Page 165 - ASHG 2013 Program Guide

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POSTER SESSIONS
W=W
ednesday authors will present; T=Thursday authors will present; F=Friday authors will pr
esent
934
T Systemic sclerosis and systemic lupus
erythematosus pan-meta-GWAS reveals new shared
susceptibility loci.
J. E. Martin, S. Assassi, L. M. Diaz-
Gallo, J. C. Broen, X. Zhou, J. D. Reveille, O. Gorlova, B. P.
C. Koeleman, T. R. D. J. Radstake, T. Vyse, M. D. Mayes,
M. E. Alarcon-Riquelme, J. Martin, SLEGEN.
935
F Replication study of age-related macular
degeneration susceptible gene using large genome-
wide association study of Japanese.
M. Miyake, K.
Yamashiro, H. Nakanishi, I. Nakata, Y. Akagi-Kurashige,
K. Kumagai, M. Oishi, A. Oishi, N. Gotoh, A. Tsujikawa,
M. Saito, Y. Kurimoto, T. Kawaguchi, C. C. Khor, C. Y.
Cheng, T. Y. Wong, R. Yamada, F. Matsuda, N. Yoshimura,
Nagahama Study Group.
936
W Imputation-based genomic coverage
assessments of current human genotyping arrays.
S.
C. Nelson, K. F. Doheny, E. W. Pugh, J. M. Romm, H. Ling,
S. R. Browning, B. S. Weir, C. C. Laurie.
937
T Understanding of
IL28B
gene associated with
treatment response for HCV patients.
N. Nishida, Y.
Tanaka, M. Sugiyama, Y. Mawatari, M. Ishii, C. Haga, K.
Tokunaga, M. Mizokami.
938
F Association of body mass-associated
polymorphisms in
FTO
intron 1 with determination of
Sasang constitutional types in Koreans.
A. Park, S. Cha,
H. Yu, J. Kim.
939
W A genome-wide association study to identify
susceptibility loci for bronchiolitis.
A. Pasanen, M. K.
Karjalainen, M. Ruotsalainen, E. Piippo-Savolainen, E.
Goksör, G. Wennergren, M. Hallman, M. Rämet, M. Korppi.
940
T The contribution of low frequency coding variants
to normal variation in adult height and BMI.
D. Pasko,
K. Stirrups, N. Masca, L. Southam, T. V. Varga, H. Zhang,
R. Mägi, D. Thompson, W. Zhang, A. Mahajan, R. A. Scott,
on behalf of UK ExomeChip Consortium.
941
F On individual genome-wide association studies
and their meta-analysis.
Y. Pei, L. Zhang, C. Papasian, Y.
Wang, H. Deng.
942
W Genome-wide association study and admixture
mapping reveals new loci associated with total IgE
levels in Latinos.
M. Pino-Yanes, C. R. Gignoux, J. M.
Galanter, A. M. Levin, R. Mathias, C. Eng, E. A. Nguyen,
L. A. Roth, S. Huntsman, K. Sandoval, A. Moreno, C. A.
Winkler, L. N. Borrell, B. A. Raby, S. T. Weiss, D. L. Nicolae,
C. Ober, D. A. Meyers, E. R. Bleecker, F. D. Martinez,
S. Sen, R. Kumar, C. Bustamante, K. C. Barnes, L. K.
Williams, D. G. Torgerson, E. G. Burchard, on behalf of
GALA II Investigators.
943
T Sequencing-based GWAS contributes to the
refinement of association signals for inflammator
markers in Sardinians.
E. Porcu, C. Sidore, M. Steri,
A. Mulas, M. Zoledziewska, F. Busonero, A. Maschio, F.
Danjou, G. Pistis, M. G. Piras, M. Dei, S. Lai, H. M. Kang,
C. Brennan, R. Berutti, M. F. Urru, M. Oppo, A. Angius, D.
Schlessinger, F. Cucca, G. Abecasis, S. Naitza, S. Sanna.
923
F Identification of multiple genetic susceptibility
loci in Takayasu’s arteritis.
T. Hughes, G. Saruhan-
Direskeneli, P. Coit, J. M. Guthridge, J. A. James, P.
A. Merkel, H. Direskeneli, A. H. Sawalha, on behalf of
Vasculitis Clinical Research Consortium and Turkish
Takayasu Study Group.
924
W Genome-wide association confirms
TCF4
as a
major locus for Fuchs endothelial corneal dystrophy
and identifies novel loci.
S. K. Iyengar, N. Afshari, R. P. Igo,
Jr., Y.-J. Li, J. L. Lass, G. Klintworth, for FECD Consortium.
925
T Sub-phenotype mapping in systemic lupus
erythematosus identifies multiple novel loci associated
with circulating interferon alpha.
S. Kariuki, Y. Ghodke-
Puranik, J. Dorschner, B. Chrabot, J. Kelly, B. Tsao, R.
Kimberly, M. Alarcón-Riquelme, C. Jacob, L. Criswell, K.
Sivils, C. Langefeld, J. Harley, A. Skol, T. Niewold.
926
F Presence of genome-wide associations for
Parkinson’s disease on the X chromosome.
M. F. Keller,
M. A. Nalls, A. B. Singleton, International Parkinson’s
Disease Genomics Consortium (IPDGC).
927
W Feasibility of routine bi- and tri-variate
exhaustive analysis of case-control GWAS.
A.
Kowalczyk, Q. Wang, B. Goudey, H. Ferra, D. Rawlinson,
J. Bedo, A. C. Kowalczyk, G. Abraham, F. Shi, L. Gor, R.
M. Campbell, C. Iglesias, A. Zarnegar, E. Kikianty, G. J.
Macintyre, I. Haviv, C. S. Ong, M. Inouye.
928
T Genetic variants associated with total lung
capacity in chronic obstructive pulmonary disease.
J.
H. Lee, G. M. Hunninghake, M. N. McDonald, M. H. Cho,
M. Hardin, E. S. Wan, P. J. Castaldi, A. Gulsvik, P. Bakke,
E. K. Silverman, C. P. Hersh, COPDGene and ECLIPSE
Investigators.
929
F The genome-wide association analysis and
meta-analysis of sciatica in two Finnish populations.
S.
Lemmelä, S. Solovieva, R. Shiri, I. Seppälä, M. Heliövaara,
M. Kähönen, M. Juonala, J. Viikari, O. Raitakari, T.
Lehtimäki, E. Viikari-Juntura, K. Husgafvel-Pursiainen.
930
W Replication of GWAS results for dental caries
in the permanent dentition.
D. Lewis, J. Shaffer, E.
Feingold, M. Cooper, R. Weyant, D. McNeil, R. Crout, S.
Reis, A. Vieira, M. Vanyukov, M. Marazita.
931
T Negative-regulation-of-apoptotic-process
identified to be associated with appendicular lean
mass through meta-analysis of pathway-based
genome-wide association analysis.
J. Li, C. Xu, Y.-F. Pei,
Q. Tian, H.-W. Deng.
932
F Cannabis dependence is associated with genetic
variants in genes linked to schizophrenia.
M. Lohsen,
R. Sherva, R. Koesterer, H. Kranzler, H. Zhao, L. Almasy, L.
Farrer, J. Gelernter.
933
W Examining genetic risk factors for progression
of chronic kidney diseases: Genome-wide pathway
analysis of PediGFR.
L. Luo, P. A. Kanetsky, J. Gupta,
N. Mitra, E. Wühl, A. Köttgen, S. L. Furth, B. A. Warady, F.
Schaefer, C. Wong.