PubRank

Andrew Crenshaw

Author PubWeight™ 64.76‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Multiple loci identified in a genome-wide association study of prostate cancer. Nat Genet 2008 17.65
2 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. Science 2010 9.61
3 SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes. Nucleic Acids Res 2006 4.63
4 Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nat Genet 2012 3.68
5 SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes. Nucleic Acids Res 2004 3.47
6 Candidate gene association resource (CARe): design, methods, and proof of concept. Circ Cardiovasc Genet 2010 2.91
7 Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancers. Hum Genet 2008 2.41
8 Epidermal growth factor receptor inhibition attenuates liver fibrosis and development of hepatocellular carcinoma. Hepatology 2014 2.40
9 Prognostic gene expression signature for patients with hepatitis C-related early-stage cirrhosis. Gastroenterology 2013 2.13
10 Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. PLoS Genet 2012 2.00
11 Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network. Hum Genet 2011 2.00
12 zCall: a rare variant caller for array-based genotyping: genetics and population analysis. Bioinformatics 2012 1.87
13 Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA. Hum Mol Genet 2011 1.77
14 High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic Arrays. BMC Genomics 2009 1.76
15 Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association. Proc Natl Acad Sci U S A 2012 1.16
16 Genetic variation associated with circulating monocyte count in the eMERGE Network. Hum Mol Genet 2013 1.05
17 Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records. PLoS One 2013 0.94
18 Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers. Hum Genet 2011 0.87
19 Feasibility of High-Throughput Genome-Wide Genotyping using DNA from Stored Buccal Cell Samples. Biomark Insights 2010 0.87
20 Evolutionary dynamics of the human NADPH oxidase genes CYBB, CYBA, NCF2, and NCF4: functional implications. Mol Biol Evol 2013 0.80
21 Genetic variants in the 8q24 locus and risk of testicular germ cell tumors. Hum Genet 2008 0.79
22 Diversity in the glucose transporter-4 gene (SLC2A4) in humans reflects the action of natural selection along the old-world primates evolution. PLoS One 2010 0.79
23 Limited clinical utility of a genetic risk score for the prediction of fracture risk in elderly subjects. J Bone Miner Res 2015 0.78