A citation-based method for searching scientific literature

Michalis Georgiou, Thomas Kane, Preena Tanna, Zaina Bouzia, Navjit Singh, Angelos Kalitzeos, Rupert W Strauss, Kaoru Fujinami, Michel Michaelides. Am J Ophthalmol 2020
Times Cited: 26







List of co-cited articles
336 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Clinical and molecular characteristics of childhood-onset Stargardt disease.
Kaoru Fujinami, Jana Zernant, Ravinder K Chana, Genevieve A Wright, Kazushige Tsunoda, Yoko Ozawa, Kazuo Tsubota, Anthony G Robson, Graham E Holder, Rando Allikmets,[...]. Ophthalmology 2015
102
46

A longitudinal study of Stargardt disease: quantitative assessment of fundus autofluorescence, progression, and genotype correlations.
Kaoru Fujinami, Noemi Lois, Rajarshi Mukherjee, Vikki A McBain, Kazushige Tsunoda, Kazuo Tsubota, Edwin M Stone, Fred W Fitzke, Catey Bunce, Anthony T Moore,[...]. Invest Ophthalmol Vis Sci 2013
91
42

A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlations.
Kaoru Fujinami, Noemi Lois, Alice E Davidson, Donna S Mackay, Chris R Hogg, Edwin M Stone, Kazushige Tsunoda, Kazuo Tsubota, Catey Bunce, Anthony G Robson,[...]. Am J Ophthalmol 2013
89
42

The Natural History of the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Studies: Design and Baseline Characteristics: ProgStar Report No. 1.
Rupert W Strauss, Alex Ho, Beatriz Muñoz, Artur V Cideciyan, José-Alain Sahel, Janet S Sunness, David G Birch, Paul S Bernstein, Michel Michaelides, Elias I Traboulsi,[...]. Ophthalmology 2016
99
34

Progression of Stargardt Disease as Determined by Fundus Autofluorescence in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 9).
Rupert W Strauss, Beatriz Muñoz, Alexander Ho, Anamika Jha, Michel Michaelides, Artur V Cideciyan, Isabelle Audo, David G Birch, Amir H Hariri, Muneeswar G Nittala,[...]. JAMA Ophthalmol 2017
55
34

Adaptive optics imaging of inherited retinal diseases.
Michalis Georgiou, Angelos Kalitzeos, Emily J Patterson, Alfredo Dubra, Joseph Carroll, Michel Michaelides. Br J Ophthalmol 2018
45
30

Clinical and molecular analysis of Stargardt disease with preserved foveal structure and function.
Kaoru Fujinami, Panagiotis I Sergouniotis, Alice E Davidson, Genevieve Wright, Ravinder K Chana, Kazushige Tsunoda, Kazuo Tsubota, Catherine A Egan, Anthony G Robson, Anthony T Moore,[...]. Am J Ophthalmol 2013
80
30

Progressive cone and cone-rod dystrophies: clinical features, molecular genetics and prospects for therapy.
Jasdeep S Gill, Michalis Georgiou, Angelos Kalitzeos, Anthony T Moore, Michel Michaelides. Br J Ophthalmol 2019
78
30

Stargardt disease: clinical features, molecular genetics, animal models and therapeutic options.
Preena Tanna, Rupert W Strauss, Kaoru Fujinami, Michel Michaelides. Br J Ophthalmol 2017
167
30

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
30

Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy.
Kamron N Khan, Melissa Kasilian, Omar A R Mahroo, Preena Tanna, Angelos Kalitzeos, Anthony G Robson, Kazushige Tsunoda, Takeshi Iwata, Anthony T Moore, Kaoru Fujinami,[...]. Ophthalmology 2018
31
30

Cross-Sectional and Longitudinal Assessment of the Ellipsoid Zone in Childhood-Onset Stargardt Disease.
Preena Tanna, Michalis Georgiou, Rupert W Strauss, Naser Ali, Neruban Kumaran, Angelos Kalitzeos, Kaoru Fujinami, Michel Michaelides. Transl Vis Sci Technol 2019
18
44

Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus.
N Lois, G E Holder, C Bunce, F W Fitzke, A C Bird. Arch Ophthalmol 2001
217
30

Clinical and genetic characteristics of late-onset Stargardt's disease.
Sarah C Westeneng-van Haaften, Camiel J F Boon, Frans P M Cremers, Lies H Hoefsloot, Anneke I den Hollander, Carel B Hoyng. Ophthalmology 2012
122
30

Macular dystrophies: clinical and imaging features, molecular genetics and therapeutic options.
Najiha Rahman, Michalis Georgiou, Kamron N Khan, Michel Michaelides. Br J Ophthalmol 2020
44
26

