Page 198 - ASHG 2012 Annual Meeting Program Guide

POSTER SESSIONS
187
POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
1885
T Genetic polymorphisms in
ESR1
and
ESR2
genes and risk of hypospadias in a multi-ethnic
study population.
S. Choudhry, E. J. Lammer, J. S.
Witte, S. Dasgupta, C. Ma, G. M. Shaw, L. S. Baskin,
S. L. Carmichael.
1886
F A missense mutation in exon 2 of adiponectin
receptor 2 is associated with serum insulin in
overweight and obese African-American subjects.
A. Doumatey, G. Chen, J. Zhou, H. Huang, A. Adeyemo,
C. Rotimi.
1887
W Common variants associated with normal
tension glaucoma and optic nerve degeneration
are also associated with glaucoma in exfoliation
syndrome.
B. Fan, S. Loomis, J. H. Kang, D. Y. Wang,
B. Yaspan, M. A. Hauser, L. R. Pasquale, J. L. Haines,
J. L. Wiggs.
1888
T Genetic variants in selenoprotein P plasma
1
gene (
SEPP1
)
are associated with fasting insulin
and first phase insulin response in Hispanics.
J. N.
Hellwege, N. D. Palmer, J. T. Ziegler, C. D. Langefeld,
C. Lorenzo, J. M. Norris, T. Takamura, D. W. Bowden.
1889
F Replication of GWAS meta-analysis associations
in a large Amish pedigree support
VWF
,
ABO
,
STXBP5
,
STAB2
,
and
SCARA5
as modifiers of VWF and FVIII
levels.
J. Hinckley, K. Wang, T. Burns, L. Law, A. Shapiro,
J. Di Paola.
1890
W Mutation analysis in zinc finger protein
isoform 1 (
ZNF644
)
in cases with moderate and high
myopia.
N. Kaur, S. Saini, V. Vanita.
1891
T To study the association of peroxisome
proliferator-activated receptor gamma (
PPARG
)
gene
polymorphism (p.Pro12Ala) with diabetic retinopathy.
R. Kaur, S. Goyal, V. Vanita.
1892
F Association of the IL17 gene polymorphisms
with lumbar disc disease.
A. Kelempisioti, I. Daavittila,
N. Noponen, S. Barral, J. Ott, J. Niinimaki, T. Koskelainen,
L. Ala-Koko, J. Karppinen, M. Männikkö.
1893
W Association and interaction of polymorphisms
in angiogenic genes with endometriosis.
M. M. Latha,
Q. Hasan, V. L. Kodati.
1894
T The
HLA-DPB1
and
DRB1
genes are
synergistically associated with Graves disease in
Han Chinese children.
Y. Lee, C. Huang, W. Ting, F. Lo,
T. Chang, C. Chu, Y. Wu, S. Chang, W. Lin, M. Lin.
1895
F Fine-mapping within regions of admixture
linkage to sarcoidosis risk in African Americans.
A. M. Levin, P. McKeigue, I. Datta, C. G. Montgomery,
I. Adrianto, M. Colombo, M. C. Iannuzzi, B. A. Rybicki.
1896
W Fine-mapping of central adiposity loci using
association results from multi-ethnic populations.
C. Liu, CHARGE, GIANT, CARe, and African American
Central Adiposity Consortia.
1874
F Evaluating laboratories’ interpretation of genetic
test results through a EuroGentest Proficiency Testing
survey.
E. Girodon, S. Berwouts, M. Rodriguez de Alba
Freiria, AF. Roux, D. Barton, L. Hoefsloot, S. Gardner,
O. Kamarainen, B. Fowler, M. A. Morris, E. Dequeker,
R. Hastings.
1875
F Interstate compatibility and emergency
preparedness of newborn screening laboratories at
the interface of clinical medicine and public health.
J. Mulvihill, P. Hopkins, S. Berberich.
1876
F Evaluation of the Bogotá Congenital
Malformations Surveillance Program.
I. Zarante,
C. Mallarino, G. Gracia.
1877
F Drivers, barriers and opportunities for genetic
testing services in emerging economies: The Genetic
Testing in Emerging Economies project.
I. Nippert,
A. Christianson, D. D. G. Horovitz, R. Raouf, C. D. Padilla,
V. Penchaszadeh, A. Rajab, I. C. Verma, N. Zhong,
L. Gribaldo, U. Kristoffersson, J. Schmidtke.
Complex Traits and Polygenic
Disorders
1878
W Genetic variation in susceptibility to
hypothyroidism induced hearing impairment.
Q. Fang,
T. J. Jones, T.-W. Gong, A. H. Mortensen, M. T. Fleming,
D. F. Dolan, M. I. Lomax, K. R. Johnson, M. Mustapha,
S. A. Camper.
1879
T Transethnic mapping of putative diabetic
nephropathy loci in African Americans.
N. D. Palmer,
M. C. Y. Ng, J. N. Cooke, M. Petrulis, B. I. Freedman,
D. W. Bowden.
1880
F The exon 3 deleted/full-lenght polymorphism
of the growth hormone receptor in the Brazilian
population: Association with idiopathic short
stature and body composition measurements in
osteoporosis.
F. A. Marques, T. C. L. Lins, C. T. Neves,
M. T. O. Cardoso, R. M. Lima, R. J. Oliveira, R. W.
Pereira, R. Pogue.
1881
W Variants in
PTPN22
and
SMOC2
genes and the
risk of thyroid disease in the Jordanian population.
A. Alkhateeb, N. Marzouka, R. Tashtosh.
1882
T Genetic associations with neonatal thyroid
stimulating hormone levels.
F. Alul, O. Shchelochkov,
S. Berberich, J. Murray, K. Ryckman.
1883
F TNF-
b
Nco1 polymorphism in relation to
postoperative sepsis outcome in joint care surgery.
K. Baghel, R. Srivastava, S. Raj, D. Sanghi.
1884
W Preeclampsia is associated with variation in
endoglin pathway genes.
M. J. Bell, J. M. Roberts, S. A.
Founds, A. Jeyabalan, L. Terhorst, Y. P. Conley.