Woodward ER - Search Results

1

Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysis.

Luchetti A, Walsh D, Rodger F, Clark G, Martin T, Irving R, Sanna M, Yao M, Robledo M, Neumann HP, Woodward ER, Latif F, Abbs S, Martin H, Maher ER. Luchetti A, et al. Among authors: woodward er. Int J Endocrinol. 2015;2015:138573. doi: 10.1155/2015/138573. Epub 2015 Mar 25. Int J Endocrinol. 2015. PMID: 25883647 Free PMC article.

2

Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.

Woodward ER, Eng C, McMahon R, Voutilainen R, Affara NA, Ponder BA, Maher ER. Woodward ER, et al. Hum Mol Genet. 1997 Jul;6(7):1051-6. doi: 10.1093/hmg/6.7.1051. Hum Mol Genet. 1997. PMID: 9215674

3

Molecular genetic analysis of von Hippel-Lindau disease.

Richards FM, Webster AR, McMahon R, Woodward ER, Rose S, Maher ER. Richards FM, et al. Among authors: woodward er. J Intern Med. 1998 Jun;243(6):527-33. doi: 10.1046/j.1365-2796.1998.00334.x. J Intern Med. 1998. PMID: 9681854 Free article. Review.

4

Familial clear cell renal cell carcinoma (FCRC): clinical features and mutation analysis of the VHL, MET, and CUL2 candidate genes.

Woodward ER, Clifford SC, Astuti D, Affara NA, Maher ER. Woodward ER, et al. J Med Genet. 2000 May;37(5):348-53. doi: 10.1136/jmg.37.5.348. J Med Genet. 2000. PMID: 10807693 Free PMC article.

5

Comparative sequence analysis of the VHL tumor suppressor gene.

Woodward ER, Buchberger A, Clifford SC, Hurst LD, Affara NA, Maher ER. Woodward ER, et al. Genomics. 2000 May 1;65(3):253-65. doi: 10.1006/geno.2000.6144. Genomics. 2000. PMID: 10857749

6

Germline SDHD mutation in familial phaeochromocytoma.

Astuti D, Douglas F, Lennard TW, Aligianis IA, Woodward ER, Evans DG, Eng C, Latif F, Maher ER. Astuti D, et al. Among authors: woodward er. Lancet. 2001 Apr 14;357(9263):1181-2. doi: 10.1016/S0140-6736(00)04378-6. Lancet. 2001. PMID: 11323050

7

Contrasting effects on HIF-1alpha regulation by disease-causing pVHL mutations correlate with patterns of tumourigenesis in von Hippel-Lindau disease.

Clifford SC, Cockman ME, Smallwood AC, Mole DR, Woodward ER, Maxwell PH, Ratcliffe PJ, Maher ER. Clifford SC, et al. Among authors: woodward er. Hum Mol Genet. 2001 May 1;10(10):1029-38. doi: 10.1093/hmg/10.10.1029. Hum Mol Genet. 2001. PMID: 11331613

8

Von Hippel-Lindau disease and endocrine tumour susceptibility.

Woodward ER, Maher ER. Woodward ER, et al. Endocr Relat Cancer. 2006 Jun;13(2):415-25. doi: 10.1677/erc.1.00683. Endocr Relat Cancer. 2006. PMID: 16728571 Review.

9

Genotype-phenotype correlations in von Hippel-Lindau disease.

Ong KR, Woodward ER, Killick P, Lim C, Macdonald F, Maher ER. Ong KR, et al. Among authors: woodward er. Hum Mutat. 2007 Feb;28(2):143-9. doi: 10.1002/humu.20385. Hum Mutat. 2007. PMID: 17024664

10

VHL mutation analysis in patients with isolated central nervous system haemangioblastoma.

Woodward ER, Wall K, Forsyth J, Macdonald F, Maher ER. Woodward ER, et al. Brain. 2007 Mar;130(Pt 3):836-42. doi: 10.1093/brain/awl362. Epub 2007 Jan 29. Brain. 2007. PMID: 17264095

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