Woodward E - Search Results

1

Cancer Variant Interpretation Group UK (CanVIG-UK): an exemplar national subspecialty multidisciplinary network.

Garrett A, Callaway A, Durkie M, Cubuk C, Alikian M, Burghel GJ, Robinson R, Izatt L, Talukdar S, Side L, Cranston T, Palmer-Smith S, Baralle D, Berry IR, Drummond J, Wallace AJ, Norbury G, Eccles DM, Ellard S, Lalloo F, Evans DG, Woodward E, Tischkowitz M, Hanson H, Turnbull C; CanVIG-UK. Garrett A, et al. Among authors: woodward e. J Med Genet. 2020 Dec;57(12):829-834. doi: 10.1136/jmedgenet-2019-106759. Epub 2020 Mar 13. J Med Genet. 2020. PMID: 32170000 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

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.

4

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.

5

Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screening.

Smith A, Moran A, Boyd MC, Bulman M, Shenton A, Smith L, Iddenden R, Woodward ER, Lalloo F, Maher ER, Evans DG. Smith A, et al. Among authors: woodward er. J Med Genet. 2007 Jan;44(1):10-15. doi: 10.1136/jmg.2006.043091. Epub 2006 Nov 1. J Med Genet. 2007. PMID: 17079251 Free PMC article.

6

Parity and breast cancer risk among BRCA1 and BRCA2 mutation carriers.

Antoniou AC, Shenton A, Maher ER, Watson E, Woodward E, Lalloo F, Easton DF, Evans DG. Antoniou AC, et al. Among authors: woodward e. Breast Cancer Res. 2006;8(6):R72. doi: 10.1186/bcr1630. Breast Cancer Res. 2006. PMID: 17187672 Free PMC article.

7

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

8

Penetrance estimates for BRCA1 and BRCA2 based on genetic testing in a Clinical Cancer Genetics service setting: risks of breast/ovarian cancer quoted should reflect the cancer burden in the family.

Evans DG, Shenton A, Woodward E, Lalloo F, Howell A, Maher ER. Evans DG, et al. Among authors: woodward e. BMC Cancer. 2008 May 30;8:155. doi: 10.1186/1471-2407-8-155. BMC Cancer. 2008. PMID: 18513387 Free PMC article.

9

Better life expectancy in women with BRCA2 compared with BRCA1 mutations is attributable to lower frequency and later onset of ovarian cancer.

Byrd LM, Shenton A, Maher ER, Woodward E, Belk R, Lim C, Lalloo F, Howell A, Jayson GC, Evans GD. Byrd LM, et al. Among authors: woodward e. Cancer Epidemiol Biomarkers Prev. 2008 Jun;17(6):1535-42. doi: 10.1158/1055-9965.EPI-07-2792. Cancer Epidemiol Biomarkers Prev. 2008. PMID: 18559571 Free article.

10

Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD.

Ricketts CJ, Forman JR, Rattenberry E, Bradshaw N, Lalloo F, Izatt L, Cole TR, Armstrong R, Kumar VK, Morrison PJ, Atkinson AB, Douglas F, Ball SG, Cook J, Srirangalingam U, Killick P, Kirby G, Aylwin S, Woodward ER, Evans DG, Hodgson SV, Murday V, Chew SL, Connell JM, Blundell TL, Macdonald F, Maher ER. Ricketts CJ, et al. Among authors: woodward er. Hum Mutat. 2010 Jan;31(1):41-51. doi: 10.1002/humu.21136. Hum Mutat. 2010. PMID: 19802898

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