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Details

Role Senior Research Officer
Research area Clinical Sciences

Contact

Available for student supervision
I am a post-doctoral researcher and psychologist working in the Speech and Language group at the Murdoch Children’s Research Institute. My primary research interests are to understand the clinical phenotypes of children with rare genetically determined neurodevelopmental disorders, particularly the comorbid conditions (sleep, autism, and intellectual disability) experienced by these individuals and to determine the underlying aetiology of these comorbidities.
I am a post-doctoral researcher and psychologist working in the Speech and Language group at the Murdoch Children’s Research Institute. My primary research interests are to understand the clinical phenotypes of children with rare genetically...
I am a post-doctoral researcher and psychologist working in the Speech and Language group at the Murdoch Children’s Research Institute. My primary research interests are to understand the clinical phenotypes of children with rare genetically determined neurodevelopmental disorders, particularly the comorbid conditions (sleep, autism, and intellectual disability) experienced by these individuals and to determine the underlying aetiology of these comorbidities.

Top Publications

  • Baker, EK, Richdale, AL, Hazi, A, Prendergast, LA. Assessing a hyperarousal hypothesis of insomnia in adults with autism spectrum disorder.. Autism Res 12(6) : 897 -910 2019
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  • Pandelache, A, Baker, EK, Aliaga, SM, Arpone, M, Forbes, R, Stark, Z, Francis, D, Godler, DE. Clinical and Molecular Differences between 4-Year-Old Monozygous Male Twins Mosaic for Normal, Premutation and Fragile X Full Mutation Alleles.. Genes (Basel) 10(4) : 2019
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  • Baker, EK, Richdale, AL, Hazi, A. Employment status is related to sleep problems in adults with autism spectrum disorder and no comorbid intellectual impairment.. Autism 23(2) : 531 -536 2019
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  • Baker, EK, Arpone, M, Aliaga, SM, Bretherton, L, Kraan, CM, Bui, M, Slater, HR, Ling, L, Francis, D, Hunter, MF, et al. Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features.. Mol Autism 10: 21 2019
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  • Richdale, AL, Baker, EK. Circadian Rhythm Sleep Disorders. 111 -122 2019
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