Page 207 - ASHG 2013 Program Guide

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POSTER SESSIONS
W=W
ednesday authors will present; T=Thursday authors will present; F=Friday authors will pr
esent
1998
T Bayesian co-estimation of selfing rate and
locus-specific mutation rates for a partially selfin
population.
B. D. Redelings, M. K. Uyenoyama.
1999
F Geographic structure of an allele associated
with blond hair color in western Island Melanesia.
H. Norton, E. Correa.
2000
W Test of synergistic interactions among
deleterious alleles in humans.
M. Sohail, A. Kondrashov,
P. I. W. de Bakker, S. Sunyaev, GoNL Consortium.
2001
T Genetic diversity is a predictor of survival in
humans.
N. A. Bihlmeyer, A. Scaria, M. Nalls, M. Garcia,
K. L. Lunetta, J. M. Murabito, D. R. Weir, J. A. Smith, G.
Davies, M. Allerhand, L. Yu, D. A. Bennett, S. S. Mirza, N.
Direck, A. Teumer, G. Homuth, A. V. Smith, V. Gudnason,
T. Lumley, D. E. Arking, on behalf of CHARGE Aging &
Longevity Working Group.
2002
F A study on genetic diversity of ADME genes in
ethnic groups in Northwestern China.
J. Li, S. Xu.
2003
W Diversity of lactase persistence alleles in
Ethiopia: Signature of a soft selective sweep.
D. M.
Swallow, B. L. Jones, T. O. Raga, A. Liebert, P. Zmarz,
E. Bekele, E. T. Danielson, A. K. Olsen, N. Bradman,
J. T. Troelsen.
2004
T Characterization of private and highly diverged
variants among human populations from the analysis
of exome sequencing.
L. R. Botigué, D. M. Bobo,
D. Twigg, C. D. Bustamante, J. M. Kidd, B. M. Henn.
2005
F Identification of known genes in a novel gene
discovery project: Experience of the FORGE Canada
Consortium.
S. L. Sawyer, C. L. Beaulieu, D. E. Bulman,
F. P. Bernier, K. M. Boycott, FORGE Canada Consortium.
2006
W Genic intolerance to functional variation and
the interpretation of personal genomes.
S. Petrovski,
Q. Wang, E. L. Heinzen, A. S. Allen, D. B. Goldstein.
2007
T Analysis of nucleotide changes in miRNAs
genes along primate evolution.
I. Balcells, M. Mele, T.
Marques-Bonet, Y. Espinosa-Parilla.
2008
F Mitochondrial haplogroup B and oxidative stress
associations with antiretroviral-associated peripheral
neuropathy in Thai individuals.
R. Levinson, T. Hulgan, M.
Gerschenson, N. Phanuphak, J. Ananworanich, A. Baker,
V. Valcour, D. E. LiButti, T. Jadwattanakul, D. Murdock,
J. McArthur, C. Shikuma, D. C. Samuels, SEARCH 003
Study Team.
2009
W Defects in the autophagy pathway contribute
to glaucoma caused by mutant myocilin accumulation.
X. Lin, G. Zode, C. C. Searby, V. C. Sheffield.
2010
T Modeling mutation events for complex variants
in human genome.
M. Bhuyan, I. Pe’er.
2011
F Modeling variability in the population mutation
rate using 1000 Genomes data for discovery and
interpretation of rare variation.
V. Aggarwala, B. Voight.
1983
T Moving backwards in time from present-day
sequences: The paradox of sequential founder events.
M. Jeanpierre.
1984
F Effective population size — Recombination,
gene conversion and linkage disequilibrium.
D. Labuda,
J. F. Lefebvre, C. Moreau.
1985
W Analysis of linkage disequilibrium associated
with Southeast Asian ovalocytosis.
M. K. Thompson,
J. A. Wilder.
1986
T Meiotic gene conversion in humans: Rate, sex
ratio and GC bias.
A. L. Williams, G. Genovese, T. Dyer, N.
Patterson, J. Blangero, D. Reich, T2D-GENES Consortium.
1987
F Linkage disequilibrium and haplotype blocks
determined by the analysis of 250K SNPs in three
quilombo remnants communities.
E. S. Andrade, D. M.
Salvanha, R. Z. N. Vêncio, L. M. Garrido, H. Krieger, A. L.
Simões, C. T. Mendes-Junior.
1988
W A recombination map of Latino populations
inferred using local ancestry.
S. Shringarpure, S.
Gravel, C. Gignoux, A. Moreno, C. Eng, S. Huntsman, D.
Torgerson, E. Burchard, C. Bustamante.
1989
T De novo genes in evolution:
Apcdd
,
a novel
dual Wnt and Bmp inhibitor.
V. Luria, S. G. Oh, A. H.
O’Donnell, A. M. Christiano.
1990
F Detecting evolutionary strata on the human X
chromosome in the absence of gametologous Y-linked
sequences.
M. Wilson Sayres, R. Shanker Pandey, R. Azad.
1991
W
NANOGP8
:
Evolution of a human-specific
cancer-promoting retrogene.
D. J. Fairbanks, T. H.
Ogden, A. D. Fairbanks, G. J. Parker, P. J. Maughan.
1992
T Characterizing bias in population genetic
inferences from uncertain genotype data.
E. Han, J.
Sinsheimer, J. Novembre.
1993
F The evolutionary impact of GC-biased gene
conversion on human populations.
J. Lachance, S. Tishkoff.
1994
W Characterization and evolution of LAVA
elements in gibbons.
M. K. Konkel, J. A. Walker, B.
Ullmer, T. J. Meyer, A. Damert, R. Hubley, A. F. A. Smit, L.
Carbone, M. A. Batzer, for Gibbon Genome Sequencing
and Analysis Consortium.
1995
T Genetic architecture of variants affecting
splicing in human populations.
Y. Lee, E. Gamazon, H.
Im, W. Hernandez, N. Cox.
1996
F From mouse to human: Evolutionary genomics
analysis of human orthologs of essential genes.
B.
Georgi, B. F. Voight, M. Bucan.
1997
W Exploring the relationship between immune
system related genetic variants and complex traits and
disease through a phenome-wide association study.
A. Verma, H. Kuivaniemi, G. Tromp, D. J. Carey, G. S.
Gerhard, J. E. Crowe Jr., M. D. Ritchie, S. A. Pendergrass.