Published in Nat Genet on August 29, 2011
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A genome-wide association study identifies novel risk loci for type 2 diabetes. Nature (2007) 35.08
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature (2011) 13.25
Approximate Bayesian computation in population genetics. Genetics (2002) 13.06
Genome-wide association study identifies eight loci associated with blood pressure. Nat Genet (2009) 12.44
Common genetic determinants of vitamin D insufficiency: a genome-wide association study. Lancet (2010) 8.89
Epigenome-wide association studies for common human diseases. Nat Rev Genet (2011) 7.96
Simultaneous analysis of all SNPs in genome-wide and re-sequencing association studies. PLoS Genet (2008) 6.66
Identifying adaptive genetic divergence among populations from genome scans. Mol Ecol (2004) 5.31
Assessment of cumulative evidence on genetic associations: interim guidelines. Int J Epidemiol (2007) 4.96
Bayesian statistical methods for genetic association studies. Nat Rev Genet (2009) 4.37
Sequence-level population simulations over large genomic regions. Genetics (2007) 4.04
Inferring population history with DIY ABC: a user-friendly approach to approximate Bayesian computation. Bioinformatics (2008) 4.02
Identification of seven loci affecting mean telomere length and their association with disease. Nat Genet (2013) 3.87
Improved heritability estimation from genome-wide SNPs. Am J Hum Genet (2012) 3.48
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat Genet (2011) 3.40
Genome-wide significance for dense SNP and resequencing data. Genet Epidemiol (2008) 3.26
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. Nat Genet (2011) 3.18
New gene functions in megakaryopoiesis and platelet formation. Nature (2011) 3.14
AIP mutation in pituitary adenomas in the 18th century and today. N Engl J Med (2011) 3.14
Logistic regression protects against population structure in genetic association studies. Genome Res (2005) 2.94
Seventy-five genetic loci influencing the human red blood cell. Nature (2012) 2.77
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. Nat Genet (2010) 2.30
A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order. J Allergy Clin Immunol (2011) 2.24
Fregene: simulation of realistic sequence-level data in populations and ascertained samples. BMC Bioinformatics (2008) 2.23
Population structure and inbreeding from pedigree analysis of purebred dogs. Genetics (2008) 2.14
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. Diabetes (2011) 2.09
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. Proc Natl Acad Sci U S A (2011) 2.01
Genome-wide association mapping to candidate polymorphism resolution in the unsequenced barley genome. Proc Natl Acad Sci U S A (2010) 1.96
Genetic association of the major histocompatibility complex with rheumatoid arthritis implicates two non-DRB1 loci. Arthritis Rheum (2009) 1.92
Genetic determinants of height growth assessed longitudinally from infancy to adulthood in the northern Finland birth cohort 1966. PLoS Genet (2009) 1.89
Long-term leisure-time physical activity and serum metabolome. Circulation (2012) 1.81
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat Genet (2013) 1.72
Ethiopian genetic diversity reveals linguistic stratification and complex influences on the Ethiopian gene pool. Am J Hum Genet (2012) 1.60
Clinical factors and ABCB1 polymorphisms in prediction of antiepileptic drug response: a prospective cohort study. Lancet Neurol (2006) 1.54
Functional constraint and small insertions and deletions in the ENCODE regions of the human genome. Genome Biol (2007) 1.43
Confounding between recombination and selection, and the Ped/Pop method for detecting selection. Genome Res (2008) 1.42
A genome-wide association study of the metabolic syndrome in Indian Asian men. PLoS One (2010) 1.42
cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVs. Nat Methods (2010) 1.41
Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. PLoS Genet (2010) 1.40
Inferring combined CNV/SNP haplotypes from genotype data. Bioinformatics (2010) 1.35
Multipoint linkage-disequilibrium mapping narrows location interval and identifies mutation heterogeneity. Proc Natl Acad Sci U S A (2003) 1.33
On optimal selection of summary statistics for approximate Bayesian computation. Stat Appl Genet Mol Biol (2010) 1.28
Genetic screening for Niemann-Pick disease type C in adults with neurological and psychiatric symptoms: findings from the ZOOM study. Hum Mol Genet (2013) 1.24
Detailed metabolic and genetic characterization reveals new associations for 30 known lipid loci. Hum Mol Genet (2011) 1.13
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. Hum Mol Genet (2011) 1.12
Disease association tests by inferring ancestral haplotypes using a hidden markov model. Bioinformatics (2008) 1.09
Variation in estimated recombination rates across human populations. Hum Genet (2007) 1.09
A genome-wide association study of neuroticism in a population-based sample. PLoS One (2010) 1.09
Inference of haplotypic phase and missing genotypes in polyploid organisms and variable copy number genomic regions. BMC Bioinformatics (2008) 1.01
Worldwide F(ST) estimates relative to five continental-scale populations. Ann Hum Genet (2014) 1.00
Lumbar disc degeneration is linked to a carbohydrate sulfotransferase 3 variant. J Clin Invest (2013) 0.98
Response to Lee et al.: SNP-based heritability analysis with dense data. Am J Hum Genet (2013) 0.97
Exon sequencing and high resolution haplotype analysis of ABC transporter genes implicated in drug resistance. Pharmacogenet Genomics (2006) 0.97
Using penalised logistic regression to fine map HLA variants for rheumatoid arthritis. Ann Hum Genet (2011) 0.96
Storytelling and story testing in domestication. Proc Natl Acad Sci U S A (2014) 0.96
Common genetic variants regulating ADD3 gene expression alter biliary atresia risk. J Hepatol (2013) 0.90
Common ABCB1 polymorphisms are not associated with multidrug resistance in epilepsy using a gene-wide tagging approach. Pharmacogenet Genomics (2007) 0.87
Multiple single nucleotide polymorphism analysis using penalized regression in nonlinear mixed-effect pharmacokinetic models. Pharmacogenet Genomics (2013) 0.86
Clustering of protein domains in the human genome. J Mol Biol (2004) 0.85
Family-based association analysis with ordered categorical phenotypes, covariates and interactions. Genet Epidemiol (2007) 0.85
Discrimination of half-siblings when maternal genotypes are known. Forensic Sci Int (2005) 0.80
The effect of genomic inversions on estimation of population genetic parameters from SNP data. Genetics (2012) 0.79
The association between polymorphisms in RLIP76 and drug response in epilepsy. Pharmacogenomics (2007) 0.79
Fine-scale estimation of location of birth from genome-wide single-nucleotide polymorphism data. Genetics (2011) 0.79
Integrating dynamic mixed-effect modelling and penalized regression to explore genetic association with pharmacokinetics. Pharmacogenet Genomics (2015) 0.77
Dysregulation of complement system and CD4+ T cell activation pathways implicated in allergic response. PLoS One (2013) 0.77
Paternity index calculations when some individuals share common ancestry. Forensic Sci Int (2004) 0.75
Corrigendum: Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. Nat Genet (2017) 0.75
Implications for DNA identification arising from an analysis of Australian forensic databases. Forensic Sci Int (2002) 0.75
Evaluation of low-template DNA profiles using peak heights. Stat Appl Genet Mol Biol (2016) 0.75