Published in PLoS One on July 18, 2013
IGENT: efficient entropy based algorithm for genome-wide gene-gene interaction analysis. BMC Med Genomics (2014) 0.85
Combinations of Genetic Data Present in Bipolar Patients, but Absent in Control Persons. PLoS One (2015) 0.78
Detecting Genetic Interactions for Quantitative Traits Using m-Spacing Entropy Measure. Biomed Res Int (2015) 0.78
Combinations of genetic data in a study of oral cancer. Genes Cancer (2015) 0.78
Transdisciplinary approaches enhance the production of translational knowledge. Transl Res (2016) 0.75
Genetic Association Analysis of Fasting and 1- and 2-Hour Glucose Tolerance Test Data Using a Generalized Index of Dissimilarity Measure for the Korean Population. Genomics Inform (2016) 0.75
Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer. Am J Hum Genet (2001) 17.43
Detecting gene-gene interactions that underlie human diseases. Nat Rev Genet (2009) 12.07
Power of multifactor dimensionality reduction for detecting gene-gene interactions in the presence of genotyping error, missing data, phenocopy, and genetic heterogeneity. Genet Epidemiol (2003) 6.31
New strategies for identifying gene-gene interactions in hypertension. Ann Med (2002) 4.19
Identifying interacting SNPs using Monte Carlo logic regression. Genet Epidemiol (2005) 4.18
Use of classification trees for association studies. Genet Epidemiol (2000) 3.67
Sample size calculation for multiple testing in microarray data analysis. Biostatistics (2005) 2.84
Exploration of gene-gene interaction effects using entropy-based methods. Eur J Hum Genet (2007) 2.42
Odds ratio based multifactor-dimensionality reduction method for detecting gene-gene interactions. Bioinformatics (2006) 2.08
Fewer permutations, more accurate P-values. Bioinformatics (2009) 1.91
Improving strategies for detecting genetic patterns of disease susceptibility in association studies. Stat Med (2008) 1.86
An entropy-based approach for testing genetic epistasis underlying complex diseases. J Theor Biol (2007) 1.56
Joint identification of multiple genetic variants via elastic-net variable selection in a genome-wide association analysis. Ann Hum Genet (2010) 1.51
Alternative contingency table measures improve the power and detection of multifactor dimensionality reduction. BMC Bioinformatics (2008) 1.50
Log-linear model-based multifactor dimensionality reduction method to detect gene gene interactions. Bioinformatics (2007) 1.44
Applications of neural networks for gene finding. Adv Genet (2001) 1.44
How accurately can we control the FDR in analyzing microarray data? Bioinformatics (2006) 1.14
Identification of gene-gene interactions in the presence of missing data using the multifactor dimensionality reduction method. Genet Epidemiol (2009) 1.00
Information-theoretic gene-gene and gene-environment interaction analysis of quantitative traits. BMC Genomics (2009) 0.93
IL-5 and IL-5 receptor alpha polymorphisms are associated with atopic dermatitis in Koreans. Allergy (2007) 0.91
A multigene assay to predict recurrence of tamoxifen-treated, node-negative breast cancer. N Engl J Med (2004) 41.02
Biological, clinical and population relevance of 95 loci for blood lipids. Nature (2010) 28.21
A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. Nat Genet (2009) 7.65
Human Proteinpedia enables sharing of human protein data. Nat Biotechnol (2008) 4.21
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. PLoS Genet (2012) 3.21
Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits. Nat Genet (2011) 2.27
Odds ratio based multifactor-dimensionality reduction method for detecting gene-gene interactions. Bioinformatics (2006) 2.08
Longitudinal data analysis in pedigree studies. Genet Epidemiol (2003) 2.06
Identification of conversion from mild cognitive impairment to Alzheimer's disease using multivariate predictors. PLoS One (2011) 1.66
Identification of novel reference genes using multiplatform expression data and their validation for quantitative gene expression analysis. PLoS One (2009) 1.55
Field evaluation of a rapid immunochromatographic dipstick test for the diagnosis of cholera in a high-risk population. BMC Infect Dis (2006) 1.53
Identification of 15 loci influencing height in a Korean population. J Hum Genet (2009) 1.52
Joint identification of multiple genetic variants via elastic-net variable selection in a genome-wide association analysis. Ann Hum Genet (2010) 1.51
Log-linear model-based multifactor dimensionality reduction method to detect gene gene interactions. Bioinformatics (2007) 1.44
Integrative analysis of multi-omics data for identifying multi-markers for diagnosing pancreatic cancer. BMC Genomics (2015) 1.44
Risk analysis of aseptic meningitis after measles-mumps-rubella vaccination in Korean children by using a case-crossover design. Am J Epidemiol (2003) 1.43
arrayQCplot: software for checking the quality of microarray data. Bioinformatics (2006) 1.41
Smoking and genetic risk variation across populations of European, Asian, and African American ancestry--a meta-analysis of chromosome 15q25. Genet Epidemiol (2012) 1.34
