Fleur O'Hare (F O'Hare)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 13

Top Topics

Optical Coherence Tomography

Top Venues

Orphanet journal of rare diseases

Clinical & experimental optometry

Acta ophthalmologica

This page only lists publications with an associated author ORCID identifier.

Publications

Lauren Johansen, Fleur O'Hare, Emily R Shepard, Lauren N Ayton, Lemuel J Pelentsov, L S Kearns, Karyn L Galvin
Correction to: Exploring the support needs of Australian parents of young children with Usher syndrome: a qualitative thematic analysis. Orphanet journal of rare diseases 19 (1) (2024)
Lauren Johansen, Fleur O'Hare, Emily R Shepard, Lauren N Ayton, Lemuel J Pelentsov, L S Kearns, Karyn L Galvin
Correction to: Exploring the support needs of Australian parents of young children with Usher syndrome: a qualitative thematic analysis. Orphanet journal of rare diseases 19 (1) (2024)
Lauren Johansen, Fleur O'Hare, Emily R Shepard, Lauren N Ayton, Lemuel J Pelentsov, L S Kearns, Karyn L Galvin
Exploring the support needs of Australian parents of young children with Usher syndrome: a qualitative thematic analysis. Orphanet journal of rare diseases 19 (1) (2024)
Lauren Johansen, Fleur O'Hare, Emily R Shepard, Lauren N Ayton, Lemuel J Pelentsov, L S Kearns, Karyn L Galvin
Correction to: Exploring the support needs of Australian parents of young children with Usher syndrome: a qualitative thematic analysis. Orphanet journal of rare diseases 19 (1) (2024)
Lauren Johansen, Fleur O'Hare, Emily R Shepard, Lauren N Ayton, Lemuel J Pelentsov, L S Kearns, Karyn L Galvin
Exploring the support needs of Australian parents of young children with Usher syndrome: a qualitative thematic analysis. Orphanet journal of rare diseases 19 (1) (2024)
Lauren Johansen, Fleur O'Hare, Emily R Shepard, Lauren N Ayton, Lemuel J Pelentsov, L S Kearns, Karyn L Galvin
Exploring the support needs of Australian parents of young children with Usher syndrome: a qualitative thematic analysis. Orphanet journal of rare diseases 19 (1) (2024)
Lauren Johansen, Fleur O'Hare, Emily R Shepard, Lauren N Ayton, Lemuel J Pelentsov, L S Kearns, Karyn L Galvin
Exploring the support needs of Australian parents of young children with Usher syndrome: a qualitative thematic analysis. Orphanet journal of rare diseases 19 (1) (2024)
Lauren N Ayton, Karyn L Galvin, Lauren Johansen, Fleur O'Hare, Emily R Shepard
Awareness of Usher Syndrome and the Need for Multidisciplinary Care: A Cross-Occupational Survey of Allied Health Clinicians. Journal of multidisciplinary healthcare 16 (2023)
Alexis Ceecee Zhang, Fleur O'Hare, Thomas L Edwards, Lauren N Ayton, null null
Victorian evolution of inherited retinal diseases natural history registry (VENTURE study): Rationale, methodology and initial participant characteristics. Clinical & experimental ophthalmology 50 (7) (2022)
Heather G Mack, Alexis Ceecee Zhang, Myra B McGuiness, Fred K Chen, John R B Grigg, Robyn V Jamieson, Thomas L Edwards, John N De Roach, Fleur O'Hare, Keith R Martin, Lauren N Ayton
Survey of perspectives of people with inherited retinal diseases on ocular gene therapy in Australia. Gene therapy (2022)
Zhengyang Liu, Luke A Perry, Jahan C Penny-Dimri, Dev Raveendran, Monica L Hu, Janan Arslan, Alexis Ceecee Zhang, Fleur O'Hare, Lauren N Ayton, Thomas L Edwards
The association of neutrophil-lymphocyte ratio and platelet-lymphocyte ratio with retinal vein occlusion: a systematic review and meta-analysis. Acta ophthalmologica (2021)
Fleur O'Hare, Thomas L Edwards, Monica L Hu, Doron G Hickey, Alexis Ceecee Zhang, Jiang-Hui Wang, Zhengyang Liu, Lauren N Ayton
An optometrist's guide to the top candidate inherited retinal diseases for gene therapy. Clinical & experimental optometry 104 (4) (2021)
Monica L Hu, Thomas L Edwards, Fleur O'Hare, Doron G Hickey, Jiang-Hui Wang, Zhengyang Liu, Lauren N Ayton
Gene therapy for inherited retinal diseases: progress and possibilities. Clinical & experimental optometry 104 (4) (2021)