Page 211 - 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
2100
T Mitochondrial genome database for Saudi
community.
I. Alabdulkareem, M. Albalwi, M. Alharbi, A.
Alghamdi, B. Alhamad, M. Aljumah.
2101
F Evolutionary insights into genetic and
environmental factors for Crohn’s disease in Ryuku
and Northern Kyushu.
S. Nakagome, H. Chinen, H.
Said, W. Suda, A. Iraha, A. Hokama, F. Kinjo, J. Fujita,
Y. Takeyama, S. Sakisaka, T. Matsui, J. Kidd, K. Kidd, S.
Kawamura, T. Hanihara, R. Kimura, H. Ishida, H. Morita, M.
Hattori, S. Mano, H. Oota.
2102
W The demographic and genetic dynamics of the
human sex ratio from conception to birth.
S. Orzack.
2103
T Critical illness from pandemic influenza A/H1N1
and
Streptococcus pneumoniae
co-infection in Nuevo
León, Mexico.
B. Silva, A. Padrón-Rocha, D. Reséndez-
Pérez, M. Bermúdez-de León.
2104
F Quantitative genetic analysis of reactivity
to three distinct behavioral challenges in an infant
primate model of susceptibility to anxiety disorders
and depression.
G. L. Fawcett, A. M. Dettmer, D. Kay, M.
Raveendran, J. D. Higley, N. D. Ryan, J. L. Cameron, J.
Rogers.
2105
W Genetic and environmental variables
contribute to genome-wide methylation variation
in geographically diverse Africans.
S. Soi, L. B.
Scheinfeldt, D. Diep, W. Beggs, N. Plongthongkum, S. A.
Tishkoff, K. Zhang.
Cardiovascular Genetics
2106
W The myocardial infarction-associated gene
PHACTR1
is controlled by MEF2.
M. Beaudoin, S.
Langlois, K. S. Lo, A. N’Diaye, J. C. Tardif, G. Lettre.
2107
T Association of variants in inflammatory gene
with disease severity in familial cerebral cavernous
malformations type 1.
H. Choquet, L. Pawlikowska,
J. Nelson, C. E. McCulloch, A. Akers, B. Baca, B.
Hart, L. Morrison, H. Kim, Brain Vascular Malformation
Consortium (BVMC).
2108
F Are loci associated with low density lipoprotein
cholesterol (LDL-C) in non-diabetics similarly
associated with LDL-C in type 1 diabetes?
K. M. Eny, L.
Sun, A. J. Canty, S. B. Bull, A. P. Boright, S. M. Hosseini,
P. A. Cleary, J. M. Lachin, A. D. Paterson, DCCT/EDIC
Research Group.
2109
W Sequencing candidate genes associated with
conotruncal heart defects.
K. Osoegawa, C. Parodi, N.
Mohammed, K. Schultz, D. Noonan, M. Ladner, G. Shaw,
E. Trachtenberg, E. Lammer.
2110
T Identification of sequence variants of hepatic
lipase (
LIPC
)
gene in individuals with extreme
HDL-C/TG levels.
D. Pirim, F. Y. Demirci, X. Wang, J. E.
Hokanson, R. F. Hamman, C. H. Bunker, M. M. Barmada,
M. I. Kamboh.
2087
W Risks for Mendelian disorders in the Bronx.
K.
Upadhyay, H. Ostrer, C. Oddoux.
2088
T
MAK
gene Alu element insertion: High carrier
frequency among Ashkenazi Jews most likely due to
founder effect.
L. Shi, M. Luo, L. Edelmann, R. Kornreich.
2089
F Whole exome sequencing reveals a rapid
change in the frequency of rare functional variants in
a founding population of humans.
A. Hodgkinson, F.
Casals, J. Hussin, Y. Idaghdour, V. Bruat, T. de Malliard, J.
C. Grenier, E. Gbeha, F. Hamdan, S. Girard, J. F. Spinella,
M. Lariviere, V. Saillour, J. Healy, I. Fernandez, D. Sinnett,
J. Michaud, G. Rouleau, E. Haddad, F. Le Deist, P.
Awadalla.
2090
W Whole exome sequencing in families with rare
perinatal onset immunodysregulatory diseases present
with fever and systemic inflammation
Z. Deng, Y. Liu,
A. Almeida de Jesus, H. Sun, M. Gadina, R. Goldbach-
Mansky.
2091
T The impact of population demography and
selection on the genetic architecture of complex traits.
K. E. Lohmueller.
2092
F Regional rare allele sharing in a homogeneous,
geographically clustered population.
S. L. Pulit, A.
Menelaou, C. C. Elbers, L. C. Francioli, P. I. W. de Bakker,
The Genome of the Netherlands Consortium.
2093
W Estimation of migration rates and patterns
based on distributions of rare variants.
R. Rothwell, M.
Ehm, P. St. Jean, M. Nelson, J. Novembre, S. Zöllner.
2094
T Exome sequencing revealing unique genetic
profile of Quebec Nunavik Inuit population
S. Zhou,
L. Xiong, A. Ambalavanan, A. Dionne-Laporte, D.
Spiegelman, E. Henrion, O. Diallo, C. Bourassa, N. Dupré,
M.-P. Dubé, P. Dion, G. Rouleau.
2095
F Inference of population structure using
sequence data.
G. Bhatia, A. Gusev, N. Zaitlen, B. J.
Vilhjalmsson, D. Diogo, P. K. Gregersen, J. Worthington,
L. Padyukov, S. Raychaudhuri, R. M. Plenge, B. Pasaniuc,
A. L. Price.
2096
W Population-specific variants in whole exome
sequencing of American Indians: The Strong Heart
Family Study.
S. A. Cole, P. E. Melton, K. Haack, C. Bizon,
J. K. Sailsbery, K. C. Wilhelmsen, E. T. Lee, L. G. Best, L.
A. Almasy, N. Franceschini.
2097
T Forward-in-time simulation of recombination,
quantitative traits, and selection.
D. Kessner, J.
Novembre.
2098
F A low frequency of copy number polymorphism
for the
NPEPPS
,
POLR2J4
,
and
PCDHB13
genes in a
sample of admixed Brazilian population.
D. Jimenez, T.
Lins, P. Taveira, R. Pereira.
2099
W Amylase gene copy number polymorphism
in ethnically admixed sample from Brazil.
T. Lins, D.
Jimenez, P. Taveira, R. Pereira.