Emma R. Woodward
Emma R. Woodward
Manchester Centre for Genomic Medicine
Verified email at mft.nhs.uk - Homepage
Cited by
Cited by
Contrasting effects on HIF-1α regulation by disease-causing pVHL mutations correlate with patterns of tumourigenesis in von Hippel-Lindau disease
SC Clifford, ME Cockman, AC Smallwood, DR Mole, ER Woodward, ...
Human molecular genetics 10 (10), 1029-1038, 2001
Tumor risks and genotype–phenotype–proteotype analysis in 358 patients with germline mutations in SDHB and SDHD
CJ Ricketts, JR Forman, E Rattenberry, N Bradshaw, F Lalloo, L Izatt, ...
Human mutation 31 (1), 41-51, 2010
Germline SDHB mutations and familial renal cell carcinoma
C Ricketts, ER Woodward, P Killick, MR Morris, D Astuti, F Latif, ER Maher
Journal of the National Cancer Institute 100 (17), 1260-1262, 2008
Germline SDHD mutation in familial phaeochromocytoma
D Astuti, F Douglas, TWJ Lennard, IA Aligianis, ER Woodward, ...
The Lancet 357 (9263), 1181-1182, 2001
Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutations
A Moran, C O’hara, S Khan, L Shack, E Woodward, ER Maher, F Lalloo, ...
Familial cancer 11 (2), 235-242, 2012
Genotype-phenotype correlations in von Hippel-Lindau disease
MER Ong KR, Woodward ER, Killick P, Lim C, Macdonald F
Human mutation 28 (2), 143-9, 2007
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 …
DG Evans, A Shenton, E Woodward, F Lalloo, A Howell, ER Maher
BMC cancer 8 (1), 1-9, 2008
Genetic Predisposition to Phaeochromocytoma: Analysis of Candidate Genes GDNF, RET and VHL
ER Woodward, C Eng, R McMahon, R Voutilainen, NA Affara, BAJ Ponder, ...
Human Molecular Genetics 6 (7), 1051-1056, 1997
Germline FH Mutations Presenting With Pheochromocytoma
GR Clark, M Sciacovelli, E Gaude, DM Walsh, G Kirby, MA Simpson, ...
The Journal of Clinical Endocrinology & Metabolism 99 (10), E2046-E2050, 2014
Annual surveillance by CA125 and transvaginal ultrasound for ovarian cancer in both high‐risk and population risk women is ineffective
ER Woodward, HV Sleightholme, AM Considine, S Williamson, ...
BJOG: An International Journal of Obstetrics & Gynaecology 114 (12), 1500-1509, 2007
Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screening
A Smith, A Moran, MC Boyd, M Bulman, A Shenton, L Smith, R Iddenden, ...
Journal of medical genetics 44 (1), 10-15, 2007
Risk of breast cancer in male BRCA2 carriers
DGR Evans, I Susnerwala, J Dawson, E Woodward, ER Maher, F Lalloo
Journal of medical genetics 47 (10), 710-711, 2010
Parity and breast cancer risk among BRCA1 and BRCA2 mutation carriers
AC Antoniou, A Shenton, ER Maher, E Watson, E Woodward, F Lalloo, ...
Breast Cancer Research 8 (6), 1-6, 2006
Von Hippel-Lindau disease and endocrine tumour susceptibility
ER Woodward, ER Maher
Endocrine-related cancer 13 (2), 415-425, 2006
A comprehensive next generation sequencing–based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma
E Rattenberry, L Vialard, A Yeung, H Bair, K McKay, M Jafri, N Canham, ...
The Journal of Clinical Endocrinology & Metabolism 98 (7), E1248-E1256, 2013
Molecular genetic analysis of von Hippel-Lindau disease.
FM Richards, AR Webster, R McMahon, ER Woodward, S Rose, ...
Journal of internal medicine 243 (6), 527-533, 1998
Tumour risks and genotype–phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD
KA Andrews, DB Ascher, DEV Pires, DR Barnes, L Vialard, RT Casey, ...
Journal of medical genetics 55 (6), 384-394, 2018
Germline selection shapes human mitochondrial DNA diversity
W Wei, S Tuna, MJ Keogh, KR Smith, TJ Aitman, PL Beales, DL Bennett, ...
Science 364 (6442), 2019
Localisation of a gene for chondrocalcinosis to chromosome 5p
AE Hughes, D McGibbon, E Woodward, J Dixey, M Doherty
Human molecular genetics 4 (7), 1225-1228, 1995
Familial clear cell renal cell carcinoma (FCRC): clinical features and mutation analysis of the VHL, MET, and CUL2candidate genes
ER Woodward, SC Clifford, D Astuti, NA Affara, ER Maher
Journal of medical genetics 37 (5), 348-353, 2000
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