Helen R. Davies

Molecular Biology · 2002–2018

A researcher in the Science corpus: 14 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 161 citations into it

Whom Helen R. Davies trusts

Their strongest outbound trust, strongest first, inferred from their citations.

1. Heng Li (in Molecular Biology)

Papers from Helen R. Davies's perspective

Ordered by how strongly the researchers Helen R. Davies trusts endorse each paper. Same corpus, a different order for every researcher.

1. Tumour evolution inferred by single-cell sequencing (Nature)
2. Hallmarks of cancer: the next generation. (Cell)
3. Pan-cancer patterns of somatic copy-number alteration (Nature Genetics)
4. Mutations of the BRAF gene in human cancer (Nature)
5. The Life History of 21 Breast Cancers (Cell)
6. Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM
7. Anaplastic Lymphoma Kinase Inhibition in Non–Small-Cell Lung Cancer (New England Journal of Medicine)
8. Statistical methods for detecting molecular adaptation (Trends in Ecology & Evolution)
9. The Population Genetics of dN/dS (PLoS Genetics)
10. Meaningful relationships: the regulation of the Ras/Raf/MEK/ERK pathway by protein interactions. (Biochemical Journal)

Their papers

• Signatures of mutational processes in human cancer (2013) — 9,146 citations
• Systematic identification of genomic markers of drug sensitivity in cancer cells (2012) — 2,417 citations
• Mutations of the BRAF gene in human cancer (2002) — 10,701 citations
• Mutational Processes Molding the Genomes of 21 Breast Cancers (2012) — 1,882 citations
• Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma (2011) — 1,262 citations
• A small cell lung cancer genome reports complex tobacco exposure signatures (2009) — 880 citations
• The Life History of 21 Breast Cancers (2012) — 1,476 citations
• Signatures of mutation and selection in the cancer genome (2010) — 715 citations
• Universal Patterns of Selection in Cancer and Somatic Tissues (2018) — 854 citations
• Subclonal diversification of primary breast cancer revealed by multiregion sequencing (2015) — 764 citations
• Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone (2013) — 775 citations
• Somatic SF3B1 Mutation in Myelodysplasia with Ring Sideroblasts (2011) — 1,243 citations
• Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes (2010) — 1,210 citations
• BRAF and RAS mutations in human lung cancer and melanoma. (2002) — 1,126 citations