PubRank

Guimin Gao

Author PubWeight™ 35.41‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Mutation in CUL4B, which encodes a member of cullin-RING ubiquitin ligase complex, causes X-linked mental retardation. Am J Hum Genet 2007 1.41
2 Comprehensive association analysis of nine candidate genes with serum 25-hydroxy vitamin D levels among healthy Caucasian subjects. Hum Genet 2010 1.31
3 Weighted multiple hypothesis testing procedures. Stat Appl Genet Mol Biol 2009 1.14
4 Characterization of nuclear localization signal in the N terminus of CUL4B and its essential role in cyclin E degradation and cell cycle progression. J Biol Chem 2009 1.12
5 A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42). Am J Hum Genet 2008 1.09
6 Resveratrol augments the canonical Wnt signaling pathway in promoting osteoblastic differentiation of multipotent mesenchymal cells. Exp Cell Res 2009 1.08
7 MethylPCA: a toolkit to control for confounders in methylome-wide association studies. BMC Bioinformatics 2013 1.06
8 Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants. Genet Epidemiol 2013 1.04
9 Haplotype-based methods for detecting uncommon causal variants with common SNPs. Genet Epidemiol 2012 1.04
10 Berberine induces p53-dependent cell cycle arrest and apoptosis of human osteosarcoma cells by inflicting DNA damage. Mutat Res 2008 1.04
11 Practical Consideration of Genotype Imputation: Sample Size, Window Size, Reference Choice, and Untyped Rate. Stat Interface 2011 1.01
12 Apolipoprotein B genetic variants modify the response to fenofibrate: a GOLDN study. J Lipid Res 2010 1.00
13 Pharmacogenetic association of the APOA1/C3/A4/A5 gene cluster and lipid responses to fenofibrate: the genetics of lipid-lowering drugs and diet network study. Pharmacogenet Genomics 2009 0.97
14 Resveratrol modulates angiogenesis through the GSK3β/β-catenin/TCF-dependent pathway in human endothelial cells. Biochem Pharmacol 2010 0.92
15 Evaluation of pooled association tests for rare variant identification. BMC Proc 2011 0.91
16 Estimation of deleterious genomic mutation parameters in natural populations by accounting for variable mutation effects across loci. Genetics 2002 0.91
17 Rank-based robust tests for quantitative-trait genetic association studies. Genet Epidemiol 2013 0.91
18 The SCARB1 gene is associated with lipid response to dietary and pharmacological interventions. J Hum Genet 2008 0.90
19 Case-control association analysis of rheumatoid arthritis with candidate genes using related cases. BMC Proc 2007 0.87
20 Serum withdrawal up-regulates human SIRT1 gene expression in a p53-dependent manner. J Cell Mol Med 2009 0.87
21 Association study between vitamin D receptor gene polymorphisms and asthma in the Chinese Han population: a case-control study. BMC Med Genet 2009 0.86
22 Capitalizing on admixture in genome-wide association studies: a two-stage testing procedure and application to height in African-Americans. Front Genet 2011 0.86
23 Kernel-machine testing coupled with a rank-truncation method for genetic pathway analysis. Genet Epidemiol 2014 0.85
24 Detecting epistatic interactions contributing to human gene expression using the CEPH family data. BMC Proc 2007 0.84
25 Sp1 and CREB regulate basal transcription of the human SNF2L gene. Biochem Biophys Res Commun 2008 0.84
26 Discussing gene-gene interaction: warning--translating equations to English may result in jabberwocky. Genet Epidemiol 2007 0.82
27 Genome-wide association studies of rheumatoid arthritis data via multiple hypothesis testing methods for correlated tests. BMC Proc 2009 0.80
28 A Sequence Kernel Association Test for Dichotomous Traits in Family Samples under a Generalized Linear Mixed Model. Hum Hered 2015 0.80
29 Similarity-based multimarker association tests for continuous traits. Ann Hum Genet 2012 0.79
30 Rare-Variant Kernel Machine Test for Longitudinal Data from Population and Family Samples. Hum Hered 2016 0.78
31 Application of imputation methods to the analysis of rheumatoid arthritis data in genome-wide association studies. BMC Proc 2009 0.78
32 A rapid association test procedure robust under different genetic models accounting for population stratification. Hum Hered 2013 0.78
33 Rank-based tests for identifying multiple genetic variants associated with quantitative traits. Ann Hum Genet 2014 0.78
34 A novel mutation of keratin 9 in epidermolytic palmoplantar keratoderma combined with knuckle pads. Am J Med Genet A 2003 0.75
35 Improving the signal-to-noise ratio in genome-wide association studies. Genet Epidemiol 2009 0.75
36 Rare SERINC2 variants are specific for alcohol dependence in individuals of European descent. Pharmacogenet Genomics 2013 0.75
37 A Generalized Sequential Bonferroni Procedure for GWAS in Admixed Populations Incorporating Admixture Mapping Information into Association Tests. Hum Hered 2015 0.75
38 Double genomic control is not effective to correct for population stratification in meta-analysis for genome-wide association studies. Front Genet 2012 0.75
39 A locus for nonspecific X-linked mental retardation mapped to a 22.3 cM region of Xp11.3-q22.3. Am J Med Genet A 2004 0.75
40 [Gene mapping of a nonsyndromic hearing impairmint family]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2003 0.75
41 [The C677T mutation in the methylenetetrahydrofolate reductase gene and its association with deep vein thrombophilia in Shandong Hans]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2002 0.75