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

Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation. by Griffin, H, Hall, D, Topf, A, Eden, J, Stuart, A, Parsons, J, Peart, I, Deanfield, J, O'Sullivan, J, Babu-Narayan, S, Gatzoulis, M, Bu'lock, F, Bhattacharya, S, Bentham, J, Farrall, M, Granados Riveron, J, Brook, J, Burn, J, Cordell, H, Goodship, J, 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

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease by Soemedi, R, Wilson, I, Bentham, J, Darlay, R, Töpf, A, Zelenika, D, Cosgrove, C, Setchfield, K, Thornborough, C, Granados-Riveron, J, Blue, G, Breckpot, J, Hellens, S, Zwolinkski, S, Glen, E, Mamasoula, C, Rahman, T, Hall, D, Rauch, A, Devriendt, K, Gewillig, M, O'sullivan, J, Winlaw, D, Bu'lock, F, Brook, J

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease. by Soemedi, R, Wilson, I, Bentham, J, Darlay, R, Töpf, A, Zelenika, D, Cosgrove, C, Setchfield, K, Thornborough, C, Granados-Riveron, J, Blue, G, Breckpot, J, Hellens, S, Zwolinkski, S, Glen, E, Mamasoula, C, Rahman, T, Hall, D, Rauch, A, Devriendt, K, Gewillig, M, O' Sullivan, J, Winlaw, D, Bu'Lock, F, Brook, J

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls. by Soemedi, R, Topf, A, Wilson, I, Darlay, R, Rahman, T, Glen, E, Hall, D, Huang, N, Bentham, J, Bhattacharya, S, Cosgrove, C, Brook, J, Granados-Riveron, J, Setchfield, K, Bu'lock, F, Thornborough, C, Devriendt, K, Breckpot, J, Hofbeck, M, Lathrop, M, Rauch, A, Blue, G, Winlaw, D, Hurles, M, Santibanez-Koref, M

Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot. by Cordell, H, Töpf, A, Mamasoula, C, Postma, A, Bentham, J, Zelenika, D, Heath, S, Blue, G, Cosgrove, C, Granados Riveron, J, Darlay, R, Soemedi, R, Wilson, I, Ayers, K, Rahman, T, Hall, D, Mulder, B, Zwinderman, A, van Engelen, K, Brook, J, Setchfield, K, Bu'Lock, F, Thornborough, C, O'Sullivan, J, Stuart, A

Rare variants in NR2F2 cause congenital heart defects in humans. by Al Turki, S, Manickaraj, A, Mercer, C, Gerety, S, Hitz, M, Lindsay, S, D'Alessandro, L, Swaminathan, G, Bentham, J, Arndt, A, Low, J, Breckpot, J, Gewillig, M, Thienpont, B, Abdul-Khaliq, H, Harnack, C, Hoff, K, Kramer, H, Schubert, S, Siebert, R, Toka, O, Cosgrove, C, Watkins, H, Lucassen, A, O'Kelly, I, Salmon, A, Bu'lock, F, Granados-Riveron, J, Setchfield, K, Thornborough, C, Brook, J, Mulder, B, Klaassen, S, Bhattacharya, S, Devriendt, K, Fitzpatrick, D, Wilson, D, Mital, S, Hurles, M

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing. by Sifrim, A, Hitz, M, Wilsdon, A, Breckpot, J, Al Turki, S, Thienpont, B, McRae, J, Fitzgerald, T, Singh, T, Swaminathan, G, Prigmore, E, Rajan, D, Abdul-Khaliq, H, Banka, S, Bauer, U, Bentham, J, Berger, F, Bhattacharya, S, Bu'Lock, F, Canham, N, Colgiu, I, Cosgrove, C, Cox, H, Daehnert, I, Daly, A, Danesh, J, Fryer, A, Gewillig, M, Hobson, E, Hoff, K, Homfray, T, Kahlert, A, Ketley, A, Kramer, H, Lachlan, K, Lampe, A, Louw, J, Manickara, A, Manase, D, McCarthy, K, Metcalfe, K, Moore, C, Newbury-Ecob, R, Omer, S, Ouwehand, W, Park, S, Parker, M, Pickardt, T, Pollard, M, Robert, L, Roberts, D, Sambrook, J, Setchfield, K, Stiller, B, Thornborough, C, Toka, O, Watkins, H, Williams, D, Wright, M, Mital, S, Daubeney, P, Keavney, B, Goodship, J, Abu-Sulaiman, R, Klaassen, S, Wright, C, Firth, H, Barrett, J, Devriendt, K, FitzPatrick, D, Brook, J, Hurles, M