Victoria Murday - Concepedia

Author

Victoria Murday

Also Known As

Andrew Norman, Carole Brewer, Helen Murphy, Hood Mugalaasi, Jenny Chang-Claude, Nicola Williams, Ruth McGowan, V Murday, V. K. Ajith Kumar, V. MURDAY

Publications

8.7K

Citations

H-Index

Concepts

All Affiliations

Institute of Cancer Research St George's, University of London St George's Hospital University College London St George's Hospital

About

Victoria Murday is an author at Institute of Cancer Research specializing in medicine, genetics, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	20	3K
2	Public Health	8	8	409
3	Nursing	1	1	37
4	Social Sciences	1	1	97
5	Biology	1	1	44

Victoria Murday

Publications

5.6K

Citations

H-Index

Page 1

	Year	Citations
Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial John Burn, Anne‐Marie Gerdes, Finlay Macrae, The Lancet Long-term EffectOncologyCancer EpidemiologyCancer RiskMedicine	2011	940
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures Andrew J. Sharp, Heather C. Mefford, Kelly Li, Nature Genetics Mendelian DisorderGenetic DisorderPsychiatric GeneticsRecurrent 15Q13.3Mental Retardation	2008	588
Clinical Presentation and Penetrance of Pheochromocytoma/Paraganglioma Syndromes Diana E. Benn, Anne‐Paule Gimenez‐Roqueplo, Jennifer Reilly, The Journal of Clinical Endocrinology & Metabolism	2006	566
The impact of genetic counselling on risk perception and mental health in women with a family history of breast cancer Maggie Watson, Samuel Lloyd, J. Davidson, British Journal of Cancer	1999	243
Tumour risks and genotype–phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes <i>SDHB</i>, <i>SDHC</i> and <i>SDHD</i> Katrina Andrews, David B. Ascher, Douglas E. V. Pires, Journal of Medical Genetics	2018	243
Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development Michael A. Simpson, Ray C. J. Hsu, Lindsay Keir, The American Journal of Human Genetics Bone DiseaseGenetic DisorderGeneticsFam20c Are AssociatedBone Development	2007	225
The mutational spectrum in Waardenburg syndrome Mayada Tassabehji, Valerie Newton, X.-Z. Liu, Human Molecular Genetics Developmental AnomalyType 1Mendelian DisorderGenetic DisorderMedicine	1995	223
Balancing autonomy and responsibility: the ethics of generating and disclosing genetic information Nina Hallowell, Claire Foster, Rosalind A. Eeles, Journal of Medical Ethics	2003	190
Familial dilated cardiomyopathy in the United Kingdom. Patrick J. Keeling, Gillian Smith, Heewon Seo, Heart	1995	186
Further observations on LKB1/STK11 status and cancer risk in Peutz–Jeghers syndrome Wendy Lim, Nicholas Hearle, Bindiya Shah, British Journal of Cancer	2003	173

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