Contributions of intrinsic mutation rate and selfish selection to levels of de novo HRAS mutations in the paternal germline. od Giannoulatou, E, McVean, G, Taylor, I, McGowan, S, Maher, G, Iqbal, Z, Pfeifer, S, Turner, I, Burkitt Wright, E, Shorto, J, Itani, A, Turner, K, Gregory, L, Buck, D, Rajpert-De Meyts, E, Looijenga, L, Kerr, B, Wilkie, A, Goriely, A

Delineation of dominant and recessive forms of LZTR1‐associated Noonan syndrome od Pagnamenta, A, Kaisaki, P, Bennett, F, Burkitt-Wright, E, Martin, H, Ferla, M, Taylor, J, Gompertz, L, Lahiri, N, Tatton-Brown, K, Newbury-Ecob, R, Henderson, A, Joss, S, Weber, A, Carmichael, J, Turnpenny, P, McKee, S, Forzano, F, Ashraf, T, Bradbury, K, Shears, D, Kini, U, De Burca, A, The DDD Study, Blair, E, Taylor, J, Stewart, H

The Fourth International Symposium on Genetic Disorders of the Ras/MAPK pathway. od Stevenson, DA, Schill, L, Schoyer, L, Andresen, BS, Bakker, A, Bayrak-Toydemir, P, Burkitt-Wright, E, Chatfield, K, Elefteriou, F, Elgersma, Y, Fisher, MJ, Franz, D, Gelb, BD, Goriely, A, Gripp, KW, Hardan, AY, Keppler-Noreuil, KM, Kerr, B, Korf, B, Leoni, C, McCormick, F, Plotkin, SR, Rauen, KA, Reilly, K, Roberts, A, Sandler, A, Siegel, D, Walsh, K, Widemann, BC