S. Myers
Genetics · Science · 2004–2019
A researcher in the Science corpus: 14 papers; trusts 18 researchers and is trusted by 17 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 186 citations into it; #776 of 6,854 by trust here, #80 by citations
- Molecular Biology — 89 citations into it
- Artificial Intelligence — 6 citations into it
Whom S. Myers trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Matthew Stephens
- J. K. Pritchard
- Paul Scheet
- Na Li
- Sharon R. Browning
- David J. Balding
- Peter Donnelly
- Alkes L Price
- J. Pella
- Nick Patterson
Who trusts S. Myers overall
- Bryan N. Howie
- Jonathan Marchini
- Joseph K. Pickrell
- Matthew Stephens
- Brian L. Browning
- Peter Donnelly
- Jerome Kelleher
- Shaun Purcell
- Sharon R. Browning
- Matthew D. Rasmussen
Papers from S. Myers's perspective
Ordered by how strongly the researchers S. Myers trusts endorse each paper. Same corpus, a different order for every researcher.
- Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies. (Genetics)
- Generating samples under a Wright-Fisher neutral model of genetic variation (Bioinform.)
- A new statistical method for haplotype reconstruction from population data. (American Journal of Human Genetics)
- Maximum likelihood from incomplete data via the EM - algorithm plus discussions on the paper
- Genotype, haplotype and copy-number variation in worldwide human populations (Nature)
- Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data. (Genetics)
- A Draft Sequence of the Neandertal Genome (Science)
- Faculty Opinions recommendation of Interpreting principal component analyses of spatial population genetic variation.
- Reconstructing Indian Population History (Nature)
- 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)
Their papers
- 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
- 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
- Multiple regions within 8q24 independently affect risk for prostate cancer (2007) — 676 citations
- A method for genome-wide genealogy estimation for thousands of samples (2019) — 488 citations
- A genetic atlas of human admixture history (2014) — 742 citations
- Great ape genetic diversity and population history (2013) — 858 citations
- Bayesian refinement of association signals for 14 loci in 3 common diseases (2012) — 508 citations
- Inference of Population Structure using Dense Haplotype Data (2012) — 1,159 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
- Drive Against Hotspot Motifs in Primates Implicates the PRDM9 gene in Meiotic Recombination (2009) — 676 citations
- Long-range LD can confound genome scans in admixed populations. (2008) — 455 citations
- A new multipoint method for genome-wide association studies by imputation of genotypes (2007) — 2,734 citations