Bryan N. Howie

Genetics · 2007–2015

A researcher in the Science corpus: 13 papers; trusts 16 researchers and is trusted by 50 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 159 citations into it; #144 of 6,854 by trust here, #38 by citations
• Molecular Biology — 88 citations into it

Whom Bryan N. Howie trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Jonathan Marchini
2. Matthew Stephens
3. Paul Scheet
4. Brian L. Browning
5. Sharon R. Browning
6. Na Li
7. Peter Donnelly
8. Yun Li
9. S. Myers
10. Gonçalo R. Abecasis

Who trusts Bryan N. Howie overall

1. Brian L. Browning
2. Olivier Delaneau
3. Jonathan Marchini
4. Sharon R. Browning
5. Christian Fuchsberger
6. Po-Ru Loh
7. Matthew Stephens
8. Heng Li
9. Gonçalo R. Abecasis
10. Rina Foygel Barber

Papers from Bryan N. Howie's perspective

Ordered by how strongly the researchers Bryan N. Howie trusts endorse each paper. Same corpus, a different order for every researcher.

1. A new statistical method for haplotype reconstruction from population data. (American Journal of Human Genetics)
2. A comparison of bayesian methods for haplotype reconstruction from population genotype data. (American Journal of Human Genetics)
3. A new multipoint method for genome-wide association studies by imputation of genotypes (Nature Genetics)
4. Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
5. Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data. (Genetics)
6. MaCH: Using Sequence and Genotype Data to Estimate Haplotypes and Unobserved Genotypes (Genetic Epidemiology)
7. Calibrating a coalescent simulation of human genome sequence variation. (Genome Research)
8. Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation. (American Journal of Human Genetics)
9. Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies. (Genetics)
10. 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
• The UK10K project identifies rare variants in health and disease (2015) — 1,063 citations
• Haplotype estimation using sequencing reads. (2013) — 388 citations
• Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel (2015) — 384 citations
• Human polymorphism at microRNAs and microRNA target sites. (2013) — 605 citations
• An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations
• Fast and accurate genotype imputation in genome-wide association studies through pre-phasing (2012) — 1,829 citations
• Genotype Imputation with Thousands of Genomes (2011) — 1,027 citations
• Genotype imputation for genome-wide association studies (2010) — 1,730 citations
• A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies (2009) — 4,153 citations
• Identification of loci associated with schizophrenia by genome-wide association and follow-up (2008) — 1,107 citations
• A new multipoint method for genome-wide association studies by imputation of genotypes (2007) — 2,734 citations
• Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (2007) — 9,550 citations