Published in Genetics on November 01, 2002
Influence of dominance, leptokurtosis and pleiotropy of deleterious mutations on quantitative genetic variation at mutation-selection balance. Genetics (2004) 1.40
Deleterious mutations and the genetic variance of male fitness components in Mimulus guttatus. Genetics (2003) 1.08
Redistribution of gene frequency and changes of genetic variation following a bottleneck in population size. Genetics (2004) 1.01
Analysis of the estimators of the average coefficient of dominance of deleterious mutations. Genetics (2004) 0.90
The effect of antagonistic pleiotropy on the estimation of the average coefficient of dominance of deleterious mutations. Genetics (2005) 0.82
Is urbanization scrambling the genetic structure of human populations? A case study. Heredity (Edinb) (2006) 0.82
Fitness Effects of Spontaneous Mutations in Picoeukaryotic Marine Green Algae. G3 (Bethesda) (2016) 0.76
Rates of spontaneous mutation. Genetics (1998) 14.89
Mutation rate and dominance of genes affecting viability in Drosophila melanogaster. Genetics (1972) 12.05
The molecular basis of dominance. Genetics (1982) 11.35
Mutations affecting fitness in Drosophila populations. Annu Rev Genet (1977) 9.39
Deleterious mutations and the evolution of sexual reproduction. Nature (1988) 8.89
The dominance theory of Haldane's rule. Genetics (1995) 5.93
Effects of P element insertions on quantitative traits in Drosophila melanogaster. Genetics (1992) 4.65
The distribution of mutation effects on viability in Drosophila melanogaster. Genetics (1994) 4.06
Nature of deleterious mutation load in Drosophila. Genetics (1996) 3.62
Comparing mutational variabilities. Genetics (1996) 3.54
How much do we know about spontaneous human mutation rates? Environ Mol Mutagen (1993) 2.34
Mathematical limits of multilocus models: the genetic transmission of bipolar disorder. Am J Hum Genet (1995) 2.24
Inference of genome-wide mutation rates and distributions of mutation effects for fitness traits: a simulation study. Genetics (1998) 1.97
Allozyme-associated heterosis in Drosophila melanogaster. Genetics (1989) 1.71
Estimation of deleterious-mutation parameters in natural populations. Genetics (1996) 1.54
Inbreeding depression and inferred deleterious-mutation parameters in Daphnia. Genetics (1997) 1.52
Marker-based inferences about epistasis for genes influencing inbreeding depression. Genetics (1996) 1.26
Spontaneous mutation as a risk factor. Exp Clin Immunogenet (1995) 1.07
On the three methods for estimating deleterious genomic mutation parameters. Genet Res (1998) 1.03
On the experimental design and data analysis of mutation accumulation experiments. Genet Res (1999) 1.02
Estimating within-locus nonadditive coefficient and discriminating dominance versus overdominance as the genetic cause of heterosis. Genetics (1998) 0.97
Inferring the major genomic mode of dominance and overdominance. Genetica (1998) 0.95
Characterization of deleterious mutations in outcrossing populations. Genetics (1998) 0.89
Estimation of parameters of deleterious mutations in partial selfing or partial outcrossing populations and in nonequilibrium populations. Genetics (2000) 0.80
Maternal malaria and gravidity interact to modify infant susceptibility to malaria. PLoS Med (2005) 2.72
A genomewide linkage scan for quantitative-trait loci for obesity phenotypes. Am J Hum Genet (2002) 1.91
Mutation patterns at dinucleotide microsatellite loci in humans. Am J Hum Genet (2002) 1.71
Chinese herbal medicine for osteoporosis: a systematic review of randomized controlled trails. Evid Based Complement Alternat Med (2013) 1.49
Upper limit of the rate and per generation effects of deleterious genomic mutations. Genet Res (2006) 1.41
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
A whole-genome linkage scan suggests several genomic regions potentially containing QTLs underlying the variation of stature. Am J Med Genet (2002) 1.39
