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exaly
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Schools
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Department of Ophthalmology
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top-articles
Department of Ophthalmology
403
(top 1%)
papers
19.6K
(top 1%)
citations
70
(top 1%)
h
-index
126
(top 1%)
g
-index
413
all documents
21.3K
doc citations
2.4K
citing journals
Top Articles
#
Title
Journal
Year
Citations
1
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
Nature Genetics
2016
1,167
2
The Prevalence of Age-related Maculopathy in the Rotterdam Study
Ophthalmology
1995
729
3
The Rotterdam Study: objectives and design update
European Journal of Epidemiology
2007
644
4
International Photographic Classification and Grading System for Myopic Maculopathy
American Journal of Ophthalmology
2015
549
5
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Nature Genetics
2013
398
6
The Rotterdam Study: 2018 update on objectives, design and main results
European Journal of Epidemiology
2017
379
7
Distribution of Central Corneal Thickness and Its Association With Intraocular Pressure: The Rotterdam Study
American Journal of Ophthalmology
1997
378
8
Age-related macular degeneration
Nature Reviews Disease Primers
2021
340
9
Prevalence of Age-Related Macular Degeneration in Europe
Ophthalmology
2017
337
10
Increasing Prevalence of Myopia in Europe and the Impact of Education
Ophthalmology
2015
329
11
Primary Open-angle Glaucoma, Intraocular Pressure, and Systemic Blood Pressure in the General Elderly Population
Ophthalmology
1995
324
12
Objectives, design and main findings until 2020 from the Rotterdam Study
European Journal of Epidemiology
2020
314
13
Prevalence of refractive error in Europe: the European Eye Epidemiology (E3) Consortium
European Journal of Epidemiology
2015
306
14
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus
Nature Genetics
2013
269
15
Age-Related Macular Degeneration and Smoking
JAMA Ophthalmology
1996
254
16
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Nature Genetics
2018
239
17
Three Genome-wide Association Studies and a Linkage Analysis Identify HERC2 as a Human Iris Color Gene
American Journal of Human Genetics
2008
220
18
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
Nature Genetics
2014
212
19
Association of Axial Length With Risk of Uncorrectable Visual Impairment for Europeans With Myopia
JAMA Ophthalmology
2016
211
20
A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25
Nature Genetics
2010
204
21
A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14
Nature Genetics
2010
200
22
Homozygosity Mapping Reveals PDE6C Mutations in Patients with Early-Onset Cone Photoreceptor Disorders
American Journal of Human Genetics
2009
194
23
Determinants of optic disc characteristics in a general population☆The Rotterdam study1
Ophthalmology
1999
192
24
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression
Nature Genetics
2020
192
25
The Generation R Study: Biobank update 2015
European Journal of Epidemiology
2014
189
26
Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia
Nature Genetics
2020
180
27
Epidemiology of age-related maculopathy: a review
European Journal of Epidemiology
2003
174
28
Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma
Modern Pathology
2014
174
29
Comprehensive Study of the Clinical Phenotype of Germline
BAP1
Variant-Carrying Families Worldwide
Journal of the National Cancer Institute
2018
164
30
A functional variant in the CFI gene confers a high risk of age-related macular degeneration
Nature Genetics
2013
162
31
Incidence of Open-Angle Glaucoma in a General Elderly Population
Ophthalmology
2005
161
32
Association of Retinal Neurodegeneration on Optical Coherence Tomography With Dementia
JAMA Neurology
2018
160
33
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration
Nature Genetics
2013
158
34
IMI – Myopia Genetics Report
2019
156
35
Sclerotherapy for low-flow vascular malformations of the head and neck: A systematic review of sclerosing agents
Journal of Plastic, Reconstructive and Aesthetic Surgery
2016
155
36
Reliability of intraocular pressure measurement with the Goldmann applanation tonometer in epidemiological studies
Graefe's Archive for Clinical and Experimental Ophthalmology
1994
152
37
Effects of blood pressure lowering and intensive glucose control on the incidence and progression of retinopathy in patients with type 2 diabetes mellitus: a randomised controlled trial
Diabetologia
2009
150
38
Progressive Loss of Cones in Achromatopsia: An Imaging Study Using Spectral-Domain Optical Coherence Tomography
2010
149
39
Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides
Genetics in Medicine
2019
147
40
Uveal melanoma: Towards a molecular understanding
Progress in Retinal and Eye Research
2020
147
41
IMI Risk Factors for Myopia
2021
143
42
Oncogenic GNAQ mutations are not correlated with disease-free survival in uveal melanoma
British Journal of Cancer
2009
139
43
RETOUCH: The Retinal OCT Fluid Detection and Segmentation Benchmark and Challenge
IEEE Transactions on Medical Imaging
2019
139
44
Clinical and Cytogenetic Analyses in Uveal Melanoma
2006
138
45
Heterozygous NTF4 Mutations Impairing Neurotrophin-4 Signaling in Patients with Primary Open-Angle Glaucoma
American Journal of Human Genetics
2009
134
46
Epidemiology of Age-related Maculopathy
Epidemiologic Reviews
1995
133
47
Long-term Follow-up of Endothelial Cell Change after Artisan Phakic Intraocular Lens Implantation
Ophthalmology
2008
131
48
GPR179 Is Required for Depolarizing Bipolar Cell Function and Is Mutated in Autosomal-Recessive Complete Congenital Stationary Night Blindness
American Journal of Human Genetics
2012
131
49
Concurrent Loss of Chromosome Arm 1p and Chromosome 3 Predicts a Decreased Disease-Free Survival in Uveal Melanoma Patients
2005
129
50
Risk of bilateral visual impairment in individuals with amblyopia: the Rotterdam study
British Journal of Ophthalmology
2007
121
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