| Macular recovery after retinal detachment H Abouzeid, TJ Wolfensberger Acta ophthalmologica Scandinavica 84 (5), 597-605, 2006 | 137 | 2006 |
| Mutations in the SPARC-related modular calcium-binding protein 1 gene, SMOC1, cause waardenburg anophthalmia syndrome H Abouzeid, G Boisset, T Favez, M Youssef, I Marzouk, N Shakankiry, ... The American Journal of Human Genetics 88 (1), 92-98, 2011 | 83 | 2011 |
| 106Ruthenium brachytherapy for retinoblastoma H Abouzeid, R Moeckli, MC Gaillard, M Beck-Popovic, A Pica, L Zografos, ... International Journal of Radiation Oncology* Biology* Physics 71 (3), 821-828, 2008 | 82 | 2008 |
| Femtosecond‐laser assisted cataract surgery: a review H Abouzeid, W Ferrini Acta ophthalmologica 92 (7), 597-603, 2014 | 81 | 2014 |
| ALDH1A3 loss of function causes bilateral anophthalmia/microphthalmia and hypoplasia of the optic nerve and optic chiasm M Yahyavi, H Abouzeid, G Gawdat, AS De Preux, T Xiao, T Bardakjian, ... Human molecular genetics 22 (16), 3250-3258, 2013 | 79 | 2013 |
| New developments in external beam radiotherapy for retinoblastoma: from lens to normal tissue‐sparing techniques FL Munier, J Verwey, A Pica, A Balmer, L Zografos, H Abouzeid, ... Clinical & experimental ophthalmology 36 (1), 78-89, 2008 | 78 | 2008 |
| VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: The first description of a VAX1 phenotype in humans AM Slavotinek, R Chao, T Vacik, M Yahyavi, H Abouzeid, T Bardakjian, ... Human mutation 33 (2), 364-368, 2012 | 72 | 2012 |
| PAX6 aniridia and interhemispheric brain anomalies H Abouzeid, MA Youssef, N ElShakankiri, P Hauser, FL Munier, ... Molecular vision 15, 2074, 2009 | 72 | 2009 |
| Mutations in the spliceosome component CWC27 cause retinal degeneration with or without additional developmental anomalies M Xu, YA Xie, H Abouzeid, CT Gordon, A Fiorentino, Z Sun, A Lehman, ... The American Journal of Human Genetics 100 (4), 592-604, 2017 | 70 | 2017 |
| Submacular fluid after encircling buckle surgery for inferior macula‐off retinal detachment in young patients H Abouzeid, K Becker, FG Holz, TJ Wolfensberger Acta ophthalmologica 87 (1), 96-99, 2009 | 44 | 2009 |
| Germline mutations in retinoma patients: relevance to low-penetrance and low-expressivity molecular basis H Abouzeid, DF Schorderet, A Balmer, FL Munier Molecular vision 15, 771, 2009 | 40 | 2009 |
| Phenotypic variability of retinocytomas: preregression and postregression growth patterns H Abouzeid, A Balmer, AP Moulin, A Mataftsi, L Zografos, FL Munier British journal of ophthalmology 96 (6), 884-889, 2012 | 34 | 2012 |
| Modern cataract surgery for radiation-induced cataracts in retinoblastoma IM Osman, H Abouzeid, A Balmer, MC Gaillard, P Othenin-Girard, A Pica, ... British journal of ophthalmology 95 (2), 227-230, 2011 | 34 | 2011 |
| RAX and anophthalmia in humans: evidence of brain anomalies H Abouzeid, MA Youssef, N Bayoumi, N ElShakankiri, I Marzouk, ... Molecular vision 18, 1449, 2012 | 33 | 2012 |
| Anterior uveitis and cataract after rubella vaccination: a case report of a 12-month-old girl W Ferrini, V Aubert, A Balmer, FL Munier, H Abouzeid Pediatrics 132 (4), e1035-e1038, 2013 | 28 | 2013 |
| Trilateral retinoblastoma with suprasellar tumor and associated pineal cyst MB Popovic, M Diezi, H Kuchler, H Abouzeid, P Maeder, A Balmer, ... Journal of pediatric hematology/oncology 29 (1), 53-56, 2007 | 28 | 2007 |
| Mutations in ALDH1A3 Represent a Frequent Cause of Microphthalmia/Anophthalmia in Consanguineous Families H Abouzeid, T Favez, A Schmid, C Agosti, M Youssef, I Marzouk, ... Human mutation 35 (8), 949-953, 2014 | 26 | 2014 |
| A G1103R Mutation in CRB1 is Co-Inherited with High Hyperopia and Leber Congenital Amaurosis H Abouzeid, Y Li, IH Maumenee, S Dharmaraj, O Sundin Ophthalmic genetics 27 (1), 15-20, 2006 | 25 | 2006 |
| Ten novel RB1 gene mutations in patients with retinoblastoma H Abouzeid, FL Munier, F Thonney, DF Schorderet Mol Vis 13 (1740), 5, 2007 | 24 | 2007 |
| A new locus for congenital cataract, microcornea, microphthalmia, and atypical iris coloboma maps to chromosome 2 H Abouzeid, FM Meire, I Osman, N ElShakankiri, S Bolay, FL Munier, ... Ophthalmology 116 (1), 154-162. e1, 2009 | 21 | 2009 |
Daniel SchorderetProfessor, faculty of Biology and Medicine, Lausanne, SwitzerlandBestätigte E-Mail-Adresse bei unil.ch
