Paul C. Boutros
Molecular Biology · 2009–2020
A researcher in the Science corpus: 13 papers; trusts 3 researchers and is trusted by 12 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 212 citations into it; #3,867 of 17,773 by trust here, #2,571 by citations
Whom Paul C. Boutros trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Paul C. Boutros overall
Papers from Paul C. Boutros's perspective
Ordered by how strongly the researchers Paul C. Boutros trusts endorse each paper. Same corpus, a different order for every researcher.
- Classification of human lung carcinomas by mRNA expression profiling reveals distinct adenocarcinoma subclasses (Proceedings of the National Academy of Sciences of the United States of America)
- Standards and Guidelines for the Interpretation of Sequence Variants: A Joint Consensus Recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular…
- Signatures of mutational processes in human cancer (Nature)
- The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. (Genome Research)
- A method and server for predicting damaging missense mutations
- Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer (Nature Genetics)
- ClinVar: public archive of interpretations of clinically relevant variants
- Analysis of protein-coding genetic variation in 60,706 humans
- Cancer Genome Landscapes (Science)
- Integrative Genomics Viewer (Nature Biotechnology)
Their papers
- Best Practices for Benchmarking Germline Small Variant Calls in Human Genomes (2019) — 350 citations
- A robust benchmark for detection of germline large deletions and insertions (2020) — 358 citations
- International network of cancer genome projects (2010) — 2,229 citations
- Pathway and Network Analysis of Cancer Genomes (2015) — 319 citations
- The evolutionary history of 2,658 cancers (2017) — 937 citations
- Combining tumor genome simulation with crowdsourcing to benchmark somatic single-nucleotide-variant detection (2015) — 314 citations
- VennDiagram: a package for the generation of highly-customizable Venn and Euler diagrams in R (2011) — 2,780 citations
- Prognostic gene signatures for non-small-cell lung cancer (2009) — 208 citations
- Analyses of non-coding somatic drivers in 2,658 cancer whole genomes (2020) — 508 citations
- Pathogenic germline variants in 10,389 adult cancers (2018) — 734 citations
- Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing (2018) — 609 citations
- Comprehensive genomic characterization of head and neck squamous cell carcinomas (2015) — 3,702 citations
- The molecular taxonomy of primary prostate cancer (2015) — 2,751 citations