Page 214 - ASHG 2013 Program Guide

POSTER SESSIONS
  201
POSTER SESSIONS
W=W
ednesday authors will present; T=Thursday authors will present; F=Friday authors will pr
esent
2170
T An extreme phenotype approach to identify
genes in Caribbean Hispanics for carotid intima-medial
thickness, a preclinical marker of atherosclerosis.
S. H.
Blanton, A. H. Beecham, L. Wang, C. Dong, D. Cabral, R.
L. Sacco, T. Rundek.
2171
F The link between hepcidin, iron and
atherosclerosis: A Mendelian randomization approach.
T. E. Galesloot, L. L. Janss, D. W. Swinkels, S. H. Vermeulen.
2172
W Eleven novel loci influencing blood p essure.
B. Keating, V. Tragante, M. Barnes, S. Ganesh, I. H. Gho,
X. Zhu, D. Levy, H. Hakonarson, P. I. W. de Bakker, F. W.
Asselbergs, P. B. Munroe, IBC BP Consortium.
2173
T Genetic and phenotypic architecture of coronary
artery disease in a diverse population.
I. Konidari, L.
Wang, Z. Liu, N. Sikka, P. Goldschmidt, M. A. Pericak-
Vance, D. Seo, G. W. Beecham.
2174
F Local ancestry inference in a genome-wide
association study of a genetically diverse population
with coronary artery disease.
Z. Liu, L. Wang, N.
Vasudeva, P. J. Goldschmidt-Clermont, M. A. Pericak-
Vance, D. M. Seo, G. W. Beecham.
2175
W Genetic variants affecting the expression of
DRAM2
at 1p13.3 are associated with acute myocardial
infarction with different effects for STEMI and NSTEMI.
P. Salo, J. Sinisalo, J. Kettunen, A. Havulinna, A. Sarin,
T. Hiekkalinna, S. Ripatti, P. J. Karhunen, H. Huikuri, M.
Lokki, V. Salomaa, M. Nieminen, M. Perola.
2176
T A novel MMP12 locus is associated with large
artery atherosclerotic stroke using a genome-wide
age-at-onset informed approach.
M. Traylor, K.-M.
Mäkelä, L. L. Kilarski, E. G. Holliday, W. J. Devan, M. A.
Nalls, K. L. Wiggins, Y.-C. Cheng, S. Achterberg, R. Malik,
C. Sudlow, E. Raitoharju, V. Thijs, A. Lindgren, A. Slowik,
M. Walters, P. Sharma, J. R. Attia, G. B. Boncoraglio, P.
M. Rothwell, P. I. W. de Bakker, J. C. Bis, S. J. Kittner, J.
Rosand, J. F. Meschia, C. Levi, M. Dichgans, T. Lehtimäki,
C. M. Lewis, H. S. Markus, METASTROKE, WTCCC2.
2177
F Genetic architecture of hypertension in a multi-
ethnic population.
N. Vasudeva, L. Wang, A. Beecham,
P. Goldschmidt, M. Pericak-Vance, D. Seo, G. Beecham.
2178
W 12 Novel genome wide associations for
human cardiac repolarization.
N. Verweij, W. G.
Wieringa, I. Mateo Leach, D. J. van Veldhuisen, W. H. van
Gilst, H. L. Hillege, R. S. N. Fehrmann, P. I. W. de Bakker,
R. A. de Boer, L. Franke, P. van der Harst.
2179
T A three-stage genome-wide association study
combining multilocus test and gene expression
analysis for young-onset hypertension on Taiwan Han
Chinese.
K. Chiang, H. Yang, J. Chen, W. Pan.
2180
F Genetic effects on levels of growth
differentiation factor 15: A PLATO genomics study.
N. Eriksson, A. Johansson, E. Hagström, T. Axelsson, B. J.
Barratt, R. C. Becker, M. Bertilsson, A. Himmelmann, S. K.
James, H. A. Katus, A. Siegbahn, P. G. Steg, R. F. Storey,
A.-C. Syvänen, C. Varenhorst, A. Åkerblom, L. Wallentin.
