Ambulatory blood pressure is associated with polymorphic variation in P2X receptor genes. by Palomino-Doza, J, Rahman, T, Avery, P, Mayosi, B, Farrall, M, Watkins, H, Edwards, C, Keavney, B

Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to congenital heart disease by Palomino Doza, J, Topf, A, Bentham, J, Bhattacharya, S, Cosgrove, C, Granados-Riveron, J, Goodship, J, Henderson, D, O'Sullivan, J, Keavney, B

Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of Fallot. by Palomino Doza, J, Topf, A, Bentham, J, Bhattacharya, S, Cosgrove, C, Brook, J, Granados-Riveron, J, Bu'Lock, F, O'Sullivan, J, Stuart, A, Parsons, J, Relton, C, Goodship, J, Henderson, D, Keavney, B

Aetiological Role Of Folate Deficiency In Congenital Cardiovascular Malformation: Evidence From "Mendelian Randomisation" And Meta-Analysis by Mamasoula, C, Pierscionek, T, Hall, D, Topf, A, Doza, J, Rahman, T, Tan, A, Bentham, J, Bhattacharya, S, Cosgrove, C, Brook, D, Riveron, J, Bu'Lock, F, O'Sullivan, J, Wren, C, Goodship, J, Cordell, H, Keavney, B

A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot. by Goodship, J, Hall, D, Topf, A, Mamasoula, C, Griffin, H, Rahman, T, Glen, E, Tan, H, Palomino Doza, J, Relton, C, Bentham, J, Bhattacharya, S, Cosgrove, C, Brook, D, Granados-Riveron, J, Bu'Lock, F, O'Sullivan, J, Stuart, A, Parsons, J, Cordell, H, Keavney, B

Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls. by Mamasoula, C, Prentice, R, Pierscionek, T, Pangilinan, F, Mills, J, Druschel, C, Pass, K, Russell, M, Hall, D, Töpf, A, Brown, D, Zelenika, D, Bentham, J, Cosgrove, C, Bhattacharya, S, Riveron, J, Setchfield, K, Brook, J, Bu'Lock, F, Thornborough, C, Rahman, T, Doza, J, Tan, H, O'Sullivan, J, Stuart, A