Richard K. Wilson
Molecular Biology · 2001–2018
A researcher in the Science corpus: 90 papers; trusts 4 researchers and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 1,181 citations into it; #12,794 of 17,773 by trust here, #9 by citations
- Genetics — 639 citations into it; #5,567 of 6,854 by trust here, #8 by citations
Whom Richard K. Wilson trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Richard K. Wilson overall
Papers from Richard K. Wilson's perspective
Ordered by how strongly the researchers Richard K. Wilson trusts endorse each paper. Same corpus, a different order for every researcher.
- Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. (American Journal of Human Genetics)
- A method and server for predicting damaging missense mutations
- Exome sequencing as a tool for Mendelian disease gene discovery
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- The Pfam protein families database
- The Human Gene Mutation Database: 2008 update
- A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic (PLoS Genetics)
- BLAT--the BLAST-like alignment tool. (Genome Research)
- Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing (Nature Genetics)
Their papers
- Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes. (2005) — 4,049 citations
- Evolution of Symbiotic Bacteria in the Distal Human Intestine (2007) — 608 citations
- Identification of a CpG island methylator phenotype that defines a distinct subgroup of glioma. (2010) — 2,267 citations
- A global reference for human genetic variation (2015) — 16,925 citations
- Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007) — 5,374 citations
- A framework for human microbiome research (2012) — 2,418 citations
- The Genome Sequence of Caenorhabditis briggsae: A Platform for Comparative Genomics (2003) — 1,019 citations
- Structure, Function and Diversity of the Healthy Human Microbiome (2012) — 10,771 citations
- Initial sequence of the chimpanzee genome and comparison with the human genome (2005) — 2,343 citations
- A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
- BreakDancer: An algorithm for high resolution mapping of genomic structural variation (2009) — 1,513 citations
- Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly (2016) — 1,005 citations
- Mapping and sequencing of structural variation from eight human genomes (2008) — 1,208 citations
- An integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR and NF1 (2010) — 7,152 citations
- Recurring Mutations Found by Sequencing an Acute Myeloid Leukemia Genome (2009) — 2,302 citations
- Mutational landscape and significance across 12 major cancer types (2013) — 4,262 citations
- VarScan: variant detection in massively parallel sequencing of individual and pooled samples (2009) — 1,343 citations
- Initial sequencing and comparative analysis of the mouse genome. (2002) — 4,291 citations
- Somatic mutations affect key pathways in lung adenocarcinoma (2008) — 2,751 citations
- The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes (2003) — 2,172 citations