Lisa S. Kearns

32 Gisborne Street
East Melbourne, VIC 3002, Australia

Last Updated: 09/26/2026

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Found 54 publications

Family and genetic counseling in Leber hereditary optic neuropathy.

Family and genetic counseling in Leber hereditary optic neuropathy.

Journal: Ophthalmic genetics

Published: January 20, 2025

Leber Hereditary Optic Neuropathy: Support, Genetic Prediction and Accurate Genetic Counselling Enhance Family Planning Choices.

Leber Hereditary Optic Neuropathy: Support, Genetic Prediction and Accurate Genetic Counselling Enhance Family Planning Choices.

Journal: Clinical & experimental ophthalmology

Published: August 30, 2024

Correction to: Exploring the support needs of Australian parents of young children with Usher syndrome: a qualitative thematic analysis.

Correction to: Exploring the support needs of Australian parents of young children with Usher syndrome: a qualitative thematic analysis.

Journal: Orphanet journal of rare diseases

Published: April 18, 2024

Patient experiences and perceived value of genetic testing in inherited retinal diseases: a cross-sectional survey.

Patient experiences and perceived value of genetic testing in inherited retinal diseases: a cross-sectional survey.

Journal: Scientific reports

Published: July 12, 2023

Exploring the support needs of Australian parents of young children with Usher syndrome: a qualitative thematic analysis.

Exploring the support needs of Australian parents of young children with Usher syndrome: a qualitative thematic analysis.

Journal: Orphanet journal of rare diseases

Published: June 05, 2023

Is the disease risk and penetrance in Leber hereditary optic neuropathy actually low?

Is the disease risk and penetrance in Leber hereditary optic neuropathy actually low?

Journal: American journal of human genetics

Published: October 08, 2022

Diagnostic yield of candidate genes in an Australian corneal dystrophy cohort.

Diagnostic yield of candidate genes in an Australian corneal dystrophy cohort.

Journal: Molecular genetics & genomic medicine

Published: July 15, 2022

Pathogenic genetic variants identified in Australian families with paediatric cataract.

Pathogenic genetic variants identified in Australian families with paediatric cataract.

Journal: BMJ open ophthalmology

Published: May 11, 2022

Transcriptomic and proteomic retinal pigment epithelium signatures of age-related macular degeneration.

Transcriptomic and proteomic retinal pigment epithelium signatures of age-related macular degeneration.

Journal: Nature communications

Published: August 04, 2021

Establishing risk of vision loss in Leber hereditary optic neuropathy.

Establishing risk of vision loss in Leber hereditary optic neuropathy.

Journal: American journal of human genetics

Published: July 12, 2021

Patient care standards for primary mitochondrial disease in Australia: an Australian adaptation of the Mitochondrial Medicine Society recommendations.

Patient care standards for primary mitochondrial disease in Australia: an Australian adaptation of the Mitochondrial Medicine Society recommendations.

Journal: Internal medicine journal

Published: April 13, 2021

Adherence to home-based videogame treatment for amblyopia in children and adults.

Adherence to home-based videogame treatment for amblyopia in children and adults.

Journal: Clinical & experimental optometry

Published: March 10, 2021

Showing 1-12 of 54

Last Updated: 09/26/2026