Institution
Moorfields Eye Hospital
Healthcare•London, United Kingdom•
About: Moorfields Eye Hospital is a healthcare organization based out in London, United Kingdom. It is known for research contribution in the topics: Visual acuity & Glaucoma. The organization has 3721 authors who have published 6790 publications receiving 246004 citations.
Papers published on a yearly basis
Papers
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TL;DR: Inhibition of IDO activity improved the ability of HUVECs to stimulate allogeneic T‐cell responses and induce anergy in allospecific T cells (which can also act as regulatory cells).
90 citations
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Queen's University Belfast1, University of Regensburg2, University of Würzburg3, Oregon Health & Science University4, Erasmus University Rotterdam5, Netherlands Institute for Neuroscience6, Centra7, National Institutes of Health8, University of Melbourne9, University of Pennsylvania10, Tufts University11, Icahn School of Medicine at Mount Sinai12, Southampton General Hospital13, University of Southampton14, University of California, Los Angeles15, University of Pittsburgh16, University College London17, Moorfields Eye Hospital18, University of Michigan19, University of Cambridge20, Stavanger University Hospital21, Aristotle University of Thessaloniki22, Universidad Miguel Hernández de Elche23, University of London24
TL;DR: This study provides strong support for an association of the APOE gene with human longevity and the association with age was strongest in ε4 homozygotes.
Abstract: Variation in the apolipoprotein E gene (APOE) has been reported to be associated with longevity in humans. The authors assessed the allelic distribution of APOE isoforms e2, e3, and e4 among 10,623 participants from 15 case-control and cohort studies of age-related macular degeneration (AMD) in populations of European ancestry (study dates ranged from 1990 to 2009). The authors included only the 10,623 control subjects from these studies who were classified as having no evidence of AMD, since variation within the APOE gene has previously been associated with AMD. In an analysis stratified by study center, gender, and smoking status, there was a decreasing frequency of the APOE e4 isoform with increasing age (χ(2) for trend = 14.9 (1 df); P = 0.0001), with a concomitant increase in the e3 isoform (χ(2) for trend = 11.3 (1 df); P = 0.001). The association with age was strongest in e4 homozygotes; the frequency of e4 homozygosity decreased from 2.7% for participants aged 60 years or less to 0.8% for those over age 85 years, while the proportion of participants with the e3/e4 genotype decreased from 26.8% to 17.5% across the same age range. Gender had no significant effect on the isoform frequencies. This study provides strong support for an association of the APOE gene with human longevity.
90 citations
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TL;DR: Eyes with open-angle glaucoma showed twice as much loss of sensitivity in the spared hemifield as compared to eyes with low-tension glauca, and these differences were statistically significant.
90 citations
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TL;DR: Results indicate that mutations in the rds gene can be expressed as a macular dystrophy, with evidence of primary cone dysfunction and preservation of peripheral rod function.
90 citations
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TL;DR: Patients with a uveal melanoma too large for plaque therapy and an associated retinal detachment run a very high risk of developing rubeosis after proton beam radiotherapy and one third of individuals developing rubosis required enucleation for pain even if local tumour control was satisfactory.
Abstract: AIMS/BACKGROUND—Proton beam radiotherapy can effectively treat primary uveal melanomas of any size Some patients, however, develop adverse late effects following treatment and the purpose of this study was to determine which factors give rise to a poor local outcome
METHODS—The hospital records from a first cohort of 127 patients treated by protons from 1989 to 1992 were reviewed retrospectively The presence of rubeosis was selected as a measure of significant ocular damage Split file analysis was performed with 73 cases forming a test group with the remaining 54 cases acting as a validation group
RESULTS—Large tumour size and the presence of retinal detachment were significant, independent risk factors for developing rubeosis for both the test and validation groups These factors also predicted subsequent enucleation for uncontrolled ocular pain Patients with tumours too large to plaque and with an associated retinal detachment had a 90% chance of developing rubeosis within 4 years of proton beam radiotherapy
CONCLUSIONS—Patients with a uveal melanoma too large for plaque therapy and an associated retinal detachment run a very high risk of developing rubeosis after proton beam radiotherapy and one third of individuals developing rubeosis required enucleation for pain even if local tumour control was satisfactory
90 citations
Authors
Showing all 3754 results
Name | H-index | Papers | Citations |
---|---|---|---|
Rakesh K. Jain | 200 | 1467 | 177727 |
David Baker | 173 | 1226 | 109377 |
Nilesh J. Samani | 149 | 779 | 113545 |
Paul Mitchell | 146 | 1378 | 95659 |
Andrew J. Lees | 140 | 877 | 91605 |
Nick C. Fox | 139 | 748 | 93036 |
Alan J. Thompson | 131 | 718 | 82324 |
Martin N. Rossor | 128 | 670 | 95743 |
Nicholas W. Wood | 123 | 614 | 66270 |
Peter J. Goadsby | 123 | 946 | 73783 |
James A. Wells | 112 | 462 | 50847 |
Simon Cousens | 102 | 361 | 54579 |
Kailash P. Bhatia | 102 | 892 | 44372 |
Stafford L. Lightman | 98 | 714 | 36735 |
Simon Shorvon | 98 | 485 | 30672 |