PubRank

Hyun Min Kang

Author PubWeight™ 178.27‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 An integrated map of genetic variation from 1,092 human genomes. Nature 2012 59.82
2 Evolution and functional impact of rare coding variation from deep sequencing of human exomes. Science 2012 17.12
3 A global reference for human genetic variation. Nature 2015 12.85
4 Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nat Genet 2012 11.09
5 Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants. Nature 2012 8.91
6 A sequence-based variation map of 8.27 million SNPs in inbred mouse strains. Nature 2007 6.77
7 The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits. PLoS Genet 2012 6.15
8 Loss-of-function mutations in APOC3, triglycerides, and coronary disease. N Engl J Med 2014 5.47
9 Low-coverage sequencing: implications for design of complex trait association studies. Genome Res 2011 5.34
10 Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. Nat Genet 2012 4.73
11 Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nat Genet 2014 4.13
12 A high-resolution association mapping panel for the dissection of complex traits in mice. Genome Res 2010 3.81
13 Leveraging the HapMap correlation structure in association studies. Am J Hum Genet 2007 3.57
14 Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion. Nat Genet 2012 2.55
15 Rapid and accurate multiple testing correction and power estimation for millions of correlated markers. PLoS Genet 2009 2.30
16 Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease. Neuroimage 2010 1.94
17 Detecting and estimating contamination of human DNA samples in sequencing and array-based genotype data. Am J Hum Genet 2012 1.94
18 Fine mapping in 94 inbred mouse strains using a high-density haplotype resource. Genetics 2010 1.71
19 Low-pass DNA sequencing of 1200 Sardinians reconstructs European Y-chromosome phylogeny. Science 2013 1.70
20 Mouse genome-wide association and systems genetics identify Asxl2 as a regulator of bone mineral density and osteoclastogenesis. PLoS Genet 2011 1.68
21 Identification and functional validation of the novel antimalarial resistance locus PF10_0355 in Plasmodium falciparum. PLoS Genet 2011 1.68
22 Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study. PLoS One 2012 1.65
23 Hybrid mouse diversity panel: a panel of inbred mouse strains suitable for analysis of complex genetic traits. Mamm Genome 2012 1.43
24 A genome-wide association study of gestational diabetes mellitus in Korean women. Diabetes 2012 1.41
25 Identification of a rare coding variant in complement 3 associated with age-related macular degeneration. Nat Genet 2013 1.39
26 Genotype calling and haplotyping in parent-offspring trios. Genome Res 2012 1.27
27 Identification of novel genes that mediate innate immunity using inbred mice. Genetics 2009 1.22
28 Imputation of coding variants in African Americans: better performance using data from the exome sequencing project. Bioinformatics 2013 1.05
29 Inference and analysis of haplotypes from combined genotyping studies deposited in dbSNP. Genome Res 2005 1.05
30 Increased power of mixed models facilitates association mapping of 10 loci for metabolic traits in an isolated population. Hum Mol Genet 2010 0.98
31 Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences. Genome Biol 2014 0.98
32 Linkage effects and analysis of finite sample errors in the HapMap. Hum Hered 2009 0.96
33 QPLOT: a quality assessment tool for next generation sequencing data. Biomed Res Int 2013 0.95
34 The benefits of using genetic information to design prevention trials. Am J Hum Genet 2013 0.91
35 Mixed-model coexpression: calculating gene coexpression while accounting for expression heterogeneity. Bioinformatics 2011 0.91
36 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Psychophysiology 2014 0.91
37 Cell-targeting and cell-penetrating peptides for delivery of therapeutic and imaging agents. Wiley Interdiscip Rev Nanomed Nanobiotechnol 2010 0.90
38 Genetic associations of nonsynonymous exonic variants with psychophysiological endophenotypes. Psychophysiology 2014 0.88
39 Accurate local-ancestry inference in exome-sequenced admixed individuals via off-target sequence reads. Am J Hum Genet 2013 0.86
40 Correction: Assessing Mitochondrial DNA Variation and Copy Number in Lymphocytes of ~2,000 Sardinians Using Tailored Sequencing Analysis Tools. PLoS Genet 2015 0.79
41 Mapping genetic variants associated with beta-adrenergic responses in inbred mice. PLoS One 2012 0.78
42 Gene-level integrated metric of negative selection (GIMS) prioritizes candidate genes for nephrotic syndrome. PLoS One 2013 0.78