Page 264 - ASHG 2012 Annual Meeting Program Guide

POSTER SESSIONS
253
POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
molecular diagnosis of pseudohypoparathyroidism
type 1a.
G. S. Charames, S. J. Steinberg, B. A. Karczeski,
M. A. Levine, G. R. Cutting.
3449
T DNA methylation of
ADCYAP1R1
is associated
with childhood asthma in Puerto Ricans.
W. Chen, N.
Boutaoui, Y. Y. Han, J. Brehm, C. Schmitz, E. Acosta-
Perez, M. Cloutier, D. Calvert, S. Thornton-Thompson, D.
B. Wakefield, M. Alvarez, A. Colón-Semidey, G. Canino, J.
C. Celedón.
3450
T The role of DNA methylation in cognitive decline
and Alzheimer’s disease.
L. B. Chibnik, B. T. Keenan, G.
Srivastava, M. L. Eaton, A. Meissner, J. A. Schneider, M.
Kellis, D. Bennett, P. L. De Jager.
3451
T Distinct DNA methylation signature in ovarian
cancer histological subtypes.
M. S. Cicek, D. C.
Koestler, B. L. Fridley, S. M. Armasu, K. R. Kalli, M. C.
Larson, R. A. Vierkant, B. J. Winterhoff, J. Chien, J. B.
Fan, M. Bibikova, B. Klotzle, G. Konecny, V. Shridhar, J. M.
Cunningham, E. L. Goode.
3452
T Identifying new biomarkers for alcohol use
behaviors in a methylome-wide MBD-seq study.
S.
L. Clark, K. A. Aberg, S. Nerella, G. Kumar, J. L. McClay,
W. Chen, L. Y. Xie, A. Hudson, G. Gao, J. Bukszar, C. M.
Hultman, P. K. E. Magnusson, P. F. Sullivan, E. J. C. G. van
den Oord, Swedish Schizophrenia Consortium.
3453
T Smoking reduces DNA methylation levels at
multiple genomic loci.
P. Deloukas, L. Tsaprouni, T.-P.
Yang, J. Bell, K. J. Dick, S. Kanoni, C. Nelson, E. Meduri, F.
Cambien, C. Hengstenberg, J. Erdmann, H. Schunkert, A.
H. Goodall, W. H. Ouwehand, T. Spector, N. J. Samani.
3454
T DNA hypomethylation of
INS-IGF2
and
BACH2
in affected individuals within discordant monozygotic
twins supports a role for epigenetic influences in type
1
diabetes susceptibility.
E. Elboudwarej, H. Quach, P.
Ramsay, J. Lane, E. Sinclair, L. Criswell, P. Fain, J. Jeffrey,
G. Eisenbarth, L. Barcellos, J. Noble.
3455
T Migration and DNA methylation: A comparison
of methylation patterns in type 2 diabetes
susceptibility genes between Indians and Europeans.
H. R. Elliott, G. K. Walia, A. Duggirala, A. Groom, S. U.
Reddy, G. R. Chandak, V. Gupta, M. Laakso, J. M. Dekker,
M. Walker, S. Ebrahim, G. Davey Smith, C. L. Relton, RISC
Consortium.
3456
T DNA methylation alterations associated
with autism spectrum disorders.
D. Grafodatskaya,
R. Rajendram, Y. Lou, D. T. Butcher, L. Senman, C.
Windpassinger, W. Roberts, S. W. Scherer, R. Weksberg.
3457
T A population-based method for identification of
differential methylation regions among samples.
C. L.
Hsiao, C. S. J. Fann, C. J. Chang.
3458
T Genetics and epigenetics of PON1 in Mexican-
American children.
K. Huen, K. Harley, P. Yousefi, A.
Bradman, L. Barcellos, B. Eskenazi, N. Holland.
3459
T Comprehensive DNA methylation profiling
genes related to metabolic pathways.
H. Kitajima, K.
Yamamoto.
3437
T Alterations in methylation status of immune
response genes promoters in cell-free DNA during
a hemodialysis procedure in patients with diabetic
nephropathy and in non-diabetic subjects.
M.
Korabecna, E. Pazourkova, A. Horinek, M. Mokrejsova, V.
Tesar.
3438
T Genome-wide DNA methylation study of obesity
and type 2 diabetes.
D. Zhou, D. Zhang, Z. Zhang.
3439
T Density of inter-individual epigenome variation
uncovered by integrative epigenome mapping at single
base resolution.
J. J. Lambourne, S. Busche, V. Adoue, T.
Kwan, M. Caron, G. Bourque, M. Lathrop, T. Pastinen.
3440
T Allelic-dropout during PCR in the promoter of
an imprinted gene potentially caused by interaction
between G-quadruplex structures and DNA
methylation.
M. A. Kennedy, A. J. Stevens, S. Stuffrein-
Roberts, A. Gibb, K. Doudney, A. Bagshaw, A. Aitchison,
M. R. Eccles, V. V. Filichev, P. R. Joyce.
3441
T Genetics of global DNA methylation patterns
in adipose tissue from twins and its effect on gene
expression and disease: The MuTHER Study.
E.
Grundberg, E. Meduri, J. K. Sandling, A. K. Hedman, S.
Keildson, J. Nisbet, M. Sekowska, A. Wilk, A. Barett, K.
S. Small, J. T. Bell, E. T. Dermitzakis, M. I. McCarthy, T. D.
Spector, P. Deloukas.
3442
T A methylome-wide MBD-seq study followed by
replication in a total of 3,000 schizophrenia case-
control samples identifies new disease biomarkers.
K.
A. Aberg, J. L. McClay, S. Nerella, S. L. Clark, G. Kumar,
W. Chen, A. N. Khachane, G. Gao, L. Y. Xie, A. Hudson, J.
Bukszar, C. M. Hultman, P. F. Sullivan, P. K. E. Magnusson,
E. J. C. G. van den Oord, Swedish Schizophrenia
Consortium.
3443
T Genome-wide estimation of DNA methylation
heritability in CD4 T-cells from 80 families.
D. Absher, L.
Waite, H. Tiwari, D. Arnett.
3444
T Epigenetic second hit on gene body of
PKD1
leads to cystic kidney in ADPKD.
J. Bae, Y. Woo, J. Lee,
J. Park, Y. Kim.
3445
T Altered DNA methylation in preeclamptic
placentas.
J. D. Blair, R. K. C. Yuen, P. von Dadelszen, W.
P. Robinson.
3446
T Highly abnormal methylation of the placental
genome in the CBAXDBA model of pregnancy failure.
S. Brown, E. Bonney, L. Brown.
3447
T DNA methylation profiles of paediatric obsessive
compulsive disorder.
D. T. Butcher, G. L. Hanna, D. R.
Rosenberg, R. Weksberg, P. D. Arnold.
3448
T Complete or partial loss of methylation at
the
GNAS
locus identified in patients referred for