Palmer, Elizabeth E
UNSW Sydney · Sydney Children's Hospital · Sydney Children’s Hospitals Network
8 papers on CoChatORCID 0000-0003-1844-215X
Most cited papers
- Verified
Artificial Intelligence Enabled Personalised Assistive Tools to Enhance Education of Children with Neurodevelopmental Disorders—A Review
Barua, P. D., Vicnesh, J., Gururajan, R., Oh, S. L., Palmer, E., Azizan, M. M., Kadri, N. A., & Acharya, U. R. (2022) · International Journal of Environmental Research and Public Health
Artificial Intelligence in EducationIntelligent Tutoring Systems and Adaptive Learning
Cited by 270
- Verified
GaborPDNet: gabor transformation and deep neural network for Parkinson's disease detection using EEG signals
Loh, H. W., Ooi, C. P., Palmer, E., Barua, P. D., Dogan, S., Tuncer, T., Baygin, M., & Acharya, U. R. (2021) · Electronics
EEG and Brain-Computer InterfacesArtificial Intelligence in Healthcare
Cited by 144
- Verified
Integrating exome sequencing into a diagnostic pathway for epileptic encephalopathy: Evidence of clinical utility and cost effectiveness
Palmer, E. E., Schofield, D., Shrestha, R., Kandula, T., Macintosh, R., Lawson, J. A., Andrews, I., Sampaio, H., Johnson, A. M., Farrar, M. A., et al. (2018) · Molecular Genetics & Genomic Medicine
Genomics and Rare DiseasesEpilepsy research and treatment
Cited by 113
- Verified
The molecular and phenotypic spectrum of IQSEC 2‐related epilepsy
Zerem, A., Haginoya, K., Lev, D., Blumkin, L., Kivity, S., Linder, I., Shoubridge, C., Palmer, E. E., Field, M., Boyle, J., et al. (2016) · Epilepsia
Epilepsy research and treatmentGenetics and Neurodevelopmental Disorders
Cited by 59
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Siblings of young people with chronic illness: Caring responsibilities and psychosocial functioning.
Kelada, L., Wakefield, C. E., Drew, D., Ooi, C. Y., Palmer, E. E., Bye, A., De Marchi, S., Jaffe, A., & Kennedy, S. (2022) · Journal of Child Health Care
Family Support in IllnessFamily and Disability Support Research
Cited by 59
- Verified
Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum
Smogavec, M., Cleall, A., Hoyer, J., Lederer, D., Nassogne, M.-C., Palmer, E. E., Deprez, M., Benoit, V., Maystadt, I., Noakes, C., et al. (2016) · Journal of Medical Genetics
Genetics and Neurodevelopmental DisordersEpilepsy research and treatment
Cited by 56
- Verified
Natural History Studies and Clinical Trial Readiness for Genetic Developmental and Epileptic Encephalopathies
Palmer, E. E., Howell, K., & Scheffer, I. E. (2021) · Neurotherapeutics
Epilepsy research and treatmentGenetics and Neurodevelopmental Disorders
Cited by 53
- Verified
Hope in the uncertainties and certainty for parents of children with rare neurological disorders: Part 2 (of 3): Certainty
Nevin, S. M., Beavis, E., Macintosh, R., Palmer, E. E., Sachdev, R., Le Marne, F. A., Bye, A. M., & Nunn, K. (2022) · Journal of Paediatrics and Child Health
Ethics and Legal Issues in Pediatric HealthcarePalliative Care and End-of-Life Issues
Cited by 9
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