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Helen Hanson
Helen Hanson
Royal Devon University Healthcare NHS Foundation Trust and University of Exeter
Verified email at nhs.net
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Cited by
Cited by
Year
Interim results from the IMPACT study: evidence for prostate-specific antigen screening in BRCA2 mutation carriers
EC Page, EK Bancroft, MN Brook, M Assel, MH Al Battat, S Thomas, ...
European urology 76 (6), 831-842, 2019
2482019
Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patients
A George, D Riddell, S Seal, S Talukdar, S Mahamdallie, E Ruark, ...
Scientific reports 6 (1), 29506, 2016
2352016
Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants
S Li, V Silvestri, G Leslie, TR Rebbeck, SL Neuhausen, JL Hopper, ...
Journal of Clinical Oncology 40 (14), 1529-1541, 2022
2302022
Germline-focussed analysis of tumour-only sequencing: recommendations from the ESMO Precision Medicine Working Group
D Mandelker, M Donoghue, S Talukdar, C Bandlamudi, P Srinivasan, ...
Annals of Oncology 30 (8), 1221-1231, 2019
2032019
Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D
X Yang, H Song, G Leslie, C Engel, E Hahnen, B Auber, J Horváth, K Kast, ...
JNCI: Journal of the National Cancer Institute 112 (12), 1242-1250, 2020
1832020
Clinical practice guidelines for BRCA1 and BRCA2 genetic testing
P Pujol, M Barberis, P Beer, E Friedman, JM Piulats, ED Capoluongo, ...
European Journal of Cancer 146, 30-47, 2021
1582021
A novel HER2-positive breast cancer phenotype arising from germline TP53 mutations
JRF Wilson, AC Bateman, H Hanson, Q An, G Evans, N Rahman, ...
Journal of medical genetics 47 (11), 771-774, 2010
1492010
BRCA1 testing should be offered to individuals with triple-negative breast cancer diagnosed below 50 years
L Robertson, H Hanson, S Seal, M Warren-Perry, D Hughes, I Howell, ...
British journal of cancer 106 (6), 1234-1238, 2012
1332012
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants
DR Barnes, MA Rookus, L McGuffog, G Leslie, TM Mooij, J Dennis, ...
Genetics in Medicine 22 (10), 1653-1666, 2020
1272020
Consensus for genes to be included on cancer panel tests offered by UK genetics services: guidelines of the UK Cancer Genetics Group
A Taylor, AF Brady, IM Frayling, H Hanson, M Tischkowitz, C Turnbull, ...
Journal of medical genetics 55 (6), 372-377, 2018
1192018
Hereditary leiomyomatosis and renal cell cancer: clinical, molecular, and screening features in a cohort of 185 affected individuals
C Forde, DHK Lim, Y Alwan, G Burghel, L Butland, R Cleaver, A Dixit, ...
European urology oncology 3 (6), 764-772, 2020
862020
A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study
EK Bancroft, EC Page, MN Brook, S Thomas, N Taylor, J Pope, J McHugh, ...
The Lancet Oncology 22 (11), 1618-1631, 2021
752021
Deletion of the distal long arm of chromosome 10; is there a characteristic phenotype? A report of 15 de novo and familial cases
M Irving, H Hanson, P Turnpenny, C Brewer, CM Ogilvie, A Davies, J Berg
American Journal of Medical Genetics Part A 123 (2), 153-163, 2003
732003
Baseline results from the UK SIGNIFY study: a whole-body MRI screening study in TP53 mutation carriers and matched controls
S Saya, E Killick, S Thomas, N Taylor, EK Bancroft, J Rothwell, S Benafif, ...
Familial cancer 16, 433-440, 2017
652017
Telomere shortening in Fanconi anaemia demonstrated by a direct FISH approach
H Hanson, CG Mathew, Z Docherty, C Mackie Ogilvie
Cytogenetics and cell genetics 93 (3-4), 203-206, 2001
652001
Germline-focused analysis of tumour-detected variants in 49,264 cancer patients: ESMO Precision Medicine Working Group recommendations
Z Kuzbari, C Bandlamudi, C Loveday, A Garrett, M Mehine, A George, ...
Annals of Oncology 34 (3), 215-227, 2023
632023
Comprehensive cancer-predisposition gene testing in an adult multiple primary tumor series shows a broad range of deleterious variants and atypical tumor phenotypes
J Whitworth, PS Smith, JE Martin, H West, A Luchetti, F Rodger, G Clark, ...
The American Journal of Human Genetics 103 (1), 3-18, 2018
632018
Clinical likelihood ratios and balanced accuracy for 44 in silico tools against multiple large-scale functional assays of cancer susceptibility genes
C Cubuk, A Garrett, S Choi, L King, C Loveday, B Torr, GJ Burghel, ...
Genetics in Medicine 23 (11), 2096-2104, 2021
572021
The value of clinical criteria in identifying patients with X-linked Alport syndrome
H Hanson, H Storey, J Pagan, F Flinter
Clinical Journal of the American Society of Nephrology 6 (1), 198-203, 2011
552011
Combining evidence for and against pathogenicity for variants in cancer susceptibility genes: CanVIG-UK consensus recommendations
A Garrett, M Durkie, A Callaway, GJ Burghel, R Robinson, J Drummond, ...
Journal of medical genetics 58 (5), 297-304, 2021
502021
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