Relevance of the genes for bone mass variation to susceptibility to osteoporotic fractures and its implications to gene search for complex human diseases. Genet Epidemiol (2002) 1.34
A whole-genome linkage scan suggests several genomic regions potentially containing quantitative trait Loci for osteoporosis. J Clin Endocrinol Metab (2002) 1.33
Comprehensive association analysis of nine candidate genes with serum 25-hydroxy vitamin D levels among healthy Caucasian subjects. Hum Genet (2010) 1.31
SNPP: automating large-scale SNP genotype data management. Bioinformatics (2004) 1.31
Genome-wide scan identified QTLs underlying femoral neck cross-sectional geometry that are novel studied risk factors of osteoporosis. J Bone Miner Res (2005) 1.16
Weighted multiple hypothesis testing procedures. Stat Appl Genet Mol Biol (2009) 1.14
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
Genetic linkage of human height is confirmed to 9q22 and Xq24. Hum Genet (2006) 1.10
A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42). Am J Hum Genet (2008) 1.09
Resveratrol augments the canonical Wnt signaling pathway in promoting osteoblastic differentiation of multipotent mesenchymal cells. Exp Cell Res (2009) 1.08
MethylPCA: a toolkit to control for confounders in methylome-wide association studies. BMC Bioinformatics (2013) 1.06
Haplotype-based methods for detecting uncommon causal variants with common SNPs. Genet Epidemiol (2012) 1.04
Berberine induces p53-dependent cell cycle arrest and apoptosis of human osteosarcoma cells by inflicting DNA damage. Mutat Res (2008) 1.04
Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants. Genet Epidemiol (2013) 1.04
Practical Consideration of Genotype Imputation: Sample Size, Window Size, Reference Choice, and Untyped Rate. Stat Interface (2011) 1.01
Apolipoprotein B genetic variants modify the response to fenofibrate: a GOLDN study. J Lipid Res (2010) 1.00
Genetic dissection of human stature in a large sample of multiplex pedigrees. Ann Hum Genet (2004) 1.00
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
Air quality in passenger cars of the ground railway transit system in Beijing, China. Sci Total Environ (2006) 0.96
Resveratrol modulates angiogenesis through the GSK3β/β-catenin/TCF-dependent pathway in human endothelial cells. Biochem Pharmacol (2010) 0.92
Mapping quantitative trait loci for cross-sectional geometry at the femoral neck. J Bone Miner Res (2005) 0.92
Evaluation of pooled association tests for rare variant identification. BMC Proc (2011) 0.91
Rank-based robust tests for quantitative-trait genetic association studies. Genet Epidemiol (2013) 0.91
The SCARB1 gene is associated with lipid response to dietary and pharmacological interventions. J Hum Genet (2008) 0.90
A follow-up linkage study for quantitative trait loci contributing to obesity-related phenotypes. J Clin Endocrinol Metab (2004) 0.88
Genome scan for QTLs underlying bone size variation at 10 refined skeletal sites: genetic heterogeneity and the significance of phenotype refinement. Physiol Genomics (2004) 0.88
Case-control association analysis of rheumatoid arthritis with candidate genes using related cases. BMC Proc (2007) 0.87
Serum withdrawal up-regulates human SIRT1 gene expression in a p53-dependent manner. J Cell Mol Med (2009) 0.87
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
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
Decreased circulating microRNA-223 level predicts high on-treatment platelet reactivity in patients with troponin-negative non-ST elevation acute coronary syndrome. J Thromb Thrombolysis (2014) 0.86
Kernel-machine testing coupled with a rank-truncation method for genetic pathway analysis. Genet Epidemiol (2014) 0.85
Sp1 and CREB regulate basal transcription of the human SNF2L gene. Biochem Biophys Res Commun (2008) 0.84
Detecting epistatic interactions contributing to human gene expression using the CEPH family data. BMC Proc (2007) 0.84
