Florian Sennlaub

Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness.

Olivier Poch, Xavier Zanlonghi, Odile Lecompte, 2013, American journal of human genetics.

The 3D Retinal Capillary Circulation in Pigs Reveals a Predominant Serial Organization.

Michel Paques, M. Pâques, F. Sennlaub, 2017, Investigative ophthalmology & visual science.

Choroidal involution is a key component of oxygen-induced retinopathy.

Pierre Lachapelle, Swathi Seshadri, Przemyslaw Sapieha, 2011, Investigative ophthalmology & visual science.

CCR2+ monocytes infiltrate atrophic lesions in age-related macular disease and mediate photoreceptor degeneration in experimental subretinal inflammation in Cx3cr1 deficient mice

José-Alain Sahel, Jean-Louis Bourges, Francine Behar-Cohen, 2013, EMBO molecular medicine.

Spectral-Domain Optical Coherence Tomography of the Rodent Eye: Highlighting Layers of the Outer Retina Using Signal Averaging and Comparison with Histology

Michel Paques, José-Alain Sahel, Alexis-Pierre Bemelmans, 2014, PloS one.

Adaptive optics imaging of geographic atrophy.

Michel Paques, José-Alain Sahel, Kiyoko Gocho, 2013, Investigative ophthalmology & visual science.