Page 216 - ASHG 2012 Annual Meeting Program Guide

POSTER SESSIONS
205
POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
2276
F Genetic association to ERAP1 in psoriasis
is confined to disease onset after puberty and not
dependent on HLA-C*06.
P. Nikamo, J. Lysell,
L. Padyukov, I. Kockum, M. Ståhle.
2277
W On the association of common polygenic variation
with body mass index across adolescent development:
A longitudinal twin study.
R. E. Peterson, B. T. Webb, E. C.
Prom-Wormley, J. L. Silberg, L. J. Eaves, H. H. Maes.
2278
T Absence of the chromosome 16p11.2
duplication in metabolically normal, constitutionally
thin individuals with extremely low BMI.
J. Hager,
N. Germain, E. Meugnier, B. Galusca, H. Vidal, B. Estour.
2279
F Lack of association of genetic variants in
PROX1
,
ADCY5
,
SLC2A2
,
DGKB-TMEM195
,
ADRA2A
,
CRY2
,
FADS1
,
IGF1
and
C2CD4B
with glucose- and
insulin-related traits in Chinese adolescents.
R. C. W.
Ma, C. Tam, G. Jiang, J. Ho, V. Lam, Y. Wang, H. M. Lee,
A. Kong, W. Y. So, J. Chan.
2280
W Combined effects of genetic variants identified
from genome-wide association studies increased risk
of type 2 diabetes in Chinese.
C. Tam, J. Ho, Y. Wang,
V. Lam, M. Ng, R. Ma, W. So, J. Chan.
2281
T
AGRP
SNPs and gender effects on obesity in
African Americans.
E. Shah, A. Patterson, U. Al-Alem,
R. A. Kittles.
2282
F Pleiotropic effects of obesity-susceptibility loci
on metabolic traits: A meta-analysis of up to 37,874
individuals.
J. van Vliet-Ostaptchouk, M. den Hoed, J.
Luan, J.-H. Zhao, K. K. Ong, P. J. van der Most, A. Wong, R.
Hardy, D. Kuh, M. M. van der Klauw, M. Bruinenberg, B. H. R.
Wolffenbuttel, N. J. Wareham, H. Snieder, R. J. F. Loos.
2283
W Investigation of celiac disease susceptibility
variants in the Irish population using the immunochip.
C. Coleman, E. Quinn, A. W. Ryan, J. Conroy, S. Ennis,
V. Trimble, R. McManus.
2284
T Risk alleles associated with ANA production in
healthy population or transition to autoimmunity.
E.
Wakeland, P. Raj, E. Rai, Q. Z. Li, D. Karp, P. Doshi,
N. Olsen, K. M. Sivils, J. James, J. Kelly, B. Lauwerys.
2285
F Interleukin-18 genetic polymorphism and
Kawasaki disease in Han Chinese children.
H. Chi,
M.-R. Chen, N.-C. Chiu, F.-Y. Huang, H.-W. Chan, S.-C.
Chang, C.-L. Lin, Y.-J. Lee.
2286
W Association between IL1A, IL1B and TNFA
polymorphisms and glaucoma in a Brazilian population.
M. B. Oliveira, J. P. C. Vasconcellos, V. P. Costa, M. B. Melo.
2287
T Evaluation of new classification criteria for
HLA-DRB1 alleles based on three amino acid positions
(11, 71
and 74) in Japanese RA patients: Disease
susceptibility and severity.
S. Yoshida, K. Ikari, K. Yano,
Y. Toyama, A. Taniguchi, H. Yamanaka, S. Momohara.
2288
F Genetic susceptibility to leptospirosis in the
Azorean island of São Miguel population.
L. M. Esteves,
S. M. Bulhıes, M. J. Brilhante, C. C. Branco, F. M. Mota, C.
Paiva, M. L. Vieira, L. Mota-Vieira.
2264
F Possible roles of miRNA to regulate effective
signaling network in controlling cell fate.
M. Nomura,
S. Kondo, T. Nagashima, Y. Suzuki, M. Okada-
Hatakeyama.
2265
W Unraveling the molecular mechanisms
underlying the teratogenicity of Topamax (topiramate).
S. K. Rafi, A. J. Olm-Shipman, I. Saadi.
2266
T The CARTaGENE Genomics Project: Systems
genetics of cardiometabolic phenotypes.
Y. Idaghdour,
J.-P. Goulet, J. Hussin, A. Hodgkinson, E. Gbeha, J.-C.
Grenier, T. de Malliard, V. Bruat, E. Hip-Ki, C. Boileau, Y.
Payette, P. Awadalla.
2267
F Association of insulin-like growth factor-1
gene polymorphism in Kuwaiti Arab patients with
rheumatoid arthritis.
M. Haider, G. S. Dhaunsi,
S. S. Uppal.
2268
W Variations within
ARID5B, CEBPE
,
and
IKZF1
and risk of childhood leukemia.
L. Hsu,
A. Chokkalingam, C. Metayer, J. Wiemels, P. Buffler.
2269
T Contribution of common
PCSK1
genetic variants
to obesity in a sample of 8,359 subjects from two
multi-ethnic American populations.
H. Choquet,
J. Kasberger, A. Hamidovic, M. Fornage, E. Jorgenson.
2270
F Association between
IRF6
gene and non-
syndromic cleft lip and/or palate in Brazil.
T. Felix,
L. T. Souza, T. W. Kowalski, I. L. Monlleó, E. M. Ribeiro, J.
Souza, G. F. Leal, A. C. Fett-Conte, V. Gil-da-Silva-Lopes.
2271
W Validation of the
PPP1R12B
as a candidate gene
for childhood asthma susceptibility.
M. B. Freidin, A. V.
Polonikov.
2272
T Association of the SNP rs 9939609 of the fat
mass and obesity associated gene (
FTO
)
with the risk
for obesity in children from Yucatan, Mexico.
L. Gonzalez-Herrera, N. Mendez-Dominguez, F. Herrera-
Sanchez, G. Uicab-Pool, V. Hernandez-Escalante, L. Ruiz-
Ortiz, G. Storey-Montalvo, J. Zavala-Castro.
2273
F Shared genetic loci between leprosy and
inflammatory bowel disease in Korean patients.
Y. Jung, M. Hong, J. Baek, S. Yang, K. Song.
2274
W Fatness related allelic variant near insulin
receptor substrate 1 gene is associated with low
low-density lipoprotein cholesterol in childhood and
a better cardiometabolic profile in their adulthood:
The Bogalusa Heart Study.
S. Li, W. Chen, E. N. Smith,
S. S. Murray, C. Fernandez, J. Xu, S. R. Srinivasan, N. J.
Schork, G. S. Berenson.
2275
T Genetic variants associate with nonalcoholic
fatty liver disease in African and Hispanic Americans.
S. K. Musani, N. D. Palmer, M. F. Feitosa, M. A. Jhun, L. M.
Yerges-Armstrong, R. Hernaez, J. Liu, B. Kahali, J. J. Carr,
T. B. Harris, A. V. Smith, L. E. Wagenknecht, I. B. Borecki,
E. K. Speliotes, L. F. Bielak for Genetics of Obesity-Related
Liver Disease Consortium.