PubRank

Christelle Borel

Author PubWeight™ 39.30‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Common regulatory variation impacts gene expression in a cell type-dependent manner. Science 2009 11.28
2 Genetic structure of Europeans: a view from the North-East. PLoS One 2009 3.46
3 Passive and active DNA methylation and the interplay with genetic variation in gene regulation. Elife 2013 2.70
4 Human microRNA-155 on chromosome 21 differentially interacts with its polymorphic target in the AGTR1 3' untranslated region: a mechanism for functional single-nucleotide polymorphisms related to phenotypes. Am J Hum Genet 2007 2.62
5 New class of gene-termini-associated human RNAs suggests a novel RNA copying mechanism. Nature 2010 1.78
6 Synaptojanin 1-linked phosphoinositide dyshomeostasis and cognitive deficits in mouse models of Down's syndrome. Proc Natl Acad Sci U S A 2008 1.54
7 DYRK1A-dosage imbalance perturbs NRSF/REST levels, deregulating pluripotency and embryonic stem cell fate in Down syndrome. Am J Hum Genet 2008 1.45
8 Evidence for transcript networks composed of chimeric RNAs in human cells. PLoS One 2012 1.16
9 Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity. Eur J Hum Genet 2012 1.12
10 ARF1 regulates Nef-induced CD4 degradation. Curr Biol 2004 1.06
11 Different mechanisms preclude mutant CLDN14 proteins from forming tight junctions in vitro. Hum Mutat 2005 1.03
12 Regulation of fibrinogen production by microRNAs. Blood 2010 0.99
13 Three common polymorphisms in the CYBA gene form a haplotype associated with decreased ROS generation. Hum Mutat 2009 0.95
14 Peutz-Jeghers LKB1 mutants fail to activate GSK-3beta, preventing it from inhibiting Wnt signaling. Mol Genet Genomics 2005 0.93
15 Rapid multiplexed genotyping of simple tandem repeats using capture and high-throughput sequencing. Hum Mutat 2013 0.93
16 The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome. Genome Res 2013 0.92
17 A mouse embryonic stem cell bank for inducible overexpression of human chromosome 21 genes. Genome Biol 2010 0.86
18 DNA methylation profiling in X;autosome translocations supports a role for L1 repeats in the spread of X chromosome inactivation. Hum Mol Genet 2013 0.82
19 Effects of liver growth factors on hepadnavirus replication in chronically infected duck hepatocytes. J Hepatol 2005 0.80
20 Detection of parent-of-origin specific expression quantitative trait loci by cis-association analysis of gene expression in trios. PLoS One 2012 0.79
21 Transcriptional and post-transcriptional profile of human chromosome 21. Genome Res 2009 0.78
22 Extensive natural variation for cellular hydrogen peroxide release is genetically controlled. PLoS One 2012 0.77
23 Research resource: the dynamic transcriptional profile of sertoli cells during the progression of spermatogenesis. Mol Endocrinol 2015 0.76
24 Corrigendum: Domains of genome-wide gene expression dysregulation in Down's syndrome. Nature 2015 0.75
25 A Case of Wiedemann-Steiner Syndrome Associated with a 46,XY Disorder of Sexual Development and Gonadal Dysgenesis. Sex Dev 2015 0.75