Moore GE - Search Results

1

Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies.

Zhou H, Brockington M, Jungbluth H, Monk D, Stanier P, Sewry CA, Moore GE, Muntoni F. Zhou H, et al. Among authors: moore ge. Am J Hum Genet. 2006 Nov;79(5):859-68. doi: 10.1086/508500. Epub 2006 Sep 21. Am J Hum Genet. 2006. PMID: 17033962 Free PMC article.

2

Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region.

Monk D, Bentley L, Hitchins M, Myler RA, Clayton-Smith J, Ismail S, Price SM, Preece MA, Stanier P, Moore GE. Monk D, et al. Among authors: moore ge. Hum Genet. 2002 Oct;111(4-5):376-87. doi: 10.1007/s00439-002-0777-4. Epub 2002 Aug 16. Hum Genet. 2002. PMID: 12384779

3

Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark.

Arnaud P, Monk D, Hitchins M, Gordon E, Dean W, Beechey CV, Peters J, Craigen W, Preece M, Stanier P, Moore GE, Kelsey G. Arnaud P, et al. Among authors: moore ge. Hum Mol Genet. 2003 May 1;12(9):1005-19. doi: 10.1093/hmg/ddg110. Hum Mol Genet. 2003. PMID: 12700169

4

Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts.

Stanier P, Moore GE. Stanier P, et al. Among authors: moore ge. Hum Mol Genet. 2004 Apr 1;13 Spec No 1:R73-81. doi: 10.1093/hmg/ddh052. Epub 2004 Jan 13. Hum Mol Genet. 2004. PMID: 14722155 Review.

5

Intrauterine growth restriction--genetic causes and consequences.

Monk D, Moore GE. Monk D, et al. Among authors: moore ge. Semin Fetal Neonatal Med. 2004 Oct;9(5):371-8. doi: 10.1016/j.siny.2004.03.002. Semin Fetal Neonatal Med. 2004. PMID: 15691772 Review.

6

A screen for retrotransposed imprinted genes reveals an association between X chromosome homology and maternal germ-line methylation.

Wood AJ, Roberts RG, Monk D, Moore GE, Schulz R, Oakey RJ. Wood AJ, et al. Among authors: moore ge. PLoS Genet. 2007 Feb 9;3(2):e20. doi: 10.1371/journal.pgen.0030020. Epub 2006 Dec 18. PLoS Genet. 2007. PMID: 17291163 Free PMC article.

7

Dynamic variation in allele-specific gene expression of Paraoxonase-1 in murine and human tissues.

Parker-Katiraee L, Bousiaki E, Monk D, Moore GE, Nakabayashi K, Scherer SW. Parker-Katiraee L, et al. Among authors: moore ge. Hum Mol Genet. 2008 Nov 1;17(21):3263-70. doi: 10.1093/hmg/ddn222. Epub 2008 Aug 4. Hum Mol Genet. 2008. PMID: 18678600 Free PMC article.

8

Transcript- and tissue-specific imprinting of a tumour suppressor gene.

Schulz R, McCole RB, Woodfine K, Wood AJ, Chahal M, Monk D, Moore GE, Oakey RJ. Schulz R, et al. Among authors: moore ge. Hum Mol Genet. 2009 Jan 1;18(1):118-27. doi: 10.1093/hmg/ddn322. Epub 2008 Oct 4. Hum Mol Genet. 2009. PMID: 18836209 Free PMC article.

9

Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression.

Monk D, Arnaud P, Frost J, Hills FA, Stanier P, Feil R, Moore GE. Monk D, et al. Among authors: moore ge. Hum Mol Genet. 2009 Aug 15;18(16):3066-74. doi: 10.1093/hmg/ddp248. Epub 2009 Jun 1. Hum Mol Genet. 2009. PMID: 19487367

10

Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weight.

Ishida M, Monk D, Duncan AJ, Abu-Amero S, Chong J, Ring SM, Pembrey ME, Hindmarsh PC, Whittaker JC, Stanier P, Moore GE. Ishida M, et al. Among authors: moore ge. Am J Hum Genet. 2012 Apr 6;90(4):715-9. doi: 10.1016/j.ajhg.2012.02.021. Epub 2012 Mar 22. Am J Hum Genet. 2012. PMID: 22444668 Free PMC article.

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