Clara W T Chung

6PUBLICATIONS
38CO-AUTHORS
Solid tumoursInfant and child healthNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Gene mapping
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Publications (6)

|Mar 01, 2026
Multicystic Kidney Disease in a Family With Tuberous Sclerosis Complex.

Julia S Donald, Caitlin Edmonstone, Denise L Chan

|Nov 22, 2025
Diagnosis and Management of Children With Tuberous Sclerosis Complex.

Celia Dewell, Denise L Chan, Vanessa Sarkozy

|Nov 19, 2025
Pathogenic Variants in RNU2-2, a Non-coding Spliceosomal RNA, Cause a Distinctive Developmental and Epileptic Encephalopathy.

Annie T G Chiu, Mark F Bennett, Harshini Thiyagarajah

|Dec 31, 2024
RICTOR variants are associated with neurodevelopmental disorders.

Raphael Carapito, Anne Molitor, Lisa Pavinato

|Oct 01, 2024
Deep Sequencing and Phenotyping in an Australian Tuberous Sclerosis Complex "No Mutations Identified" Cohort.

Clara W T Chung, Adam M Bournazos, Lok Chi Denise Chan

|Jan 27, 2023
A cell-based functional assay that accurately links genotype to phenotype in familial HLH.

Tahereh Noori, Jesse A Rudd-Schmidt, Alisa Kane

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