Sebastian Lunke

29PUBLICATIONS
159CO-AUTHORS
Medical molecular engineering of nucleic acids and proteinsGene expression (incl. microarray and other genome-wide approaches)Infant and child healthEvolutionary computationEpigenetics (incl. genome methylation and epigenomics)
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Publications (29)

|Aug 17, 2026
Scaling up Genomics: A Mainstream Model of Care in Nephrology.

|Jul 23, 2026
Scaling up genomic newborn screening: implementation lessons from the BabyScreen+ study.

|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.

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Frequent Collaborators

17 joint publications

Zornitza Stark

10 joint publications

John Christodoulou

6 joint publications

David R Thorburn

6 joint publications

Stephanie Best