Moore GE - Search Results

1

Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome.

Monk D, Wakeling EL, Proud V, Hitchins M, Abu-Amero SN, Stanier P, Preece MA, Moore GE. Monk D, et al. Among authors: moore ge. Am J Hum Genet. 2000 Jan;66(1):36-46. doi: 10.1086/302717. Am J Hum Genet. 2000. PMID: 10631135 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

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

5

Maternal uniparental disomy 7 in Silver-Russell syndrome.

Preece MA, Price SM, Davies V, Clough L, Stanier P, Trembath RC, Moore GE. Preece MA, et al. Among authors: moore ge. J Med Genet. 1997 Jan;34(1):6-9. doi: 10.1136/jmg.34.1.6. J Med Genet. 1997. PMID: 9032641 Free PMC article.

6

Lack of hemizygosity for the insulin-like growth factor I receptor gene in a quantitative study of 33 Silver Russell syndrome probands and their families.

Abu-Amero S, Price S, Wakeling E, Stanier P, Trembath R, Preece MA, Moore GE. Abu-Amero S, et al. Among authors: moore ge. Eur J Hum Genet. 1997 Jul-Aug;5(4):235-41. Eur J Hum Genet. 1997. PMID: 9359045

7

Genetics of Silver-Russell syndrome.

Wakeling EL, Abu-Amero S, Price SM, Stanier P, Trembath RC, Moore GE, Preece MA. Wakeling EL, et al. Among authors: moore ge. Horm Res. 1998;49 Suppl 2:32-6. doi: 10.1159/000053085. Horm Res. 1998. PMID: 9730670 Review.

8

Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues.

Wakeling EL, Abu-Amero SN, Stanier P, Preece MA, Moore GE. Wakeling EL, et al. Among authors: moore ge. Eur J Hum Genet. 1998 Mar-Apr;6(2):158-64. doi: 10.1038/sj.ejhg.5200179. Eur J Hum Genet. 1998. PMID: 9781061

9

An analysis of common isodisomic regions in five mUPD 16 probands.

Abu-Amero SN, Ali Z, Abu-Amero KK, Stanier P, Moore GE. Abu-Amero SN, et al. Among authors: moore ge. J Med Genet. 1999 Mar;36(3):204-7. J Med Genet. 1999. PMID: 10204845 Free PMC article.

10

The search for the gene for Silver-Russell syndrome.

Moore GE, Abu-Amero S, Wakeling E, Hitchins M, Monk D, Stanier P, Preece M. Moore GE, et al. Acta Paediatr Suppl. 1999 Dec;88(433):42-8. doi: 10.1111/j.1651-2227.1999.tb14402.x. Acta Paediatr Suppl. 1999. PMID: 10626544 Review.

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