Progression of Stargardt Disease as Determined by Fundus Autofluorescence Over a 12-Month Period: ProgStar Report No. 11.
Rupert W Strauss, Xiangrong Kong, Alexander Ho, Anamika Jha, Sheila West, Michael Ip, Paul S Bernstein, David G Birch, Artur V Cideciyan, Michel Michaelides,[...]. JAMA Ophthalmol 2019
35
26

Quantitative fundus autofluorescence in recessive Stargardt disease.
Tomas R Burke, Tobias Duncker, Russell L Woods, Jonathan P Greenberg, Jana Zernant, Stephen H Tsang, R Theodore Smith, Rando Allikmets, Janet R Sparrow, François C Delori. Invest Ophthalmol Vis Sci 2014
123
26

Early-onset stargardt disease: phenotypic and genotypic characteristics.
Stanley Lambertus, Ramon A C van Huet, Nathalie M Bax, Lies H Hoefsloot, Frans P M Cremers, Camiel J F Boon, B Jeroen Klevering, Carel B Hoyng. Ophthalmology 2015
82
26

Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions.
Neruban Kumaran, Anthony T Moore, Richard G Weleber, Michel Michaelides. Br J Ophthalmol 2017
145
23

Adaptive Optics Retinal Imaging in CNGA3-Associated Achromatopsia: Retinal Characterization, Interocular Symmetry, and Intrafamilial Variability.
Michalis Georgiou, Katie M Litts, Angelos Kalitzeos, Christopher S Langlo, Thomas Kane, Navjit Singh, Melissa Kassilian, Nashila Hirji, Neruban Kumaran, Alfredo Dubra,[...]. Invest Ophthalmol Vis Sci 2019
30
23


Human embryonic stem cell-derived retinal pigment epithelium in patients with age-related macular degeneration and Stargardt's macular dystrophy: follow-up of two open-label phase 1/2 studies.
Steven D Schwartz, Carl D Regillo, Byron L Lam, Dean Eliott, Philip J Rosenfeld, Ninel Z Gregori, Jean-Pierre Hubschman, Janet L Davis, Gad Heilwell, Marc Spirn,[...]. Lancet 2015
753
23

Progression of retinal pigment epithelial atrophy in stargardt disease.
Vikki A McBain, John Townend, Noemi Lois. Am J Ophthalmol 2012
66
23

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy.
R Allikmets, N Singh, H Sun, N F Shroyer, A Hutchinson, A Chidambaram, B Gerrard, L Baird, D Stauffer, A Peiffer,[...]. Nat Genet 1997
23

Flecks in Recessive Stargardt Disease: Short-Wavelength Autofluorescence, Near-Infrared Autofluorescence, and Optical Coherence Tomography.
Janet R Sparrow, Marcela Marsiglia, Rando Allikmets, Stephen Tsang, Winston Lee, Tobias Duncker, Jana Zernant. Invest Ophthalmol Vis Sci 2015
76
23

Functional Relevance and Structural Correlates of Near Infrared and Short Wavelength Fundus Autofluorescence Imaging in ABCA4-Related Retinopathy.
Philipp L Müller, Johannes Birtel, Philipp Herrmann, Frank G Holz, Peter Charbel Issa, Martin Gliem. Transl Vis Sci Technol 2019
20
30

ULTRAWIDEFIELD AUTOFLUORESENCE IN ABCA4 STARGARDT DISEASE.
Michael A Klufas, Irena Tsui, SriniVas R Sadda, Hamid Hosseini, Steven D Schwartz. Retina 2018
22
27

Impact of segmentation density on spectral domain optical coherence tomography assessment in Stargardt disease.
Swetha Bindu Velaga, Muneeswar Gupta Nittala, Dennis Jenkins, J Melendez, Alexander Ho, R W Strauss, H P Scholl, SriniVas R Sadda. Graefes Arch Clin Exp Ophthalmol 2019
9
66

Residual Foveal Cone Structure in CNGB3-Associated Achromatopsia.
Christopher S Langlo, Emily J Patterson, Brian P Higgins, Phyllis Summerfelt, Moataz M Razeen, Laura R Erker, Maria Parker, Frederick T Collison, Gerald A Fishman, Christine N Kay,[...]. Invest Ophthalmol Vis Sci 2016
68
19

Quantitative Analysis of Retinal Structure Using Spectral-Domain Optical Coherence Tomography in RPGR-Associated Retinopathy.
James J L Tee, Joseph Carroll, Andrew R Webster, Michel Michaelides. Am J Ophthalmol 2017
25
20

Quantifying the Rate of Ellipsoid Zone Loss in Stargardt Disease.
Cindy X Cai, Jacob G Light, James T Handa. Am J Ophthalmol 2018
23
21

