Page 182 - ASHG 2012 Annual Meeting Program Guide

POSTER SESSIONS
171
POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
1498
F Genetic pathways for ADHD show association to
hyperactive/impulsive symptoms.
A. Arias Vásquez, J.
Bralten, B. Franke, I. Waldan, S. Faraone, J. Buitelaar.
1499
W Graphical models and intervention calculus for
causal inference of genetic epidemiology studies.
P.
Wang, L. Jin, M. Xiong.
1500
T Multi-SNP analysis of GWAS reveals important
gene-gene interactions and gene networks implicated
in breast cancer.
L. Briollais, A. Dobra, H. Massam, H.
Ozcelik.
1501
F Connecting genome-wide association studies
with a biological gene interaction network to
uncover epistasis.
D. S. Himmelstein, J. S. Witte, O. G.
Troyanskaya, C. S. Greene.
1502
W Gene-based collapsing methods may not be
powerful for pathway-based association analysis for
exome sequencing data.
G. Wu, D. Zhi.
1503
T Gene function prediction based on 80,000
expression samples identifies downstream effects
of many trait-associated SNPs in an eQTL dataset
of 5,311 samples.
J. Karjalainen, H. Westra, R. S. N.
Fehrmann, T. Esko, M. J. Peters, E. M. Festen, G. J. te
Meerman, S. B. Felix, H. Yaghootkar, J. Kettunen, M. W.
Christiansen, A. Hofman, F. Rivadeneira, E. Reinmaa, R.
C. Jansen, J. Brody, S. A. Gharib, A. Suchy-Dicey, D.
Enquobahrie, A. G. Uitterlinden, C. Wijmenga, B. M. Psaty,
S. Ripatti, T. Frayling, A. Teumer, A. Metsepalu, J. B. J. van
Meurs, L. Franke.
1504
F Constructing biological network using RNA-seq
data.
Y. Choi, M. Coram, H. Tang.
1505
W Network inference, integrative dynamic
omics and personalized medicine.
G. I. Mias, H. Im, E.
Mitsunaga, R. Chen., J. Li-Pook-Than, L. Jiang, M. Snyder.
1506
T Stress-induced changes in gene interactions in
human cells.
R. Nayak, M. Kearns, V. G. Cheung.
1507
F An exploration of the use of low coverage whole
genome sequencing datasets as additional controls
for exome sequenced case series.
D. Gurdasani, M. S.
Sandhu, P. Kellam, P. J. Openshaw, J. K. Baillie, MOSAIC
and GenISIS Investigators.
1508
W Genome profile-based disease risk prediction.
P. Hu, E. Boerwinkle, L. Jin, M. Xiong.
1509
T Whole genome sequencing-based imputation: A
comparison between the 1000 Genomes data and the
UK10K sequencing data.
J. Huang.
1510
F EPACTS : A flexible and efficient sequence-
based genetic analysis software package.
H. M. Kang,
X. Zhan, X. Sim, C. Ma.
1511
W A Monte Carlo procedure for assessing co-
occurring and anti-co-occurring gene mutations in
cancer genome sequencing studies.
P. Liu, X. Hua, H.
Xu, Y. Lu.
O’Connell, O. Delaneau, N. Pirastu, S. Ulivi, P. Gasparini,
J. Marchini.
1485
T Local ancestry inference using identity by
descent.
Z. Cai, B. L. Browning, S. R. Browning.
1486
F Detection of identity by descent based on rare
variants.
G. Povysil, G. Klambauer, S. Hochreiter.
1487
W Refined IBD: A new method for detecting
identity by descent in population samples.
B. L.
Browning, S. R. Browning.
1488
T IBD estimation with whole-genome sequence
data.
L. Han, M. Abney.
1489
F Evaluating type 1 error and power for
association and linkage in large complex pedigrees.
A.
C. Cummings, E. Torstenson, M. F. Davis, L. N. D’Aoust,
W. K. Scott, M. A. Pericak-Vance, W. S. Bush, J. L. Haines.
1490
W Loss-of-co-homozygosity mapping: a novel
non-parametric linkage analysis leveraging exome
sequencing data.
Y. Okada, N. Gupta, D. Mirel, S. Gabriel,
T. Arayssi, F. Mouassess, W. A. L. Achkar, L. A. Kazkaz, R.
M. Plenge.
1491
T Patterns of indel variation: Comparison of
calling methods and LD with SNPs.
K. Huang, M. Ehm,
N. Bing, Y. Liu, J. Xu, A. Slater, D. Fraser, J. Novembre, J.
Li, M. Neison, Y. Li.
1492
F Estimating disease associations with common,
low-risk alleles using pedigree data: Applications to
breast cancer.
D. R. Barnes, D. Barrowdale, J. Hopper, D.
Goldgar, G. Chenevix-Trench, A. C. Antoniou, G. Mitchell,
kConFab Investigators, AOCS Group.
1493
W Improving association tests by learning mode
of inheritance from parental data.
Z. Yu, D. Gillen, C. Li,
M. Demetriou.
1494
T Enhanced maternal origin of the 22q11.2
deletion in velo-cardio-facial/DiGeorge syndrome.
M.
Delio, T. Guo, D. McDonald-McGinn, E. Zackai, S. Herman,
A. Higgins, K. Coleman, T. Wang, A. Auton, R. Shprintzen,
B. Emanuael, B. Morrow.
1495
F Connection between heritability and polygenic
risk score: Implications for the genetic architecture of
complex traits.
V. V. Trubetskoy, E. R. Gamazon, M. E.
Dolan, N. J. Cox, H. K. Im.
1496
W Genetic variants in DNA repair pathway genes
and upper aerodigestive tract cancers: Combined
analysis of data from genome-wide association
studies.
M.-C. Babron, R. Kazma, V. Gaborieau, J. D.
McKay, P. Brennan, A. Sarasin, S. Benhamou, INHANCE
Consortium.
1497
T Venous thromboembolism-susceptibility
pathways by gene set analyses.
J. Heit, S. M. Armasu, J.
P. Sinnwell, D. J. Schaid, M. de Andrade.