The epidemiology of acute pyelonephritis in South Korea, 1997-1999. Am J Epidemiol (2004) 1.29
Elastic-net regularization approaches for genome-wide association studies of rheumatoid arthritis. BMC Proc (2009) 1.26
Diagnostic application of targeted resequencing for familial nonsyndromic hearing loss. PLoS One (2013) 1.24
Associations of variants in CHRNA5/A3/B4 gene cluster with smoking behaviors in a Korean population. PLoS One (2010) 1.21
New evaluation measures for multifactor dimensionality reduction classifiers in gene-gene interaction analysis. Bioinformatics (2009) 1.20
Comparative analyses of DNA methylation and sequence evolution using Nasonia genomes. Mol Biol Evol (2011) 1.20
Feasibility of two-dimensional global longitudinal strain and strain rate imaging for the assessment of left atrial function: a study in subjects with a low probability of cardiovascular disease and normal exercise capacity. Echocardiography (2009) 1.19
Large-scale genome-wide association study of Asian population reveals genetic factors in FRMD4A and other loci influencing smoking initiation and nicotine dependence. Hum Genet (2011) 1.19
Boolean networks using the chi-square test for inferring large-scale gene regulatory networks. BMC Bioinformatics (2007) 1.19
A functional annotation of subproteomes in human plasma. Proteomics (2005) 1.15
Auxin stimulates DWARF4 expression and brassinosteroid biosynthesis in Arabidopsis. Plant J (2011) 1.14
Molecular time-course and the metabolic basis of entry into dauer in Caenorhabditis elegans. PLoS One (2009) 1.13
DNA methylation and transcriptional noise. Epigenetics Chromatin (2013) 1.09
A novel method to identify high order gene-gene interactions in genome-wide association studies: gene-based MDR. BMC Bioinformatics (2012) 1.06
Efficient prefractionation of low-abundance proteins in human plasma and construction of a two-dimensional map. Proteomics (2005) 1.04
Association of GABRB3 polymorphisms with autism spectrum disorders in Korean trios. Neuropsychobiology (2007) 1.02
Identification of differentially expressed subnetworks based on multivariate ANOVA. BMC Bioinformatics (2009) 1.01
Gene-gene interaction analysis for the survival phenotype based on the Cox model. Bioinformatics (2012) 1.00
Identification of gene-gene interactions in the presence of missing data using the multifactor dimensionality reduction method. Genet Epidemiol (2009) 1.00
Quantitative analysis of phosphopeptides in search of the disease biomarker from the hepatocellular carcinoma specimen. Proteomics (2009) 0.99
Novel 48-membered hexadecanuclear and 60-membered icosanuclear manganese metallamacrocycles. Inorg Chem (2008) 0.97
Identification of multiple gene-gene interactions for ordinal phenotypes. BMC Med Genomics (2013) 0.96
Biomarker discovery from the plasma proteome using multidimensional fractionation proteomics. Curr Opin Chem Biol (2006) 0.96
What are the determinants of gene expression levels and breadths in the human genome? Hum Mol Genet (2011) 0.96
Family-based association study between GRIK2 polymorphisms and autism spectrum disorders in the Korean trios. Neurosci Res (2007) 0.94
Analysis of human disease genes in the context of gene essentiality. Genomics (2008) 0.93
Multiphasic analysis of whole exome sequencing data identifies a novel mutation of ACTG1 in a nonsyndromic hearing loss family. BMC Genomics (2013) 0.93
Meta-analysis of homogeneous subgroups reveals association between PDE4D gene variants and ischemic stroke. Neuroepidemiology (2011) 0.93
Genome-scale DNA methylation pattern profiling of human bone marrow mesenchymal stem cells in long-term culture. Exp Mol Med (2012) 0.92
-759 C/T polymorphism of 5-HT2C receptor gene and early phase weight gain associated with antipsychotic drug treatment. Prog Neuropsychopharmacol Biol Psychiatry (2007) 0.92
An integrated proteome database for two-dimensional electrophoresis data analysis and laboratory information management system. Proteomics (2002) 0.90
Pathway-based evaluation in early onset colorectal cancer suggests focal adhesion and immunosuppression along with epithelial-mesenchymal transition. PLoS One (2012) 0.90
Age-related distributions of anti-Müllerian hormone level and anti-Müllerian hormone models. Acta Obstet Gynecol Scand (2012) 0.90
External cross-validation of bioelectrical impedance analysis for the assessment of body composition in Korean adults. Nutr Res Pract (2011) 0.89
Family-based association study of 5-HTTLPR and the 5-HT2A receptor gene polymorphisms with autism spectrum disorder in Korean trios. Brain Res (2007) 0.89
Association of the glutamate transporter gene SLC1A1 with atypical antipsychotics-induced obsessive-compulsive symptoms. Arch Gen Psychiatry (2009) 0.88
Selective gas sorption property of an interdigitated 3-D metal-organic framework with 1-D channels. Chem Commun (Camb) (2007) 0.88
Family- and population-based association studies of monoamine oxidase A and autism spectrum disorders in Korean. Neurosci Res (2008) 0.88
