Genetics and cardiovascular risk

Por Day, Ian N M, Wilson, David I
Publicado em 2001

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 em 2005

A novel medium throughput quantitative competitive PCR technology to simultaneously measure mRNA levels from multiple genes

Por Zhang, Junlong, Day, Ian N. M., Byrne, Christopher D.
Publicado em 2002

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

Por Rodriguez, Santiago, Gaunt, Tom R., Day, Ian N. M.
Publicado em 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 em 2010

Manual 768 or 384 well microplate gel ‘dry’ electrophoresis for PCR checking and SNP genotyping

Por Gaunt, Tom R., Hinks, Lesley J., Rassoulian, Hamid, Day, Ian N. M.
Publicado em 2003

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 em 2014

An efficient procedure for genotyping single nucleotide polymorphisms

Por Ye, Shu, Dhillon, Sahar, Ke, Xiayi, Collins, Andrew R., Day, Ian N. M.
Publicado em 2001

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 em 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 no PLoS One (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 em 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 em 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 no Ann Hum Genet (2016)

The association of the paraoxonase (PON1) Q192R polymorphism with depression in older women: findings from the British Women's Heart and Health Study

Por Lawlor, Debbie A, Day, Ian N M, Gaunt, Tom R, Hinks, Lesley J, Timpson, Nick, Ebrahim, Shah
Publicado em 2007

Lactase persistence-related genetic variant: population substructure and health outcomes

Por Smith, George Davey, Lawlor, Debbie A, Timpson, Nic J, Baban, Jamil, Kiessling, Matt, Day, Ian N M, Ebrahim, Shah
Publicado em 2009

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 em 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 em 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 no Biomed Res Int (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 em 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 no Bioinformatics (2015)