PubRank

Andrew J Lotery

Author PubWeight™ 62.53‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet 2011 13.25
2 Ranibizumab versus bevacizumab to treat neovascular age-related macular degeneration: one-year findings from the IVAN randomized trial. Ophthalmology 2012 4.70
3 Alternative treatments to inhibit VEGF in age-related choroidal neovascularisation: 2-year findings of the IVAN randomised controlled trial. Lancet 2013 4.35
4 Seven new loci associated with age-related macular degeneration. Nat Genet 2013 3.81
5 Missense variations in the fibulin 5 gene and age-related macular degeneration. N Engl J Med 2004 3.15
6 Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. Nat Genet 2010 2.75
7 Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders. Am J Hum Genet 2009 1.72
8 Common genetic variants associated with open-angle glaucoma. Hum Mol Genet 2011 1.58
9 Missense mutations in a retinal pigment epithelium protein, bestrophin-1, cause retinitis pigmentosa. Am J Hum Genet 2009 1.53
10 Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. Nat Genet 2013 1.49
11 Association of HLA class I and class II polymorphisms with age-related macular degeneration. Invest Ophthalmol Vis Sci 2005 1.40
12 Clinical course, genetic etiology, and visual outcome in cone and cone-rod dystrophy. Ophthalmology 2012 1.34
13 Support for the involvement of complement factor I in age-related macular degeneration. Eur J Hum Genet 2010 1.20
14 Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people. Am J Epidemiol 2011 1.19
15 Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3. Hum Mol Genet 2012 1.18
16 Evidence of association of APOE with age-related macular degeneration: a pooled analysis of 15 studies. Hum Mutat 2011 1.17
17 Common spectral domain OCT and electrophysiological findings in different pattern dystrophies. Br J Ophthalmol 2013 1.13
18 Allelic variation of the FRMD7 gene in congenital idiopathic nystagmus. Arch Ophthalmol 2007 1.02
19 Localization of complement 1 inhibitor (C1INH/SERPING1) in human eyes with age-related macular degeneration. Exp Eye Res 2009 0.99
20 Ranibizumab in myopic choroidal neovascularization: the 12-month results from the REPAIR study. Ophthalmology 2013 0.92
21 The complement component 5 gene and age-related macular degeneration. Ophthalmology 2009 0.92
22 Optimisation of polymer scaffolds for retinal pigment epithelium (RPE) cell transplantation. Br J Ophthalmol 2009 0.88
23 Clinical implications of old and new genes for open-angle glaucoma. Ophthalmology 2011 0.88
24 Fcγ receptor upregulation is associated with immune complex inflammation in the mouse retina and early age-related macular degeneration. Invest Ophthalmol Vis Sci 2014 0.87
25 Idiopathic juxtafoveolar retinal telangiectasis in monozygotic twins. Br J Ophthalmol 2007 0.86
26 Electroretinographic abnormalities in parents of patients with Leber congenital amaurosis who have heterozygous GUCY2D mutations. Arch Ophthalmol 2002 0.85
27 Age-related macular degeneration is associated with the HLA-Cw*0701 Genotype and the natural killer cell receptor AA haplotype. Invest Ophthalmol Vis Sci 2008 0.84
28 Structural effects of fibulin 5 missense mutations associated with age-related macular degeneration and cutis laxa. Invest Ophthalmol Vis Sci 2009 0.83
29 Case of Stargardt disease caused by uniparental isodisomy. Arch Ophthalmol 2006 0.83
30 Fibulin 5 forms a compact dimer in physiological solutions. J Biol Chem 2009 0.83
31 Successful treatment of choroidal neovascularization secondary to sorsby fundus dystrophy with intravitreal bevacizumab. Retin Cases Brief Rep 2011 0.82
32 Age-related macular degeneration and modification of systemic complement factor H production through liver transplantation. Ophthalmology 2013 0.80
33 Developing methacrylate-based copolymers as an artificial Bruch's membrane substitute. J Biomed Mater Res A 2012 0.80
34 A novel GUCY2D mutation, V933A, causes central areolar choroidal dystrophy. Invest Ophthalmol Vis Sci 2012 0.80
35 Characterization of rabbit myocilin: Implications for human myocilin glycosylation and signal peptide usage. BMC Genet 2003 0.79
36 Generation of light-sensitive photoreceptor phenotypes by genetic modification of human adult ocular stem cells with Crx. Invest Ophthalmol Vis Sci 2009 0.79
37 The chemistry of retinal transplantation: the influence of polymer scaffold properties on retinal cell adhesion and control. Br J Ophthalmol 2010 0.79
38 Vitamin A deficiency-related retinopathy after bariatric surgery. Graefes Arch Clin Exp Ophthalmol 2011 0.78
39 Retinal pigment epithelial tear following intravitreal bevacizumab for choroidal neovascular membrane due to age-related macular degeneration. Br J Ophthalmol 2007 0.75
40 Genetic variants within chromosome 4q28.3 are not reproducibly associated with age-related macular degeneration (AMD). Acta Ophthalmol 2010 0.75
41 Autosomal dominant early onset aponeurotic ptosis and corneal limbal vascularization in a three-generation family. Ophthal Plast Reconstr Surg 2007 0.75
42 [Familial choroideremia--case report]. Oftalmologia 2009 0.75
43 Diagnostic and therapeutic challenges. Retina 2009 0.75
44 Genetics update of macular diseases. Ophthalmol Clin North Am 2002 0.75