Dr Kraan (BBNSc (Hons), PhD) is a cognitive neuroscientist with expertise in genetic neurodevelopmental disorders. Held appointments are in GenV, Prevention Innovation, Murdoch Children’s Research Institute (MCRI), the Australian Institute of Health Innovation, Macquarie University, and University of Melbourne (Honorary Level C). She has a PhD in Advanced Behavioural Neuroscience from the School of Psychology, Monash University and a recently completed a NHMRC fellowship in Genomic Medicine at MCRI.
As of 2024, Dr Kraan is undertaking two new roles. (1) GenV School Entry Wave project overseeing selection of the wearable technology and digital neurodevelopment phenotyping approaches. (2) Genomics in Primary care project via Centre for Healthcare Resilience and Implementation Science (CHRIS), Macquarie University / seconded to Genomics in Society, MCRI. She also holds positions as Vice chair of the Fragile X Association of Australia (FXAA) Scientific, Clinical and Research Committee (since Feb 2023) and Founder and Chair of Annual Fragile X Roundtable.
Dr Kraan (BBNSc (Hons), PhD) is a cognitive neuroscientist with expertise in genetic neurodevelopmental disorders. Held appointments are in GenV, Prevention Innovation, Murdoch Children’s Research Institute (MCRI), the Australian Institute of Health...
Dr Kraan (BBNSc (Hons), PhD) is a cognitive neuroscientist with expertise in genetic neurodevelopmental disorders. Held appointments are in GenV, Prevention Innovation, Murdoch Children’s Research Institute (MCRI), the Australian Institute of Health Innovation, Macquarie University, and University of Melbourne (Honorary Level C). She has a PhD in Advanced Behavioural Neuroscience from the School of Psychology, Monash University and a recently completed a NHMRC fellowship in Genomic Medicine at MCRI.
As of 2024, Dr Kraan is undertaking two new roles. (1) GenV School Entry Wave project overseeing selection of the wearable technology and digital neurodevelopment phenotyping approaches. (2) Genomics in Primary care project via Centre for Healthcare Resilience and Implementation Science (CHRIS), Macquarie University / seconded to Genomics in Society, MCRI. She also holds positions as Vice chair of the Fragile X Association of Australia (FXAA) Scientific, Clinical and Research Committee (since Feb 2023) and Founder and Chair of Annual Fragile X Roundtable.
Top Publications
Baker, EK, Arpone, M, Kraan, C, Bui, M, Rogers, C, Field, M, Bretherton, L, Ling, L, Ure, A, Cohen, J, et al.
FMR1 mRNA from full mutation alleles is associated with ABC-CFX scores in males with fragile X syndrome..
Sci Rep
10(1)
:
11701
2020
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Baker, EK, Arpone, M, Vera, SA, Bretherton, L, Ure, A, Kraan, CM, Bui, M, Ling, L, Francis, D, Hunter, MF, et al.
Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome..
J Neurodev Disord
11(1)
:
41
2019
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Kraan, CM, Godler, DE, Amor, DJ.
Epigenetics of fragile X syndrome and fragile X-related disorders..
Dev Med Child Neurol
61(2)
:
121 -127
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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Kraan, CM, Bui, QM, Field, M, Archibald, AD, Metcalfe, SA, Christie, LM, Bennetts, BH, Oertel, R, Smith, MJ, du Sart, D, et al.
FMR1 allele size distribution in 35,000 males and females: a comparison of developmental delay and general population cohorts..
Genet Med
20(12)
:
1627 -1634
2018
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