PubRank

Kelly A Frazer

Author PubWeight™ 234.62‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 A second generation human haplotype map of over 3.1 million SNPs. Nature 2007 85.39
2 Whole-genome patterns of common DNA variation in three human populations. Science 2005 21.22
3 Genome-wide detection and characterization of positive selection in human populations. Nature 2007 17.27
4 Common sequence polymorphisms shaping genetic diversity in Arabidopsis thaliana. Science 2007 9.85
5 Common deletions and SNPs are in linkage disequilibrium in the human genome. Nat Genet 2005 9.61
6 Evaluation of next generation sequencing platforms for population targeted sequencing studies. Genome Biol 2009 9.59
7 High-resolution whole-genome association study of Parkinson disease. Am J Hum Genet 2005 6.86
8 Common vs. rare allele hypotheses for complex diseases. Curr Opin Genet Dev 2009 6.85
9 9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response. Nature 2011 6.25
10 Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. Nat Genet 2008 6.06
11 Fine-scale recombination patterns differ between chimpanzees and humans. Nat Genet 2005 5.00
12 Implementing genomic medicine in the clinic: the future is here. Genet Med 2013 4.89
13 Microdroplet-based PCR enrichment for large-scale targeted sequencing. Nat Biotechnol 2009 4.80
14 Genomewide SNP variation reveals relationships among landraces and modern varieties of rice. Proc Natl Acad Sci U S A 2009 4.65
15 Identification of liver cancer progenitors whose malignant progression depends on autocrine IL-6 signaling. Cell 2013 3.08
16 Analysis of allelic differential expression in human white blood cells. Genome Res 2006 3.07
17 Accurate detection and genotyping of SNPs utilizing population sequencing data. Genome Res 2010 2.84
18 The genomics gold rush. JAMA 2007 2.35
19 Enrichment of sequencing targets from the human genome by solution hybridization. Genome Biol 2009 2.32
20 Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels. Hum Genomics 2004 1.71
21 Fine mapping in 94 inbred mouse strains using a high-density haplotype resource. Genetics 2010 1.71
22 Detection of low prevalence somatic mutations in solid tumors with ultra-deep targeted sequencing. Genome Biol 2011 1.60
23 Experimental selection of hypoxia-tolerant Drosophila melanogaster. Proc Natl Acad Sci U S A 2011 1.60
24 A Pan-BCL2 inhibitor renders bone-marrow-resident human leukemia stem cells sensitive to tyrosine kinase inhibition. Cell Stem Cell 2013 1.59
25 Sensitive gene fusion detection using ambiguously mapping RNA-Seq read pairs. Bioinformatics 2011 1.58
26 Allele-specific KRT1 expression is a complex trait. PLoS Genet 2006 1.41
27 Identification of high-confidence somatic mutations in whole genome sequence of formalin-fixed breast cancer specimens. Nucleic Acids Res 2012 1.27
28 ADAR1 promotes malignant progenitor reprogramming in chronic myeloid leukemia. Proc Natl Acad Sci U S A 2012 1.25
29 Population sequencing of two endocannabinoid metabolic genes identifies rare and common regulatory variants associated with extreme obesity and metabolite level. Genome Biol 2010 1.12
30 Whole-genome sequencing uncovers the genetic basis of chronic mountain sickness in Andean highlanders. Am J Hum Genet 2013 1.06
31 The resequencing imperative. Nat Genet 2007 1.05
32 Genetic determinants of phenotypic diversity in humans. Genome Biol 2008 1.00
33 In vitro human keratinocyte migration rates are associated with SNPs in the KRT1 interval. PLoS One 2007 0.99
34 Whole genome sequencing of Ethiopian highlanders reveals conserved hypoxia tolerance genes. Genome Biol 2014 0.94
35 Elucidating the role of 8q24 in colorectal cancer. Nat Genet 2009 0.93
36 Mutascope: sensitive detection of somatic mutations from deep amplicon sequencing. Bioinformatics 2013 0.92
37 Evaluation of the SNP tagging approach in an independent population sample--array-based SNP discovery in Sami. Hum Genet 2007 0.92
38 High-resolution mutational profiling suggests the genetic validity of glioblastoma patient-derived pre-clinical models. PLoS One 2013 0.90
39 Variation in conserved non-coding sequences on chromosome 5q and susceptibility to asthma and atopy. Respir Res 2005 0.88
40 Evaluation of ultra-deep targeted sequencing for personalized breast cancer care. Breast Cancer Res 2013 0.88
41 Transcriptome sequencing of tumor subpopulations reveals a spectrum of therapeutic options for squamous cell lung cancer. PLoS One 2013 0.83
42 Biased estimates of clonal evolution and subclonal heterogeneity can arise from PCR duplicates in deep sequencing experiments. Genome Biol 2014 0.83
43 Genetic ancestry of participants in the National Children's Study. Genome Biol 2014 0.80
44 Whole transcriptome sequencing enables discovery and analysis of viruses in archived primary central nervous system lymphomas. PLoS One 2013 0.78
45 Homozygous GNAS 393C-allele carriers with locally advanced esophageal cancer fail to benefit from platinum-based preoperative chemoradiotherapy. Ann Surg Oncol 2014 0.78
46 Corrigendum: PI3Kγ is a molecular switch that controls immune suppression. Nature 2016 0.75
47 The nature, pattern and function of human sequence variation. Genome Biol 2004 0.75