Cooper WN - Search Results

1

Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome.

Cooper WN, Luharia A, Evans GA, Raza H, Haire AC, Grundy R, Bowdin SC, Riccio A, Sebastio G, Bliek J, Schofield PN, Reik W, Macdonald F, Maher ER. Cooper WN, et al. Eur J Hum Genet. 2005 Sep;13(9):1025-32. doi: 10.1038/sj.ejhg.5201463. Eur J Hum Genet. 2005. PMID: 15999116

2

An association between variants in the IGF2 gene and Beckwith-Wiedemann syndrome: interaction between genotype and epigenotype.

Murrell A, Heeson S, Cooper WN, Douglas E, Apostolidou S, Moore GE, Maher ER, Reik W. Murrell A, et al. Among authors: cooper wn. Hum Mol Genet. 2004 Jan 15;13(2):247-55. doi: 10.1093/hmg/ddh013. Epub 2003 Nov 25. Hum Mol Genet. 2004. PMID: 14645199

3

Mitotic recombination and uniparental disomy in Beckwith-Wiedemann syndrome.

Cooper WN, Curley R, Macdonald F, Maher ER. Cooper WN, et al. Genomics. 2007 May;89(5):613-7. doi: 10.1016/j.ygeno.2007.01.005. Epub 2007 Mar 6. Genomics. 2007. PMID: 17337339 Free article.

4

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART).

Maher ER, Brueton LA, Bowdin SC, Luharia A, Cooper W, Cole TR, Macdonald F, Sampson JR, Barratt CL, Reik W, Hawkins MM. Maher ER, et al. J Med Genet. 2003 Jan;40(1):62-4. doi: 10.1136/jmg.40.1.62. J Med Genet. 2003. PMID: 12525545 Free PMC article. No abstract available.

5

Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome.

Diaz-Meyer N, Day CD, Khatod K, Maher ER, Cooper W, Reik W, Junien C, Graham G, Algar E, Der Kaloustian VM, Higgins MJ. Diaz-Meyer N, et al. J Med Genet. 2003 Nov;40(11):797-801. doi: 10.1136/jmg.40.11.797. J Med Genet. 2003. PMID: 14627666 Free PMC article.

6

Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumour.

Astuti D, Latif F, Wagner K, Gentle D, Cooper WN, Catchpoole D, Grundy R, Ferguson-Smith AC, Maher ER. Astuti D, et al. Among authors: cooper wn. Br J Cancer. 2005 Apr 25;92(8):1574-80. doi: 10.1038/sj.bjc.6602478. Br J Cancer. 2005. PMID: 15798773 Free PMC article.

7

Frequent RASSF1A tumour suppressor gene promoter methylation in Wilms' tumour and colorectal cancer.

Wagner KJ, Cooper WN, Grundy RG, Caldwell G, Jones C, Wadey RB, Morton D, Schofield PN, Reik W, Latif F, Maher ER. Wagner KJ, et al. Among authors: cooper wn. Oncogene. 2002 Oct 17;21(47):7277-82. doi: 10.1038/sj.onc.1205922. Oncogene. 2002. PMID: 12370819

8

Beckwith Weidemann syndrome: a behavioral phenotype-genotype study.

Kent L, Bowdin S, Kirby GA, Cooper WN, Maher ER. Kent L, et al. Among authors: cooper wn. Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1295-7. doi: 10.1002/ajmg.b.30729. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18314872

9

Multigene methylation analysis of Wilms' tumour and adult renal cell carcinoma.

Morris MR, Hesson LB, Wagner KJ, Morgan NV, Astuti D, Lees RD, Cooper WN, Lee J, Gentle D, Macdonald F, Kishida T, Grundy R, Yao M, Latif F, Maher ER. Morris MR, et al. Among authors: cooper wn. Oncogene. 2003 Oct 2;22(43):6794-801. doi: 10.1038/sj.onc.1206914. Oncogene. 2003. PMID: 14555992

10

Epigenetic analysis of HIC1, CASP8, FLIP, TSP1, DCR1, DCR2, DR4, DR5, KvDMR1, H19 and preferential 11p15.5 maternal-allele loss in von Hippel-Lindau and sporadic phaeochromocytomas.

Margetts CD, Astuti D, Gentle DC, Cooper WN, Cascon A, Catchpoole D, Robledo M, Neumann HP, Latif F, Maher ER. Margetts CD, et al. Among authors: cooper wn. Endocr Relat Cancer. 2005 Mar;12(1):161-72. doi: 10.1677/erc.1.00865. Endocr Relat Cancer. 2005. PMID: 15788647

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