Claudine M Kraan

10PUBLICATIONS
41CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Counselling psychologyInfant and child healthMicroelectromechanical systems (MEMS)Epigenetics (incl. genome methylation and epigenomics)
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Publications (10)

|Jun 30, 2026
Scoping review and recommendations for development and delivery of education resources for reproductive genetic carrier screening.

|Jun 16, 2026
Developing general practitioner and consumer supports for genomics in Australian primary care: a mixed-methods protocol.

|Feb 17, 2025
Parents' Experiences and Views About Use of Wearable Technology for Research and Treatment Monitoring of Children with Neurodevelopmental Disorders.

Rachel Xifaras, David J Amor, Erin Turbitt

|Jan 17, 2025
Parents' Experiences and Views About Use of Wearable Technology for Research and Treatment Monitoring of Children with Neurodevelopmental Disorders.

Rachel Xifaras, David J Amor, Erin Turbitt

|Sep 28, 2023
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.

Flora Tassone, Dragana Protic, Emily Graves Allen

|Nov 09, 2022
Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome.

Emma K Baker, Marta Arpone, Minh Bui

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Frequent Collaborators

3 joint publications

David J Amor

3 joint publications

David E Godler

2 joint publications

Janet C Long

2 joint publications

Alison D Archibald