Page 218 - ASHG 2012 Annual Meeting Program Guide

POSTER SESSIONS
207
POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
Than, K. Nadeau, M. Snyder.
2323
T Whole-genome deep-coverage sequencing
of asthma genomes.
M. A. R. Ferreira, C. S. Tang, G.
Chenevix-Trench.
2324
F Rare non-coding variant prioritization and
burden testing in whole genome sequencing of
complex traits.
K. J. Gaulton, M. A. Rivas, M. van de
Bunt, C. M. Lindgren, M. I. McCarthy, GoT2D Consortium.
2325
W Deep sequencing of genomic regions
associated with cleft lip susceptibility.
C. Harris,
E. Leslie, R. Fulton, T. Miner, E. Appelbaum, C. Fronick,
M. Mead, D. Larson, M. Adela Mansilla, A. Lidral,
L. Moreno, J. Hecht, M. Marazita, A. Scott, T. Beaty,
J. Murray, R. Wilson, G. Weinstock.
2326
T Exome sequencing identifies rare variants
associated with the common pain disorder
fibromyalgia.
H. Hor, E. Docampo, R. Rabionet, M. Gut,
M. Bayés, I. Gut, A. Collado, S. Ossowski, X. Estivill.
2327
F Application of whole genome sequencing
to identify susceptibility loci for polycystic ovary
syndrome.
G. Kosova, R. S. Legro, A. Dunaif, M. Urbanek.
2328
W
CYP1B1
,
MYOC
and
LTBP2
mutations in primary
congenital glaucoma patients in the United States.
S.
Lim, K. Tran-Viet, T. Yanovitch, S. Freedman,
T. Klemm, W. Call, C. Powell, A. Ravichandran, R.
Metlapally, E. Nading, S. Rozen, T. Young.
2329
T Enhancing sequencing lab workflows in the
SardiNIA project.
A. Maschio, F. Busonero, C. Sidore,
E. A. Ketterer, E. B. Pedersen, A. M. Chidester, A. M.
Gurkan, M. R. Coon, M. Dei, S. Lai, A. Mulas, M. G. Piras,
M. Lobina, B. Tarrier, S. Sanna, C. A. Brennan, G. R.
Abecasis, F. Cucca, R. H. Lyons.
2330
F Whole-exome sequencing identifies novel risk
variants for thrombotic storm.
P. Whitehead, N. D.
Dueker, G. Beecham, D. Hedges, A. Beecham, S. Hahn,
N. Hofmann, J. W. Lawson, D. Erkan, L. R. Brandao, A. H.
James, M. J. Manco-Johnson, R. Kulkarni, C. S. Kitchens,
T. L. Ortel, J. M. Vance, M. A. Pericak-Vance.
2331
W Identification of genetic modifiers associated
with risk of stroke in children with sickle cell anemia.
J. M. Flanagan, H. Linder, V. Sheehan, T. A. Howard, B.
Aygun, J. S. Hankins, M. Wang, G. A. Neale, R. E. Ware.
2332
T Implication of rare variants from European-derived
adiposity loci in African Americans.
J. Hester, P. Mudgal, J.
Li, J. Xu, P. Hicks, B. Freedman, D. Bowden, M. Ng.
2333
F Assessing the effect of rare variants on cancer
drug-induced cytotoxicity phenotypes using whole
genome sequence data.
A. Tikhomirov, A. Pluzhnikov, C.
R. King, A. Konkashbaev, E. Gamazon, M. E. Dolan, D. L.
Nicolae, N. J. Cox.
2334
W Detecting rare variant effects using extreme
phenotype sampling in sequencing association
studies.
I. Barnett, S. Lee, X. Lin.
2335
T Whole genome sequencing to identify rare genetic
K. Kristiansen, T. Hansen, G. Sanchez, I. Hallgrímsdóttir,
J. Wang, R. Nielsen, O. Pedersen.
2312
F Whole exome sequencing identifies a novel
mutation within the
FOXP3
gene in 2-generational
family with inflammatory bowel disease.
D. T. Okou,
K. Mondal, L. J. Kobrynski, J. G. Mulle, D. Ramachandran,
V. C. Patel, P. Bose, J. P. Waters, P. Sampath, D. J. Cutler,
M. E. Zwick, S. Kugathasan.
2313
W Identification of rare genetic variants that
contribute to diabetic nephropathy in type 2 diabetes
through family-based targeted exome sequencing.
M. G. Pezzolesi, J. Jeong, A. M. Smiles, J. Skupien, J. C.
Mychaleckyj, S. S. Rich, J. H. Warram, A. S. Krolewski.
2314
T Exome sequencing and functional data identify
PRDM1 and NPD52 as susceptibility factors in
Crohn’s disease.
A. Franke, D. Ellinghaus,
H. Zhang, S. Schreiber, M. Parkes.
2315
F Exome sequencing for Crohn’s disease
pedigrees.
B.-S. Petersen, Y. Zeissig, M. Kohl, S.
Schreiber, S. Zeissig, A. Franke.
2316
W Whole-exome sequencing of patients with
isolated biliary atresia.
E. A.-L. Tsai, S. Sukhadia,
C. Grochowski, C.-F. Lin, O. Valladares, L.-S. Wang,
L. Leonard, G. D. Schellenberg, K. M. Loomes, B. A.
Haber, M. Devoto, N. B. Spinner.
2317
T Identification of low-frequency and common
variants associated with circulating levels of vitamin
B
12
and folate.
N. Grarup, C. H. Sandholt, P. Sulem,
T. S. Ahluwalia, T. Sparsø, A. Albrechtsen, L. Husemoen,
D. R. Witte, Y. Li, A. Linneberg, R. Nielsen, T. Jørgensen, J.
Wang, T. Hansen, U. Thorsteinsdottir, K. Stefansson,
O. Pedersen.
2318
F Whole-exome sequencing in age-related
macular degeneration (AMD) using a highly-discordant
phenotype and genotype design: Evidence for novel
loci underlying bilateral late AMD.
W. K. Scott, W. H.
Cade, M. D. Courtenay, P. L. Whitehead, I. Konidari,
W. F. Hulme, S. G. Schwartz, J. L. Kovach, G. Wang,
A. Agarwal, J. L. Haines, M. A. Pericak-Vance.
2319
W Deep resequencing of GWAS loci identifies a
novel rare variant in
RNF186
associated with ulcerative
colitis.
P. Goyette, M. Beaudoin, G. Boucher, C. Stevens,
K. S. Sin Lo, A. Alikashani, M. Ladouceur, M. A. Rivas,
S. R. Brant, R. H. Duerr, D. P. McGovern, M. S. Silverberg,
M. D’Amato, A. Franke, S. Vermeire, G. Lettre, J. H.
Cho, R. J. Xavier, M. J. Daly, J. D. Rioux, NIDDK and
International IBD Genetics Consortia.
2320
T Traits of human disease significance segregating in
the non-human primate vervet.
W. Warren, A. J. Jasinska,
N. Tran, Y. Huang, K. Dewar, J. Kaplan, P. Minx, L. Hillier, R. K.
Wilson, M. Nordborg, G. M. Weinstock, N. B. Freimer.
2321
F Association and replication of rare allele
windows within cis-regulatory regions to nearby gene
expression.
A. Fish, L. Wiley, W. Bush.
2322
W Asthma: An omics view through discordant
monozygotic twins.
R. Chen, S. Runyon, J. Li-Pook-