| Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout mice J Weng, NL Mata, SM Azarian, RT Tzekov, DG Birch, GH Travis Cell 98 (1), 13-23, 1999 | 993 | 1999 |
| A randomized controlled trial of early dietary supply of long-chain polyunsaturated fatty acids and mental development in term infants EE Birch, S Garfield, DR Hoffman, R Uauy, DG Birch Developmental medicine and child neurology 42 (3), 174-181, 2000 | 942 | 2000 |
| Effect of dietary omega-3 fatty acids on retinal function of very-low-birth-weight neonates RD Uauy, DG Birch, EE Birch, JE Tyson, DR Hoffman Pediatric research 28 (5), 485-492, 1990 | 753 | 1990 |
| Visual acuity and the essentiality of docosahexaenoic acid and arachidonic acid in the diet of term infants EE Birch, DR Hoffman, R Uauy, DG Birch, C Prestidge Pediatric research 44 (2), 201-209, 1998 | 704 | 1998 |
| Essential fatty acids in visual and brain development R Uauy, DR Hoffman, P Peirano, DG Birch, EE Birch Lipids 36 (9), 885-895, 2001 | 624 | 2001 |
| Dietary essential fatty acid supply and visual acuity development. EE Birch, DG Birch, DR Hoffman, R Uauy Investigative ophthalmology & visual science 33 (11), 3242-3253, 1992 | 550 | 1992 |
| Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness NT Bech-Hansen, MJ Naylor, TA Maybaum, RL Sparkes, B Koop, ... Nature genetics 26 (3), 319-323, 2000 | 421 | 2000 |
| Retinal development in very-low-birth-weight infants fed diets differing in omega-3 fatty acids. DG Birch, EE Birch, DR Hoffman, RD Uauy Investigative Ophthalmology & Visual Science 33 (8), 2365-2376, 1992 | 407 | 1992 |
| Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies MM Sohocki, SP Daiger, SJ Bowne, JA Rodriquez, H Northrup, ... Human mutation 17 (1), 42-51, 2001 | 396 | 2001 |
| Five-year safety and performance results from the Argus II retinal prosthesis system clinical trial L da Cruz, JD Dorn, MS Humayun, G Dagnelie, J Handa, PO Barale, ... Ophthalmology 123 (10), 2248-2254, 2016 | 393 | 2016 |
| Natural course of retinitis pigmentosa over a three-year interval EL Berson, MA Sandberg, B Rosner, DG Birch, AH Hanson American journal of ophthalmology 99 (3), 240-251, 1985 | 377 | 1985 |
| Ciliary neurotrophic factor delivered by encapsulated cell intraocular implants for treatment of geographic atrophy in age-related macular degeneration K Zhang, JJ Hopkins, JS Heier, DG Birch, LS Halperin, TA Albini, ... Proceedings of the National Academy of Sciences 108 (15), 6241-6245, 2011 | 361 | 2011 |
| A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene MM Sohocki, LS Sullivan, HA Mintz-Hittner, D Birch, JR Heckenlively, ... The American Journal of Human Genetics 63 (5), 1307-1315, 1998 | 344 | 1998 |
| Standardized full-field electroretinography: normal values and their variation with age DG Birch, JL Anderson Archives of ophthalmology 110 (11), 1571-1576, 1992 | 337 | 1992 |
| Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families LS Sullivan, SJ Bowne, DG Birch, D Hughbanks-Wheaton, ... Investigative ophthalmology & visual science 47 (7), 3052-3064, 2006 | 331 | 2006 |
| Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis MM Sohocki, SJ Bowne, LS Sullivan, S Blackshaw, CL Cepko, AM Payne, ... Nature genetics 24 (1), 79-83, 2000 | 324 | 2000 |
| Visual and brain function measurements in studies of n-3 fatty acid requirements of infants R Uauy, E Birch, D Birch, P Peirano The Journal of pediatrics 120 (4), S168-S180, 1992 | 308 | 1992 |
| Breast-feeding and optimal visual development E Birch, D Birch, D Hoffman, L Hale, M Everett, R Uauy Journal of Pediatric Ophthalmology & Strabismus 30 (1), 33-38, 1993 | 305 | 1993 |
| Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice Z Yang, Y Chen, C Lillo, J Chien, Z Yu, M Michaelides, M Klein, ... The Journal of clinical investigation 118 (8), 2908-2916, 2008 | 301 | 2008 |
| Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa SJ Bowne, LS Sullivan, SH Blanton, CL Cepko, S Blackshaw, DG Birch, ... Human molecular genetics 11 (5), 559-568, 2002 | 295 | 2002 |
