Publications

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Author Title [ Year(Desc)]
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2013
Issa, P. Charbel et al. Macular telangiectasia type 2. Prog Retin Eye Res 34, 49-77 (2013).
2014
Xie, Y. Angela et al. New syndrome with retinitis pigmentosa is caused by nonsense mutations in retinol dehydrogenase RDH11. Hum Mol Genet 23, 5774-80 (2014).
2015
Wolfson, Y., Applegate, C. D., Strauss, R. W., Han, I. C. & Scholl, H. P. CRB1-Related Maculopathy With Cystoid Macular Edema. JAMA Ophthalmol 133, 1357-60 (2015).
Scholl, H. P. N. et al. Safety and Proof-of-Concept Study of Oral QLT091001 in Retinitis Pigmentosa Due to Inherited Deficiencies of Retinal Pigment Epithelial 65 Protein (RPE65) or Lecithin:Retinol Acyltransferase (LRAT). PLoS One 10, e0143846 (2015).
Collison, F. T. et al. Whole Exome Sequencing Identifies an Adult-Onset Case of Methylmalonic Aciduria and Homocystinuria Type C (cblC) with Non-Syndromic Bull's Eye Maculopathy. Ophthalmic Genet 36, 270-5 (2015).
2016
Strauss, R. W. et al. Assessment of estimated retinal atrophy progression in Stargardt macular dystrophy using spectral-domain optical coherence tomography. Br J Ophthalmol 100, 956-962 (2016).
Wolfson, Y., Fletcher, E., Strauss, R. W. & Scholl, H. P. N. Evidence of macular pigment in the central macula in albinism. Exp Eye Res 145, 468-471 (2016).