{"id":4424,"date":"2025-11-25T11:24:13","date_gmt":"2025-11-25T00:24:13","guid":{"rendered":"https:\/\/kollinginstitute.org.au\/?post_type=research-group&p=4424"},"modified":"2026-03-17T11:11:17","modified_gmt":"2026-03-17T00:11:17","slug":"neurogenetics-research-group","status":"publish","type":"research-group","link":"https:\/\/kollinginstitute.org.au\/news_demo\/research-group\/neurogenetics-research-group\/","title":{"rendered":"Neurogenetics Research Group"},"content":{"rendered":"\n
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The Neurogenetics Research Group is dedicated to unraveling the genetic underpinnings of neurogenetic disorders, with a particular focus on Parkinson\u2019s disease and mitochondrial diseases. The group employs a multidisciplinary approach, integrating fundamental and clinical research. By integrating molecular biology techniques, genomic analysis, and omic approaches they aim to identify disease-causing variants, develop biomarkers and identify therapeutic targets to address the underlying pathological mechanisms.<\/p>\n\n\n\n

The group’s work spans from discovery research into disease mechanisms, to clinical studies aimed at improving diagnostic capabilities, and translation of findings into clinical capability that supports innovations in precision and personalized medicine. The Neurogenetics Research Group has strong collaborative links with clinical teams across Sydney, Australia and globally in order to link their findings with clinical care and patient outcomes.<\/p>\n\n\n\n

By combining cutting-edge research with clinical insights, the group aims to improve the lives of individuals affected by inherited neurological disorders.<\/p>\n<\/div>\n\n\n\n

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