Dr Claudine Kraan
Honorary (Senior Fellow)
Department of Paediatrics
40 Scholarly works
0 Projects
HIGHLIGHTS
2026
Journal article
Developing general practitioner and consumer supports for genomics in Australian primary care: a mixed-methods protocol
DOI: 10.1136/bmjopen-2025-1051002026
Journal article
Scoping review and recommendations for development and delivery of education resources for reproductive genetic carrier screening
DOI: 10.1038/s41431-026-02152-42025
Journal article
Parents' Experiences and Views About Use of Wearable Technology for Research and Treatment Monitoring of Children with Neurodevelopmental Disorders.
DOI: 10.1097/DBP.00000000000013372025
Journal article
Parents' Experiences and Views about Use of Wearable Technology for Research and Treatment Monitoring of Children with Neurodevelopmental Disorders
DOI: 10.1097/DBP.00000000000013372024
Journal article
Comparability between wearable inertial sensors and an electronic walkway for spatiotemporal and relative phase data in young children aged 6–11 years
DOI: 10.1016/j.gaitpost.2024.04.0032023
Journal article
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation
DOI: 10.3390/cells121823302023
Journal article
Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome
DOI: 10.1002/ajmg.a.63027
RECENT SCHOLARLY WORKS
2023
Journal article
Social and physical predictors of mental health impact in adult women who have an FMR1 premutation
DOI: 10.1016/j.gimo.2023.1008292022
Journal article
Feasibility of wearable technology for ‘real-world’ gait analysis in children with Prader–Willi and Angelman syndromes
DOI: 10.1111/jir.129552022
Journal article
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)
DOI: 10.1136/jmedgenet-2021-107758