Search Results - "Raistrick, Christopher A."

Genome-wide data-mining of candidate human splice translational efficiency polymorphisms (STEPs) and an online database by Raistrick, Christopher A, Day, Ian N M, Gaunt, Tom R

“…Variation in pre-mRNA splicing is common and in some cases caused by genetic variants in intronic splicing motifs. Recent studies into the insulin gene (INS)…”
Get full text

PhenoSpD: an integrated toolkit for phenotypic correlation estimation and multiple testing correction using GWAS summary statistics by Zheng, Jie, Richardson, Tom G, Millard, Louise A C, Hemani, Gibran, Elsworth, Benjamin L, Raistrick, Christopher A, Vilhjalmsson, Bjarni, Neale, Benjamin M, Haycock, Philip C, Smith, George Davey, Gaunt, Tom R

“…Identifying phenotypic correlations between complex traits and diseases can provide useful etiological insights. Restricted access to much individual-level…”
Get full text

Analysis of Potential Genomic Confounding in Genetic Association Studies and an Online Genomic Confounding Browser (GCB) by Raistrick, Christopher A., Alharbi, Khalid K., Day, Ian N. M., Gaunt, Tom R.

“…Summary Genome‐wide association studies have transformed genetic studies of disease susceptibility, identifying many variants that may tag functional…”
Get full text

Genome-Wide Data-Mining of Candidate Human Splice Translational Efficiency Polymorphisms by Raistrick, Christopher A, Day, Ian N. M, Gaunt, Tom R

“…Background Variation in pre-mRNA splicing is common and in some cases caused by genetic variants in intronic splicing motifs. Recent studies into the insulin…”
Get full text

Analysis of Potential Genomic Confounding in Genetic Association Studies and an Online Genomic Confounding Browser (GCB): Analysis of Genomic Confounding by Raistrick, Christopher A., Alharbi, Khalid K., Day, Ian N. M., Gaunt, Tom R.

Get full text