| Preview | Issue Date | Title | Author(s) |
| 2013 | Autosomal dominant vasovagal syncope: clinical features and linkage to chromosome 15q26 | Klein, K.; Bromhead, C.; Smith, K.; O'Callaghan, C.; Corcoran, S.; Heron, S.; Iona, X.; Hodgson, B.; McMahon, J.; Lawrence, K.; Scheffer, I.; Dibbens, L.; Bahlo, M.; Berkovic, S. |
| 2016 | De novo mutations in SLC1A2 and CACNA1A are important causes of epileptic encephalopathies | Myers, C.; McMahon, J.; Schneider, A.; Petrovski, S.; Allen, A.; Carvill, G.; Zemel, M.; Saykally, J.; LaCroix, A.; Heinzen, E.; Hollingsworth, G.; Nikanorova, M.; Corbett, M.; Gecz, J.; Coman, D.; Freeman, J.; Calvert, S.; Gill, D.; Carney, P.; Lerman-Sagie, T.; et al. |
| 2018 | Exploring general practitioners' views and experiences of providing care to people with borderline personality disorder in primary care: A qualitative study in Australia | Wlodarczyk, J.; Lawn, S.; Powell, K.; Crawford, G.B.; McMahon, J.; Burke, J.; Woodforde, L.; Kent, M.; Howell, C.; Litt, J. |
| 2012 | Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations | Carranza Rojo, D.; Simon Harvey, A.; Iona, X.; Dibbens, L.; Damiano, J.; Arsov, T.; Gill, D.; Freeman, J.; Leventer, R.; Vincent, A.; Berkovic, S.; McMahon, J.; Scheffer, I. |
| 2015 | Mutations in KCNT1 cause a spectrum of focal epilepsies | Møller, R.; Heron, S.; Larsen, L.; Lim, C.; Ricos, M.; Bayly, M.; Van Kempen, M.; Klinkenberg, S.; Andrews, I.; Kelley, K.; Ronen, G.; Callen, D.; McMahon, J.; Yendle, S.; Carvill, G.; Mefford, H.; Nabbout, R.; Poduri, A.; Striano, P.; Baglietto, M.; et al. |
| 2013 | Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies | Heron, S.; Ong, Y.; Yendle, S.; McMahon, J.; Berkovic, S.; Scheffer, I.; Dibbens, L. |
