Davies, Helen
University of Cambridge · Wellcome Sanger Institute · MRC Cancer Unit · Seven Bridges Genomics (United States) · Addenbrooke's Hospital
27 papers on CoChatORCID 0000-0001-6381-3664
Most cited papers
- Verified
Mutations in the DLG3 Gene Cause Nonsyndromic X-Linked Mental Retardation
Tarpey, P., Parnau, J., Blow, M., Woffendin, H., Bignell, G., Cox, C., Cox, J., Davies, H., Edkins, S., Holden, S., et al. (2004) · The American Journal of Human Genetics
Genetics and Neurodevelopmental DisordersDown syndrome and intellectual disability research
Cited by 176
- Verified
Whole-Genome Sequencing Reveals Breast Cancers with Mismatch Repair Deficiency
Davies, H., Morganella, S., Purdie, C. A., Jang, S. J., Borgen, E., Russnes, H., Glodzik, D., Zou, X., Viari, A., Richardson, A. L., et al. (2017) · Cancer Research
Cancer Genomics and DiagnosticsGenetic factors in colorectal cancer
Cited by 99
- Verified
A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers
Glodzik, D., Morganella, S., Davies, H., Simpson, P. T., Li, Y., Zou, X., Diez-Perez, J., Staaf, J., Alexandrov, L. B., Smid, M., et al. (2017) · Nature Genetics
Cancer Genomics and DiagnosticsBRCA gene mutations in cancer
Cited by 84
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