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Email

claudine.kraan@unimelb.edu.au

Credentials


Position
Honorary (Senior Fellow)
Department of Paediatrics
ORCID

0000-0003-1805-6339

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-2025-105100
  • 2026

    Journal article

    Scoping review and recommendations for development and delivery of education resources for reproductive genetic carrier screening
    DOI: 10.1038/s41431-026-02152-4
  • 2025

    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.0000000000001337
  • 2025

    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.0000000000001337
  • 2024

    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.2024.04.003
  • 2023

    Journal article

    Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation
    DOI: 10.3390/cells12182330
  • 2023

    Journal article

    Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome
    DOI: 10.1002/ajmg.a.63027
Claudine Kraan

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.2023.100829
  • 2022

    Journal article

    Feasibility of wearable technology for ‘real-world’ gait analysis in children with Prader–Willi and Angelman syndromes
    DOI: 10.1111/jir.12955
  • 2022

    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

Acknowledgement of Country

We acknowledge Aboriginal and Torres Strait Islander people as the Traditional Owners of the unceded lands on which we work, learn and live. We pay respect to Elders past, present and future, and acknowledge the importance of Indigenous knowledge in the Academy.

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