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About
Gil McVean
Author PubWeight™ 231.51
‹?›
Top papers
Rank
Title
Journal
Year
PubWeight™
‹?›
1
A new multipoint method for genome-wide association studies by imputation of genotypes.
Nat Genet
2007
52.68
2
Integrating common and rare genetic variation in diverse human populations.
Nature
2010
32.30
3
A fine-scale map of recombination rates and hotspots across the human genome.
Science
2005
26.82
4
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.
Nat Genet
2006
15.63
5
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Nature
2011
13.23
6
Mapping copy number variation by population-scale genome sequencing.
Nature
2011
12.55
7
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.
Nature
2010
12.27
8
A common sequence motif associated with recombination hot spots and genome instability in humans.
Nat Genet
2008
8.64
9
Drive against hotspot motifs in primates implicates the PRDM9 gene in meiotic recombination.
Science
2009
7.35
10
De novo assembly and genotyping of variants using colored de Bruijn graphs.
Nat Genet
2012
5.61
11
Differential confounding of rare and common variants in spatially structured populations.
Nat Genet
2012
5.28
12
A statistical method for predicting classical HLA alleles from SNP data.
Am J Hum Genet
2008
4.65
13
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.
Nat Genet
2013
4.62
14
The influence of recombination on human genetic diversity.
PLoS Genet
2006
4.04
15
Human genome sequence variation and the influence of gene history, mutation and recombination.
Nat Genet
2002
3.24
16
A fine-scale chimpanzee genetic map from population sequencing.
Science
2012
2.83
17
HLA*IMP--an integrated framework for imputing classical HLA alleles from SNP genotypes.
Bioinformatics
2011
2.21
18
The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes.
Genome Res
2013
1.83
19
Recombination rate estimation in the presence of hotspots.
Genome Res
2007
1.83
20
Recombination and population structure in Salmonella enterica.
PLoS Genet
2011
1.61
21
Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3.
Nat Genet
2012
1.53
22
A structured ancestral population for the evolution of modern humans.
Curr Opin Genet Dev
2004
1.48
23
Multi-population classical HLA type imputation.
PLoS Comput Biol
2013
1.43
24
Estimating selection coefficients in spatially structured populations from time series data of allele frequencies.
Genetics
2013
1.29
25
Arabidopsis meiotic crossover hot spots overlap with H2A.Z nucleosomes at gene promoters.
Nat Genet
2013
1.29
26
Whole-exome sequencing studies of nonhereditary (sporadic) parathyroid adenomas.
J Clin Endocrinol Metab
2012
1.12
27
Psoriasis patients are enriched for genetic variants that protect against HIV-1 disease.
PLoS Genet
2012
1.10
28
Screening for recently selected alleles by analysis of human haplotype similarity.
Am J Hum Genet
2005
1.10
29
High-throughput microbial population genomics using the Cortex variation assembler.
Bioinformatics
2012
1.04
30
PRDM9 marks the spot.
Nat Genet
2010
0.98
31
Genomewide association studies and common disease--realizing clinical utility.
N Engl J Med
2012
0.95
32
Hypervariable antigen genes in malaria have ancient roots.
BMC Evol Biol
2013
0.90
33
Estimating recombination rates from genetic variation in humans.
Methods Mol Biol
2012
0.81
34
Experiments with the site frequency spectrum.
Bull Math Biol
2010
0.81
35
Integrating genealogical and dynamical modelling to infer escape and reversion rates in HIV epitopes.
Proc Biol Sci
2013
0.80
36
Reply to: "FaST-LMM-Select for addressing confounding from spatial structure and rare variants".
Nat Genet
2013
0.80
37
The comings and goings of a Y polymorphism.
Nat Genet
2003
0.77
38
Corrigendum: Rapid antibiotic-resistance predictions from genome sequence data for Staphylococcus aureus and Mycobacterium tuberculosis.
Nat Commun
2016
0.75