Page 257 - 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
3273
T Ascertainment bias in microsatellites: Impact on
estimates of mutation rates.
B. Li, M. Kimmel.
3274
F Characterizing recent evolutionary changes on
the human lineage using the high-coverage Denisovan
genome.
F. Racimo, M. Kircher, J. Kelso, S. Pääbo,
Archaic Genome Analysis Consortium.
3275
W Recurrent tissue-specific mtDNA mutations are
common in humans.
S. M. Williams, D. C. Samuels, B. Li,
Z. Song, E. Torstenson, A. Rokas, T. A. Thornton-Wells, J.
H. Moore, T. M. Hughes, R. D. Hoffman, J. L. Haines, D. P.
Mortlock, C. Li.
3276
T Associations of human leukocyte antigen G with
resistance and susceptibility to HIV-1 infection in the
Pumwani Sex Worker Cohort.
M. Luo, W. Turk, J. Kimani,
C. Wachihi, T. Bielawny, T. Ball, F. Plummer.
3277
F Alleles at the rs3212368 SNP at the 3’UTR of the
MC1R
gene are associated with human pigmentation
by possible microRNA influence.
L. A. Marano, A. L.
Simões, E. A. Donadi, C. T. Mendes-Junior.
3278
W Targeted re-sequencing of 328 inherited
disease-associated genes in a family trio and HapMap
populations using the Ion AmpliSeq™ Inherited
Disease Panel and Ion PGM™ semiconductor
sequencing.
I. Casuga, B. Kong, D. Joun, S.-M. Chen,
C.-Y. Li, D. Ruff, R. Bennet, M. Shannon.
3279
T Sequencing of an extended pedigree in Western
chimpanzees.
O. Venn, I. Turner, Z. Iqbal, I. Mathieson, N.
de Groot, G. McVean.
3280
F Allelic and genotypic associations of SNPs of
the
OCA2
and
HERC2
genes with eye, hair and skin
pigmentation and the presence of freckles in Brazil.
E.
S. Andrade, N. C. A. Fracasso, P. S. Strazza Júnior, A. L.
Simões, C. T. Mendes-Junior.
3281
W
AKT3, ANGPTL4, eNOS3
,
and
VEGFA
associations with high altitude sickness in Han and
Tibetan Chinese at the Qinghai-Tibetan Plateau.
N.
Buroker, X.-H. Ning, Z.-N. Zhou, K. Li, W.-J. Cen, X.-F. Wu,
W.-Z. Zhu, C. R. Scott, S.-H. Chen.
3282
T A population genetic measure of the de novo
mutation rate using identity-by-descent estimates.
C. W.
K. Chiang, J. Li, M. G. Ehm, M. R. Nelson, J. Novembre.
3283
F Determination of
PON1
and
P2RY12
polymorphisms distribution in Hungary living
population samples.
B. Melegh, I. Janicsek, Cs. Sipeky,
B. Duga, B. I. Melegh, L. Jaromi, L. Magyari, J. Bene.
3284
W Mapping the genetic diversity of HLA haplotype
in Asia populations.
W. Y. Saw, R. T. H. Ong, C. C. Khor,
N. Kato, Y. Y. Teo.
3285
T Long runs of homozygosity contain a higher
fraction of all genome-wide deleterious homozygotes
relative to the fraction of all genome-wide non-
damaging homozygotes.
Z. A. Szpiech, J. Xu, T. J.
Pemberton, W. Peng, S. Zöllner, N. A. Rosenberg, J. Z. Li.
3260
W Heterogeneity in recombination among African
populations.
M. Capredon, J. Hussin, J. Quinlan, Y.
Idaghdour, L. Barreiro, T. de Malliard, J. C. Grenier, E.
Gbeha, P. Awadalla.
3261
T Linkage disequilibrium patterns in a Brazilian
population: A comparison of X chromosome STR
markers with autosomal and Y chromosome STR
markers.
S. Oliveira, C. Mendes-Júnior, A. Trindade-Filho.
3262
F Association of (CCTTT)n polymorphism in the
NOS2A
gene with tuberculosis in two population
groups of India.
M. Jena, P. Das, R. Bamezai.
3263
W Purifying selection in mitochondrial protein-
coding genes is highly effective in mammals and
congruent with evolution of nuclear genes.
S. I.
Nikolaev, K. Popadin, T. Junier, M. Baranova, S. E.
Antonarakis.
3264
T Molecular phylogeny of an autosomal region
under natural selection.
V. A. Canfield, A. Berg, S.
Peckins, S. Oppenheimer, K. C. Cheng.
3265
F MtDNA analysis of global populations supports
that major population expansions began before
Neolithic time.
H. Zheng, S. Yan, Z. Qin, L. Jin.
3266
W Different DNA methylation of
FOXP2
target
genes in adult cortices of humans and chimpanzees.
U. Zechner, D. Seifert, E. Schneider, N. El Hajj, B. Navarro,
I. Kondova, R. E. Bontrop, O. Bartsch, T. Haaf.
3267
T Skin color variation in the Orang Asli Tribes of
Peninsular Malaysia.
K. C. Ang, M. S. Ngu, K. P. Reid,
M. S. Teh, A. S. Zamzuraida, D. X. R. Koh, A. Berg, S.
Oppenheimer, S. Hood, M. M. Clyde, B. M. Md-Zain, V. A.
Canfield, K. C. Cheng.
3268
F Exome and RNA sequencing of French-
Canadians reveals an excess of rare variants that are
enriched at functionally important sites.
A. Hodgkinson,
F. Casals, Y. Idaghdour, J. Hussin, V. Bruat, T. de Malliard,
J.-C. Grenier, J.-P. Goulet, E. Gbeha, E. Hip-Ki, S. Girard,
J.-F. Spinella, V. Saillour, D. Sinnett, G. Rouleau, P.
Awadalla.
3269
W Evidence for selection at the
BDNF
Val66Met
polymorphism in 1000 Genomes Project populations.
C. V. Van Hout, A. G. Clark.
3270
T Mobile element evolution of the
Callithrix
jacchus
(
common marmoset).
M. K. Konkel, J. A.
Walker, B. Ullmer, R. Hubley, A. F. A. Smit, M. A. Batzer for
Marmoset Genome Sequencing and Analysis Consortium.
3271
F Association of GSTT1, MI and M3 gene
polymorphism with age and quantity of smoke in
Northern Indian COPD patients.
R. K. Shukla, S. Kant, S.
Bhattacharya, B. Mittal.
3272
W Polymorphic miRNA genomic sequences
embedded in CNV sites: A prospective screening in
Brazilian admixed population sample.
T. C. L. Lins, D. E.
Jimenez, A. P. M. Barbosa, R. W. Pereira.