Lisa Kearns is a Research Genetic Counsellor and Orthoptist in CERA’s Clinical Genetics team.

Lisa coordinates research studies focused on the genetics of inherited eye diseases, including Leber Hereditary Optic Neuropathy (LHON), Autosomal Dominant Optic Atrophy (ADOA), glaucoma, inherited retinal diseases (IRDs), congenital cataracts and strabismus. She also provides guidance to patients and families about relevant clinical trials and research opportunities.

Lisa provides research-based genetic counselling and support to individuals and families affected by inherited eye conditions. Lisa is part of the team who specialises in LHON and committed to raising awareness of the condition among healthcare professionals to improve understanding and reduce misconceptions about the condition.

Her work focuses on connecting people to appropriate services and support organisations to address both practical and psychosocial needs, helping them cope with the life-changing impact of vision loss. Lisa’s ensures that those at risk are informed about potential trigger factors and supported in making appropriate healthcare and lifestyle choices. Lisa recognises that accurate risk information is particularly vital for family planning, enabling individuals and families to understand their options and make informed decisions about their future.

In 2024, Lisa was awarded the Mito Foundation Health Professional Award in recognition of her work with individuals and families affected by LHON.

In addition to her work in genetic eye research, Lisa practices as an orthoptist and clinic coordinator in the Ocular Diagnostic and Ocular Genetics Clinic at The Royal Victorian Eye and Ear Hospital. Her clinical practice translates research findings into practical care, improving patient outcomes while ensuring the latest knowledge and best practices are shared across the field.