Maher ER - Search Results

1

Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scan.

Kemp Z, Carvajal-Carmona L, Spain S, Barclay E, Gorman M, Martin L, Jaeger E, Brooks N, Bishop DT, Thomas H, Tomlinson I, Papaemmanuil E, Webb E, Sellick GS, Wood W, Evans G, Lucassen A, Maher ER, Houlston RS; ColoRectal tumour Gene Identification (CoRGI) Study Consortium. Kemp Z, et al. Among authors: maher er. Hum Mol Genet. 2006 Oct 1;15(19):2903-10. doi: 10.1093/hmg/ddl231. Epub 2006 Aug 21. Hum Mol Genet. 2006. PMID: 16923799

2

TaqI and PstI RFLPs in the von Hippel-Lindau disease gene (VHL).

Richards FM, Latif F, Lerman MI, Zbar B, Maher ER. Richards FM, et al. Among authors: maher er. Hum Mol Genet. 1993 Oct;2(10):1750. doi: 10.1093/hmg/2.10.1750. Hum Mol Genet. 1993. PMID: 7903582 No abstract available.

3

A PCR generated AccI RFLP in the 3' untranslated region of the von Hippel-Lindau disease (VHL) tumour suppressor gene.

Payne SJ, Richards FM, Maher ER. Payne SJ, et al. Among authors: maher er. Hum Mol Genet. 1994 Feb;3(2):390. doi: 10.1093/hmg/3.2.390. Hum Mol Genet. 1994. PMID: 7911705 No abstract available.

4

Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome.

Reik W, Brown KW, Slatter RE, Sartori P, Elliott M, Maher ER. Reik W, et al. Among authors: maher er. Hum Mol Genet. 1994 Aug;3(8):1297-301. doi: 10.1093/hmg/3.8.1297. Hum Mol Genet. 1994. PMID: 7987305

5

Physical mapping of chromosome 3p25-p26 by fluorescence in situ hybridisation (FISH).

Phipps ME, Maher ER, Affara NA, Latif F, Leversha MA, Ferguson-Smith ME, Nakamura Y, Lerman M, Zbar B, Ferguson-Smith MA. Phipps ME, et al. Among authors: maher er. Hum Genet. 1993 Aug;92(1):18-22. doi: 10.1007/BF00216139. Hum Genet. 1993. PMID: 8365722

6

Genetic linkage between von Hippel-Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locus.

Crossey PA, Maher ER, Jones MH, Richards FM, Latif F, Phipps ME, Lush M, Foster K, Tory K, Green JS, et al. Crossey PA, et al. Among authors: maher er. Hum Mol Genet. 1993 Mar;2(3):279-82. doi: 10.1093/hmg/2.3.279. Hum Mol Genet. 1993. PMID: 8499917

7

A pericentric inversion of chromosome six in a patient with Peutz-Jeghers' syndrome and the use of FISH to localise the breakpoints on a genetic map.

Markie D, Huson S, Maher E, Davies A, Tomlinson I, Bodmer WF. Markie D, et al. Hum Genet. 1996 Aug;98(2):125-8. doi: 10.1007/s004390050173. Hum Genet. 1996. PMID: 8698325

8

Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway.

Brown KW, Villar AJ, Bickmore W, Clayton-Smith J, Catchpoole D, Maher ER, Reik W. Brown KW, et al. Among authors: maher er. Hum Mol Genet. 1996 Dec;5(12):2027-32. doi: 10.1093/hmg/5.12.2027. Hum Mol Genet. 1996. PMID: 8968759

9

Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.

Paulsen M, Davies KR, Bowden LM, Villar AJ, Franck O, Fuermann M, Dean WL, Moore TF, Rodrigues N, Davies KE, Hu RJ, Feinberg AP, Maher ER, Reik W, Walter J. Paulsen M, et al. Among authors: maher er. Hum Mol Genet. 1998 Jul;7(7):1149-59. doi: 10.1093/hmg/7.7.1149. Hum Mol Genet. 1998. PMID: 9618174

10

A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancer.

Froggatt NJ, Green J, Brassett C, Evans DG, Bishop DT, Kolodner R, Maher ER. Froggatt NJ, et al. Among authors: maher er. J Med Genet. 1999 Feb;36(2):97-102. J Med Genet. 1999. PMID: 10051005 Free PMC article.

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