| Retinitis pigmentosa and allied diseases: numerous diseases, genes, and inheritance patterns C Rivolta, D Sharon, MM DeAngelis, TP Dryja Human molecular genetics 11 (10), 1219-1227, 2002 | 429 | 2002 |
| Worldwide carrier frequency and genetic prevalence of autosomal recessive inherited retinal diseases M Hanany, C Rivolta, D Sharon Proceedings of the National Academy of Sciences 117 (5), 2710-2716, 2020 | 292 | 2020 |
| The olfactory receptor gene superfamily: data mining, classification, and nomenclature G Glusman, A Bahar, D Sharon, Y Pilpel, J White, D Lancet Mammalian genome 11, 1016-1023, 2000 | 267 | 2000 |
| RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosa D Sharon, MA Sandberg, VW Rabe, M Stillberger, TP Dryja, EL Berson The American Journal of Human Genetics 73 (5), 1131-1146, 2003 | 259 | 2003 |
| Profile of the genes expressed in the human peripheral retina, macula, and retinal pigment epithelium determined through serial analysis of gene expression (SAGE) D Sharon, S Blackshaw, CL Cepko, TP Dryja Proceedings of the National Academy of Sciences 99 (1), 315-320, 2002 | 199 | 2002 |
| Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration D Sharon, MA Sandberg, RC Caruso, EL Berson, TP Dryja Archives of ophthalmology 121 (9), 1316-1323, 2003 | 186 | 2003 |
| Primate evolution of an olfactory receptor cluster: diversification by gene conversion and recent emergence of pseudogenes D Sharon, G Glusman, Y Pilpel, M Khen, F Gruetzner, T Haaf, D Lancet Genomics 61 (1), 24-36, 1999 | 153 | 1999 |
| Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness I Audo, K Bujakowska, E Orhan, CM Poloschek, S Defoort-Dhellemmes, ... The American Journal of Human Genetics 90 (2), 321-330, 2012 | 148 | 2012 |
| A missense mutation in DHDDS, encoding dehydrodolichyl diphosphate synthase, is associated with autosomal-recessive retinitis pigmentosa in Ashkenazi Jews L Zelinger, E Banin, A Obolensky, L Mizrahi-Meissonnier, A Beryozkin, ... The American Journal of Human Genetics 88 (2), 207-215, 2011 | 143 | 2011 |
| Whole genome sequencing in patients with retinitis pigmentosa reveals pathogenic DNA structural changes and NEK2 as a new disease gene KM Nishiguchi, RG Tearle, YP Liu, EC Oh, N Miyake, P Benaglio, ... Proceedings of the National Academy of Sciences 110 (40), 16139-16144, 2013 | 142 | 2013 |
| An integrated genetic linkage map of avocado D Sharon, PB Cregan, S Mhameed, M Kusharska, J Hillel, E Lahav, ... Theoretical and Applied Genetics 95, 911-921, 1997 | 135 | 1997 |
| Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics M Khan, SS Cornelis, MD Pozo-Valero, L Whelan, EH Runhart, K Mishra, ... Genetics in Medicine 22 (7), 1235-1246, 2020 | 134 | 2020 |
| Gene augmentation therapy restores retinal function and visual behavior in a sheep model of CNGA3 achromatopsia E Banin, E Gootwine, A Obolensky, R Ezra-Elia, A Ejzenberg, L Zelinger, ... Molecular therapy 23 (9), 1423-1433, 2015 | 133 | 2015 |
| BBS1 mutations in a wide spectrum of phenotypes ranging from nonsyndromic retinitis pigmentosa to Bardet-Biedl syndrome A Estrada-Cuzcano, RK Koenekoop, A Senechal, EBW De Baere, ... Archives of ophthalmology 130 (11), 1425-1432, 2012 | 131 | 2012 |
| Inherited retinal diseases: linking genes, disease-causing variants, and relevant therapeutic modalities N Schneider, Y Sundaresan, P Gopalakrishnan, A Beryozkin, M Hanany, ... Progress in retinal and eye research 89, 101029, 2022 | 122 | 2022 |
| Exome sequencing and cis-regulatory mapping identify mutations in MAK, a gene encoding a regulator of ciliary length, as a cause of retinitis pigmentosa RK Özgül, AM Siemiatkowska, D Yücel, CA Myers, RWJ Collin, ... The American Journal of Human Genetics 89 (2), 253-264, 2011 | 121 | 2011 |
| Application of DNA fingerprints for identification and genetic analyses of mango (Mangifera indica) genotypes A Adato, D Sharon, U Lavi, J Hillel, S Gazit Journal of the American Society for Horticultural Science 120 (2), 259-264, 1995 | 121 | 1995 |
| Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosa D Bandah-Rozenfeld, L Mizrahi-Meissonnier, C Farhy, A Obolensky, ... The American Journal of Human Genetics 87 (3), 382-391, 2010 | 120 | 2010 |
| Mutations in IMPG2, encoding interphotoreceptor matrix proteoglycan 2, cause autosomal-recessive retinitis pigmentosa D Bandah-Rozenfeld, RWJ Collin, E Banin, LI Van Den Born, KLM Coene, ... The American Journal of Human Genetics 87 (2), 199-208, 2010 | 119 | 2010 |
| X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual function D Sharon, GAP Bruns, TL McGee, MA Sandberg, EL Berson, TP Dryja Investigative ophthalmology & visual science 41 (9), 2712-2721, 2000 | 115 | 2000 |
Samer KhatebOphthalmologist - Hadassah Medical CenterCorreu electrònic verificat a mail.huji.ac.il
