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371W Genome-wide association study for resting heart
rate: Variants detection and replication.
B. Gombojav,
D. H. Lee, Y. S. Ju, J. I. Kim, J. S. Seo, M. Lee, Y. M.
Song, K. Lee, J. Sung.
372W Salt-sensitivity of blood pressure is strongly
associated with polymorphisms in the sodium-
bicarbonate symporter.
L. Gordon, R. Carey, C.
Schoeffel, J. Gildea, J. Jones, H. McGrath, M. Park, S.
Williams, P. Jose, R. Felder.
373W ENPP1 polymorphisms influence the risk of
developing calcific aortic valve stenosis.
S. Guauque-
Olarte, V. Ducharme, N. Gaudreault, P. Pibarot, P. Mathieu,
Y. Bossé.
374W
ABCA1
gene promoter DNA methylation is
associated with a deterioration of HDL-cholesterol
metabolism in familial hypercholesterolemia.
S. Guay,
D. Brisson, J. Munger, D. Gaudet, L. Bouchard.
375W LQTS in Northern BC: A more severe cardiac
phenotype but minimal impact on auditory function
with homozygosity for KCNQ1 V205M rules out Jervell
and Lange Nielson syndrome.
H. Jackson, S. Lauson, R.
Rupps, S. McIntosh, B. Casey, A. Tang, L. Arbour.
376W Assumption-free heritability estimates of
electrocardiographic measures in the TwinsUK study.
Y. Jamshidi, I. M. Nolte, H. Riese, P. van der Harst, F. W.
Asselbergs, T. D. Spector, H. Snieder.
377W Genes and viruses in idiopathic (dilated)
cardiomyopathy: A pilot study.
I. P. C. Krapels, Y. H. J.
M. Arens, A. T. J. M. Helderman-van den Enden, C.
Eurlings, R. Jongbloed, A. van den Wijngaard, S. R. B.
Heymans.
378W Genetic testing for dilated cardiomyopathy in the
United States: A health technology assessment.
A. Lea,
S. Levine, D. Allingham-Hawkins.
379W MYLK and INK4/ARF genes are the susceptibility
genes of cerebral small vessel disease in Chinese
population.
W. Li, G. Li, X. Zhao, B. Xin, J. Lin, Y. Shen,
X. Liang, H. Gao, X. Liao, Z. Liang, Y. Wang.
380W Novel
ACTA2
mutation in a large family with
familial thoracic aortic aneurysms and dissections
exhibiting reduced penetrance in a female carrier.
M.
A. McGinniss, H. Wang, J. N. Young, R. Calhoun, S.
Mayberg, J. Martinezmoles, A. W. Grix, B. A. Westerfield,
L. S. Pena, D. J. Penny, Y. Fan, S. A. Boyadjiev.
Complex Traits: Theory and Methods
381W Single nucleotide polymorphisms analysis of
INSL3 and RXFP2 genes in Mexican patients with
idiopathic cryptorchidism.
M. D. Chávez-Saldaña, J. C.
Gutiérrez, I. Zamora, O. Cuevas, J. Rojas, O. Gutiérrez, E.
Yokoyama, R. M. Vigueras.
Wednesday Poster Authors are reminded to remove posters from the boards at 6:30 pm.
382W Molecular markers for effective prognosis in
systemic lupus erythematosus patients at risk of re
and cardiovascular diseases.
R. Chandirasekar, K.
Sasikala, D. Nedumaran, K. Suresh, R. Jayakumar, R.
Venkatesan, B. Laksmankumar, G. Karthik, S. Arun.
383W Dynamic modularity beyond “date” and “party
hubs in protein-protein interaction networks.
X. Cha
K. Wang.
384W Testing for a mixture of effects on either disea
or quantitative traits across a set of rare variants.
G.
Clarke, A. Morris.
385W Pathway association analysis using an overall
test for the most promising SNPs.
M. Mattheisen, W.
Yip, P. Lipman, C. Lange.
386W Modeling of the interaction between the
serotonin regulation pathway and the stress respon
mediated by the hypothalamic-pituitary-adrenal axis
using a Boolean approximation: A novel study for
depression.
O. A. Moreno-Ramos, M. C. Lattig, A. F.
Gonzalez.
387W Large-scale transcriptome study in the Sardin
founder population.
M. Pala, M. Marongiu, A. Mulas,
Cusano, F. Crobu, F. Reinier, R. Berutti, M. G. Piras, C.
Jones, D. Schlessinger, G. Abecasis, A. Angius, S. San
F. Cucca.
388W Development and use of a pipeline to generat
strand and position information for common
genotyping chips.
N. W. Rayner, M. I. McCarthy.
389W Association of endothelial nitric oxide synthas
gene haplotypes with systemic lupus erythematosus
Kuwaiti Arabs.
M. Haider, S. Alfadhli, B. Altamimy, K.
Alsaeid.
390W
FRIZZLED
mutations in patients with neural tu
defects.
V. Capra, P. De Marco, E. Merello, G. Piatelli,
Cama, Z. Kibar.
391W Replication of a FOXP2 association with moto
sequencing during an oral task in families with famil
speech sound disorder.
B. Peter, M. Matsushita, K. O
W. Raskind.
392W Relative impact of genetic and epigenetic
factors on gene expression in tumor tissue samples
H. Dong, L. Jin, M. Xiong.
393W
eNOS
(27bp deletion/insertion in intron 4) and
Mn-SOD
(p.Val16Ala) polymorphisms analysis in typ
diabetic retinopathy patients from North India.
P.
Badhan, V. Vanita.
394W NTF4 mutations in primary open-angle
glaucoma.
L. Chen, T. Ng, P. Tam, A. Fan, M. Zhang, C
Tham, N. Wang, D. Lam, C. Pang.