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Nicola Bradshaw

Guidelines for the management of hereditary colorectal cancer from the British Society of Gastroenterology (BSG)/Association of Coloproctology of Great Britain and Ireland (ACPGBI)/United Kingdom Cancer Genetics Group (UKCGG)
2019 · Kevin J Monahan, Nicola Bradshaw, et al. · Gut · 484
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Tumor risks and genotype–phenotype–proteotype analysis in 358 patients with germline mutations inSDHBandSDHD
2009 · Christopher J. Ricketts, Julia R. Forman, et al. · Human Mutation · 337
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Tumour risks and genotype–phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD
2018 · Katrina A Andrews, David B Ascher, et al. · Journal of Medical Genetics · 249
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A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study
2021 · Elizabeth K Bancroft, Elizabeth C Page, et al. · The Lancet Oncology · 99
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Molecular Analysis of Pheochromocytoma after Maternal Transmission of SDHD Mutation Elucidates Mechanism of Parent-of-Origin Effect
2011 · Phey M. Yeap, Edward S. Tobias, et al. · The Journal of Clinical Endocrinology & Metabolism · 63
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers
2011 · David G. Cox, Jacques Simard, et al. · Human Molecular Genetics · 44
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Colonoscopy surveillance of individuals at risk of familial colorectal cancer
2003 · N Bradshaw, S Holloway, et al. · Gut · 37
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Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing
2022 · Lynne J. Hocking, Claire Andrews, et al. · European Journal of Human Genetics · 12
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Guidelines and care pathways for genetic diseases: the Scottish collaborative project on tuberous sclerosis
1998 · Nicola Bradshaw, Carole Brewer, et al. · European Journal of Human Genetics · 10
Urinary free (unconjugated) metadrenalines in different hereditary forms of catecholamine-secreting phaeochromocytoma/paraganglioma
2012 · D Fraser Davidson, Nicola Bradshaw, et al. · Annals of Clinical Biochemistry International Journal of Laboratory Medicine · 8
Use of Vandetanib in Metastatic Medullary Carcinoma of Thyroid in a Pediatric Patient With Multiple Endocrine Neoplasia 2B
2015 · Vidya K. Narayanan, Milind Ronghe, et al. · Journal of Pediatric Hematology/Oncology · 7
Prospective surveillance of women with a family history of breast cancer: auditing the risk threshold
2008 · E Anderson, J Berg, et al. · British Journal of Cancer · 7
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Predicting breast cancer risk: implications of a “weak” family history
2008 · Elaine Anderson, Jonathan Berg, et al. · Familial Cancer · 5
Tumour risks and genotype–phenotype–proteotype analysis of patients with germline mutations in the succinate dehydrogenase subunit genes SDHB, SDHC, and SDHD
2016 · Katrina A Andrews, Lindsey Vialard, et al. · The Lancet · 4
A succinate dehydrogenase B (SDHB) founder mutation
2008 · Katherine Hughes, Lindsay McDougall, et al. · Society for Endocrinology BES 2008 · 1
Follow up of patients with SDHB mutations attending a tertiary endocrine service in Greater Glasgow and Clyde
2016 · Stefanie Lip, Claire Middleton, et al. · Endocrine Abstracts
MIBG-avidity in genetically distinct phaeochromocytoma and paraganglioma populations
2014 · Ross Jack, Robert Lindsay, et al. · Endocrine Abstracts
Abstract 3673: Molecular analysis of pheochromocytoma after maternal transmission of SDHD mutation elucidates mechanism of parent-of-origin effect.
2012 · Edward S. Tobias, Phey M. Yeap, et al. · Cancer Research
Use of Vandetenib in metastatic medullary carcinoma of thyroid in a paediatric patient with Multiple Endocrine Neoplasia (MEN)2B
2012 · Vidya Kanamkote Narayanan, Nicola Bradshaw, et al.
Impact of national guidelines on family history breast cancer surveillance
2011 · J D Saldanha, R M Garrett, et al. · Scottish Medical Journal
Genetic counsellor contribution to the MEN patient
2007 · Nicola Bradshaw · Society for Endocrinology BES
Works count: 21
Citation count: 1,367
H-index: 9
I10-index: 9
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