Robust imputation method for missing values in microarray data. BMC Bioinformatics (2007) 0.87
An integrated approach to infer causal associations among gene expression, genotype variation, and disease. Genomics (2009) 0.87
Possible association of the alpha-2A-adrenergic receptor gene with response time variability in attention deficit hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet (2008) 0.87
cuGWAM: Genome-wide association multifactor dimensionality reduction using CUDA-enabled high-performance graphics processing unit. Int J Data Min Bioinform (2012) 0.86
IDMap: facilitating the detection of potential leads with therapeutic targets. Bioinformatics (2008) 0.86
Multiple pathway-based genetic variations associated with tobacco related multiple primary neoplasms. PLoS One (2012) 0.86
An anion receptor with NH and OH groups for hydrogen bonds. Chem Commun (Camb) (2008) 0.85
Association study between single nucleotide polymorphisms in promoter region of AVPR1A and Korean autism spectrum disorders. Neurosci Lett (2010) 0.85
IGENT: efficient entropy based algorithm for genome-wide gene-gene interaction analysis. BMC Med Genomics (2014) 0.85
Family history of diabetes and risk of atherosclerotic cardiovascular disease in Korean men and women. Atherosclerosis (2007) 0.85
DRAK2 participates in a negative feedback loop to control TGF-β/Smads signaling by binding to type I TGF-β receptor. Cell Rep (2012) 0.85
Genome-wide analysis of haplotype interaction for the data from the North American Rheumatoid Arthritis Consortium. BMC Proc (2009) 0.85
Multivariate generalized multifactor dimensionality reduction to detect gene-gene interactions. BMC Syst Biol (2013) 0.84
Cognitive profiles of healthy siblings of schizophrenia patients: application of the cognitive domains of the MATRICS consensus battery. World J Biol Psychiatry (2009) 0.84
Overview and introduction to clinical proteomics. Methods Mol Biol (2008) 0.84
Association tests based on the principal-component analysis. BMC Proc (2007) 0.84
No evidence of an association between norepinephrine transporter gene polymorphisms and attention deficit hyperactivity disorder: a family-based and case-control association study in a Korean sample. Neuropsychobiology (2008) 0.84
Family based association of GRIN2A and GRIN2B with Korean autism spectrum disorders. Neurosci Lett (2012) 0.84
Association study of polymorphisms in N-methyl-D-aspartate receptor 2B subunits (GRIN2B) gene with Korean alcoholism. Neurosci Res (2006) 0.84
Dropout rate and associated factors in patients with bipolar disorders. J Affect Disord (2012) 0.84
Two-stage normalization using background intensities in cDNA microarray data. BMC Bioinformatics (2004) 0.83
A prognostic model for lymph node-negative breast cancer patients based on the integration of proliferation and immunity. Breast Cancer Res Treat (2011) 0.83
Inference of large-scale gene regulatory networks using regression-based network approach. J Bioinform Comput Biol (2009) 0.83
Family-based association study between NOS-I and -IIA polymorphisms and autism spectrum disorders in Korean trios. Am J Med Genet B Neuropsychiatr Genet (2009) 0.83
Lineage-specific variation in slow- and fast-X evolution in primates. Evolution (2012) 0.83
Randomized controlled trial for Salvia sclarea or Lavandula angustifolia: differential effects on blood pressure in female patients with urinary incontinence undergoing urodynamic examination. J Altern Complement Med (2013) 0.83
Family-based association study of microsatellites in the 5' flanking region of AVPR1A with autism spectrum disorder in the Korean population. Psychiatry Res (2010) 0.83
No association of the norepinephrine transporter gene (SLC6A2) and cognitive and behavioural phenotypes of patients with autism spectrum disorder. Eur Arch Psychiatry Clin Neurosci (2014) 0.82
Network graph analysis of gene-gene interactions in genome-wide association study data. Genomics Inform (2012) 0.82
Discussing gene-gene interaction: warning--translating equations to English may result in jabberwocky. Genet Epidemiol (2007) 0.82
Modulation of biological processes in the nucleus by delivery of DNA oligonucleotides conjugated with gold nanoparticles. Biomaterials (2011) 0.82
Interaction between genetic variants of DLGAP3 and SLC1A1 affecting the risk of atypical antipsychotics-induced obsessive-compulsive symptoms. Am J Med Genet B Neuropsychiatr Genet (2011) 0.82
The Asia Oceania Human Proteome Organisation Membrane Proteomics Initiative. Preparation and characterisation of the carbonate-washed membrane standard. Proteomics (2010) 0.82
A set of stage-specific gene transcripts identified in EK stage X and HH stage 3 chick embryos. BMC Dev Biol (2007) 0.82
Association analysis of sphingomyelinase 2 polymorphisms for the extrinsic type of atopic dermatitis in Koreans. J Dermatol Sci (2007) 0.82
A Bayesian hierarchical model for categorical data with nonignorable nonresponse. Biometrics (2003) 0.82