Page 161 - 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
840
W Mild deficiency of methylenetetrahyd ofolate
reductase (
MTHFR
)
increases resistance to malaria in
mice.
D. N. Meadows, M. Pyzik, Q. Wu, S. Torre, P. Gros,
S. Vidal, R. Rozen.
841
T In vivo modeling of genetic mechanisms
associated with sickle cell disease nephropathy.
B. R.
Anderson, E. E. Davis, M. J. Telen, A. E. Ashley-Koch.
842
F Evolution and functional genomics of host-
pathogen interaction in Crohn’s disease.
B. M. P.
Bowen, W. Zhang, K. Hui, J. H. Cho, TAGC.
843
W Identification of a egulatory variant that binds a
transcriptional activator complex including FOXA1 and
FOXA2 at the
CDC123/CAMKD
type 2 diabetes GWAS
locus.
M. P. Fogarty, S. Vadlamudi, M. E. Cannon, K. J.
Gaulton, K. L. Mohlke.
844
T Gene-gene interaction and RNA splicing profile
of
MAP2K4
gene in rheumatoid arthritis.
K. Shchetynsky,
M. Roninnger, D. Protsyuk, L. Klareskog, L. Padyukov.
845
F A polymorphism in human estrogen-related
receptor beta associated with physiologic measures
of noise-induced hearing loss.
I. Bhatt, S. Phillips, S.
Richter, R. Morehouse, D. Tucker, K. Lundgren, V. Henrich.
846
W Genetic risk variants for autoimmune diseases
regulate gene expression in thymus.
I. S. M. Gabrielsen,
S. Svanstrøm Amundsen, H. Helgeland, S. Tennebø Flåm,
N. Hatinoor, K. Holm, M. K. Viken, B. A. Lie.
847
T The apical sodium-dependent bile acid
transporter ASBT (
SLC10A2
)
affects the progression
of primary biliary cirrhosis in Japanese patients via its
transcriptional activity.
K. Taira, T. Inamine, A. Kawauchi,
S. Kondo, M. Nakamura, K. Tsukamoto.
848
F Comprehensive functional assays for variants of
unknown significance
J. O. Kitzman, L. Starita, R. Lo, R.
Qiu, S. Fields, J. Shendure.
849
W Expression of two genes from the candidate
locus of chromosome X in rheumatoid arthritis and
systemic sclerosis.
L. M. Diaz-Gallo, K. Shchetynsky, A.
Nordin, A. I. Catrina, J. Martín, L. Padyukov.
850
T An enhancer element harboring variants
associated with systemic lupus erythematosus engages
the
TNFAIP3
promoter to influence A20 exp ession.
S.
Wang, F. Wen, G. B. Wiley, M. T. Kinter, P. M. Gaffney.
851
F Gene-gene interactions of
EG-VEGF, PKR1
and
PKR2
genes and the risk of recurrent miscarriages.
M.
Su, P. Kuo, S. Lin.
852
W Gene-asbestos exposure interactions on lung
cancer risk.
C. Liu, I. Stücker, C. Chen, G. Goodman, M.
K. McHugh, A. M. D’Amelio, C. J. Etzel, S. Li, X. Lin, D. C.
Christiani.
853
T
RBMS1
genotype strongly influences adiposity
and liver function in rural but not urban dwellers.
M. E.
S. Bailey, C. A. Celis-Morales, M. Staunton, N. Ulloa, C.
Calvo, F. Perez-Bravo, J. M. R. Gill.
827
F A role for
IRF6
in cell cycle regulation and DNA
damage response in mesenchymal stem cells.
G. S.
Kobayashi, L. Alvizi, B. V. P. Almada, L. C. Andrade-Lima,
C. F. Menck, M. R. Passos-Bueno.
828
W Novel regulatory variants in family studies with
adult chronic atopic dermatitis.
W. B. Jones, T. C.
Pansuriya, K. J. Gulewicz, I. Oh, B. Borgo, A. Shemer, J.
G. Krueger, E. Guttman-Yassky, C. de Guzman Strong.
829
T Meta-analysis on eQTL mapping identify insertion
and deletion specific eQTLs in LCL, PBMC and skin
tissues.
J. Huang, J. Chen, J. Esparza, J. Ding, J. Elder, Y.
Lee, M. Moffatt, W. Cookson, L. Liang.
830
F Integrative genomics approach to unravel the
molecular mechanisms underlying genome-wide
association results for lung function measures.
M.
Obeidat, K. Hao, Y. Bossé, D. Nickle, D. Postma, M.
Laviolette, A. Sandford, D. Daley, C. Brandsma, M. Berge,
R. Vessey, G. Opitec, W. Timens, D. Sin, P. Paré.
831
W Identifying the molecular mechanisms at the
vascular
PLXND1
locus associated with human waist-
hip ratio.
T. S. Roman, J. E. N. Minchin, J. F. Rawls, K. L.
Mohlke.
832
T Genome-wide enrichments for regulatory regions
across thousands of unlinked disease-associated
variants.
A. K. Sarkar, L. Ward, M. Kellis.
833
F Enabling phenomics with high-throughput whole-
organism 3D pan-cellular imaging at cell resolution.
K.
Cheng, P. La Riviere.
834
W Genetic variants and regulation in human
complex diseases and traits.
C. Yao, R. Joehanes, A. D.
Johnson, B. Chen, T. Huan, J. E. Freedman, P. J. Munson,
D. Levy.
835
T READ1, a regulatory element within
DCDC2
,
epistatically affects reading and language with both
deleterious and protective alleles.
N. R. Powers, J. D.
Eicher, Y. Kong, L. L. Miller, S. M. Ring, J. R. Gruen.
836
F A computational framework for identifying
genes perturbed by MS associated variants through
regulatory element disruption.
P. Shooshtari, C.
Cotsapas.
837
W TNF-
b
Nco1 polymorphism and sepsis
susceptibility following major elective surgery.
R. N.
Srivastava, K. Baghel, S. Raj, A. Chandra, S. K. Goel.
838
T Genetic variation in the serotonin receptor gene
affects immune responses in rheumatoid arthritis.
E. Hesselberg, O. Snir, P. Amoudruz, L. Klareskog, I.
Zarea-Ganji, A. I. Catrina, L. Padyukov, V. Malmström, M.
Seddighzadeh.
839
F Regulation by the asthma susceptibility gene
DENND1B
of Rab35 and TNF
a
signaling.
M. E. March,
P. M. A. Sleiman, C. Hou, J. Bradfield, C. E. Kim, J. T.
Glessner, H. Hakonarson.