Page 152 - ASHG 2013 Program Guide

POSTER SESSIONS
  139
POSTER SESSIONS
W=W
ednesday authors will present; T=Thursday authors will present; F=Friday authors will pr
esent
624
T Predicting the impact of non-coding genetic
variants on complex traits.
F. Luca, G. Moyerbrailean, R.
Pique-Regi.
625
F Mutation profiling of exonic-enhancers using
massively parallel reporter assays.
R. Y. Birnbaum, R.
P. Patwardhan, M. J. Kim, G. Finlay, J. Zhao, R. Bell, R. P.
Smith, A. A. Ku, J. Shendure, N. Ahituv.
626
W HSA21 single-minded 2 binding sites co-localize
with super-enhancers and pioneer transcription
factors in pluripotent mouse ES cells.
A. Letourneau, G.
Cobellis, F. Santoni, E. Falconnet, A. Vannier, M. Guipponi,
C. Borel, S. E. Antonarakis.
627
T Splicing QTL analysis from primary immune cells
identifies egulatory effects putatively associated with
autism and Alzheimer’s disease.
J. M. Replogle, T. Raj,
K. L. Rothamel, C. Benoist, B. E. Stranger, P. L. De Jager,
Immunological Variation Consortium.
628
F Transcription in the human brain: DNA
methylation in a single nucleosome may regulate an
opioid gene as a region-specific “epigenetic switch”
G. Bakalkin, T. Yakovleva, H. Watanabe, O. Kononenko, R.
Henriksson, I. Bazov.
629
W Sex chromosomes and sexual dimorphism in
human transcriptome.
D. Nguyen, C. Disteche.
630
T
FREM1
regulates genes important for HIV-1
replication and cell migration.
M. Luo, J. Sainsbury, P.
Lacap, F. Plummer.
631
F In vivo UAS
Gal
gene regulation analysis using a
novel approach.
H. Guillen Ahlers, A. Ludwig-Kubinski,
K. Lazarova, A. M. Greene, J. Kennedy-Darling, M.
Levenstein, C. Anderson, J. Barfknecht, R. Knoener, M.
Scalf, Y. Yuan, R. Cole, M. Shortreed, L. Cirillo, L. Smith,
M. Olivier.
632
W Functional impact of polymorphic inversions
on gene expression in humans.
M. Oliva, S. Villatoro, L.
Pantano, C. Aguado, D. Vicente-Salvador, D. Izquierdo, M.
Puig, T. Marques-Bonet, J. I. Lucas Lledó, R. Castelo, M.
Cáceres.
633
T Targeted sequencing of promoter-associated
tandem repeats identifies common functional e fects
on gene expression levels in the human genome.
A. J.
Sharp, A. Guilmatre, P. Garg, G. Highnam, D. Mittelman.
634
F Targeted CD4
1
effector memory T-cell gene
expression profiling identifies state-specific c
eQTLs among rheumatoid arthritis and celiac disease
risk variants.
X. Hu, H. Kim, C. Baecher-Allan, T. Raj, P.
Brennan, P. De Jager, M. Brenner, S. Raychaudhuri.
635
W Mapping the genetic architecture of gene
regulation in whole blood in the KORA study.
K.
Schramm, C. Marzi, C. Schurmann, M. Carstensen, E.
Reinmaa, C. Gieger, E. Mihhailov, R. Mägi, A. Peters, K.
Strauch, M. Roden, T. Illig, T. Meitinger, A. Metspalu, C.
Herder, H. Grallert, H. Prokisch.
610
F MicroRNA regulation in the inner ear and link
to deafness.
K. Avraham, A. Rudnicki, K. Ushakov, O.
Isakov, N. Shomron.
611
W Integrated microRNA and mRNA signature
associated with the transition from the locally confined
to the metastasized renal cell carcinoma.
J. Billaud, Z.
Wotschofsky, K. Jung, H. Meyer.
612
T Global patterns of miRNA variation and
population-specific di ferentiation based on whole
genome sequence data.
R. A. Rawlings-Goss, S.
Tishkoff.
613
F Evaluation and identification of master egulatory
microRNAs on protein levels.
A. L. Stark, R. J. Hause,
Jr., R. B. Jones, M. E. Dolan.
614
W Study of microRNAs regulated by hypoxia in
cells latently infected by Kaposi’s sarcoma-associated
virus.
C. Viollet-Djelassi, D. Davis, C. Camps, M. Reczko,
F. Pezzella, R. Yarchoan, I. Ragoussis.
615
T Functional assessment of snoRNA-derived
microRNAs in Prader-Willi syndrome.
V. Williamson, M.
Mamdani, G. McMichael, V. Vladimirov.
616
F New clues that shape microRNA expression
in human neurospheres.
C. Palacios, A. Espinoza, A.
Contreras, N. Najera, I. Rubio, A. Conejo, I. Ita, I. Palma.
617
W LncRNAs regulation in insulin resistance of the
adipose tissue.
M. Pradas-Juni, X. Bofill, F. Hanzu, C.
Fillat, R. Gomis, E. Fernandez-Rebollo.
618
T Characterization of piRNA genomic distribution
and expression variation in human individuals.
J. Xing,
H. Ha, J. Song, S. Wang, K. C. Chen.
619
F Alternative splicing of MAP/microtubule affinity
regulating kinase 4 in glioma: Search for involvement
of polypyrimidine-tract binding protein.
L. Fontana, D.
Rovina, C. Novielli, I. Magnani, L. Larizza.
620
W A synonymous change, p.Gly16Gly in
MECP2
exon 1, causes a cryptic splice event in a Rett
syndrome patient.
T. I. Sheikh, J. Vincent.
621
T Role of RNA editing in ER stress response.
A.
Richards, I. Wang, V. Cheung.
622
F Understanding translational regulation using
RNA-seq of ribosome protected mRNA fragments.
J.
Pease, S. Kuersten, P. De Araujo, D. Vo, S. Burs, M. Qiao,
A. Radek, E. Bahrami, P. Uren, A. Smith, L. Penalva.
623
W Integrator Complex Subunit 8 mutation
associated with cortical and cerebellar malformations
results in disruption of the Integrator complex and
spliceosomal defects.
G. M. Mancini, R. Oegema,
D. Baillat, R. Schot, D. Heijsman, L. van Unen, S.
Kheradmand Kia, J. Hoogeboom, A. Kremer, F. W.
Verheijen, P. van der Spek, R. M. Hofstra, E. Wagner, M.
Fornerod.