Showing 1 - 6 results of 6 for search 'Winlaw, D', query time: 0.02s
Refine Results
-
1
A screening approach to identify clinically actionable variants causing congenital heart disease in exome data by Szot, J, Cuny, H, Blue, G, Humphreys, D, Ip, E, Harrison, K, Sholler, G, Giannoulatou, E, Leo, P, Duncan, E, Sparrow, D, Ho, J, Graham, R, Pachter, N, Chapman, G, Winlaw, D, Dunwoodie, S
Published 2018Journal article -
2
Functional genomics and gene-environment interaction highlight the complexity of Congenital Heart Disease caused by Notch pathway variants by Chapman, G, Moreau, J, Ip, E, Szot, J, Iyer, K, Shi, H, Yam, M, O'Reilly, V, Enriquez, A, Greasby, J, Alankarage, D, Martin, E, Hanna, B, Edwards, M, Monger, S, Blue, G, Winlaw, D, Ritchie, H, Grieve, S, Giannoulatou, E, Sparrow, D, Dunwoodie, S
Published 2019Journal article -
3
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
Published 2012Journal article -
4
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
Published 2012Journal article -
5
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
Published 2012Journal article -
6
NAD deficiency, congenital malformations and niacin supplementation by Shi, H, Enriquez, A, Rapadas, M, Martin, E, Wang, R, Moreau, J, Lim, C, Szot, J, Ip, E, Hughes, J, Sugimoto, K, Humphreys, D, McInerney-Leo, A, Leo, P, Maghzal, G, Halliday, J, Smith, J, Colley, A, Mark, P, Collins, F, Sillence, D, Winlaw, D, Ho, J, Guillemin, G, Brown, M, Kikuchi, K, Thomas, P, Stocker, R, Giannoulatou, E, Chapman, G, Duncan, E, Sparrow, D, Dunwoodie, S
Published 2017Journal article