Page 145 - ASHG 2012 Annual Meeting Program Guide

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POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
Deiros, G. L. Fawcett, Z. Johnson, N. H. Kalin, R. W.
Wiseman, B. Ferguson, E. Vallender, S. Kanthaswamy, D.
M. Muzny, R. Gibbs, J. Rogers.
596
W Whole genome haplotyping by dilution,
amplification and sequencing.
F. Kaper, S. Swamy, B.
Klotzle, J. Cottrell, S. Munchel, M. Bibikova, S. Kruglyak,
M. Ronaghi, M. A. Eberle, J. B. Fan.
597
F Mechanism and potential diversity of T-cell
receptor rearrangement from sequence repertoires.
A. Murugan, T. Mora, A. Walczak, C. Callan.
598
W Expression of mouse acidic mammalian
chitinase in
Escherichia coli
and characterization of its
properties.
A. Kashimura, Y. Kida, M. Ohno, K. Ishikawa,
M. Sakaguchi, F. Oyama.
599
F Functional analysis of mouse chitinase-like
protein Ym1.
Y. Kida, M. Sakaguchi, Y. Sugahara, F.
Oyama.
600
F Targeted deep sequencing by mobile element
scanning (ME-Scan) reveals Alu insertions throughout
the genome and around the world.
D. J. Witherspoon,
W. S. Watkins, Y. Zhang, J. Xing, M. A. Batzer, L. B. Jorde.
Pharmacogenetics
601
T Identification of
HNRNPA1
as a novel regulator
of cholesterol metabolism.
C. Yu, E. Theusch, D. A.
Nickerson, K. Lo, M. Kutilova, R. M. Krauss, M. W. Medina.
602
T Novel association of dual anti-platelet drug
response with a functional variant in
PPARG
.
A. S.
Fisch, J. Liu, J. P. Lewis, L. M. Yerges-Armstrong, J. R.
O’Connell, B. D. Mitchell, R. B. Horenstein, N. Ambulos, K.
Ryan, Q. Gibson, J. Shelton, A. R. Shuldiner.
603
T Genetic variations associated with gemcitabine
treatment outcome in pancreatic cancer.
L. Li, B.
Fridley, G. Jenkins, E. Carlson, K. Kalari, G. Petersen, R.
McWilliams, L. Wang.
604
T Large scale phenotyping using the 1000 Genomes
Project lymphoblastoid cell line panel.
D. Spacek, M.
Kaganovich, M. Snyder.
605
T The association of
SLC6A4
with antidepressant-
induced mania: The long and the short of it.
J. M.
Biernacka, D. L. Walker, J. Geske, S. Winham, S. Crow, M.
Chauhan, S. McElroy, M. Frye.
606
T Interactions between polymorphisms in
eicosanoid metabolism genes and vasodilator
responses in humans.
L. N. Gordon, C. R. Lee, M.
Pretorius, R. N. Schuck, L. H. Burch, D. C. Zeldin, S. M.
Williams, N. J. Brown.
607
T Pharmacogenetics of schizophrenia: Predicting
early response to antipsychotic therapy.
M. Gupta, S.
Jain, R. Kukreti.
K. Ahmadi, E. Schadt, K. Stefansson, G. Davey Smith,
M. McCarthy, P. Deloukas, E. Dermitzakis, T. Spector,
MuTHER Consortium.
584
W Identifying age- and sex-associated gene
expression profiles in
.
7,000
whole-blood samples.
M. J. Peters, R. Joehanes, T. Esko, K. Heim, H. Völzke,
L. Pilling, J. Brody, Y. F. Ramos, B. E. Stranger, M. W.
Christiansen, S. Gharib, R. Hanson, A. Hofman, J.
Kettunen, D. Levy, P. Munson, C. O’Donnell, B. Psaty, F.
Rivadeneira, A. Suchy-Dicey, A. G. Uitterlinden, H. Westra,
I. Meulenbelt, D. Enquobahrie, T. Frayling, A. Teumer, H.
Prokisch, A. Metspalu, J. B. J. Van Meurs, A. D. Johnson
on behalf of CHARGE Gene Expression Working Group.
585
F Simplified sample preparation and streamlined
library preparation method for deep sequencing
ribosome protected mRNA fragments.
R. Vaidyanathan,
S. Kuersten, A. Radek, S. Swami, D. Vo, L. Penalva.
586
W Genetics and epigenetic regulation of eukaryotic
transcriptome.
Y. Wakabayashi, T. Ni, D. Corcoran, W.
Yang, U. Ohler, W. Peng, C. O’Donnell, J. Zhu.
587
F Differential protein expression in human-induced
pluripotent and embryonic stem cells.
S. Brown-Ford,
M. Pellitteri-Hahn, A. De La Forest, B. Halligan, S. Duncan,
M. Olivier.
588
W Understanding the molecular mechanisms
underlying autism spectrum disorders using iPSC-
derived neurons.
B. A. DeRosa, J. M. Van Baaren, G.
K. Dubey, J. M. Lee, M. L. Cuccaro, J. M. Vance, M. A.
Pericak-Vance, D. M. Dykxhoorn.
589
F Whole exome sequencing in familial non-HHT
brain arteriovenous malformations.
N. Bendjilali,
L. Tang, D. E. Guo, R. Hernandez, M. Segal, C. E.
McCulloch, S. Inoue, A. Koizumi, W. L. Young, L.
Pawlikowska, H. Kim.
590
W The investigation of angiotensin converting
enzyme I/D and plasminogen activator inhibitor-1
4
G/5G polymorphisms in venous thromboembolism
patients in Turkish patients.
H. Salifoglu, H. Kaya, M.
Karkucak, D. Torun, Y. Tunca.
591
F Organization of alphoid sequence clusters on
human chromosome 21.
W. Ziccardi, C. Putonti, J.
Doering.
592
W A high-resolution genome-wide map of meiotic
double-strand breaks in humans.
F. Pratto, K. Brick, P.
Khil, F. Smagulova, G. Petukhova, R. D. Camerini-Otero.
593
F Genome-wide scan of disease-inversion
association.
J. Ma, C. I. Amos.
594
W
HOXA11
and
MMP2
gene expressions in women
with pelvic organ prolapsus.
N. Yilmaz, G. Ozaksit, Y. K.
Terzi, S. Yilmaz, B. Budak, O. Aksakal, F. I. Sahin.
595
F Large scale whole genome and whole exome
sequencing of rhesus monkeys (
Macaca mulatta
)
in
five primate research centers.
M. Raveendran, D. Rio