1
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Stem cell-related "self-renewal" signature and high epidermal growth factor receptor expression associated with resistance to concomitant chemoradiotherapy in glioblastoma.
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J Clin Oncol
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2008
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6.41
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2
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Validation of real-time methylation-specific PCR to determine O6-methylguanine-DNA methyltransferase gene promoter methylation in glioma.
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J Mol Diagn
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2008
|
2.71
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3
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Coordinated effects of sequence variation on DNA binding, chromatin structure, and transcription.
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Science
|
2013
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2.66
|
4
|
Genome-wide RNA polymerase II profiles and RNA accumulation reveal kinetics of transcription and associated epigenetic changes during diurnal cycles.
|
PLoS Biol
|
2012
|
2.12
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5
|
DNA methylation profiles of human active and inactive X chromosomes.
|
Genome Res
|
2011
|
1.68
|
6
|
Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts.
|
Genome Res
|
2010
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1.67
|
7
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Modulation of angiogenic and inflammatory response in glioblastoma by hypoxia.
|
PLoS One
|
2009
|
1.19
|
8
|
Elevated levels of MIC-1/GDF15 in the cerebrospinal fluid of patients are associated with glioblastoma and worse outcome.
|
Int J Cancer
|
2009
|
1.16
|
9
|
The Wnt inhibitory factor 1 (WIF1) is targeted in glioblastoma and has a tumor suppressing function potentially by induction of senescence.
|
Neuro Oncol
|
2011
|
1.10
|
10
|
A multiplicity of factors contributes to selective RNA polymerase III occupancy of a subset of RNA polymerase III genes in mouse liver.
|
Genome Res
|
2012
|
1.00
|
11
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A recurrent 14q32.2 microdeletion mediated by expanded TGG repeats.
|
Hum Mol Genet
|
2010
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1.00
|
12
|
Regulation of fibrinogen production by microRNAs.
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Blood
|
2010
|
0.99
|
13
|
Methylation profiling in individuals with uniparental disomy identifies novel differentially methylated regions on chromosome 15.
|
Genome Res
|
2010
|
0.97
|
14
|
Comprehensive spatiotemporal transcriptomic analyses of the ganglionic eminences demonstrate the uniqueness of its caudal subdivision.
|
Mol Cell Neurosci
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2008
|
0.94
|
15
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The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome.
|
Genome Res
|
2013
|
0.92
|
16
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Multiple imputations applied to the DREAM3 phosphoproteomics challenge: a winning strategy.
|
PLoS One
|
2010
|
0.91
|
17
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Tandem repeat sequence variation as causative cis-eQTLs for protein-coding gene expression variation: the case of CSTB.
|
Hum Mutat
|
2012
|
0.88
|
18
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Infrequent promoter methylation of the MGMT gene in liver metastases from uveal melanoma.
|
Int J Cancer
|
2008
|
0.83
|
19
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A fish-specific transposable element shapes the repertoire of p53 target genes in zebrafish.
|
PLoS One
|
2012
|
0.83
|
20
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Structural variation-associated expression changes are paralleled by chromatin architecture modifications.
|
PLoS One
|
2013
|
0.82
|
21
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Identification and removal of low-complexity sites in allele-specific analysis of ChIP-seq data.
|
Bioinformatics
|
2013
|
0.77
|
22
|
Extensive natural variation for cellular hydrogen peroxide release is genetically controlled.
|
PLoS One
|
2012
|
0.77
|
23
|
Corrigendum: Domains of genome-wide gene expression dysregulation in Down's syndrome.
|
Nature
|
2015
|
0.75
|