2158
T
KLF15
regulates circadian cardiac susceptibility
to ischemia reperfusion injury.
L. Zhang, D. Prosdocimo,
M. Jain.
2159
F Interactions among depressive symptoms and
genetic influences on ca diac outcomes.
L. Frazier,
J. Sanner, T.-Y. Yu, A. Morrison, E. Boerwinkle.
2160
W A genome-wide interaction study identifies
PDE1C
genetic variants and renal function as jointly
associated with coronary artery disease.
C. Ward-
Caviness, M. Winn, C. Blach, C. Haynes, E. Dowdy, S.
Gregory, S. Shah, W. Kraus, E. Hauser.
2161
T A 62 variant type 2 diabetes genetic risk score
is not associated with subclinical atherosclerosis in
the Framingham Heart Study - SNP Health Association
Resource (FHS SHARe Study).
M. Dauriz, B. Porneala,
J. L. Vassy, M. F. Hivert, J. M. Murabito, J. C. Florez,
J. Dupuis, C. J. O’Donnell, J. B. Meigs.
2162
F Saturated fat intake modulates the association
between an obesity genetic risk score and BMI.
P. Casas-Agustench, D. K. Arnett, C. E. Smith, C.-Q. Lai,
L. D. Parnell, I. B. Borecki, Y.-C. Lee, J. M. Ordovás.
2163
W GxE GWAS and path analysis identify a
cardiovascular and metabolic risk gene
EBF1
.
A. Singh,
M. B. Babyak, D. K. Nolan, B. H. Brummett, R. Jiang, I. C.
Siegler, S. H. Shah, R. B. Williams, E. R. Hauser.
2164
T Influences of SNPs of
LIPC
,
LIPG
,
APO E
,
PLTP
and
PON1
genes on plasma high-density lipoprotein,
cholesterol and paraoxonase-1 activity.
D. Z. Scherrer, V. H.
S. Zago, R. Secolin, E. S. Parra, N. B. Panzoldo, F. Alexandre,
I. V. Calanca, E. Nakandakare, E. C. R. Quintão, E. C. de Faria.
2165
F Analysis of allele specific exp ession and
transcription factor activity identifies potential gene
by-environment mechanisms of coronary heart disease
risk.
O. V. Sazonova, A. Raiesdana, S. T. Nurnberg, K. S.
Smith, V. Anaya, T. Quertermous, S. B. Montgomery.
2166
W A genome-wide association study reveals novel
susceptibility loci for coronary artery disease in Saudi
Arabs.
N. Dzimiri, C. Nguyen, S. M. Wakil, N. P. Muiya,
E. Andres, N. Mahzar, B. Baz, S. Hagos, M. Alshahid,
G. Morahan, B. F. Meyer.
2167
T A genome-wide association study reveals
novel susceptibility loci for obesity in Saudi Arabs.
N. P. Muiya, C. Nguyen, S. M. Wakil, E. Andres, N. Mazhar,
B. Baz, D. Gueco, M. Najai, O. Alboudary, S. Hawari, S.
Hagos, M. Alshahid, G. Morahan, B. F. Meyer, N. Dzimiri.
2168
F Investigation of genome-wide DNA methylation
marks associated with FV Leiden mutation in patients
with venous thrombosis.
D. Aïssi, M. Ladouceur, J.
Dennis, F. Gagnon, P. E. Morange, D. A. Trégouët.
2169
W Sex-specific e fects of CAD SNPs in sudden
cardiac death.
F. N. Ashar, C. Albert, S. S. Chugh, A.
Cupples, M. Eigelsheim, P. Goyette, A. Huertas-Vazquez,
H. Huikuri, J. Jintilla, X. Jouven, S. Kääb, M. Kortelainen, P.
Kwok, T. Lehtimäki, L. Lyytikäinen, M. Müller-Nurasyid, C.
Newton-Cheh, B. Psaty, S. Pulit, D. Siscovick, B. Stricker,
N. Sotoodehnia, D. E. Arking, CHARGE-SCD.