Response of sulfide:quinone oxidoreductase to sulfide exposure in the echiuran worm Urechis unicinctus. Mar Biotechnol (NY) (2011) 0.83
Linkage and association of the CA repeat polymorphism of the IL6 gene, obesity-related phenotypes, and bone mineral density (BMD) in two independent Caucasian populations. J Hum Genet (2003) 0.83
Discussing gene-gene interaction: warning--translating equations to English may result in jabberwocky. Genet Epidemiol (2007) 0.82
Epistasis between loci on chromosomes 2 and 6 influences human height. J Clin Endocrinol Metab (2006) 0.82
A Sequence Kernel Association Test for Dichotomous Traits in Family Samples under a Generalized Linear Mixed Model. Hum Hered (2015) 0.80
Genome-wide association studies of rheumatoid arthritis data via multiple hypothesis testing methods for correlated tests. BMC Proc (2009) 0.80
Sulfide:quinone oxidoreductase from echiuran worm Urechis unicinctus. Mar Biotechnol (NY) (2010) 0.80
A follow-up linkage study for bone size variation in an extended sample. Bone (2004) 0.79
Quality of reporting of systematic reviews published in "evidence-based" Chinese journals. Syst Rev (2014) 0.79
Similarity-based multimarker association tests for continuous traits. Ann Hum Genet (2012) 0.79
Several genomic regions potentially containing QTLs for bone size variation were identified in a whole-genome linkage scan. Am J Med Genet A (2003) 0.79
Rare-Variant Kernel Machine Test for Longitudinal Data from Population and Family Samples. Hum Hered (2016) 0.78
Rank-based tests for identifying multiple genetic variants associated with quantitative traits. Ann Hum Genet (2014) 0.78
A novel immunotherapy for superficial bladder cancer by the immobilization of streptavidin-tagged bioactive IL-2 on the biotinylated mucosal surface of the bladder wall. Chin J Cancer (2010) 0.78
A rapid association test procedure robust under different genetic models accounting for population stratification. Hum Hered (2013) 0.78
A web services choreography scenario for interoperating bioinformatics applications. BMC Bioinformatics (2004) 0.78
Application of imputation methods to the analysis of rheumatoid arthritis data in genome-wide association studies. BMC Proc (2009) 0.78
Surgical mortality in patients with malignant obstructive jaundice: a multivariate discriminant analysis. Hepatobiliary Pancreat Dis Int (2003) 0.75
A novel mutation of keratin 9 in epidermolytic palmoplantar keratoderma combined with knuckle pads. Am J Med Genet A (2003) 0.75
Improving the signal-to-noise ratio in genome-wide association studies. Genet Epidemiol (2009) 0.75
A Generalized Sequential Bonferroni Procedure for GWAS in Admixed Populations Incorporating Admixture Mapping Information into Association Tests. Hum Hered (2015) 0.75
Systematic review of randomized clinical trials of acupressure therapy for primary dysmenorrhea. Evid Based Complement Alternat Med (2013) 0.75
Rare SERINC2 variants are specific for alcohol dependence in individuals of European descent. Pharmacogenet Genomics (2013) 0.75
Double genomic control is not effective to correct for population stratification in meta-analysis for genome-wide association studies. Front Genet (2012) 0.75
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
[Gene mapping of a nonsyndromic hearing impairmint family]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi (2003) 0.75
Effects on liver hydrogen peroxide metabolism induced by dietary selenium deficiency or excess in chickens. Biol Trace Elem Res (2014) 0.75
Dietary selenium regulation of transcript abundance of selenoprotein N and selenoprotein W in chicken muscle tissues. Biometals (2011) 0.75
Effects of dietary selenium on selenoprotein W gene expression in the chicken immune organs. Biol Trace Elem Res (2011) 0.75
[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
Modeling of air quality with a modified two-dimensional Eulerian model: a case study in the Pearl River Delta (PRD) region of China. J Environ Sci (China) (2007) 0.75