Published in Nat Rev Genet on January 01, 2001
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Combined deficiency of Tet1 and Tet2 causes epigenetic abnormalities but is compatible with postnatal development. Dev Cell (2013) 3.31
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In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene. Am J Hum Genet (2003) 2.21
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Short interspersed transposable elements (SINEs) are excluded from imprinted regions in the human genome. Proc Natl Acad Sci U S A (2001) 2.14
Maternal periconceptional folic acid intake and risk of autism spectrum disorders and developmental delay in the CHARGE (CHildhood Autism Risks from Genetics and Environment) case-control study. Am J Clin Nutr (2012) 2.14
Transgenerational epigenetic programming of the brain transcriptome and anxiety behavior. PLoS One (2008) 2.07
Regulation of supply and demand for maternal nutrients in mammals by imprinted genes. J Physiol (2003) 2.01
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Adaptation of nutrient supply to fetal demand in the mouse involves interaction between the Igf2 gene and placental transporter systems. Proc Natl Acad Sci U S A (2005) 1.90
Bidirectional action of the Igf2r imprint control element on upstream and downstream imprinted genes. Genes Dev (2001) 1.89
Maternal effects as the cause of parent-of-origin effects that mimic genomic imprinting. Genetics (2008) 1.88
Dnmt1 expression in pre- and postimplantation embryogenesis and the maintenance of IAP silencing. Mol Cell Biol (2004) 1.86
DNA methylation dynamics during the mammalian life cycle. Philos Trans R Soc Lond B Biol Sci (2013) 1.85
Programming and inheritance of parental DNA methylomes in mammals. Cell (2014) 1.85
Discovery of imprinted transcripts in the mouse transcriptome using large-scale expression profiling. Genome Res (2003) 1.82
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Novel epigenetic mechanisms that control pluripotency and quiescence of adult bone marrow-derived Oct4(+) very small embryonic-like stem cells. Leukemia (2009) 1.80
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Transcriptional interferences in cis natural antisense transcripts of humans and mice. Genetics (2007) 1.79
Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution. PLoS Genet (2007) 1.79
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Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS. J Clin Invest (2003) 1.77
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Imprinting disorders and assisted reproductive technology. Fertil Steril (2009) 1.73
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Reprogramming DNA methylation in the mammalian life cycle: building and breaking epigenetic barriers. Philos Trans R Soc Lond B Biol Sci (2013) 1.70
Antisense transcripts with rice full-length cDNAs. Genome Biol (2003) 1.69
DNA methylation is critical for Arabidopsis embryogenesis and seed viability. Plant Cell (2006) 1.64
An intragenic methylated region in the imprinted Igf2 gene augments transcription. EMBO Rep (2001) 1.63
Genome-wide analysis reveals a complex pattern of genomic imprinting in mice. PLoS Genet (2008) 1.63
Relics of repeat-induced point mutation direct heterochromatin formation in Neurospora crassa. Genome Res (2008) 1.61
Two distinct mechanisms of silencing by the KvDMR1 imprinting control region. EMBO J (2007) 1.59
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome. Eur J Hum Genet (2008) 1.59
Duplicated fie genes in maize: expression pattern and imprinting suggest distinct functions. Plant Cell (2003) 1.59
Imputation of missing genotypes from sparse to high density using long-range phasing. Genetics (2011) 1.57
Random monoallelic expression of three genes clustered within 60 kb of mouse t complex genomic DNA. Genome Res (2001) 1.56
Imprinting regulation of the murine Meg1/Grb10 and human GRB10 genes; roles of brain-specific promoters and mouse-specific CTCF-binding sites. Nucleic Acids Res (2003) 1.54
Epigenetic profiling at mouse imprinted gene clusters reveals novel epigenetic and genetic features at differentially methylated regions. Genome Res (2009) 1.52
Distinct physiological and behavioural functions for parental alleles of imprinted Grb10. Nature (2011) 1.52
The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region. J Med Genet (2006) 1.51
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Epigenetic properties and identification of an imprint mark in the Nesp-Gnasxl domain of the mouse Gnas imprinted locus. Mol Cell Biol (2003) 1.47
Somatically acquired hypomethylation of IGF2 in breast and colorectal cancer. Hum Mol Genet (2008) 1.47
Analysis and accurate quantification of CpG methylation by MALDI mass spectrometry. Nucleic Acids Res (2003) 1.46
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Impaired glucose homeostasis in transgenic mice expressing the human transient neonatal diabetes mellitus locus, TNDM. J Clin Invest (2004) 1.44
Identification of the control region for tissue-specific imprinting of the stimulatory G protein alpha-subunit. Proc Natl Acad Sci U S A (2005) 1.43
The parental non-equivalence of imprinting control regions during mammalian development and evolution. PLoS Genet (2010) 1.41
Dynamic usage of transcription start sites within core promoters. Genome Biol (2006) 1.41
Stage-specific roles for tet1 and tet2 in DNA demethylation in primordial germ cells. Cell Stem Cell (2013) 1.40
Genomic imprinting and parent-of-origin effects on complex traits. Nat Rev Genet (2013) 1.40
The mouse Murr1 gene is imprinted in the adult brain, presumably due to transcriptional interference by the antisense-oriented U2af1-rs1 gene. Mol Cell Biol (2004) 1.40
Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumour. Br J Cancer (2005) 1.39
Global changes in genomic methylation levels during early development of the zebrafish embryo. Dev Genes Evol (2004) 1.39
A Common Polymorphism within the IGF2 Imprinting Control Region Is Associated with Parent of Origin Specific Effects in Infantile Hemangiomas. PLoS One (2015) 1.38
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Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci. Eur J Hum Genet (2010) 1.37
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A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus. Hum Genet (2006) 1.35
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Demethylation of the zygotic paternal genome. Nature (2000) 8.52
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