Page 113 - ASHG 2012 Annual Meeting Program Guide

102
INVITED AND PLATFORM SESSIONS
Taking photographs or sound recordings in all meeting rooms is strictly prohibited. Thank you for your cooperation.
Friday, November 9
8:00
AM
–10:15
AM
Concurrent Platform (abstract-driven)
Session D (47-55)
SESSION 49 – Common Variants, Rare Variants, and
Everything in Between
Room 135, Lower Level North, Moscone Center
Moderators
:
Steve Rich, Univ. of Virginia; Rasika
Mathias, Johns Hopkins Univ. Sch. of Med.
268
/8:00
Minimal differences in single nucleotide
variation calls between blood- and cell line-derived
DNA from the same individuals.
C. M. Schafer, N. G.
Campbell, G. Cai, J. S. Sutcliffe, J. D. Buxbaum, K.
Roeder, ARRA Autism Sequencing Consortium.
269
/8:15
The impact of genetic variation on
diabetes-related quantitative traits from whole
exome sequences: The T2D-GENES Consortium.
H. M. Highland, X. Sim, A. Manning, M. Rivas, G.
Atzmon, S. Choi, B. K. Cornes, J. Dupuis, J. C. Florez,
P. Fontanillas, T. Frayling, E. R. Gamazon, I.-S. Huh,
H. K. Im, J. Kim, Y. J. Kim, C. M. Lindgren, A. E. Locke,
J. B. Meigs, A. P. Morris, N. Palmer, I. Prokopenko,
T. M. Teslovich, T2D-GENES Consortium.
270
/8:30
Whole-exome sequencing in multiplex
families identifies novel rare variants in multiple
sclerosis.
A. H. Beecham, J. L. McCauley, A.
Hadjixenofontos, P. L. Whitehead, I. Konidari, A.
Aviram, Y. Pasco, S. L. Hauser, J. R. Oksenberg,
D. J. Hedges, J. M. Vance, J. L. Haines, M. A. Pericak-
Vance.
271
/8:45
A Mendelian randomization study on
vitamin D status and blood pressure: A meta-
analysis in up to 89,042 individuals.
K. S.
Vimaleswaran, D. J. Berry, A. Cavadino, M. R. Järvelin,
E. Hyppönen, D-CarDia Collaboration.
272
/9:00
APOE
modulates the relationship among
triglycerides, cholesterol, and CHD through
pleiotropy and gene-gene interactions.
T . J. Maxwell, C. M. Ballantyne, J. M. Cheverud,
C. S. Guild, C. E. Ndumele, E. Boerwinkle.
273
/9:15
Statistical inference of tissue-consistent
and tissue-specific eQTLs.
T. Flutre, X. Wen,
J. Pritchard, M. Stephens.
274
/9:30
Estimates of penetrance for common
pathogenic copy number variations.
J. A. Rosenfeld,
B. P. Coe, E. E. Eichler, H. Cuckle, L. G. Shaffer.
275
/9:45
Combining Illumina gene expression
microarrays from different tissues: Methodological
aspects.
K. Heim, C. Schurmann, A. Schillert,
C. Müller, T. Zeller, C. Herder, J. Kruppa, T. Illig,
G. Homuth, K. Strauch, A. Peters, H. Wallaschofski,
M. Dörr, T. Meitinger, P. S. Wild, S. Blankenberg,
U. Völker, M. Roden, A. Teumer, H. Prokisch, A. Ziegler
on behalf of MetaXpress Consortium.
276
/10:00
A DNA variant caller adapted to assess
mitochondrial DNA variation in lymphocytes from
1,000
Sardinians.
J. Ding, C. Sidore, O. Meirelles,
M. K. Trost, F. Busonero, R. Nagaraja, F. Cucca,
G. R. Abecasis, D. Schlessinger.