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

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Ingrid E. Scheffer

Florey Neuroscience Institutes

245 Burgundy Street

Heidelberg

Victoria 3084

Australia

[email]@unimelb.edu.au

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Florey Neuroscience Institutes, 245 Burgundy Street, Heidelberg, Victoria 3084, Australia. 2011
  • Epilepsy Research Centre, Department of Medicine, University of Melbourne, Heidelberg Repatriation Hospital, Australia. 2008 - 2010
  • Department of Medicine and Paediatrics, The University of Melbourne, Epilepsy Research Centre, Melbourne, Australia. 2005 - 2010
  • Epilepsy Research Institute, University of Melbourne, Austin and Repatriation Medical Centre and Royal Children's Hospital, Melbourne, Australia. 2001 - 2002

References

  1. De novo SCN1A mutations in migrating partial seizures of infancy. Carranza Rojo, D., Hamiwka, L., McMahon, J.M., Dibbens, L.M., Arsov, T., Suls, A., Stödberg, T., Kelley, K., Wirrell, E., Appleton, B., Mackay, M., Freeman, J.L., Yendle, S.C., Berkovic, S.F., Bienvenu, T., De Jonghe, P., Thorburn, D.R., Mulley, J.C., Mefford, H.C., Scheffer, I.E. Neurology (2011) [Pubmed]
  2. Copy number variants--an unexpected risk factor for the idiopathic generalized epilepsies. Scheffer, I.E., Berkovic, S.F. Brain (2010) [Pubmed]
  3. Genetics of the epilepsies: genetic twists in the channels and other tales. Scheffer, I.E., Zhang, Y.H., Gecz, J., Dibbens, L. Epilepsia (2010) [Pubmed]
  4. Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?. Scheffer, I.E., Zhang, Y.H., Jansen, F.E., Dibbens, L. Brain Dev. (2009) [Pubmed]
  5. Epilepsy and mental retardation limited to females: an under-recognized disorder. Scheffer, I.E., Turner, S.J., Dibbens, L.M., Bayly, M.A., Friend, K., Hodgson, B., Burrows, L., Shaw, M., Wei, C., Ullmann, R., Ropers, H.H., Szepetowski, P., Haan, E., Mazarib, A., Afawi, Z., Neufeld, M.Y., Andrews, P.I., Wallace, G., Kivity, S., Lev, D., Lerman-Sagie, T., Derry, C.P., Korczyn, A.D., Gecz, J., Mulley, J.C., Berkovic, S.F. Brain (2008) [Pubmed]
  6. Classification and clinical features of absence epilepsies: how evidence leads to changing concepts. Scheffer, I.E., Berg, A.T. Epilepsia (2008) [Pubmed]
  7. Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations. Scheffer, I.E., Harkin, L.A., Grinton, B.E., Dibbens, L.M., Turner, S.J., Zielinski, M.A., Xu, R., Jackson, G., Adams, J., Connellan, M., Petrou, S., Wellard, R.M., Briellmann, R.S., Wallace, R.H., Mulley, J.C., Berkovic, S.F. Brain (2007) [Pubmed]
  8. The role of genetics and ethnicity in epilepsy management. Scheffer, I.E. Acta Neurol. Scand., Suppl. (2005) [Pubmed]
  9. Neonatal epilepsy syndromes and generalized epilepsy with febrile seizures plus (GEFS+). Scheffer, I.E., Harkin, L.A., Dibbens, L.M., Mulley, J.C., Berkovic, S.F. Epilepsia (2005) [Pubmed]
  10. X-linked myoclonic epilepsy with spasticity and intellectual disability: mutation in the homeobox gene ARX. Scheffer, I.E., Wallace, R.H., Phillips, F.L., Hewson, P., Reardon, K., Parasivam, G., Stromme, P., Berkovic, S.F., Gecz, J., Mulley, J.C. Neurology (2002) [Pubmed]
  11. Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome). Scheffer, I.E., Wallace, R., Mulley, J.C., Berkovic, S.F. Brain Dev. (2001) [Pubmed]
 
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