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Jessica Clarke

Senior Genetic Scientist, Douglass Hanly Moir Pathology; NSW Branch representative, Australasian Society of Diagnostic Genomics (ASDG)
Jess Clarke is a Senior Genetic Scientist at Douglass Hanly Moir Pathology with over 10 years of expertise in germline genetic testing and non-invasive prenatal screening. After working on the 100,000 genome project in London between 2018 and 2020, Jess returned to Australia and to DHM to launch new genomic services as part of a collaborative and innovative team. Soon after, she started training for the faculty of science fellowship in Genetic Pathology offered through the RCPA. Jess is an active member in the field of genomics and is currently the NSW Branch representative for the Australasian Society of Diagnostic Genomics (ASDG). Jess has a passion for providing equitable service for the Australians population and beyond and enjoys mentoring new scientists in the field of genomics.

More from this expert

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This episode explores the evolving landscape of fetal Rhesus screening in pregnancy care, featuring expert insights from A/Prof Marina Berbic and Jessica Clarke. Learn how advances in cell-free DNA testing are reshaping anti-D immunoglobulin use, why updated national guidelines matter, and what healthcare professionals need to know about ordering, timing, and interpreting results.

This episode explores the evolving landscape of fetal Rhesus screening in pregnancy care, featuring expert insights from A/Prof Marina Berbic and Jessica Clarke. Learn how advances in cell-free DNA testing are reshaping anti-D immunoglobulin use, why updated national guidelines matter, and what healthcare professionals need to know about ordering, timing, and interpreting results.

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Upcoming Healthed Webcast

Abnormal Liver Function Test Interpretation

Tuesday 31st March, 7pm - 9pm AEDT

Speaker

Dr Emily Nash

Gastroenterologist and Hepatologist; Chris O'Brien Lifehouse; Clinical Associate Lecturer, University of Sydney

Join Dr Emily Nash for their lecture where they will offer a framework to interpret abnormal LFTS and suggest diagnostic algorithms to help determine the most appropriate next step.