A. Caignard

Improved Locus‐Specific Database for OPA1 Mutations Allows Inclusion of Advanced Clinical Data

D. Milea, D. Bonneau, P. Amati‐Bonneau, 2015, Human mutation.

Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophy.

M. Larsen, D. Milea, G. Lenaers, 2016, Human molecular genetics.

MOG-Ab prevalence in optic neuritis and clinical predictive factors for diagnosis

P. Lebranchu, A. Caignard, R. Marignier, 2019, British Journal of Ophthalmology.

OPA1: 516 unique variants and 831 patients registered in an updated centralized Variome database

Dan Milea, Johan T den Dunnen, Xavier Zanlonghi, 2019, Orphanet journal of rare diseases.

[Neuro-ophthalmic emergencies].

D. Milea, S. Leruez, A. Caignard, 2016, Journal Francais d'Ophtalmologie.

Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophy.

M. Larsen, D. Milea, G. Lenaers, 2017, Human molecular genetics.

Educational Concerns About the Safety of Cataract Surgery During Residency: The E3CAPS Pedagogic Study

P. Lebranchu, P. Pladys, P. Gohier, 2023, Ophthalmology and Therapy.