Cyril Chapman - Concepedia

Author

Cyril Chapman

Birmingham Women's Hospital

Also Known As

Cyril Chapman, Cyril J. Chapman

Publications

Citations

H-Index

Concepts

All Affiliations

Birmingham Women's Hospital University College London University of Oxford University of Birmingham Churchill Hospital

About

Cyril Chapman is an author at Birmingham Women's Hospital specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	1K
2	Public Health	2	2	53
3	Nursing	1	1	11
4	Counseling	1	1	11
5	Epidemiology	1	1	25

Cyril Chapman

Publications

Citations

H-Index

Page 1

	Year	Citations
Germline mutations in RAD51D confer susceptibility to ovarian cancer Chey Loveday, Clare Turnbull, Emma Ramsay, Nature Genetics GeneticsGermline MutationsCancer GeneticsMedicineOvarian Cancer	2011	526
Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer Elise Ruark, Katie Snape, Peter Humburg, Nature Breast OncologyCancer PathologyTumor HeterogeneityGeneticsMosaic Ppm1d Mutations	2012	256
Population Testing for Cancer Predisposing BRCA1/BRCA2 Mutations in the Ashkenazi-Jewish Community: A Randomized Controlled Trial Ranjit Manchanda, K Loggenberg, Saskia C. Sanderson, JNCI Journal of the National Cancer Institute	2014	184
Cost-effectiveness of Population Screening for BRCA Mutations in Ashkenazi Jewish Women Compared With Family History–Based Testing Ranjit Manchanda, Rosa Legood, Matthew Burnell, JNCI Journal of the National Cancer Institute	2014	175
Microarray based analysis of 3p25‐p26 deletions (3p‐ syndrome) Salwati Shuib, Dominic McMullan, Eleanor Rattenberry, American Journal of Medical Genetics Part A	2009	148
Autosomal Recessive Cerebellar Ataxia with Oculomotor Apraxia (Ataxia-Telangiectasia–Like Syndrome) Is Linked to Chromosome 9q34 Andrea H. Németh, Elena G. Bochukova, Eimear Dunne, The American Journal of Human Genetics Genetic DisorderMedicineGeneticsChromosome 9Q34Clinical Genetics	2000	89
A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study Elizabeth Bancroft, Elizabeth Page, Mark N. Brook, The Lancet Oncology	2021	89
Congenital Defects and Miscarriages among New Zealand 2,4,5-T Sprayers Allan H. Smith, David O. Fisher, Neil Pearce, Archives of Environmental Health An International Journal	1982	84
Familial Non-VHL Clear Cell (Conventional) Renal Cell Carcinoma: Clinical Features, Segregation Analysis, and Mutation Analysis of <i>FLCN</i> Emma R. Woodward, Christopher J. Ricketts, Pip Killick, Clinical Cancer Research	2008	69
Cluster-randomised non-inferiority trial comparing DVD-assisted and traditional genetic counselling in systematic population testing for BRCA1/2 mutations Ranjit Manchanda, Matthew Burnell, K Loggenberg, Journal of Medical Genetics	2016	53

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