photo of Dr Claudine Kraan

Dr Claudine Kraan

Dr Claudine Kraan

Details

Role Research Officer
Research area Genetics

Top Publications

  • Kraan, CM, Date, P, Rattray, A, Sangeux, M, Bui, QM, Baker, EK, Morison, J, Amor, DJ, Godler, DE. Feasibility of wearable technology for ‘real‐world’ gait analysis in children with Prader–Willi and Angelman syndromes. Journal of Intellectual Disability Research 2022
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  • Carroll, K, Kennedy, RA, Koutoulas, V, Bui, M, Kraan, CM. Validation of shoe-worn Gait Up Physilog®5 wearable inertial sensors in adolescents. Gait & Posture 91: 19 -25 2021
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  • Martin, EM, Zhu, Y, Kraan, CM, Kumar, KR, Godler, DE, Field, M. Men with FMR1 premutation alleles of less than 71 CGG repeats have low risk of being affected with fragile X-associated tremor/ataxia syndrome (FXTAS). Journal of Medical Genetics 59(7) : 706 -709 2021
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  • Kraan, CM, Baker, EK, Arpone, M, Bui, M, Ling, L, Gamage, D, Bretherton, L, Rogers, C, Field, MJ, Wotton, TL, et al. DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome. International Journal of Molecular Sciences 21(20) : 7735 2020
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  • 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. Scientific Reports 10(1) : 11701 2020
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