Karin S Kassahn

8PUBLICATIONS
90CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Evolutionary computationNeonatologyEpigenetics (incl. genome methylation and epigenomics)Artificial life and complex adaptive systems
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Publications (8)

|Sep 24, 2026
The Australian PreGen Study: Results From Prospective Prenatal Exome Sequencing in 275 Pregnancies.

|Jun 24, 2026
Automated reanalysis of genomic data for rare disease diagnostics at scale.

|Mar 11, 2026
NewbornsInSA multi-omic newborn screening: protocol for a prospective cohort study.

Lucy Anastasi, Ayesha Chowdhury, Alex Ashenden

|Jul 11, 2024
Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition.

Jiarna R Zerella, Claire C Homan, Peer Arts

|May 25, 2024
Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services.

Stephanie Best, Zoe Fehlberg, Christopher Richards

|Apr 05, 2024
Extending the new era of genomic testing into pregnancy management: A proposed model for Australian prenatal services.

Alice Rogers, Lucas De Jong, Wendy Waters

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Frequent Collaborators

6 joint publications

Hamish Scott

4 joint publications

Sebastian Lunke

3 joint publications

Peer Arts

3 joint publications

Zornitza Stark