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716F Association analysis of LRRC20 polymorphisms
with aspirin exacerbated respiratory disease.
J. Kim, B.
Park, C. Park, H. Shin.
717F Polymorphisms in genes participating in the
oxidative stress pathway are associated with airway
reactivity in patients with COPD.
N. M. Rafaels, I.
Ruczinski, T. Murray, R. A. Mathias, L. Huang, V. Mantese,
C. Vergara, L. Gao, A. E. Berger, J. Connett, P. D. Paré, D.
Sin, A. Sandford, D. Daley, T. H. Beaty, K. C. Barnes, N.
N. Hansel.
718F Examining the relationship between smoking
history and genetic susceptibility on pancreatic cancer
risk.
E. J. Childs, L. Wang, S. Chen, A. Blackford, G.
Parmigiani, A. P. Klein.
719F Influence of genetic variants on response to
vitamin D administration.
Z. Dastani, D. Goltzman, T.
Wang, L. Fu, D. P. Kiel, D. Cole, B. Richards.
720F Genome-wide linkage scan for QTL influencing
quantitative ultrasound measures of bone strength in
children from the Jirel ethnic group in Eastern Nepal.
K. D. Williams, J. Blangero, M. C. Mahaney, T. D. Dyer, J.
Subedi, B. Jha, J. L. VandeBerg, S. Williams-Blangero, B.
Towne.
721F Sliding-window based testing of rare variant
associations.
A. Brisbin, K. A. Ellsworth, L. Wang, B. L.
Fridley.
722F Joint modeling of repeated measures and time-
to-event data in genetic association analysis of type 1
diabetes.
Z. Chen, A. D. Paterson, A. J. Canty, L. Sun, S.
B. Bull.
723F A generalized pooled association statistic for
analyzing rare variants.
A. Derkach, J. F. Lawless, L.
Sun.
724F Genetic associations of inflammatory diseases
with the gene encoding septin 6.
M. Kong, Y. Kim, J.
Ryu, C. Lee.
725F Combining SNP and HLA AIMs for ancestry
analysis for an immunogenetic transplantation
outcome association study.
A. Madbouly, L. Gragert, M.
Maiers, M. Malkki, E. Petersdorf.
726F A model that combines array and sequence data
to improve genotype accuracy.
J. O'Connell, J.
Marchini.
727F Making the most of case-sibling studies.
M. Shi,
D. M. Umbach, C. R. Weinberg.
728F The role of thromboxane A2 receptor gene
polymorphisms in lung function and severity in
childhood-onset asthma.
K. Takeuchi, Y. Mashimo, S.
Hattori, N. Shimojo, M. Tomita, T. Arima, Y. Morita, K.
Sato, S. Suzuki, T. Nishimuta, H. Watanabe, A. Hoshioka,
A. Yamaide, M. Watanabe, Y. Kohno, A. Hata, Y. Suzuki.
Friday Poster Authors are reminded to remove posters from the boards at 4:00 pm.
The Exhibit Hall will close at 4:30 pm.
729F Extensions of bootstrap bias-reduction to
address the winner's curse in genome-wide
association analysis of time-to-event phenotypes.
J.
Taleban, L. L. Faye, A. Dimitromanolakis, A. D. Paterso
L. Sun, S. B. Bull.
730F Discovery and replication of gene-gene
interactions in multiple independent Alzheimer's
Disease Genetics Consortium datasets.
T. A. Thornto
Wells, K. D. Brown-Gentry, E. S. Torstenson, S. M. Dud
L. Jiang, M. D. Ritchie, E. R. Martin, M. A. Pericak-Vanc
J. L. Haines, Alzheimer's Disease Genetics Consortium.
731F An evaluation of the informativeness of
population genetics when making genotype calls in
exome-captured next-generation sequencing data.
Vattathil, F. A. San Lucas, Y. Fan, W. Yang, W. Wang, S.
Hunger, M. Loh, M. Devidas, C.-H. Pui, E. Mardis, M. V.
Relling, P. Scheet.
732F Further replication of the TRAF1/C5 genetic
association with radiological damage in patients wit
rheumatoid arthritis.
S. Viatte, D. Plant, M. Lunt, B. Fu
B. Parker, J. Galloway, C. Solymossy, J. Worthington, D
Symmons, J. Dixey, A. Young, A. Barton.
733F Association of
matrix metalloproteinase-7
and
-12
genes polymorphisms with asthma: A case-cont
study of
MMP-7
and
-12
in a Japanese population.
F
Yamaide, Y. Mashimo, N. Shimojo, T. Arima, Y. Morita,
Hirota, S. Doi, K. Sato, S. Suzuki, T. Nishimuta, H.
Watanabe, A. Hoshioka, M. Tomiita, A. Yamaide, M.
Watanabe, Y. Okamoto, Y. Kohno, M. Tamari, A. Hata,
Suzuki.
734F RVTests: Rare-variant test package.
X. Zhan, Y.
Hu, G. Abecasis.
735F Combining association tests for rare variant
analysis.
H. Zhou, K. Hao, C. Molony.
736F Critical comparison of deep resequencing
analysis methods in a population sample of over 30
subjects.
L. Li, L. Warren, J. Shen, V. E. Mooser, D. M.
Waterworth, J. C. Whittaker, M. R. Nelson.
737F Keloid susceptibility loci 1q41, 3q22.3, and
15q21.3 replicated in a Nigerian population.
S. Hook
Jr., P. B. Olaitan, O. M. Oluwatosin, S. A. Fadiora, S.
Ademola, V. Odesina, S. M. Leal, E. J. Reichenberger.
738F Genotype at the NOS3 G894T SNP is not
associated with acute mountain sickness upon asce
to 4380 m or during brief exposure to an equivalent
normobaric hypoxia.
M. J. MacInnis, E. A. Carter, M.
Koehle, J. L. Rupert.
739F The functional MICA-129 polymorphism is
associated with psoriatic disease independently of
HLA-B and C.
R. A. Pollock, V. Chandran, J. Barrett, L.
Eder, F. Pellett, C. Yao, M. Lino, S. Shanmugarajah, V. T
Farewell, D. D. Gladman.