Page 203 - ASHG 2012 Annual Meeting Program Guide

192
POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
2001
W Post GWAS analysis of the
BCL11A
intronic
region to define its role in regulating HbF levels.
F. Anedda, S. Sanna, I. Asunis, G. Usala, F. Danjou,
L. Perseu, A. Cabriolu, C. A. Caria, L. Porcu, M. G. Marini,
M. Marongiu, C. Sidore, R. Berutti, M. Pala, A. Angius,
F. Busonero, A. Maschio, S. Satta, F. Demartis, L. Maccioni,
A. Meloni, R. Nagaraja, G. Abecasis, D. Schlessinger,
M. S. Ristaldi, R. Galanello, P. Moi, F. Cucca, S. Sanna,
M. Uda.
2002
T Additional patients and an association study
support a role of SOX9 in CD-ACD-PRS phenotypic
continuum and in CPO.
M. Quentric, L. Desmyter,
M. Ghassibe, W. Courtens, S. Kivirikko, H. Antoine-Poirel,
G. Ameye, B. Bayet, G. Francois, R. Vanwijck, O. Boute,
P. Pellerin, M. Rubini, M. Vikkula.
2003
F The impact of amino acid polymorphisms
in four genes of the tumor necrosis factor (TNF)
and interferon-gamma pathways on BCG-triggered
production of TNF.
T. Yu, L. de Léséleuc, A. Cobat,
L. Simkin, G. F. Black, K. Stanley, P. van Helden, L. Abel,
A. AlcaÔs, E. G. Hoal, E. Schurr.
2004
W Functional variants of
NFKBIE
and
RTKN2
genes
are associated with rheumatoid arthritis susceptibility
in Japanese.
K. Myouzen, Y. Kochi,
Y. Okada, C. Terao, A. Suzuki, K. Ikari, T. Tsunoda,
A. Takahashi, M. Kubo, A. Taniguchi, F. Matsuda,
K. Ohmura, S. Momohara, T. Mimori, H. Yamanaka,
N. Kamatani, R. Yamada, Y. Nakamura, K. Yamamoto.
2005
T Resequencing
ITGAM
reveals two functionally
deleterious rare variants in systemic lupus
erythematosus cases.
A. L. Roberts, E. R. A. Thomas,
S. Bhosle, L. Game, O. Obraztsova, T. J. Aitman,
T. J. Vyse, B. Rhodes.
2006
F
DcR3
mutations in systemic lupus
erythematosus patients lead to enhanced lymphocyte
proliferation.
K. Suphapeetiporn, C. Chokdeemeeboon,
P. Ammarinthnukrowh, S. Tongkobpetch, C. Srichomthong,
T. Deekajorndech, P. Rianthavorn, P. Kingwattanakul,
Y. Avihingsanon, V. Hoven, S. Edwards, N. Hirankarn,
V. Shotelersuk.
2007
W A
CD14
promoter polymorphism is implicated
in tuberculosis susceptibility in a South African
population.
M. Möller, C. Wagman, M. Daya,
C. Kok, L. van der Merwe, P. D. van Helden, E. G. Hoal.
2008
T Effects of IL9 and IL9 receptor gene
polymorphisms on allergic rhinitis in Iranian females.
F. Fatahi, H. Khazraee, K. Ghatreh, M. Hashemzadeh.
2009
F
TRIB1
is involved in the susceptibility of non-
alcoholic fatty liver disease.
S. Iwamoto, Y. Ishizuka, Y.
Kitamura, S. Makishima, S. Boonvisut, K. Nakayama.
2010
W Alleles of a rapidly-evolving ETV6 binding
site in
DCDC2
confer risk of reading and language
impairment.
N. R. Powers, J. D. Eicher, F. Butter,
L. L. Miller, S. M. Ring, M. Mann, J. R. Gruen.
1988
F Functional assessment of
CRY2
type II diabetes
variants using a targeted circadian luciferase assay.
J. Lane, A. Tare, C. Cowan, R. Saxena.
1989
W Modification of endothelial progenitor
cell recruitment by tyrosinase in oxygen-induced
retinopathy.
B. E. O’Bryhim, R. S. White, R. C. A. Symons.
1990
T Understanding the impact of body mass index
and associated SNPs on serum metabolites.
J. Kumar,
R. Karlsson, J. Prince, M. Hong, C. Broeckling, J. Prenni,
E. Ingelsson, F. Wiklund.
1991
F Biological processes of human development and
genome-wide linkage disequilibrium.
I. Culminskaya,
A. Kulminski, A. Yashin.
1992
W The type 1 diabetes gene
CLEC16A
functions
in NK cells to restrain secretory functions including
cytokine release and cytotoxicity.
M. Bakay, R. Pandey,
A. Mohamed-Hadley, P. Banerjee, H. H. Hakonarson.
1993
T Influence of ethnicity with type 2 diabetes in
association of UCP2 -866G/A, PGC1
a
(
Gly 482 Ser) and
SIRT1 -1400T/C polymorphisms in North Indian Punjabi
population groups.
A. Bhanwer, N. Kaul, R. N. K. Bamezai.
1994
F Allelic variation in the protein stability of
HLA shapes genetic association of HLA with type 1
diabetes.
H. Miyadera, J. Ohashi, K. Tokunaga.
1995
W Functional characterization of gene regulatory
elements associated with epilepsy.
R. Y. Birnbaum,
Y. Zhang, C. Wei, N. Ahituv.
1996
T Differential behavior of splice isoforms of the
asthma susceptibility gene
DENND1B
.
M. E. March,
P. M. A. Sleiman, C. Hou, J. Bradfield, C. E. Kim,
E. Frackelton, J. T. Glessner, H. Hakonarson.
1997
F Targeted resequencing identifies secretion-
defective variants of decoy receptor 3 in pediatric-onset
inflammatory bowel disease.
C. J. Cardinale,
S. Panossian, F. Wang, E. Frackelton, C. E. Kim,
F. D. Mentch, R. M. Chiavacci, K. E. Kachelries, R. Pandey,
S. F. A. Grant, R. N. Baldassano, H. Hakonarson.
1998
W A population-based immunologic phenotype
study for the identification of high risk individuals to
childhood infectious diseases in Vietnam.
R. Miyahara,
L. M. Yoshida, H. Nakamura, K. Takahashi, X. M. Trinh,
D. A. Dang, N. H. Tran, K. Ariyoshi, M. Yasunami.
1999
T A birth-cohort study for the identification of
genetic risk for childhood infectious diseases in
Vietnam.
M. Yasunami, L. M. Yoshida, R. Miyahara,
H. Nakamura, K. Takahashi, H. Moriuchi, D. A. Dang,
N. H. Tran, K. Ariyoshi.
2000
F Variant genotypes of
PKR1
and
PKR2
in patients
of recurrent pregnancy loss.
M. Su, L. Wu, P. Kuo.