A. Coffey
Molecular Biology · Nature · 2005–2012
A researcher in the Science corpus: 4 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 62 citations into it
Whom A. Coffey trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts A. Coffey overall
Papers from A. Coffey's perspective
Ordered by how strongly the researchers A. Coffey trusts endorse each paper. Same corpus, a different order for every researcher.
- Diversity of Human Copy Number Variation and Multicopy Genes (Science)
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- Exome sequencing as a tool for Mendelian disease gene discovery
- Direct selection of human genomic loci by microarray hybridization (Nature Methods)
- The Human Gene Mutation Database: 2008 update
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people (Science)
- Mapping copy number variation by population scale genome sequencing (Nature)
- Integrated detection and population-genetic analysis of SNPs and copy number variation (Nature Genetics)
- Error-correcting barcoded primers for pyrosequencing hundreds of samples in multiplex (Nature Methods)
Their papers
- The DNA sequence of the human X chromosome (2005) — 1,099 citations
- Target-enrichment strategies for next-generation sequencing (2010) — 643 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations
- Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) — 710 citations