Name
Affiliation
Papers
WILLIAM S. BUSH
Vanderbilt Univ, Med Ctr, Ctr Human Genet Res, 221 Kirkland Hall, Nashville, TN 37232 USA
27
Collaborators
Citations 
PageRank 
77
161
18.45
Referers 
Referees 
References 
460
472
106
Search Limit
100472
Title
Citations
PageRank
Year
Modeling Transcriptional Regulation Using Gene Regulatory Networks Based On Multi-Omics Data Sources10.352021
Packaging Biocomputing Software to Maximize Distribution and Reuse.00.342020
Functional annotation of genomic variants in studies of late-onset Alzheimer's disease.20.512018
Three-dimensional spatial analysis of missense variants in <Emphasis Type="Italic">RTEL1</Emphasis> identifies pathogenic variants in patients with Familial Interstitial Pneumonia00.342018
INTEGRATING COMMUNITY-LEVEL DATA RESOURCES FOR PRECISION MEDICINE RESEARCH.00.342018
Local ancestry transitions modify snp-trait associations.00.342018
Transition-transversion encoding and genetic relationship metric in ReliefF feature selection improves pathway enrichment in GWAS.00.342018
Introducing COCOS: codon consequence scanner for annotating reading frame changes induced by stop-lost and frame shift variants.00.342017
Towards a phenome-wide catalog of human clinical traits impacted by genetic ancestry.00.342015
Estimating cumulative pathway effects on risk for age-related macular degeneration using mixed linear models.00.342015
Genotype Correlation Analysis Reveals Pathway-Based Functional Disequilibrium and Potential Epistasis in the Human Interactome.00.342014
Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenome-wide association studies.20.422014
Utilization of an EMR-biorepository to identify the genetic predictors of calcineurin-inhibitor toxicity in heart transplant recipients.00.342014
SecureMA: protecting participant privacy in genetic association meta-analysis.60.482014
Rapid storage and retrieval of genomic intervals from a relational database system using nested containment lists.10.372013
A comparison of cataloged variation between International HapMap Consortium and 1000 Genomes Project data.50.792012
Chapter 11: Genome-Wide Association Studies302.462012
Multivariate Analysis of Regulatory Snps: Empowering Personal Genomics by Considering Cis-Epistasis and Heterogeneity.00.342011
Visualizing SNP statistics in the context of linkage disequilibrium using LD-Plus31.442010
LD-Spline: Mapping SNPs on genotyping platforms to genomic regions using patterns of linkage disequilibrium.30.392009
Conquering the Needle-in-a-Haystack: How Correlated Input Variables Beneficially Alter the Fitness Landscape for Neural Networks40.602009
Alternative contingency table measures improve the power and detection of multifactor dimensionality reduction.411.522008
Generating linkage disequilibrium patterns in data simulations using genomeSIMLA171.782008
Association Rule Discovery Has the Ability to Model Complex Genetic Effects10.352007
Genetic programming neural networks: A powerful bioinformatics tool for human genetics261.462007
Parallel multifactor dimensionality reduction: a tool for the large-scale analysis of gene--gene interactions161.262006
Can neural network constraints in GP provide power to detect genes associated with human disease?30.562005