K. Raine
Molecular Biology · 2007–2018
A researcher in the Science corpus: 18 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 244 citations into it
- Artificial Intelligence — 10 citations into it
Whom K. Raine trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from K. Raine's perspective
Ordered by how strongly the researchers K. Raine trusts endorse each paper. Same corpus, a different order for every researcher.
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- RECURRENT MUTATIONS IN THE U2AF1 SPLICING FACTOR IN MYELODYSPLASTIC SYNDROMES (Nature Genetics)
- Pan-cancer patterns of somatic copy-number alteration (Nature Genetics)
- Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing (Nature Genetics)
- Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM
- Statistical methods for detecting molecular adaptation (Trends in Ecology & Evolution)
- Frequent pathway mutations of splicing machinery in myelodysplasia (Nature)
- Discovery and saturation analysis of cancer genes across 21 tumor types (Nature)
- Genetic variegation of clonal architecture and propagating cells in leukaemia (Nature)
- The Population Genetics of dN/dS (PLoS Genetics)
Their papers
- Signatures of mutational processes in human cancer (2013) — 9,146 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
- The landscape of cancer genes and mutational processes in breast cancer (2012) — 1,739 citations
- The Life History of 21 Breast Cancers (2012) — 1,476 citations
- Genomic Evolution of Breast Cancer Metastasis and Relapse (2017) — 605 citations
- Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia (2011) — 1,652 citations
- Genomic Classification and Prognosis in Acute Myeloid Leukemia (2016) — 3,531 citations
- HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational-signatures (2017) — 946 citations
- Universal Patterns of Selection in Cancer and Somatic Tissues (2018) — 854 citations
- Prediction of acute myeloid leukaemia risk in healthy individuals (2018) — 766 citations
- Landscape of somatic mutations in 560 breast cancer whole genome sequences (2016) — 2,045 citations
- Subclonal diversification of primary breast cancer revealed by multiregion sequencing (2015) — 764 citations
- Clinical and biological implications of driver mutations in myelodysplastic syndromes. (2013) — 1,780 citations
- Somatic CALR Mutations in Myeloproliferative Neoplasms with Nonmutated JAK2 (2013) — 1,750 citations
- Intratumor Heterogeneity and Branched Evolution Revealed by Multiregion Sequencing (2012) — 7,381 citations
- Somatic SF3B1 Mutation in Myelodysplasia with Ring Sideroblasts (2011) — 1,243 citations
- Patterns of somatic mutation in human cancer genomes (2007) — 3,189 citations