Published in Genome Res on December 08, 2004
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A differentially methylated region within the gene Kcnq1 functions as an imprinted promoter and silencer. Hum Mol Genet (2003) 1.50
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Genomic imprinting and seed development: endosperm formation with and without sex. Curr Opin Plant Biol (2001) 1.25
Insulator and silencer sequences in the imprinted region of human chromosome 11p15.5. Hum Mol Genet (2003) 1.20
Parental allele-specific chromatin configuration in a boundary-imprinting-control element upstream of the mouse H19 gene. Mol Cell Biol (1999) 1.17
Bidirectional silencing and DNA methylation-sensitive methylation-spreading properties of the Kcnq1 imprinting control region map to the same regions. J Biol Chem (2003) 1.13
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The potential role of gene duplications in the evolution of imprinting mechanisms. Hum Mol Genet (2003) 1.06
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Comparative sequence analysis of imprinted genes between human and mouse to reveal imprinting signatures. Genomics (2004) 1.02
The Tnfrh1 (Tnfrsf23) gene is weakly imprinted in several organs and expressed at the trophoblast-decidua interface. BMC Genet (2002) 0.98
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Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting. Hum Mol Genet (1999) 0.97
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Epigenomic profiling reveals DNA-methylation changes associated with major psychosis. Am J Hum Genet (2008) 4.71
The dynamics of genome-wide DNA methylation reprogramming in mouse primordial germ cells. Mol Cell (2012) 4.32
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CpG island methylation in human lymphocytes is highly correlated with DNA sequence, repeats, and predicted DNA structure. PLoS Genet (2006) 2.66
DNA methylation analysis of chromosome 21 gene promoters at single base pair and single allele resolution. PLoS Genet (2009) 2.37
Whole-genome bisulfite sequencing of two distinct interconvertible DNA methylomes of mouse embryonic stem cells. Cell Stem Cell (2013) 2.32
Dynamic link of DNA demethylation, DNA strand breaks and repair in mouse zygotes. EMBO J (2010) 2.30
Dnmt1 overexpression causes genomic hypermethylation, loss of imprinting, and embryonic lethality. Mol Cell Biol (2002) 2.24
Inter-individual variation of DNA methylation and its implications for large-scale epigenome mapping. Nucleic Acids Res (2008) 2.19
DNA-methylation analysis by the bisulfite-assisted genomic sequencing method. Methods Mol Biol (2002) 1.91
BiQ Analyzer HT: locus-specific analysis of DNA methylation by high-throughput bisulfite sequencing. Nucleic Acids Res (2011) 1.90
Epigenetic modifications in an imprinting cluster are controlled by a hierarchy of DMRs suggesting long-range chromatin interactions. Hum Mol Genet (2003) 1.73
High-resolution map and imprinting analysis of the Gtl2-Dnchc1 domain on mouse chromosome 12. Genomics (2005) 1.60
Active demethylation of the Foxp3 locus leads to the generation of stable regulatory T cells within the thymus. J Immunol (2013) 1.45
A critical control element for interleukin-4 memory expression in T helper lymphocytes. J Biol Chem (2005) 1.44
Differential dynamics of histone H3 methylation at positions K4 and K9 in the mouse zygote. BMC Dev Biol (2004) 1.30
DNA methylation analysis by bisulfite conversion, cloning, and sequencing of individual clones. Methods Mol Biol (2009) 1.26
A rapid, quantitative, non-radioactive bisulfite-SNuPE- IP RP HPLC assay for methylation analysis at specific CpG sites. Nucleic Acids Res (2002) 1.19
DNA-methylome analysis of mouse intestinal adenoma identifies a tumour-specific signature that is partly conserved in human colon cancer. PLoS Genet (2013) 1.13
Assisted reproductive technologies do not enhance the variability of DNA methylation imprints in human. J Med Genet (2009) 0.98
Adult monozygotic twins discordant for intra-uterine growth have indistinguishable genome-wide DNA methylation profiles. Genome Biol (2013) 0.97
Overexpression of the IGF2-mRNA binding protein p62 in transgenic mice induces a steatotic phenotype. J Hepatol (2010) 0.96
Dissecting the genotype in syndromic intellectual disability using whole exome sequencing in addition to genome-wide copy number analysis. Hum Genet (2013) 0.94
DNA unmethylome profiling by covalent capture of CpG sites. Nat Commun (2013) 0.91
Comprehensive analysis of DNA-methylation in mammalian tissues using MeDIP-chip. Methods (2010) 0.91
Identification of a DNA methylation-independent imprinting control region at the Arabidopsis MEDEA locus. Genes Dev (2012) 0.90
Expression profile and transcription factor binding site exploration of imprinted genes in human and mouse. BMC Genomics (2009) 0.90
Replication timing properties within the mouse distal chromosome 7 imprinting cluster. Biosci Biotechnol Biochem (2002) 0.83
Dissecting the role of H3K64me3 in mouse pericentromeric heterochromatin. Nat Commun (2013) 0.83
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Bi-PROF: bisulfite profiling of target regions using 454 GS FLX Titanium technology. Epigenetics (2013) 0.82
Patients with familial biparental hydatidiform moles have normal methylation at imprinted genes. Eur J Hum Genet (2005) 0.82
NR4A1-mediated apoptosis suppresses lymphomagenesis and is associated with a favorable cancer-specific survival in patients with aggressive B-cell lymphomas. Blood (2014) 0.82
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DNA methylation variability at growth-related imprints does not contribute to overweight in monozygotic twins discordant for BMI. Obesity (Silver Spring) (2011) 0.80
Reversible epigenetic fingerprint-mediated glutathione-S-transferase P1 gene silencing in human leukemia cell lines. Biochem Pharmacol (2011) 0.80
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AKSmooth: enhancing low-coverage bisulfite sequencing data via kernel-based smoothing. J Bioinform Comput Biol (2014) 0.75