.
1575
T Are heritability estimates of binary traits
meaningful?
P. H. Benchek, N. J. Morris.
1576
F Genetic ancestry and mammographic density
among U.S.
Caucasians. J. L. Caswell, K. Kerlikowske,
J. Shepherd, S. R. Cummings, D. Hu, S. Huntsman,
E. Ziv.
1577
W Robust partitioning of local heritability at
associated GWAS loci.
A. Gusev, G. Bhatia, B. Pasaniuc,
N. Zaitlen, A. L. Price.
1578
T Multiple mediation analysis in case-control
studies: Application to detecting joint mediating
effects of smoking and chronic obstructive
pulmonary disease on the association between
CHRNA5-A3
genetic locus and lung cancer risk.
J.