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600F Correlation between ATRA-induced and basal
CD38
expression: Clinical implications of basal
expression as a response indicator to treatment of
autism spectrum disorder with retinoids.
P. S. Lai, O. S.
Yim, S. Chhabra, H. Muralidharan, M. Monakhov, R. P.
Ebstein.
601F Increased incidence of attention deficit
hyperactivity disorder in children with nail patella
syndrome.
I. McIntosh, C. López-Arvizu, A. Diaz-Stansky,
E. P. Sparrow, M. J. Strube, C. Slavin, J. E. Hoover-Fong,
E. Tierney.
602F Generation and characterization of a WNK1/
HSN2-/- mouse model of hereditary sensory
autonomous neuropathy type II.
V. Lavastre, S.
Ramalingan, G. Houle, J. Laganiere, S. Laurent, R.
Gaudet, P. Hince, D. Rochefort, G. Castonguay, K. Huot,
P. A. Dion, G. A. Rouleau.
603F A novel transgenic mouse model of Machado-
Joseph disease: Genetic, phenotypic and pathologic
similarities with the human disease.
S. D. Silva, A. S.
Fernandes, A. N. Carvalho, A. T. Castro, C. S. Cunha, P.
Maciel.
604F Somatic mutations mediated by Alu in
schizophrenia.
M. Ueno, A. Akahane, T. Hata, S. Nanko.
605F The effect of TOMM40 poly-T length and APOE
genotype on age of onset of neurodegenerative
diseases: A pilot study of frontotemporal lobe
dementia.
I. Grossman, A. M. Saunders, M. W. Lutz, O.
Chiba-Falek, K. M. Hayden, D. G. Crenshaw, C. M.
Hulette, B. L. Plassman, K. A. Welsh-Bohmer, J. R. Burke,
A. D. Roses.
606F SCA7: Clinical and genetic analysis of an Italian
family.
D. Italiano, P. Tarantino, C. Lombardo, E. V. De
Marco, C. Pastura, P. Bramanti, A. Quattrone, G. Annesi.
607F Two new Rett syndrome families: Expanding the
knowledge of
MECP2
frameshift mutations.
K. Ravn, G.
Roende, M. Duno, K. Fuglsang, K. L. Eiklid, Z. Tümer, J.
B. Nielsen, O. H. Skjeldal.
608F Analysis of modulation of FXTAS rCGG-mediated
neurodegeneration by CUGBP1 in
Mus musculus
.
Z. A.
Zalewski, P. Jin, L. T. Timchenko, D. L. Nelson.
Statistical Genetics and Genetic
Epidemiology
609F Bayesian SNP-set analysis for case-control
genome-wide association studies.
X. Wang, D. Qian.
610F Multivariate quality control improves genotyping
accuracy and call rate.
B. T. Webb, J. E. Dellava, L. M.
Hack, M. C. Neale, A. Corvin, M. Gill, F. A. O'Neill, D.
Walsh, K. S. Kendler, B. P. Riley.
Friday Poster Authors are reminded to remove posters from the boards at 4:00 pm.
The Exhibit Hall will close at 4:30 pm.
611F Characterization of genome-wide association
epistasis signals for serum uric acid in human
population isolates.
W. Wei, G. Hemani, A. Hicks, V.
Vitart, C. Cabrera-Cardenas, P. Navarro, J. Huffman, C.
Hayward, S. Knott, I. Rudan, P. Pramstaller, S. Wild, J.
Wilson, H. Campbell, N. Hastie, A. Wright, C. Haley.
612F Analyze X: A comparison of X chromosome an
autosomal results in GWAS.
A. Wise, L. Gyi, T. Manoli
613F Detecting pleiotropy via Bayesian latent variabl
modeling.
L. Xu, R. Craiu, A. D. Paterson, L. Sun.
614F Quantitative trait prediction based on SNP-arr
data: A simulation study.
W. Yip, C. Lange.
615F Common variants near
FRK/COL10A1
and
VE
are associated with advanced age-related macular
degeneration.
Y. Yu, T. R. Bhangale, J. Fagerness, S.
Ripke, G. Thorleifsson, P. L. Tan, E. H. Souied, A. J.
Richardson, J. E. Merriam, G. H. S. Buitendijk, S.
Raychaudhuri, L. Sobrin, E. Evangelou, A. Y. Lee, R. H.
Guymer, U. Chakravarthy, T. W. Behrens, K. Stefansson
C. M. van Duijn, J. R. Vingerling, C. C. W. Klaver, R.
Allikmets, M. A. Brantley Jr., P. N. Baird, N. Katsanis, U.
Thorsteinsdottir, J. P. A. Ioannidis, M. J. Daly, R. R.
Graham, J. M. Seddon.
616F The Kaiser Permanente/UCSF Genetic
Epidemiology Research Study on Adult Health and
Aging: Design of genotyping arrays using imputatio
and a hybrid SNP selection algorithm.
Y. Zhan, T.
Hoffmann, J. Gollub, M. Kvale, Y. Lu, G. Mei, M. Shen,
Webster, P. Kwok, C. Schaefer, N. Risch.
617F Imputation reference panel selection using
maximal phylogenetic diversity.
P. Zhang, N. A.
Rosenberg, S. Zöllner.
618F A high-performance computing package for
relatedness and principal component analysis in
GWAS.
X. Zheng, D. Levine, J. Shen, C. Laurie, B. Weir
619F The effect of genome-wide autozygosity on
cognitive ability.
D. P. Howrigan, G. Davies, B. M. Neal
A. F. McRae, S. E. Harris, N. G. Martin, M. J. Wright, N.
Pendleton, A. Payton, M. Horan, W. E. Ollier, A. Tenesa,
M. Starr, I. J. Deary, P. M. Visscher, M. C. Keller.
620F Loss of accuracy when imputing genotypes in
previously phased individuals.
P. H. Keung, B. L.
Browning.
621F Next-generation imputation: Assessing the 100
Genomes Project reference panel and imputation int
multi-ethnic cohorts.
S. C. Nelson, C. C. Laurie, B. L.
Browning, S. M. Gogarten, J. Li, M. Sale, B. B. Worrall,
Doheny, E. Bookman, GARNET Collaborative Research
Group.