Exonization of AluYa5 in the human ACE gene requires mutations in both 3′ and 5′ splice sites and is facilitated by a conserved splicing enhancer

por Lei, Haixin, Day, Ian N. M., Vořechovský, Igor
Publicado 2005

Hardy-Weinberg Equilibrium Testing of Biological Ascertainment for Mendelian Randomization Studies

por Rodriguez, Santiago, Gaunt, Tom R., Day, Ian N. M.
Publicado 2009

Genome-Wide Data-Mining of Candidate Human Splice Translational Efficiency Polymorphisms (STEPs) and an Online Database

por Raistrick, Christopher A., Day, Ian N. M., Gaunt, Tom R.
Publicado 2010

Possible positive effect of the APOE ε2 allele on cognition in early to mid-adult life

por Sinclair, Lindsey I., Pleydell-Pearce, Christopher W., Day, Ian N.M.
Publicado 2017

A pathway-based data integration framework for prediction of disease progression

por Seoane, José A., Day, Ian N. M., Gaunt, Tom R., Campbell, Colin
Publicado 2014

Dependence of Deodorant Usage on ABCC11 Genotype: Scope for Personalized Genetics in Personal Hygiene

por Rodriguez, Santiago, Steer, Colin D, Farrow, Alexandra, Golding, Jean, Day, Ian N M
Publicado 2013

Possible Association of APOE Genotype with Working Memory in Young Adults

por Sinclair, Lindsey I., Button, Katherine S., Munafò, Marcus R., Day, Ian N. M., Lewis, Glyn
Publicado 2015

Predicting the functional consequences of cancer-associated amino acid substitutions

por Shihab, Hashem A., Gough, Julian, Cooper, David N., Day, Ian N. M., Gaunt, Tom R.
Publicado 2013

Canonical Correlation Analysis for Gene-Based Pleiotropy Discovery

por Seoane, Jose A., Campbell, Colin, Day, Ian N. M., Casas, Juan P., Gaunt, Tom R.
Publicado 2014

Importance of Genetic Studies in Consanguineous Populations for the Characterization of Novel Human Gene Functions

por Erzurumluoglu, A. Mesut, Shihab, Hashem A., Rodriguez, Santiago, Gaunt, Tom R., Day, Ian N.M.
Publicado 2016

Complexity of a complex trait locus: HP, HPR, haemoglobin and cholesterol

por Guthrie, Philip A.I., Rodriguez, Santiago, Gaunt, Tom R., Lawlor, Debbie A., Smith, George Davey, Day, Ian N.M.
Publicado 2012

Structural and Population-Based Evaluations of TBC1D1 p.Arg125Trp

por Richardson, Tom G., Thomas, Elaine C., Sessions, Richard B., Lawlor, Debbie A., Tavaré, Jeremy M., Day, Ian N. M.
Publicado 2013

Identifying Highly Penetrant Disease Causal Mutations Using Next Generation Sequencing: Guide to Whole Process

por Erzurumluoglu, A. Mesut, Rodriguez, Santiago, Shihab, Hashem A., Baird, Denis, Richardson, Tom G., Day, Ian N. M., Gaunt, Tom R.
Publicado 2015

Amplification ratio control system for copy number variation genotyping

por Guthrie, Philip A. I., Gaunt, Tom R., Abdollahi, Mohammed R., Rodriguez, Santiago, Lawlor, Debbie A., Smith, George Davey, Day, Ian N. M.
Publicado 2011

An integrative approach to predicting the functional effects of non-coding and coding sequence variation

por Shihab, Hashem A., Rogers, Mark F., Gough, Julian, Mort, Matthew, Cooper, David N., Day, Ian N. M., Gaunt, Tom R., Campbell, Colin
Publicado 2015

IQ, Educational Attainment, Memory and Plasma Lipids: Associations with Apolipoprotein E Genotype in 5995 Children

por Taylor, Amy E., Guthrie, Philip A.I., Smith, George Davey, Golding, Jean, Sattar, Naveed, Hingorani, Aroon D., Deanfield, John E., Day, Ian N.M.
Publicado 2011

Predicting the Functional, Molecular, and Phenotypic Consequences of Amino Acid Substitutions using Hidden Markov Models

por Shihab, Hashem A, Gough, Julian, Cooper, David N, Stenson, Peter D, Barker, Gary L A, Edwards, Keith J, Day, Ian N M, Gaunt, Tom R
Publicado 2013

Homogeneous Assay of rs4343, an ACE I/D Proxy, and an Analysis in the British Women’s Heart and Health Study (BWHHS)

por Abdollahi, Mohammad Reza, Huang, Shuwen, Rodriguez, Santiago, Guthrie, Philip Alexander Isles, Smith, George Davey, Ebrahim, Shah, Lawlor, Debbie A., Day, Ian N. M., Gaunt, Tom R.
Publicado 2008

Haptoglobin Duplicon, Hemoglobin, and Vitamin C: Analyses in the British Women's Heart and Health Study and Caerphilly Prospective Study

por Guthrie, Philip A. I., Abdollahi, Mohammad R., Gaunt, Tom, Lawlor, Debbie A., Ben-Shlomo, Yoav, Gallacher, John, Davey Smith, George, Day, Ian N. M., Rodriguez, Santiago
Publicado 2014

Carrier Status for the Common R501X and 2282del4 Filaggrin Mutations Is Not Associated with Hearing Phenotypes in 5377 Children from the ALSPAC Cohort

por Rodriguez, Santiago, Hall, Amanda J., Granell, Raquel, McLean, W. H. Irwin, Irvine, Alan D., Palmer, Colin N. A., Smith, George Davey, Henderson, John, Day, Ian N. M.
Publicado 2009