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
Green, AC, Tjin, G, Lee, SC, Chalk, AM, Straszkowski, L, Kwang, D, Baker, EK, Quach, JM, Kimura, T, Wu, JY, et al.
The characterization of distinct populations of murine skeletal cells that have different roles in B lymphopoiesis..
Blood
138(4)
:
304 -317
2021
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Jarmolowicz, AI, Baker, EK, Bartlett, E, Francis, D, Ling, L, Gamage, D, Delatycki, MB, Godler, DE.
Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program..
Am J Med Genet A
185(5)
:
1498 -1503
2021
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Hudry, K, Chetcuti, L, Boutrus, M, Pillar, S, Baker, EK, Dimov, S, Barbaro, J, Green, J, Whitehouse, AJ, Varcin, KJ, et al.
Performance of the Autism Observation Scale for Infants with community-ascertained infants showing early signs of autism..
Autism
25(2)
:
490 -501
2021
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Ballester, P, Richdale, AL, Baker, EK, Peiró, AM.
Sleep in autism: A biomolecular approach to aetiology and treatment..
Sleep Med Rev
54:
101357
2020
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Baker, EK, Butler, MG, Hartin, SN, Ling, L, Bui, M, Francis, D, Rogers, C, Field, MJ, Slee, J, Gamage, D, et al.
Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disorders..
Transl Psychiatry
10(1)
:
362
2020
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