| Nrl is required for rod photoreceptor development AJ Mears, M Kondo, PK Swain, Y Takada, RA Bush, TL Saunders, ... Nature genetics 29 (4), 447-452, 2001 | 1007 | 2001 |
| Ciliary neurotrophic factor (CNTF) for human retinal degeneration: phase I trial of CNTF delivered by encapsulated cell intraocular implants PA Sieving, RC Caruso, W Tao, HR Coleman, DJS Thompson, ... Proceedings of the National Academy of Sciences 103 (10), 3896-3901, 2006 | 702 | 2006 |
| Retinopathy induced in mice by targeted disruption of the rhodopsin gene MM Humphries, D Rancourt, GJ Farrar, P Kenna, M Hazel, RA Bush, ... Nature genetics 15 (2), 216-219, 1997 | 640 | 1997 |
| A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy K Zhang, M Kniazeva, M Han, W Li, Z Yu, Z Yang, Y Li, ML Metzker, ... Nature genetics 27 (1), 89-93, 2001 | 522 | 2001 |
| Multiple evanescent white dot syndrome: I. Clinical findings LM Jampol, PA Sieving, D Pugh, GA Fishman, H Gilbert Archives of ophthalmology 102 (5), 671-674, 1984 | 511 | 1984 |
| Push–pull model of the primate photopic electroretinogram: A role for hyperpolarizing neurons in shaping the b-wave PA Sieving, K Murayama, F Naarendorp Visual neuroscience 11 (3), 519-532, 1994 | 481 | 1994 |
| Mutations in the CNGB3 gene encoding the β-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to … S Kohl, B Baumann, M Broghammer, H Jägle, P Sieving, U Kellner, ... Human molecular genetics 9 (14), 2107-2116, 2000 | 358 | 2000 |
| PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23 ZM Ahmed, S Riazuddin, J Ahmad, SL Bernstein, Y Guo, MF Sabar, ... Human molecular genetics 12 (24), 3215-3223, 2003 | 327 | 2003 |
| A proximal retinal component in the primate photopic ERG a-wave. RA Bush, PA Sieving Investigative ophthalmology & visual science 35 (2), 635-645, 1994 | 324 | 1994 |
| Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration DA Thompson, P Gyürüs, LL Fleischer, EL Bingham, CL McHenry, ... Investigative ophthalmology & visual science 41 (13), 4293-4299, 2000 | 303 | 2000 |
| Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration PK Swain, S Chen, QL Wang, LM Affatigato, CL Coats, KD Brady, ... Neuron 19 (6), 1329-1336, 1997 | 298 | 1997 |
| Treatment with isotretinoin inhibits lipofuscin accumulation in a mouse model of recessive Stargardt's macular degeneration RA Radu, NL Mata, S Nusinowitz, X Liu, PA Sieving, GH Travis Proceedings of the National Academy of Sciences 100 (8), 4742-4747, 2003 | 292 | 2003 |
| Biology and therapy of inherited retinal degenerative disease: insights from mouse models S Veleri, CH Lazar, B Chang, PA Sieving, E Banin, A Swaroop Disease models & mechanisms 8 (2), 109-129, 2015 | 287 | 2015 |
| P23H rhodopsin transgenic rat: correlation of retinal function with histopathology S Machida, M Kondo, JA Jamison, NW Khan, LT Kononen, T Sugawara, ... Investigative ophthalmology & visual science 41 (10), 3200-3209, 2000 | 282 | 2000 |
| A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa DK Breuer, BM Yashar, E Filippova, S Hiriyanna, RH Lyons, AJ Mears, ... The American Journal of Human Genetics 70 (6), 1545-1554, 2002 | 279 | 2002 |
| CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia S Kohl, B Varsanyi, GA Antunes, B Baumann, CB Hoyng, H Jägle, ... European Journal of Human Genetics 13 (3), 302-308, 2005 | 266 | 2005 |
| CNTF and retina R Wen, W Tao, Y Li, PA Sieving Progress in retinal and eye research 31 (2), 136-151, 2012 | 249 | 2012 |
| Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage disease GR Abecasis, BM Yashar, Y Zhao, NM Ghiasvand, S Zareparsi, ... The American Journal of Human Genetics 74 (3), 482-494, 2004 | 235 | 2004 |
| Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the … A Swaroop, QL Wang, W Wu, J Cook, C Coats, S Xu, S Chen, DJ Zack, ... Human molecular genetics 8 (2), 299-305, 1999 | 231 | 1999 |
| Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophy DA Thompson, Y Li, CL McHenry, TJ Carlson, X Ding, PA Sieving, ... Nature genetics 28 (2), 123-124, 2001 | 228 | 2001 |
Samuel G. JacobsonProfessor of Ophthalmology, University of PennsylvaniaVerified email at mail.med.upenn.edu
