PubRank

David J Balding

Author PubWeight™ 137.73‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 A genome-wide association study identifies novel risk loci for type 2 diabetes. Nature 2007 35.08
2 Approximate Bayesian computation in population genetics. Genetics 2002 13.06
3 Epigenome-wide association studies for common human diseases. Nat Rev Genet 2011 7.96
4 Simultaneous analysis of all SNPs in genome-wide and re-sequencing association studies. PLoS Genet 2008 6.66
5 Identifying adaptive genetic divergence among populations from genome scans. Mol Ecol 2004 5.31
6 Assessment of cumulative evidence on genetic associations: interim guidelines. Int J Epidemiol 2007 4.96
7 Bayesian statistical methods for genetic association studies. Nat Rev Genet 2009 4.37
8 Sequence-level population simulations over large genomic regions. Genetics 2007 4.04
9 Inferring population history with DIY ABC: a user-friendly approach to approximate Bayesian computation. Bioinformatics 2008 4.02
10 Improved heritability estimation from genome-wide SNPs. Am J Hum Genet 2012 3.48
11 Genome-wide significance for dense SNP and resequencing data. Genet Epidemiol 2008 3.26
12 AIP mutation in pituitary adenomas in the 18th century and today. N Engl J Med 2011 3.14
13 Logistic regression protects against population structure in genetic association studies. Genome Res 2005 2.94
14 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
15 Fregene: simulation of realistic sequence-level data in populations and ascertained samples. BMC Bioinformatics 2008 2.23
16 Population structure and inbreeding from pedigree analysis of purebred dogs. Genetics 2008 2.14
17 Genome-wide association mapping to candidate polymorphism resolution in the unsequenced barley genome. Proc Natl Acad Sci U S A 2010 1.96
18 Genetic association of the major histocompatibility complex with rheumatoid arthritis implicates two non-DRB1 loci. Arthritis Rheum 2009 1.92
19 Ethiopian genetic diversity reveals linguistic stratification and complex influences on the Ethiopian gene pool. Am J Hum Genet 2012 1.60
20 Clinical factors and ABCB1 polymorphisms in prediction of antiepileptic drug response: a prospective cohort study. Lancet Neurol 2006 1.54
21 Functional constraint and small insertions and deletions in the ENCODE regions of the human genome. Genome Biol 2007 1.43
22 Confounding between recombination and selection, and the Ped/Pop method for detecting selection. Genome Res 2008 1.42
23 A genome-wide association study of the metabolic syndrome in Indian Asian men. PLoS One 2010 1.42
24 cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVs. Nat Methods 2010 1.41
25 Inferring combined CNV/SNP haplotypes from genotype data. Bioinformatics 2010 1.35
26 Multipoint linkage-disequilibrium mapping narrows location interval and identifies mutation heterogeneity. Proc Natl Acad Sci U S A 2003 1.33
27 On optimal selection of summary statistics for approximate Bayesian computation. Stat Appl Genet Mol Biol 2010 1.28
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
29 Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. Hum Mol Genet 2011 1.12
30 Disease association tests by inferring ancestral haplotypes using a hidden markov model. Bioinformatics 2008 1.09
31 Variation in estimated recombination rates across human populations. Hum Genet 2007 1.09
32 A genome-wide association study of neuroticism in a population-based sample. PLoS One 2010 1.09
33 Inference of haplotypic phase and missing genotypes in polyploid organisms and variable copy number genomic regions. BMC Bioinformatics 2008 1.01
34 Worldwide F(ST) estimates relative to five continental-scale populations. Ann Hum Genet 2014 1.00
35 Exon sequencing and high resolution haplotype analysis of ABC transporter genes implicated in drug resistance. Pharmacogenet Genomics 2006 0.97
36 Response to Lee et al.: SNP-based heritability analysis with dense data. Am J Hum Genet 2013 0.97
37 Using penalised logistic regression to fine map HLA variants for rheumatoid arthritis. Ann Hum Genet 2011 0.96
38 Storytelling and story testing in domestication. Proc Natl Acad Sci U S A 2014 0.96
39 Common ABCB1 polymorphisms are not associated with multidrug resistance in epilepsy using a gene-wide tagging approach. Pharmacogenet Genomics 2007 0.87
40 Multiple single nucleotide polymorphism analysis using penalized regression in nonlinear mixed-effect pharmacokinetic models. Pharmacogenet Genomics 2013 0.86
41 Family-based association analysis with ordered categorical phenotypes, covariates and interactions. Genet Epidemiol 2007 0.85
42 Clustering of protein domains in the human genome. J Mol Biol 2004 0.85
43 Discrimination of half-siblings when maternal genotypes are known. Forensic Sci Int 2005 0.80
44 The association between polymorphisms in RLIP76 and drug response in epilepsy. Pharmacogenomics 2007 0.79
45 Dysregulation of complement system and CD4+ T cell activation pathways implicated in allergic response. PLoS One 2013 0.77
46 Integrating dynamic mixed-effect modelling and penalized regression to explore genetic association with pharmacokinetics. Pharmacogenet Genomics 2015 0.77
47 Admixture provides new insights into recombination. Nat Genet 2011 0.75
48 Paternity index calculations when some individuals share common ancestry. Forensic Sci Int 2004 0.75
49 Implications for DNA identification arising from an analysis of Australian forensic databases. Forensic Sci Int 2002 0.75
50 Evaluation of low-template DNA profiles using peak heights. Stat Appl Genet Mol Biol 2016 0.75