| Genetic basis of inherited retinal disease in a molecularly characterized cohort of more than 3000 families from the United Kingdom N Pontikos, G Arno, N Jurkute, E Schiff, R Ba-Abbad, S Malka, A Gimenez, ... Ophthalmology 127 (10), 1384-1394, 2020 | 149 | 2020 |
| Postoperative complications after primary adult optical penetrating keratoplasty: prevalence and impact on graft survival MD Wagoner, R Ba-Abbad, M Al-Mohaimeed, S Al-Swailem, ... Cornea 28 (4), 385-394, 2009 | 89 | 2009 |
| Corneal transplant survival after onset of severe endothelial rejection MD Wagoner, R Ba-Abbad, JE Sutphin, MB Zimmerman Ophthalmology 114 (9), 1630-1636. e1, 2007 | 40 | 2007 |
| Mutations in CACNA2D4 Cause Distinctive Retinal Dysfunction in Humans Rola Ba-Abbad, Gavin Arno, Keren Carss, Kathleen Stirrups, Christopher J ... Ophthalmology, 2015 | 38* | 2015 |
| Penetrating keratoplasty for keratoconus with or without vernal keratoconjunctivitis MD Wagoner, R Ba-Abbad Cornea 28 (1), 14-18, 2009 | 35 | 2009 |
| Clinical characteristics of early retinal disease due to CDHR1 mutation R Ba-Abbad, PI Sergouniotis, V Plagnol, AG Robson, M Michaelides, ... Molecular vision 19, 2250, 2013 | 27 | 2013 |
| Retinal architecture in RGS9-and R9AP-associated retinal dysfunction (bradyopsia) RW Strauss, AM Dubis, RF Cooper, R Ba-Abbad, AT Moore, AR Webster, ... American Journal of Ophthalmology 160 (6), 1269-1275. e1, 2015 | 16 | 2015 |
| CNGB1‐related rod‐cone dystrophy: A mutation review and update M Nassisi, VM Smirnov, C Solis Hernandez, S Mohand‐Saïd, ... Human mutation 42 (6), 641-666, 2021 | 15 | 2021 |
| Prph2 mutations as a cause of electronegative ERG R Ba-Abbad, AG Robson, YC Yap, AT Moore, AR Webster, GE Holder Retina 34 (6), 1235-1243, 2014 | 14 | 2014 |
| Prph2 mutations as a cause of electronegative ERG R Ba-Abbad, AG Robson, YC Yap, AT Moore, AR Webster, GE Holder Retina 34 (6), 1235-1243, 2014 | 14 | 2014 |
| King Khaled Eye Specialist Hospital Corneal Transplant Study Group Postoperative complications after primary adult optical penetrating keratoplasty: prevalence and impact on … MD Wagoner, R Ba-Abbad, M Al-Mohaimeed, S Al-Swailem, ... Cornea 28 (4), 385-394, 2009 | 14 | 2009 |
| Bilateral optic disc swelling as the presenting sign of pheochromocytoma in a child RA Ba-Abbad, SR Nowilaty The Medscape Journal of Medicine 10 (7), 176, 2008 | 14 | 2008 |
| Macula-predominant retinopathy associated with biallelic variants in RDH12 R Ba-Abbad, G Arno, AG Robson, K Bouras, M Georgiou, G Wright, ... Ophthalmic Genetics 41 (6), 612-615, 2020 | 12 | 2020 |
| A genetic and clinical study of individuals with nonsyndromic retinopathy consequent upon sequence variants in HGSNAT, the gene associated with Sanfilippo C … ER Schiff, M Daich Varela, AG Robson, K Pierpoint, R Ba‐Abbad, S Nutan, ... American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2020 | 11 | 2020 |
| Clinical and genetic findings in CTNNA1-associated macular pattern dystrophy A Tanner, HW Chan, JS Pulido, G Arno, R Ba-Abbad, N Jurkute, ... Ophthalmology 128 (6), 952-955, 2021 | 10 | 2021 |
| Clinical features of a retinopathy associated with a dominant allele of the RGR gene R Ba-Abbad, M Leys, X Wang, C Chakarova, N Waseem, KJ Carss, ... Investigative Ophthalmology & Visual Science 59 (12), 4812-4820, 2018 | 10 | 2018 |
| Broadening INPP5E phenotypic spectrum: detection of rare variants in syndromic and non-syndromic IRD R Sangermano, I Deitch, VG Peter, R Ba-Abbad, EM Place, ... NPJ genomic medicine 6 (1), 53, 2021 | 9 | 2021 |
| Isolated rod dysfunction associated with a novel genotype of CNGB1 R Ba-Abbad, GE Holder, AG Robson, MM Neveu, N Waseem, G Arno, ... American journal of ophthalmology case reports 14, 83-86, 2019 | 9 | 2019 |
| King Khaled Eye Specialist Hospital Cornea Transplant Study Group. Penetrating keratoplasty for keratoconus with or without vernal keratoconjunctivitis MD Wagoner, R Ba-Abbad Cornea 28 (1), 14-18, 2009 | 9 | 2009 |
| Ceramide synthase TLCD3B is a novel gene associated with human recessive retinal dystrophy RE Bertrand, J Wang, KH Xiong, C Thangavel, X Qian, R Ba-Abbad, ... Genetics in Medicine 23 (3), 488-497, 2021 | 8 | 2021 |
Prof. Graham E HolderSingapore, UCL, Moorfields, Sydney, Kings, Brook, Astonبريد إلكتروني تم التحقق منه على moorfields.nhs.uk
