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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Samuel F. Berkovic

FRS, Epilepsy Research Centre

Department of Medicine

University of Melbourne



Name/email consistency: high



  • FRS, Epilepsy Research Centre, Department of Medicine, University of Melbourne, Australia. 2004 - 2011
  • Department of Medicine, Austin Health and Northern Health, Heidelberg, Victoria 3081, Australia. 2008
  • Epilepsy Research Center, Heidelberg Repatriation Hospital, Banksia Street, West Heidelberg, Australia. 2007
  • Epilepsy Research Institute and Department of Neurology, Austin and Repatriation Medical Centre, Heidelberg (Melbourne), Australia. 2003 - 2006


  1. Mutation of SCARB2 in a Patient With Progressive Myoclonus Epilepsy and Demyelinating Peripheral Neuropathy. Dibbens, L.M., Karakis, I., Bayly, M.A., Costello, D.J., Cole, A.J., Berkovic, S.F. Arch. Neurol. (2011) [Pubmed]
  2. Epilepsy: insights into causes and treatment dilemmas. Berkovic, S.F. Lancet. Neurol (2010) [Pubmed]
  3. The borderland of epilepsy: a clinical and molecular view, 100 years on. Berkovic, S.F., Crompton, D.E. Epilepsia (2010) [Pubmed]
  4. Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis. Berkovic, S.F., Dibbens, L.M., Oshlack, A., Silver, J.D., Katerelos, M., Vears, D.F., Lüllmann-Rauch, R., Blanz, J., Zhang, K.W., Stankovich, J., Kalnins, R.M., Dowling, J.P., Andermann, E., Andermann, F., Faldini, E., D'Hooge, R., Vadlamudi, L., Macdonell, R.A., Hodgson, B.L., Bayly, M.A., Savige, J., Mulley, J.C., Smyth, G.K., Power, D.A., Saftig, P., Bahlo, M. Am. J. Hum. Genet. (2008) [Pubmed]
  5. Placebo-controlled study of levetiracetam in idiopathic generalized epilepsy. Berkovic, S.F., Knowlton, R.C., Leroy, R.F., Schiemann, J., Falter, U. Neurology (2007) [Pubmed]
  6. De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study. Berkovic, S.F., Harkin, L., McMahon, J.M., Pelekanos, J.T., Zuberi, S.M., Wirrell, E.C., Gill, D.S., Iona, X., Mulley, J.C., Scheffer, I.E. Lancet. Neurol (2006) [Pubmed]
  7. Human epilepsies: interaction of genetic and acquired factors. Berkovic, S.F., Mulley, J.C., Scheffer, I.E., Petrou, S. Trends Neurosci. (2006) [Pubmed]
  8. Febrile seizures: traffic slows in the heat. Berkovic, S.F., Petrou, S. Trends. Mol. Med (2006) [Pubmed]
  9. A new clinical and molecular form of Unverricht-Lundborg disease localized by homozygosity mapping. Berkovic, S.F., Mazarib, A., Walid, S., Neufeld, M.Y., Manelis, J., Nevo, Y., Korczyn, A.D., Yin, J., Xiong, L., Pandolfo, M., Mulley, J.C., Wallace, R.H. Brain (2005) [Pubmed]
  10. Treatment with anti-epileptic drugs. Berkovic, S.F. Aust. Fam. Physician (2005) [Pubmed]
  11. Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy. Berkovic, S.F., Heron, S.E., Giordano, L., Marini, C., Guerrini, R., Kaplan, R.E., Gambardella, A., Steinlein, O.K., Grinton, B.E., Dean, J.T., Bordo, L., Hodgson, B.L., Yamamoto, T., Mulley, J.C., Zara, F., Scheffer, I.E. Ann. Neurol. (2004) [Pubmed]
  12. LGI1 mutations in temporal lobe epilepsies. Berkovic, S.F., Izzillo, P., McMahon, J.M., Harkin, L.A., McIntosh, A.M., Phillips, H.A., Briellmann, R.S., Wallace, R.H., Mazarib, A., Neufeld, M.Y., Korczyn, A.D., Scheffer, I.E., Mulley, J.C. Neurology (2004) [Pubmed]
  13. Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12. Berkovic, S.F., Serratosa, J.M., Phillips, H.A., Xiong, L., Andermann, E., Díaz-Otero, F., Gómez-Garre, P., Martín, M., Fernández-Bullido, Y., Andermann, F., Lopes-Cendes, I., Dubeau, F., Desbiens, R., Scheffer, I.E., Wallace, R.H., Mulley, J.C., Pandolfo, M. Epilepsia (2004) [Pubmed]
  14. Hypothalamic hamartoma and seizures: a treatable epileptic encephalopathy. Berkovic, S.F., Arzimanoglou, A., Kuzniecky, R., Harvey, A.S., Palmini, A., Andermann, F. Epilepsia (2003) [Pubmed]
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