Emma R. Woodward
Emma R. Woodward
Manchester Centre for Genomic Medicine
Verified email at mft.nhs.uk - Homepage
Title
Cited by
Cited by
Year
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
4342001
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
3702008
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
3682010
Germline SDHD mutation in familial phaeochromocytoma
D Astuti, F Douglas, TWJ Lennard, IA Aligianis, ER Woodward, ...
The Lancet 357 (9263), 1181-1182, 2001
2942001
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
2742012
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
2342007
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
2302008
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
1512014
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
1441997
Whole-genome sequencing of patients with rare diseases in a national health system
SJ Turro E, Astle WJ, Megy K, Gräf S, Greene D, Shamardina O, Allen HL ...
Nature, 2020
1432020
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
1432007
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
1222007
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
1192010
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
1162006
Germline selection shapes human mitochondrial DNA diversity
W Wei, S Tuna, MJ Keogh, KR Smith, TJ Aitman, PL Beales, DL Bennett, ...
Science 364 (6442), eaau6520, 2019
1152019
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
1132018
Von Hippel-Lindau disease and endocrine tumour susceptibility
ER Woodward, ER Maher
Endocrine-related cancer 13 (2), 415-425, 2006
972006
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
962013
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
941998
Association of mismatch repair mutation with age at cancer onset in Lynch syndrome: implications for stratified surveillance strategies
NAJ Ryan, J Morris, K Green, F Lalloo, ER Woodward, J Hill, EJ Crosbie, ...
JAMA oncology 3 (12), 1702-1706, 2017
912017
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Articles 1–20