Items where Author is "Bush, Stephen J."

Article

Wood, Katherine A. and Tong, R Spencer and Motta, Marialetizia and Cordeddu, Viviana and Scimone, Eleanor R. and Bush, Stephen J. and Maxwell, Dale W. and Giannoulatou, Eleni and Caputo, Viviana and Traversa, Alice and Mancini, Cecilia and Ferrero, Giovanni B. and Benedicenti, Francesco and Grammatico, Paola and Melis, Daniela and Steindl, Katharina and Brunetti-Pierri, Nicola and Trevisson, Eva and Wilkie, Andrew OM. and Lin, Angela E. and Cormier-Daire, Valerie and Twigg, Stephen RF. and Tartaglia, Marco and Goriely, Anne (2024) SMAD4 mutations causing Myhre syndrome are under positive selection in the male germline. The American Journal of Human Genetics, 111 (9). pp.1953-1969. ISSN 00029297

Bernkopf, Marie and Abdullah, Ummi B. and Bush, Stephen J. and Wood, Katherine A. and Ghaffari, Sahar and Giannoulatou, Eleni and Koelling, Nils and Maher, Geoffrey J. and Thibaut, Loïc M. and Williams, Jonathan and Blair, Edward M. and Kelly, Fiona Blanco and Bloss, Angela and Burkitt-Wright, Emma and Canham, Natalie and Deng, Alexander T. and Dixit, Abhijit and Eason, Jacqueline and Elmslie, Frances and Gardham, Alice and Hay, Eleanor and Holder, Muriel and Homfray, Tessa and Hurst, Jane A. and Johnson, Diana and Jones, Wendy D. and Kini, Usha and Kivuva, Emma and Kumar, Ajith and Lees, Melissa M. and Leitch, Harry G. and Morton, Jenny E. V. and Németh, Andrea H. and Ramachandrappa, Shwetha and Saunders, Katherine and Shears, Deborah J. and Side, Lucy and Splitt, Miranda and Stewart, Alison and Stewart, Helen and Suri, Mohnish and Clouston, Penny and Davies, Robert W. and Wilkie, Andrew O. M. and Goriely, Anne (2023) Personalized recurrence risk assessment following the birth of a child with a pathogenic de novo mutation. Nature Communications, 14 (1). ISSN 2041-1723