Hodgson, Bree L
University of South Australia · Centre for Cancer Biology
2 papers on CoChat
Most cited papers
- Verified
Mutations in DEPDC5 cause familial focal epilepsy with variable foci
Dibbens, L. M., de Vries, B., Donatello, S., Heron, S. E., Hodgson, B. L., Chintawar, S., Crompton, D. E., Hughes, J. N., Bellows, S. T., Klein, K. M., et al. (2013) · Nature Genetics
Epilepsy research and treatmentTuberous Sclerosis Complex Research
Cited by 373
- Verified
Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy
Ricos, M. G., Hodgson, B. L., Pippucci, T., Saidin, A., Ong, Y. S., Heron, S. E., Licchetta, L., Bisulli, F., Bayly, M. A., Hughes, J., et al. (2016) · Annals of Neurology
Epilepsy research and treatmentTuberous Sclerosis Complex Research
Cited by 246
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