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WILLIAM S. BUSH
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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
100
472
Publications (27 rows)
Collaborators (77 rows)
Referers (100 rows)
Referees (100 rows)
Title
Citations
PageRank
Year
Modeling Transcriptional Regulation Using Gene Regulatory Networks Based On Multi-Omics Data Sources
1
0.35
2021
Packaging Biocomputing Software to Maximize Distribution and Reuse.
0
0.34
2020
Functional annotation of genomic variants in studies of late-onset Alzheimer's disease.
2
0.51
2018
Three-dimensional spatial analysis of missense variants in <Emphasis Type="Italic">RTEL1</Emphasis> identifies pathogenic variants in patients with Familial Interstitial Pneumonia
0
0.34
2018
INTEGRATING COMMUNITY-LEVEL DATA RESOURCES FOR PRECISION MEDICINE RESEARCH.
0
0.34
2018
Local ancestry transitions modify snp-trait associations.
0
0.34
2018
Transition-transversion encoding and genetic relationship metric in ReliefF feature selection improves pathway enrichment in GWAS.
0
0.34
2018
Introducing COCOS: codon consequence scanner for annotating reading frame changes induced by stop-lost and frame shift variants.
0
0.34
2017
Towards a phenome-wide catalog of human clinical traits impacted by genetic ancestry.
0
0.34
2015
Estimating cumulative pathway effects on risk for age-related macular degeneration using mixed linear models.
0
0.34
2015
Genotype Correlation Analysis Reveals Pathway-Based Functional Disequilibrium and Potential Epistasis in the Human Interactome.
0
0.34
2014
Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenome-wide association studies.
2
0.42
2014
Utilization of an EMR-biorepository to identify the genetic predictors of calcineurin-inhibitor toxicity in heart transplant recipients.
0
0.34
2014
SecureMA: protecting participant privacy in genetic association meta-analysis.
6
0.48
2014
Rapid storage and retrieval of genomic intervals from a relational database system using nested containment lists.
1
0.37
2013
A comparison of cataloged variation between International HapMap Consortium and 1000 Genomes Project data.
5
0.79
2012
Chapter 11: Genome-Wide Association Studies
30
2.46
2012
Multivariate Analysis of Regulatory Snps: Empowering Personal Genomics by Considering Cis-Epistasis and Heterogeneity.
0
0.34
2011
Visualizing SNP statistics in the context of linkage disequilibrium using LD-Plus
3
1.44
2010
LD-Spline: Mapping SNPs on genotyping platforms to genomic regions using patterns of linkage disequilibrium.
3
0.39
2009
Conquering the Needle-in-a-Haystack: How Correlated Input Variables Beneficially Alter the Fitness Landscape for Neural Networks
4
0.60
2009
Alternative contingency table measures improve the power and detection of multifactor dimensionality reduction.
41
1.52
2008
Generating linkage disequilibrium patterns in data simulations using genomeSIMLA
17
1.78
2008
Association Rule Discovery Has the Ability to Model Complex Genetic Effects
1
0.35
2007
Genetic programming neural networks: A powerful bioinformatics tool for human genetics
26
1.46
2007
Parallel multifactor dimensionality reduction: a tool for the large-scale analysis of gene--gene interactions
16
1.26
2006
Can neural network constraints in GP provide power to detect genes associated with human disease?
3
0.56
2005
1