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Friday, October 14
4:15
PM
–6:15
PM
Concurrent Platform Session C (51-60)
SESSION 56 – Complex Traits I: Approaches and
Methods
Room 511, Level 5, Convention Center
Moderators:
Melanie Carless, Texas Biomed. Res.
Inst., USA; Dale Nyholt, QIMR, Herston, Australia
203
/4:15
Analysis of noncoding RNA expression in
late-onset Alzheimer’s disease.
C. E. Humphries, M.
A. Kohli, P. L. Whitehead, D. C. Mash, M. A. Pericak-
Vance, J. R. Gilbert.
204
/4:30
Components of heritability in an Icelandic
cohort.
N. Zaitlen, A. Helgason, N. Patterson, B.
Pasaniuc, D. Gudbjartsson, P. Kraft, A. Kong, A. L.
Price, K. Stefansson.
205
/4:45
Gene-phenotype relationships in a deep-
resequencing study of 202 genes in >14,000
subjects including 12 complex diseases.
M. G. Ehm,
M. R. Nelson, L. Warren, L. Li, P. L. St. Jean, J. Shen,
D. Fraser, J. L. Aponte, J. Rubio, S. Zöllner, L. R.
Cardon, J. Novembre, J. C. Whittaker, S. L. Chissoe,
V. E. Mooser.
206
/5:00
Multivariate genetic analysis of phenotypic
sets identifies 10 novel loci for systemic
metabolism.
M. Inouye, P. I. W. de Bakker, J.
Kettunen, A. J. Kangas, P. Soininen, M. J. Savolainen,
J. Viikari, M. Kahonen, T. Lehtimaki, S. Ripatti, O.
Raitakari, M. R. Jarvelin, A. Palotie, M. Ala-Korpela.
207
/5:15
Multi-ethnic fine-mapping reveals rare and
potential causal variants for a complex disease.
R.
C. Almeida, G. Trynka, J. Gutierrez-Achury, J.
Romanos, J. R. Bilbao, D. Barisani, L. Greco, M. C.
Mazilli, A. Sood, B. Cukrowska, K. Hunt, E. Urcelay, D.
van Heel, C. Wijmenga, Wellcome Trust Case Control
Consortium.
208
/5:30
Custom array genotyping identifies new
loci for type-2 diabetes, providing insight into the
biological and genetic architecture of disease.
B. F.
Voight, A. P. Morris, T. M. Teslovich, T. Ferreira, E. J.
Rossin, R. J. Strawbridge, A. V. Segrè, A. Mahajan, I.
Prokopenko, H. Grallert, M. Boehnke, M. I. McCarthy
on behalf of DIAGRAM Consortium.
209
/5:45
Search for novel susceptibility loci for type
2 diabetes using genome-wide association studies
imputed from a 1000 Genomes reference panel.
I.
Prokopenko, H. Chen, C. Ma, R. Mägi, B. F. Voight, Q.
Lu, N. Van Zuydam, H. Grallert, L. Yengo, C. Dina, G.
Thorleifsson, C. Fuchsberger, L. Liang, M. Mueller, S.
M. Willems, K. J. Gaulton, V. Steinthorsdottir, C. M.
Van Duijn, M. Boehnke, J. Dupuis, M. I. McCarthy, L.
J. Scott on behalf of DIAGRAM+ Consortium.
Cameras and all other recording devices are
strictly prohibited
in all session rooms. Thank you for your cooperati
210
/6:00
Exome sequencing to identify genes
harboring rare variants that determine lung
function decline in COPD.
R. A. Mathias, Y. Kim,
Taub, L. Huang, N. Rafaels, T. Murray, C. Vergara, M
Bamshad, M. Emond, T. H. Beaty, I. Ruczinski, N.
Hansel, K. C. Barnes on behalf of NHLBI Exome
Sequencing Program and Lung Project Team.