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627T Coexpression network analysis in abdominal and
gluteal adipose tissue reveals regulatory genetic loci
for metabolic syndrome and related phenotypes.
J. L.
Min, G. Nicholson, I. Halgrimsdottir, K. Almstrup, A. Petri,
P. Keller, A. Barrett, M. Travers, N. W. Rayner, R. Mägi, F.
H. Pettersson, J. Broxholme, M. J. Neville, Q. F. Wills, J.
Cheeseman, M. Allen, C. C. Holmes, T. D. Spector, J.
Fleckner, M. I. McCarthy, F. Karpe, C. M. Lindgren, K. T.
Zondervan, GIANT Consortium, MolPAGE Consortium.
628T Pleiotropic relationships among measures of
body composition in Afro-Caribbeans from Tobago.
R.
L. Minster, A. L. Kuipers, C. M. Kammerer, A. L. Patrick, V.
W. Wheeler, J. M. Zmuda.
629T Association tests for rare and common variants:
An approach based on genotypic and phenotypic
measures of similarity between individuals.
I.
Mukhopadhyay, J. Zhao, A. Thalamuthu.
630T The effect of plasma fibrinogen on the risk of
venous thromboembolism among African American
and White women using oral contraceptives.
C. S.
Neal, F. D. Mili, W. C. Hooper, C. Lally, H. Austin.
631T Improving discrimination of true associations
from tracking associations: A test using simulated
disease data structured by real genomic data.
G.
Nelson, P. An, C. A. Winkler.
632T Japanese population structure estimated from
the Japanese Multi-institutional Collaborative Cohort
data.
T. Nishiyama, N. Hamajima, S. Suzuki, H. Kishino,
Japan Multi-institutional Collaborative Cohort.
633T Cross-sectional gender-stratified blood pressure
analyses in children: Results from a genome-wide
association study.
P. G. Parmar, H. R. Taal, V. Aalto, E.
Thiering, N. J. Timpson, M. Bustamante, N. G. Martin, G.
Verwoert, T. Lehtimäki, A. G. Uitterlinden, L. Briollais, C.
Stoltenberg, C. Power, J. P. Newnham, D. I. Boomsma, J.
Viikari, M. W. Gillman, H. N. Lyon, J. J. Hottenga, A.
Hofman, M. Kähönen, M. J. Tobin, O. Raitakari, V. W. V.
Jaddoe, M.-R. Jarvelin, L. J. Beilin, J. Heinrich, C. M. van
Duijn, C. E. Pennell, L. J. Palmer, EArly Genetics and
Lifecourse Epidemiology and CHARGE Consortiums.
634T Meta-analysis of genome-wide association
studies on atopic dermatitis identifies three novel risk
loci.
L. Paternoster, M. Standl, C.-M. Chen, A. Ramasamy,
K. Bønnelykke, L. Duijts, M.-R. Jarvelin, M. A. Ferreira,
Australian Asthma Genetics Consortium, H.-E. Wichmann,
D. Strachan, J. P. Thyssen, E. A. Nohr, D. L. Jarvis, B.
Feenstra, P. Sleiman, D. Glass, L. J. Palmer, N. M. Probst-
Hensch, B. Jacobsson, J. A. Curtin, D. I. Boomsma, G. H.
Koppelman, A. Sääf, H. Bisgaard, J. Heinrich, D. M.
Evans, S. Weidinger on behalf of EAGLE Eczema
Consortium.
Thursday Poster Authors are reminded to remove posters from the boards at 4:00 pm.
635T Segregation analysis of isolated cleft lip in a
high-prevalence cluster of South America: Uncomm
high-risk allele and implications for genetic
association studies.
F. A. Poletta, E. E. Castilla, I. M.
Orioli, J. C. Mereb, F. M. Carvalho, C. A. Brandon, J. M
Resick, A. R. Vieira, M. L. Marazita, J. S. Lopez-Camel
636T Classification of anthropometric validated
associations from GIANT using effects on childhood
growth.
R. M. Salem, J. N. Hirschhorn, Early Growth
Genetics Consortium.
637T Imprinting and maternal genotype effects of 4
genetic variants on combined asthma-plus-rhinitis
phenotype.
C. Sarnowski, G. Malerba, C. Laprise, K.
Rohde, M. Moffatt, P. Jeannin, M.-H. Dizier, P. F. Pignat
W. O. C. Cookson, M. Lathrop, F. Demenais, E. Bouzig
638T The Kaiser Permanente Research Program on
Genes, Environment and Health: A resource for
genetic epidemiology research linking electronic
health and environmental risk data to genomics dat
in a large cohort based in a health plan.
C. Schaefer,
Rowell, L. Walter, C. Somkin, S. Van DenEeden, C.
Quesenberry, L. Croen, L. Kushi, R. Whitmer, C. Iribarre
M. Henderson, D. Smethurst, M. Sadler, D. Ranatunga,
Shen, S. Sciortino, D. Ludwig, D. Olberg, K. Lapham, J.
Lin, S. Miles, S. Hesselson, T. Hoffman, M. Kvale, E.
Blackburn, P. Kwok, N. Risch.
639T Rare variants in
ANKRD31
and
CXADR
are
associated with blood pressure in African American
P. B. Shetty, H. Tang, T. Bamidele, A. C. Morrison, C. L.
Hanis, D. C. Rao, R. S. Cooper, N. Risch, X. Zhu.
640T Gene-based tests that account for covariates
and pedigree: The GLOGS / ACR pipeline for GWAS
complex traits.
S. Stanhope, M. Abney.
641T Clinical and epidemiological analyses of
nonsyndromic craniosynostosis.
C. G. Stevens, G.
Yagnik, L. Qi, E. Cherkez, P. A. Sanchez-Lara, V. Kimoni
J. Stoler, M. Cunningham, J. M. Graham, S. A. Boyd.
642T Descriptive analysis of skeletal dysplasias in t
Utah population.
D. Stevenson, J. C. Carey, J. L. B.
Byrne, S. Srisukhumbowornchai, M. L. Feldkamp.
643T Association testing for rare variants via pooled
design.
I. Tachmazidou, M. De Iorio, M. Falchi.
644T Additive polygenic effects on longevity and the
functional meaning.
S. V. Ukraintseva, D. Wu, K. G.
Arbeev, A. I. Yashin.
645T Association of a TOMM40 variable-length
polymorphism with risk and age at onset of Alzheim
disease is notiIndependent of APOE.
B. N. Vardaraja
G. Jun, J. Buros, L. Cantwell, K. L. Lunetta, T. Foroud,
Mayuex, J. Haines, M. A. Pericak-Vance, G. Schellenbe
L. A. Farrer, Alzheimer's Disease Genetics Consortium.