Pre-symptomatic genetic testing for inherited cardiac conditions: a qualitative exploration of psychosocial and ethical implications

द्वारा Ormondroyd, Elizabeth, Oates, Stephanie, Parker, Michael, Blair, Edward, Watkins, Hugh
प्रकाशित 2014

Inpatient detection of cardiac-inherited disease: the impact of improving family history taking

द्वारा Waddell-Smith, Kathryn E, Donoghue, Tom, Oates, Stephanie, Graham, Amanda, Crawford, Jackie, Stiles, Martin K, Aitken, Andrew, Skinner, Jonathan R
में प्रकाशित Open Heart (2016)

Incorporating epilepsy genetics into clinical practice: a 360°evaluation

द्वारा Oates, Stephanie, Tang, Shan, Rosch, Richard, Lear, Rosalie, Hughes, Elaine F., Williams, Ruth E., Larsen, Line H. G., Hao, Qin, Dahl, Hans Atli, Møller, Rikke S., Pal, Deb K.
में प्रकाशित NPJ Genom Med (2018)

Clinical spectrum of STX1B-related epileptic disorders

द्वारा Wolking, Stefan, May, Patrick, Mei, Davide, Møller, Rikke S., Balestrini, Simona, Helbig, Katherine L., Altuzarra, Cecilia Desmettre, Chatron, Nicolas, Kaiwar, Charu, Stöhr, Katharina, Widdess-Walsh, Peter, Mendelsohn, Bryce A., Numis, Adam, Cilio, Maria R., Van Paesschen, Wim, Svendsen, Lene L., Oates, Stephanie, Hughes, Elaine, Goyal, Sushma, Brown, Kathleen, Sifuentes Saenz, Margarita, Dorn, Thomas, Muhle, Hiltrud, Pagnamenta, Alistair T., Vavoulis, Dimitris V., Knight, Samantha J.L., Taylor, Jenny C., Canevini, Maria Paola, Darra, Francesca, Gavrilova, Ralitza H., Powis, Zöe, Tang, Shan, Marquetand, Justus, Armstrong, Martin, McHale, Duncan, Klee, Eric W., Kluger, Gerhard J., Lowenstein, Daniel H., Weckhuysen, Sarah, Pal, Deb K., Helbig, Ingo, Guerrini, Renzo, Thomas, Rhys H., Rees, Mark I., Lesca, Gaetan, Sisodiya, Sanjay M., Weber, Yvonne G., Lal, Dennis, Marini, Carla, Lerche, Holger, Schubert, Julian
में प्रकाशित Neurology (2019)