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Items: 1 to 20 of 104

1.

Extensive variation and low heritability of DNA methylation identified in a twin study.

Gervin K, Hammerø M, Akselsen HE, Moe R, Nygård H, Brandt I, Gjessing HK, Harris JR, Undlien DE, Lyle R.

Genome Res. 2011 Nov;21(11):1813-21. doi: 10.1101/gr.119685.110. Epub 2011 Sep 26.

2.

Impact of the genome on the epigenome is manifested in DNA methylation patterns of imprinted regions in monozygotic and dizygotic twins.

Coolen MW, Statham AL, Qu W, Campbell MJ, Henders AK, Montgomery GW, Martin NG, Clark SJ.

PLoS One. 2011;6(10):e25590. doi: 10.1371/journal.pone.0025590. Epub 2011 Oct 3.

3.

Neonatal DNA methylation profile in human twins is specified by a complex interplay between intrauterine environmental and genetic factors, subject to tissue-specific influence.

Gordon L, Joo JE, Powell JE, Ollikainen M, Novakovic B, Li X, Andronikos R, Cruickshank MN, Conneely KN, Smith AK, Alisch RS, Morley R, Visscher PM, Craig JM, Saffery R.

Genome Res. 2012 Aug;22(8):1395-406. doi: 10.1101/gr.136598.111. Epub 2012 Jul 16.

4.

Increased DNA methylation at the AXIN1 gene in a monozygotic twin from a pair discordant for a caudal duplication anomaly.

Oates NA, van Vliet J, Duffy DL, Kroes HY, Martin NG, Boomsma DI, Campbell M, Coulthard MG, Whitelaw E, Chong S.

Am J Hum Genet. 2006 Jul;79(1):155-62. Epub 2006 May 22.

5.

Heritable rather than age-related environmental and stochastic factors dominate variation in DNA methylation of the human IGF2/H19 locus.

Heijmans BT, Kremer D, Tobi EW, Boomsma DI, Slagboom PE.

Hum Mol Genet. 2007 Mar 1;16(5):547-54. Epub 2007 Mar 5.

PMID:
17339271
6.

Intra-Monozygotic Twin Pair Discordance and Longitudinal Variation of Whole-Genome Scale DNA Methylation in Adults.

Zhang N, Zhao S, Zhang SH, Chen J, Lu D, Shen M, Li C.

PLoS One. 2015 Aug 6;10(8):e0135022. doi: 10.1371/journal.pone.0135022. eCollection 2015.

7.

DNA methylation analysis of multiple tissues from newborn twins reveals both genetic and intrauterine components to variation in the human neonatal epigenome.

Ollikainen M, Smith KR, Joo EJ, Ng HK, Andronikos R, Novakovic B, Abdul Aziz NK, Carlin JB, Morley R, Saffery R, Craig JM.

Hum Mol Genet. 2010 Nov 1;19(21):4176-88. doi: 10.1093/hmg/ddq336. Epub 2010 Aug 10.

PMID:
20699328
8.

Evidence for monozygotic twin (MZ) discordance in methylation level at two CpG sites in the promoter region of the catechol-O-methyltransferase (COMT) gene.

Mill J, Dempster E, Caspi A, Williams B, Moffitt T, Craig I.

Am J Med Genet B Neuropsychiatr Genet. 2006 Jun 5;141B(4):421-5.

PMID:
16583437
9.

DNA methylation and mRNA expression of SYN III, a candidate gene for schizophrenia.

Murphy BC, O'Reilly RL, Singh SM.

BMC Med Genet. 2008 Dec 22;9:115. doi: 10.1186/1471-2350-9-115.

10.

Predicting aberrant CpG island methylation.

Feltus FA, Lee EK, Costello JF, Plass C, Vertino PM.

Proc Natl Acad Sci U S A. 2003 Oct 14;100(21):12253-8. Epub 2003 Sep 30.

11.

Methylation patterns of the human beta-glucuronidase gene locus: boundaries of methylation and general implications for frequent point mutations at CpG dinucleotides.

Tomatsu S, Orii KO, Islam MR, Shah GN, Grubb JH, Sukegawa K, Suzuki Y, Orii T, Kondo N, Sly WS.

Genomics. 2002 Mar;79(3):363-75.

PMID:
11863366
12.

Aberrant methylation and silencing of ARHI, an imprinted tumor suppressor gene in which the function is lost in breast cancers.

Yuan J, Luo RZ, Fujii S, Wang L, Hu W, Andreeff M, Pan Y, Kadota M, Oshimura M, Sahin AA, Issa JP, Bast RC Jr, Yu Y.

Cancer Res. 2003 Jul 15;63(14):4174-80.

13.

LINE-1 DNA methylation: A potential forensic marker for discriminating monozygotic twins.

Xu J, Fu G, Yan L, Craig JM, Zhang X, Fu L, Ma C, Li S, Cong B.

Forensic Sci Int Genet. 2015 Nov;19:136-45. doi: 10.1016/j.fsigen.2015.07.014. Epub 2015 Jul 23.

PMID:
26223032
14.
15.

DNA methylation signatures of peripheral leukocytes in schizophrenia.

Kinoshita M, Numata S, Tajima A, Shimodera S, Ono S, Imamura A, Iga J, Watanabe S, Kikuchi K, Kubo H, Nakataki M, Sumitani S, Imoto I, Okazaki Y, Ohmori T.

Neuromolecular Med. 2013 Mar;15(1):95-101. doi: 10.1007/s12017-012-8198-6. Epub 2012 Sep 9.

PMID:
22961555
16.

Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation.

Busche S, Shao X, Caron M, Kwan T, Allum F, Cheung WA, Ge B, Westfall S, Simon MM; Multiple Tissue Human Expression Resource., Barrett A, Bell JT, McCarthy MI, Deloukas P, Blanchette M, Bourque G, Spector TD, Lathrop M, Pastinen T, Grundberg E.

Genome Biol. 2015 Dec 23;16:290. doi: 10.1186/s13059-015-0856-1.

17.
18.

Genome-wide analysis of DNA methylation differences in muscle and fat from monozygotic twins discordant for type 2 diabetes.

Ribel-Madsen R, Fraga MF, Jacobsen S, Bork-Jensen J, Lara E, Calvanese V, Fernandez AF, Friedrichsen M, Vind BF, Højlund K, Beck-Nielsen H, Esteller M, Vaag A, Poulsen P.

PLoS One. 2012;7(12):e51302. doi: 10.1371/journal.pone.0051302. Epub 2012 Dec 10.

19.

Symmetric and asymmetric DNA methylation in the human IGF2-H19 imprinted region.

Vu TH, Li T, Nguyen D, Nguyen BT, Yao XM, Hu JF, Hoffman AR.

Genomics. 2000 Mar 1;64(2):132-43.

PMID:
10729220
20.

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