STK39 polymorphisms and blood pressure: an association study in British Caucasians and assessment of cis-acting influences on gene expression

por Cunnington, Michael S, Kay, Chris, Avery, Peter J, Mayosi, Bongani M, Koref, Mauro Santibanez, Keavney, Bernard
Publicado 2009

Atrial fibrillation associated with ivabradine treatment: meta-analysis of randomised controlled trials

por Martin, Ruairidh I R, Pogoryelova, Oksana, Koref, Mauro Santibáñez, Bourke, John P, Teare, M Dawn, Keavney, Bernard D
Publicado 2014

Chromosome 16q22 variants in a region associated with cardiovascular phenotypes correlate with ZFHX3 expression in a transcript-specific manner

por Martin, Ruairidh I R, Owens, W Andrew, Cunnington, Michael S, Mayosi, Bongani M, Koref, Mauro Santibáñez, Keavney, Bernard D
Publicado 2014

AstuteClinician Report: A Novel 10 bp Frameshift Deletion in Exon 2 ofICOSCauses a Combined Immunodeficiency Associated with an Enteritis and Hepatitis

por Robertson, Nic, Engelhardt, Karin R., Morgan, Neil V., Barge, Dawn, Cant, Andrew J., Hughes, Stephen M., Abinun, Mario, Xu, Yaobo, Koref, Mauro Santibanez, Arkwright, Peter D., Hambleton, Sophie
Publicado 2015

Point of care testing for improving risk- benefit ratio of aspirin and warfarin

por Sheth, Harsh, Northwood, Emma, Elliott, Faye, Jackson, Michael, Koref, Mauro Santibanez, Tyson, John, Daly, Ann, O’Halloran, Jonathan, Sheth, Jayesh, Sheth, Frenny, Parikh, Keyur, Bishop, D Timothy, Burn, John
Publicado 2014

Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 Deficiency

por Dang, Tarana Singh, Willet, Joseph DP, Griffin, Helen R, Morgan, Neil V, O’Boyle, Graeme, Arkwright, Peter D, Hughes, Stephen M, Abinun, Mario, Tee, Louise J, Barge, Dawn, Engelhardt, Karin R, Jackson, Michael, Cant, Andrew J, Maher, Eamonn R, Koref, Mauro Santibanez, Reynard, Louise N, Ali, Simi, Hambleton, Sophie
Publicado 2016

Erratum to: Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 Deficiency

por Dang, Tarana Singh, Willet, Joseph D. P., Griffin, Helen R., Morgan, Neil V., O’Boyle, Graeme, Arkwright, Peter D., Hughes, Stephen M., Abinun, Mario, Tee, Louise J., Barge, Dawn, Engelhardt, Karin R., Jackson, Michael, Cant, Andrew J., Maher, Eamonn R., Koref, Mauro Santibanez, Reynard, Louise N., Ali, Simi, Hambleton, Sophie
Publicado 2016