G. McVean
Genetics · 2002–2018
A researcher in the Science corpus: 31 papers; trusts 34 researchers and is trusted by 27 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 354 citations into it; #564 of 6,854 by trust here, #20 by citations
- Molecular Biology — 258 citations into it; #4,084 of 17,773 by trust here, #345 by citations
- Plant Science — 69 citations into it
- Artificial Intelligence — 16 citations into it
- Statistics and Probability — 11 citations into it
- Paleontology — 5 citations into it
Whom G. McVean trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Richard Durbin
- Matthew Stephens
- Jonathan Marchini
- Heng Li
- J. K. Pritchard
- Bryan N. Howie
- Peter Donnelly
- S. Myers
- David J. Balding
- Henrik Kaessmann
Who trusts G. McVean overall
- Darren P. Martin
- Edward C. Holmes
- Matthew Stephens
- T. C. Bruen
- W. Wachowiak
- Daniel R. Schrider
- Oliver Stegle
- Sergei L. Kosakovsky Pond
- Bryan N. Howie
- Brian L. Browning
Papers from G. McVean's perspective
Ordered by how strongly the researchers G. McVean trusts endorse each paper. Same corpus, a different order for every researcher.
- Generating samples under a Wright-Fisher neutral model of genetic variation (Bioinform.)
- Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies. (Genetics)
- A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase. (American Journal of Human Genetics)
- A new statistical method for haplotype reconstruction from population data. (American Journal of Human Genetics)
- Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data. (Genetics)
- Calibrating a coalescent simulation of human genome sequence variation. (Genome Research)
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- Exome sequencing as a tool for Mendelian disease gene discovery
- The Human Gene Mutation Database: 2008 update
Their papers
- Detecting Novel Associations in Large Datasets (2011) — 3,212 citations
- A global reference for human genetic variation (2015) — 16,925 citations
- A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
- De novo assembly and genotyping of variants using colored de Bruijn graphs (2012) — 677 citations
- The Fine-Scale Structure of Recombination Rate Variation in the Human Genome (2004) — 1,002 citations
- A Fine-Scale Map of Recombination Rates and Hotspots Across the Human Genome (2005) — 1,169 citations
- Dindel: accurate indel calls from short-read data. (2011) — 455 citations
- The UK Biobank resource with deep phenotyping and genomic data (2018) — 7,745 citations
- Integrating common and rare genetic variation in diverse human populations (2010) — 3,033 citations
- Genome-wide genetic data on ~500,000 UK Biobank participants (2017) — 696 citations
- Rapid antibiotic-resistance predictions from genome sequence data for Staphylococcus aureus and Mycobacterium tuberculosis (2015) — 509 citations
- Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications (2014) — 1,029 citations
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- Multi-Population Classical HLA Type Imputation (2013) — 213 citations
- Efficient Coalescent Simulation and Genealogical Analysis for Large Sample Sizes (2015) — 638 citations
- A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigree (2016) — 352 citations
- Class II HLA interactions modulate genetic risk for multiple sclerosis (2015) — 366 citations
- Germline mutations in the proof-reading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas (2012) — 943 citations
- Bayesian refinement of association signals for 14 loci in 3 common diseases (2012) — 508 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations