Eugenia Migliavacca

Author PubWeight™ 32.43‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Stem cell-related "self-renewal" signature and high epidermal growth factor receptor expression associated with resistance to concomitant chemoradiotherapy in glioblastoma. J Clin Oncol 2008 6.41
2 Validation of real-time methylation-specific PCR to determine O6-methylguanine-DNA methyltransferase gene promoter methylation in glioma. J Mol Diagn 2008 2.71
3 Coordinated effects of sequence variation on DNA binding, chromatin structure, and transcription. Science 2013 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
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 1.67
7 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 A recurrent 14q32.2 microdeletion mediated by expanded TGG repeats. Hum Mol Genet 2010 1.00
12 Regulation of fibrinogen production by microRNAs. 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 2008 0.94
15 The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome. Genome Res 2013 0.92
16 Multiple imputations applied to the DREAM3 phosphoproteomics challenge: a winning strategy. PLoS One 2010 0.91
17 Tandem repeat sequence variation as causative cis-eQTLs for protein-coding gene expression variation: the case of CSTB. Hum Mutat 2012 0.88
18 Infrequent promoter methylation of the MGMT gene in liver metastases from uveal melanoma. Int J Cancer 2008 0.83
19 A fish-specific transposable element shapes the repertoire of p53 target genes in zebrafish. PLoS One 2012 0.83
20 Structural variation-associated expression changes are paralleled by chromatin architecture modifications. PLoS One 2013 0.82
21 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