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References from AIMER: A SNP-independent software for identifying imprinting-like allelic methylated regions from DNA methylome. Local targets link to admitted publications; unresolved targets remain external evidence.
DNA methylation reprogramming during mammalian development
10.3390/genes10040257 · 2019 · External reference
Mammalian genomic imprinting
10.1101/cshperspect.a002592 · 2011 · External reference
Genomic imprinting in mammals
10.1101/cshperspect.a018382 · 2014 · External reference
10.1101/gr.095562.109
10.1101/gr.095562.109 · External reference
10.1111/acer.13776
10.1111/acer.13776 · External reference
10.1038/nrg3032
10.1038/nrg3032 · External reference
DNA methylation of intragenic CpG islands depends on their transcriptional activity during differentiation and disease
10.1073/pnas.1703087114 · 2017 · External reference
10.1093/bfgp/elq013
10.1093/bfgp/elq013 · External reference
Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype
10.1086/502981 · 2006 · External reference
Selective methylation of CpGs at regulatory binding sites controls NNAT expression in Wilms tumors
10.1371/journal.pone.0067605 · 2013 · External reference
Genotype-phenotype correlations in central precocious puberty caused by MKRN3 mutations
10.1210/clinem/dgaa955 · 2021 · External reference
Genomic imprinting syndromes and cancer
10.1016/b978-0-12-380866-0.60006-x · 2010 · External reference
Role of DNA methylation in imprinting disorders: an updated review
10.1007/s10815-017-0895-5 · 2017 · External reference
10.1002/path.2116
10.1002/path.2116 · External reference
Congenital imprinting disorders: application of multilocus and high throughput methods to decipher new pathomechanisms and improve their management
10.1016/j.mcp.2015.05.003 · 2015 · External reference
Imprinting, genomic imprinting and physiological processes in mammals
10.1016/j.cell.2019.01.043 · 2019 · External reference
10.1038/nature08514
10.1038/nature08514 · External reference
10.1016/j.tig.2008.01.006
10.1016/j.tig.2008.01.006 · External reference
10.1016/j.cell.2011.12.035
10.1016/j.cell.2011.12.035 · External reference
10.1073/pnas.1201310109
10.1073/pnas.1201310109 · External reference
Two approaches reveal a new paradigm of 'switchable or genetics-influenced allele-specific DNA methylation' with potential in human disease
10.1038/celldisc.2017.38 · 2017 · External reference
DAMEfinder: a method to detect differential allele-specific methylation
10.1186/s13072-020-00346-8 · 2020 · External reference
10.1038/ng.174
10.1038/ng.174 · External reference
10.1016/j.ajhg.2016.08.021
10.1016/j.ajhg.2016.08.021 · External reference
10.1101/gr.1006603
10.1101/gr.1006603 · External reference
10.1126/science.1245316
10.1126/science.1245316 · External reference
Cytosine methylation and CpG, TpG (CpA) and TpA frequencies
10.1016/j.gene.2004.02.043 · 2004 · External reference
10.1038/ng.298
10.1038/ng.298 · External reference
10.1038/s41588-018-0232-7
10.1038/s41588-018-0232-7 · External reference
10.1038/ng.2746
10.1038/ng.2746 · External reference
10.1016/j.cell.2014.04.017
10.1016/j.cell.2014.04.017 · External reference
10.1073/pnas.0506580102
10.1073/pnas.0506580102 · External reference
10.1093/bioinformatics/btu170
10.1093/bioinformatics/btu170 · External reference
10.1093/bioinformatics/btr167
10.1093/bioinformatics/btr167 · External reference
10.1186/1471-2105-12-77
10.1186/1471-2105-12-77 · External reference
10.1016/j.ajhg.2010.01.014
10.1016/j.ajhg.2010.01.014 · External reference
Allele-specific epigenome maps reveal sequence-dependent stochastic switching at regulatory loci
10.1126/science.aar3146 · 2018 · External reference
10.3389/fgene.2018.00695
10.3389/fgene.2018.00695 · External reference
