Mathilda Wilding
Royal North Shore Hospital
Sydney, NSW, Australia
Sydney, NSW, Australia
Last Updated: 09/26/2026
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Found 8 publications
Bi-allelic missense variants in human GPN2 result in Perrault syndrome.
Journal: American journal of human genetics
Published: March 27, 2026
The development and evaluation of educational resources for young women with neurofibromatosis type 1 undergoing breast cancer surveillance.
Journal: Women's health (London, England)
Published: June 29, 2025
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome.
Journal: medRxiv : the preprint server for health sciences
Published: March 13, 2023
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome.
Journal: Journal of translational medicine
Published: February 09, 2023
Identifying primary and secondary MLH1 epimutation carriers displaying low-level constitutional MLH1 methylation using droplet digital PCR and genome-wide DNA methylation profiling of colorectal cancers.
Journal: Clinical epigenetics
Published: January 16, 2023
Clinical and imaging modality factors impacting radiological interpretation of breast screening in young women with neurofibromatosis type 1.
Journal: Familial cancer
Published: November 20, 2022
The psychological impact and experience of breast cancer screening in young women with an increased risk of breast cancer due to neurofibromatosis type 1.
Journal: Familial cancer
Published: March 24, 2021
Bayesian approach to determining penetrance of pathogenic SDH variants.
Journal: Journal of medical genetics
Published: April 13, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026