Page 188 - ASHG 2012 Annual Meeting Program Guide

POSTER SESSIONS
177
POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
P. Goldschmidt-Clermont, M. A. Pericak-Vance, G. W.
Beecham.
1645
T Functional relationship of the
COL4A1/COL4A2
locus on chromosome 13q34 to coronary artery disease.
A. Turner, P. Lau, S. Soubeyrand, O. Jarinova, R. McPherson.
1646
T De novo copy number variants in non-syndromic
left ventricular outflow tract obstruction.
L. A. Umana,
N. A. Hanchard, G. A. Zender, S. M. Fitzgerald-Butt, G.
Zapata, P. Hernandez, M. S. Azamian, D. J. Penny, J. W.
Belmont, K. L. McBride.
1647
T Genetic association of CVD-related loci with
lipid traits in the Heart Strategies Concentrating on
Risk Evaluation (Heart SCORE) Study.
X. B. Wang,
S. Reis, M. M. Barmada, I. Halder, F. Y. Demirci, M. I.
Kamboh.
1648
T Genetic analysis of vascular disease in the
Diabetes Heart Study.
A. J. Cox, M. C. Y. Ng, J. Xu, C. D.
Langefeld, J. J. Carr, B. I. Freedman, D. W. Bowden.
1649
T SNPs associated with plasma triglyceride levels
influence response during intensive cardiovascular risk
reduction.
D. L. Ellsworth, A. Decewicz, M. Hicks, K. A.
Mamula, A. Burke, M. J. Haberkorn, H. L. Patney, M. N.
Vernalis.
1650
T Sex-specific association of cadherin with high
density-lipoprotein cholesterol in the Long Life Family
Study.
M. F. Feitosa, A. T. Kraja, J. Lee, K. Christensen, J.
Wang, C. Kammerer, M. A. Province, I. B. Borecki.
1651
T A genome-wide association study identifies
KNG1
as a genetic determinant of plasma factor XI
level and activated partial thromboplastin time.
J.
M. Soria, M. Sabater-Lleal, A. Martinez-Perez, A. Buil,
L. Folkersen, J. C. Souto, M. Bruzelius, M. Borrell, J.
Odeberg, S. Silveira, P. Eriksson, A. Almasy, A. Hamsten.
1652
T Gene variants are associated with soft lipid-rich
coronary plaque in African Americans with replication
in European Americans.
L. R. Yanek, B. G. Kral, D.
Vaidya, T. F. Moy, L. C. Becker, D. M. Becker.
1653
T Genetic variation for leukocyte telomere
length predicts incident coronary heart disease: The
Framingham Heart Study.
S. Hwang, A. Aviv, D. Levy,
M. Mangino, S. Hunt, A. L. Fitzpatrick, J. C. Bis, E. S.
Smith.
1654
T Genome-wide association analysis of plasma
triglyceride in Korean population.
B. Gombojav, D. H.
Lee, M. K. Lee, Y. M. Song, K. Lee, J. Sung.
1655
T Genome-wide association study of calcific
aortic valve disease.
S. Guauque-Olarte, M. Lamontagne,
N. Gaudreault, P. Mathieu, P. Pibarot, Y. Bossé, D.
Messika-Zeitoun.
1656
T Genetic variants explaining sodium intake in
a population with higher sodium intake level: The
Healthy Twin Study, Korea.
M. Kho, Y.-M. Song, K. Lee,
J.-E. Lee, K. Kim, J. Sung.
1632
T The AA genotype of tumor necrosis factor
induced protein 2 rs8126 polymorphism is associated
with increased mortality in septic shock.
S. A. Thair, J.
H. Boyd, T. A. Nakada, J. A. Russell, K. R. Walley.
1633
T Significance of the
NODAL
p.H165R variant in
complex cardiovascular malformations: A report of two
lethal cases with an asymptomatic parent.
Z. Ammous,
A. Rajadhyaksha, P. Jayakar.
1634
T Parent of origin effect in HDL levels.
J. S. Lilley,
I. M. Predazzi, W. S. Bush, M. F. Linton, S. M. Williams, S.
Fazio.
1635
T Loci on chromosomes 2q12, 6p21 and 13q14
modulate the effect of smoking on carotid intima-
media thickness in whites, blacks and Hispanics.
C.
Dong, L. Wang, A. Beecham, D. Cabral, C. B. Wright, S. H.
Blanton, T. Rundek, H. Zhao, R. L. Sacco.
1636
T A genome-wide gene-by-environment scan
for mobile source air pollution in atherosclerosis and
myocardial infarction identifies
PIGR
and
HCN4
.
C. K.
Ward-Caviness, L. Neas, C. Haynes, C. Blach, E. Burns, K.
LaRocque-Abramson, E. Dowdy, W. Cascio, R. Devlin, D.
Diaz-Sanchez, W. E. Kraus, S. H. Shah, S. G. Gregory, M.
L. Miranda, E. R. Hauser.
1637
T Genome-wide association analysis of blood
pressure incorporating gene-age interactions in the
CHARGE, GBPgen, and ICBP Consortia.
J. Simino,
CHARGE, GBPgen, and ICBP Investigators.
1638
T A genome-wide association study of carotid
intima-medial thickness, a preclinical marker of
atherosclerosis.
S. H. Blanton, A. H. Beecham, L. Wang,
C. Dong, D. Cabral, B. I. Hudson, M. Kiryiya, F. Jasmine,
B. Pierce, R. Demmer, A. Habibul, M. Desvarieux, R.
Sacco, T. Rundek.
1639
T Genome-wide association analyses of long-term
blood pressure traits.
S. K. Ganesh, G. B. Ehret, A.
Chakravarti on behalf of CHARGE-BP and ICBP Consortia.
1640
T A genome-wide association study in a Lebanese
population identifies three new loci for coronary artery
disease.
M. Ghassibe, J. Hager, J. B. Cazier, D. Platt, Y.
Kamatani, M. Farrall, D. Gauguier, P. Zalloua.
1641
T An assessment of association of blood pressure
with DNA variants in the Long Life Family Study and
other studies.
A. T. Kraja, J. H. Lee, R. Straka, I. B.
Borecki, C. Kammerer, M. A. Province.
1642
T Novel tissue-specific transcriptomic signatures
revealed by experimental endotoxemia in healthy
human subjects.
Y. Liu, J. Feguson, I. Silverman, B.
Gregory, M. Li, M. Reilly.
1643
T Genome-wide association study for atrial
fibrillation in the Japanese population.
K. Ozaki, Y.
Onouchi, N. Kamatani, T. Tsunoda, M. Kubo, Y. Nakamura,
T. Tanaka.
1644
T Cardiovascular genetics.
D. Seo, Z. Liu, N. Sikka,