Thesis work
Thesis title: Phenotype-genotype studies of multiplex families with cerebral palsy and other neurodevelopmental disorders.
Supervisors: Nadia Badawi, Sarah McIntyre
Publications
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Journals
- Wilson, Y., Garrity, N., Smithers-Sheedy, H., Goldsmith, S., Karim, T., Henry, G., Paget, S., Kyriagis, M., Badawi, N., Baynam, G., McIntyre, S., et al (2024). Clinically Relevant Genes Identified in Cerebral Palsy Cohorts Following Evaluation of the Clinical Description and Phenotype: A Systematic Review. Journal of Child Neurology. [More Information]
- Wilson, Y., Smithers-Sheedy, H., Ostojic, K., Waight, E., Kruer, M., Fahey, M., Baynam, G., Gecz, J., Badawi, N., McIntyre, S. (2022). Common data elements to standardize genomics studies in cerebral palsy. Developmental Medicine and Child Neurology. [More Information]
- Wilson, Y., McIntyre, S., Waight, E., Thornton, M., Van Otterloo, S., Marmont, S., Kruer, M., Baynam, G., Gecz, J., Badawi, N. (2022). People with Cerebral Palsy and Their Family's Preferences about Genomics Research. Public Health Genomics, 25(1-Feb), 22-31. [More Information]
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2024
- Wilson, Y., Garrity, N., Smithers-Sheedy, H., Goldsmith, S., Karim, T., Henry, G., Paget, S., Kyriagis, M., Badawi, N., Baynam, G., McIntyre, S., et al (2024). Clinically Relevant Genes Identified in Cerebral Palsy Cohorts Following Evaluation of the Clinical Description and Phenotype: A Systematic Review. Journal of Child Neurology. [More Information]
2022
- Wilson, Y., Smithers-Sheedy, H., Ostojic, K., Waight, E., Kruer, M., Fahey, M., Baynam, G., Gecz, J., Badawi, N., McIntyre, S. (2022). Common data elements to standardize genomics studies in cerebral palsy. Developmental Medicine and Child Neurology. [More Information]
- Wilson, Y., McIntyre, S., Waight, E., Thornton, M., Van Otterloo, S., Marmont, S., Kruer, M., Baynam, G., Gecz, J., Badawi, N. (2022). People with Cerebral Palsy and Their Family's Preferences about Genomics Research. Public Health Genomics, 25(1-Feb), 22-31. [More Information]
2020
- Jin, S., Lewis, S., Bakhtiari, S., Zeng, X., Sierant, M., Shetty, S., Nordlie, S., Elie, A., Corbett, M., Norton, B., Novak, I., Badawi, N., Wilson, Y., McIntyre, S., et al (2020). Mutations disrupting neuritogenesis genes confer risk for cerebral palsy. Nature Genetics, 52(10), 1046-1056. [More Information]
2019
- MacLennan, A., Lewis, S., Moreno-De-Luca, A., Fahey, M., Leventer, R., McIntyre, S., Ben-Pazi, H., Corbett, M., Wang, X., Baynam, G., Smithers-Sheedy, H., Wilson, Y., Badawi, N., et al (2019). Genetic or Other Causation Should Not Change the Clinical Diagnosis of Cerebral Palsy. Journal of Child Neurology, 34(8), 472-476. [More Information]