Page 217 - ASHG 2012 Annual Meeting Program Guide

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POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
M. R. Hansen, T. T. Harkins, R. J. H. Smith.
2302
T Next-generation sequencing identifies genes
dysregulated in otosclerotic stapes bone and provides
a candidate gene set for filtering of whole exome
sequence data in familial cases.
J. L. Ziff, J. Lavy, H.
Powell, S. Khalil, K. P. Steel, S. R. Saeed, S. J. Dawson.
2303
F Dissection of healthy aging by whole genome
and exome sequencing of supercentenarian genomes.
X. Estivill, N. Badarinarayan, P. Rosenstiel, M. Bayés, S.
Ossowski, C. Tornador, H. Blanche, G. Escaramís, M. Gut,
S. Heath, F. Flachsbart, A. Nebel, M. Lathrop, A. Franke,
M. Gratacòs, S. Schreiber, I. Gut, D. Trujillano.
2304
W Whole exome sequencing cases: Fnding and
testing with external controls.
A. Hendricks on behalf of
UK10K Statistics Group.
2305
T Whole-exome sequencing study of four families
with bipolar disorder.
E. Elhaik, M. Pirooznia, F. S. Goes,
J. Parla, R. Karchin, A. Chakravarti, P. P. Zandi, W. R.
McCombie, J. B. Potash.
2306
F Whole exome sequencing of five
consanguineous families with juvenile myoclonic
epilepsy.
B. Ouled Amar Bencheikh, J. Gauthier, F.
Lahjouji, l. Jouan, P. La Chance Touchette, K. Khaldi, H.
Lamghari, C. Bourassa, D. Spiegelman, A. Dionne laporte,
H. Daoud, F. Hamdan, H. Belaidi, O. Ouazzani, P. Dion, P.
Cossette, G. Rouleau.
2307
W GEnetics of Nephropathy–an International
Effort (GENIE): CNV analysis.
Y. Meng, R. M. Salem, A.
J. McKnight, E. P. Brennan, N. Sandholm, C. Forsblom,
J. Florez, C. Godson, P.-H. Groop, A. P. Maxwell, J. N.
Hirschhorn for GENIE Consortium.
2308
T Whole genome sequencing identifies coding
variants influencing canonical lipid species in Mexican
American families.
C. Bellis, P. J. Meikle, J. M. Weir, J.
B. Jowett, T. M. Teslovich, G. Jun, S. Kumar, M. Almeida,
J. M. Peralta, E. E. Quillen, C. Fuchsberger, A. R. Wood,
T. M. Frayling, P. Cingolani, T. W. Blackwell, R. Sladek,
G. Atzmon, J. Laramie, S. Lincoln, D. M. Lehman, G.
Abecasis, M. C. Mahaney, T. D. Dyer, L. Almasy, R.
Duggirala, J. Blangero, J. E. Curran.
2309
F Identifying non-synonymous variants exhibiting
pleiotropic effects on preeclampsia and CVD risk
traits.
M. P. Johnson, S. P. Brennecke, J. M. Peralta, T.
D. Dyer, M. A. Almeida, J. M. Proffitt, C. E. East, A. G.
Comuzzie, M. C. Mahaney, L. Almasy, J. E. Curran, J.
Blangero, E. K. Moses.
2310
W Analysis of coding variants identified from
exome sequencing in diabetic and non-diabetic
nephropathy genes in African Americans.
J. N. Cooke,
N. D. Palmer, M. C. Y. Ng, P. J. Hicks, J. A. Bonomo, J. M.
Hester, C. D. Langefeld, B. I. Freedman, D. W. Bowden.
2311
T Assessing the role of low-frequency variants in
type 2 diabetes risk using exome sequencing of 2,000
Danish individuals.
K. E. Lohmueller, T. Sparso, Q. B. Li,
E. Andersson, N. Grarup, A. Albrechtsen, T. Korneliussen,
2289
W A replication study supports
NOD2
and
CCDC122
as leprosy susceptibility genes.
H. Salomão, W. L. Silva,
P. Medeiros, V. M. Fava, I. M. F. Dias-Baptista, M. L. C.
Virmond, M. O. Moraes, M. T. Mira, A. C. Pereira-Latini.
2290
T Positive association of apolipoprotein E4
polymorphism with recurrent pregnancy loss in Iranian
patients.
M. T. Akbari, N. Asgari.
2291
F Investigation of rs4236601 and rs4977756 SNPs
in a primary open-angle glaucoma Brazilian population.
H. F. Nunes, M. B. Oliveira, J. P. C. Vasconcellos, V. P.
Costa, M. B. de Melo.
2292
W Role of genetic variation at the
FTO
gene
in genetic susceptibility to osteoarthritis.
K.
Panoutsopoulou, S. Metrustry, S. Doherty, L. L. Laslett, R.
A. Maciewicz, D. J. Hart, W. Zhang, K. R. Muir, M. Wheeler,
arcOGEN Consortium, C. Cooper, T. Spector, F. M. Cicuttini,
G. Jones, N. K. Arden, M. Doherty, E. Zeggini, A. Valdes.
2293
T Association of
COX-2, IL-1b
and
IL-1 RN
gene polymorphisms with susceptibility to chronic
periodontitis in North India population.
G. Prakash,
S. Ajay, K. K. Gupta, J. Dixit, D. Bali, B. Mittal.
2294
F A variant of filaggrin are associated with
susceptibility to food allergy in the Japanese
population.
T. Hirota, M. Ebisawa, T. Imai, Y. Suzuk,
N. Shimojo, Y. Kohno, M. Kubo, M. Tamari.
2295
W
AKT1
fails to replicate as a longevity-associated
gene in Danish and German nonagenarians and
centenarians.
M. Nygaard, M. Soerensen,
F. Flachsbart, J. Mengel-From, Q. Tan, S. Schreiber,
A. Nebel, K. Christensen, L. Christiansen.
2296
T Association of
HLA-DRB1
and
HLA-DQB1
genes
with asthma in the Spanish population.
M. Pino-Yanes,
A. Corrales, M. Acosta-Herrera, J. Cumplido, F. Sánchez-
García, R. González, J. Figueroa, I. Sánchez-Machín,
O. Acosta, A. Sánchez-Palacios, J. C. García-Robaina,
J. Villar, E. G. Burchard, T. Carrillo, C. Flores.
2297
F Turning the GWAS upside down: A PheWAS
approach in studying human disease.
S. Hebbring,
S. Schrodi, Z. Ye, Z. Zhou, D. Page, M. Brilliant.
2298
W Assessment of bias in an EMR-derived cohort.
W. S. Bush, L. C. Dumitrescu, D. C. Crawford.
2299
T Defining the use of electronic medical records
in genetic studies of multiple sclerosis.
M. F. Davis, J. L.
McCauley, J. C. Denny, J. R. Oksenberg, S. L. Hauser, M.
A. Pericak-Vance, J. L. Haines.
2300
F The NINDS Repository: A public resource of
biomaterials for genetic, mechanistic and biomarker
discovery for neurological disorders.
A. Scutti, M. Self,
K. Reeves, J. Santana, S. Heil, C. Pérez, A. Nasuti, R.
Corriveau, C. Tarn.
2301
W Mutation of
SLC45A3
in familial and sporadic
Ménière’s disease.
C. A. Campbell, B. J. Boese, C. C.
Della Santina, C. Li, N. C. Meyer, L. T. TeGrootenhuis,
J. Webster, D. A. Stephan, H. Najmabadi, A. Danashi, A. P.
May, K. Fredrickson, B. J. Gantz, J. P. Carey, L. B. Minor,