PubRank

Lachlan J M Coin

Author PubWeight™ 54.37‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet 2010 17.89
2 Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. Nat Genet 2009 6.39
3 Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. PLoS Genet 2012 3.21
4 Haplotype and isoform specific expression estimation using multi-mapping RNA-seq reads. Genome Biol 2011 2.61
5 MultiPhen: joint model of multiple phenotypes can increase discovery in GWAS. PLoS One 2012 2.56
6 Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly. Nat Biotechnol 2011 2.45
7 Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. Nat Genet 2010 2.30
8 Genetic determinants of height growth assessed longitudinally from infancy to adulthood in the northern Finland birth cohort 1966. PLoS Genet 2009 1.89
9 A genome-wide association search for type 2 diabetes genes in African Americans. PLoS One 2012 1.72
10 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. PLoS Genet 2010 1.40
11 Inferring combined CNV/SNP haplotypes from genotype data. Bioinformatics 2010 1.35
12 Small deletion variants have stable breakpoints commonly associated with alu elements. PLoS One 2008 1.30
13 Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathways. Hum Mol Genet 2011 1.22
14 Disease association tests by inferring ancestral haplotypes using a hidden markov model. Bioinformatics 2008 1.09
15 Inference of haplotypic phase and missing genotypes in polyploid organisms and variable copy number genomic regions. BMC Bioinformatics 2008 1.01
16 cnvHiTSeq: integrative models for high-resolution copy number variation detection and genotyping using population sequencing data. Genome Biol 2012 0.98
17 invertFREGENE: software for simulating inversions in population genetic data. Bioinformatics 2010 0.90
18 Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity. PLoS One 2013 0.88
19 Novel association approach for variable number tandem repeats (VNTRs) identifies DOCK5 as a susceptibility gene for severe obesity. Hum Mol Genet 2012 0.83
20 A population model for genotyping indels from next-generation sequence data. Nucleic Acids Res 2012 0.81
21 Fine-scale estimation of location of birth from genome-wide single-nucleotide polymorphism data. Genetics 2011 0.79
22 Gene-targeted analysis of copy number variants identifies 3 novel associations with coronary heart disease traits. Circ Cardiovasc Genet 2012 0.79
23 Dysregulation of complement system and CD4+ T cell activation pathways implicated in allergic response. PLoS One 2013 0.77
24 YHap: a population model for probabilistic assignment of Y haplogroups from re-sequencing data. BMC Bioinformatics 2013 0.75
25 Accurate single-nucleotide polymorphism allele assignment in trisomic or duplicated regions by using a single base-extension assay with MALDI-TOF mass spectrometry. Clin Chem 2011 0.75
26 Bioinformatics: living on the edge. Genome Biol 2012 0.75