Name
Affiliation
Papers
TOM R. GAUNT
Human Genetics Division, University of Southampton, School of Medicine, Duthie Building (MP 808), Southampton General Hospital, Tremona Road, Southampton SO16 6YD, UK. Tom.Gaunt@soton.ac.uk
22
Collaborators
Citations 
PageRank 
63
61
10.36
Referers 
Referees 
References 
253
616
163
Search Limit
100616
Title
Citations
PageRank
Year
Epigraphdb: A Database And Data Mining Platform For Health Data Science10.342021
Epigraphdb: A Database And Data Mining Platform For Health Data Science (Nov, 10.1093/Bioinformatics/Btaa961, 2020)00.342021
Melodi Presto: A Fast And Agile Tool To Explore Semantic Triples Derived From Biomedical Literature10.362021
Mendelvar: Gene Prioritization At Gwas Loci Using Phenotypic Enrichment Of Mendelian Disease Genes00.342021
Prediction of driver variants in the cancer genome via machine learning methodologies00.342021
CScape-somatic: distinguishing driver and passenger point mutations in the cancer genome.00.342020
FATHMM-XF: accurate prediction of pathogenic point mutations via extended features.30.462018
HAPRAP: a haplotype-based iterative method for statistical fine mapping using GWAS summary statistics.00.342017
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis.10.362017
An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome.00.342017
GTB - an online genome tolerance browser.10.442017
HIPred: an integrative approach to predicting haploinsufficient genes.10.442017
Texture classification using feature selection and kernel-based techniques120.692015
Sequential data selection for predicting the pathogenic effects of sequence variation00.342015
Using A Random Forest Proximity Measure For Variable Importance Stratification In Genotypic Data00.342014
A pathway-based data integration framework for prediction of disease progression.110.682014
A Random Forest proximity matrix as a new measure for gene annotation.00.342014
Canonical Correlation Analysis for Gene-Based Pleiotropy Discovery.50.502014
Predicting the functional consequences of cancer-associated amino acid substitutions81.892013
Texture classification using kernel-based techniques10.352013
Cubic exact solutions for the estimation of pairwise haplotype frequencies: implications for linkage disequilibrium analyses and a web tool 'CubeX'.140.352007
MIDAS: software for analysis and visualisation of interallelic disequilibrium between multiallelic markers.20.452006