Sebastian Lunke

27PUBLICATIONS

128CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Infant and child healthEvolutionary computationEpigenetics (incl. genome methylation and epigenomics)Medical biotechnology diagnostics (incl. biosensors)

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Publications (27)

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|Jun 27, 2026

Australian parents' perspectives on extended genomic screening: what information to return and when?

|Jun 26, 2026

How parents decide whether to have genomic newborn screening: experiences from BabyScreen.

|Jun 24, 2026

Automated reanalysis of genomic data for rare disease diagnostics at scale.

|May 11, 2026

Unraveling a Diagnostic Enigma: A TECPR2 Case Solved Through Multi-Omic Genomics.

|May 04, 2026

KCNQ2 neonatal epilepsy: Impact of prompt diagnosis and treatment, and early predictors of outcome severity.

|Feb 26, 2026

Mainstreaming genomic testing for mitochondrial disease in Australia.

Megan Ball, Naomi Baker, Sze Chern Lim

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Frequent Collaborators

15 joint publications

Zornitza Stark

10 joint publications

John Christodoulou

David R Thorburn

Stephanie Best

Karin S Kassahn

Sophie E Bouffler

Fiona Lynch

Jade Caruana

Tiong Yang Tan

David J Amor

Frequent Collaborators

15 joint publications

Zornitza Stark

10 joint publications

John Christodoulou

6 joint publications

David R Thorburn

4 joint publications

Stephanie Best