The clinical effect of homozygous ABCA4 alleles in 18 patients.
Kaoru Fujinami, Panagiotis I Sergouniotis, Alice E Davidson, Donna S Mackay, Kazushige Tsunoda, Kazuo Tsubota, Anthony G Robson, Graham E Holder, Anthony T Moore, Michel Michaelides,[...]. Ophthalmology 2013
46
19

The genetics of inherited macular dystrophies.
M Michaelides, D M Hunt, A T Moore. J Med Genet 2003
120
19

ISCEV Standard for full-field clinical electroretinography (2015 update).
Daphne L McCulloch, Michael F Marmor, Mitchell G Brigell, Ruth Hamilton, Graham E Holder, Radouil Tzekov, Michael Bach. Doc Ophthalmol 2015
937
19

Incidence of Atrophic Lesions in Stargardt Disease in the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Study: Report No. 5.
Rupert W Strauss, Beatriz Muñoz, Alex Ho, Anamika Jha, Michel Michaelides, Saddek Mohand-Said, Artur V Cideciyan, David Birch, Amir H Hariri, Muneeswar G Nittala,[...]. JAMA Ophthalmol 2017
36
19

Rescue of the Stargardt phenotype in Abca4 knockout mice through inhibition of vitamin A dimerization.
Peter Charbel Issa, Alun R Barnard, Philipp Herrmann, Ilyas Washington, Robert E MacLaren. Proc Natl Acad Sci U S A 2015
82
19

Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations.
Frans P M Cremers, Winston Lee, Rob W J Collin, Rando Allikmets. Prog Retin Eye Res 2020
95
19

Centrifugal expansion of fundus autofluorescence patterns in Stargardt disease over time.
Catherine A Cukras, Wai T Wong, Rafael Caruso, Denise Cunningham, Wadih Zein, Paul A Sieving. Arch Ophthalmol 2012
61
19

COMPARISON OF MANUAL AND SEMIAUTOMATED FUNDUS AUTOFLUORESCENCE ANALYSIS OF MACULAR ATROPHY IN STARGARDT DISEASE PHENOTYPE.
Laura Kuehlewein, Amir H Hariri, Alexander Ho, Laurie Dustin, Yulia Wolfson, Rupert W Strauss, Hendrik P N Scholl, SriniVas R Sadda. Retina 2016
43
19

Fundus autofluorescence in Stargardt macular dystrophy-fundus flavimaculatus.
Noemi Lois, Anthony S Halfyard, Alan C Bird, Graham E Holder, Frederick W Fitzke. Am J Ophthalmol 2004
129
19


Deep Phenotyping of PDE6C-Associated Achromatopsia.
Michalis Georgiou, Anthony G Robson, Navjit Singh, Nikolas Pontikos, Thomas Kane, Nashila Hirji, Caterina Ripamonti, Tryfon Rotsos, Alfredo Dubra, Angelos Kalitzeos,[...]. Invest Ophthalmol Vis Sci 2019
28
19

Retinal Structure in RPE65-Associated Retinal Dystrophy.
Neruban Kumaran, Michalis Georgiou, James W B Bainbridge, Mette Bertelsen, Michael Larsen, Fiona Blanco-Kelly, Carmen Ayuso, Hoai Viet Tran, Francis L Munier, Angelos Kalitzeos,[...]. Invest Ophthalmol Vis Sci 2020
16
31

Characterization of Retinal Structure in ATF6-Associated Achromatopsia.
Rebecca R Mastey, Michalis Georgiou, Christopher S Langlo, Angelos Kalitzeos, Emily J Patterson, Thomas Kane, Navjit Singh, Ajoy Vincent, Anthony T Moore, Stephen H Tsang,[...]. Invest Ophthalmol Vis Sci 2019
24
20

Assessment of estimated retinal atrophy progression in Stargardt macular dystrophy using spectral-domain optical coherence tomography.
Rupert W Strauss, Beatriz Muñoz, Yulia Wolfson, Raafay Sophie, Emily Fletcher, Millena G Bittencourt, Hendrik P N Scholl. Br J Ophthalmol 2016
33
19

Natural History Study of Retinal Structure, Progression, and Symmetry Using Ellipzoid Zone Metrics in RPGR-Associated Retinopathy.
James J L Tee, Yesa Yang, Angelos Kalitzeos, Andrew Webster, James Bainbridge, Michel Michaelides. Am J Ophthalmol 2019
29
15

Quantification of Ellipsoid Zone Changes in Retinitis Pigmentosa Using en Face Spectral Domain-Optical Coherence Tomography.
Amir H Hariri, Hong Yang Zhang, Alexander Ho, Peter Francis, Richard G Weleber, David G Birch, Frederick L Ferris, SriniVas R Sadda. JAMA Ophthalmol 2016
48
15

Lack of fundus autofluorescence to 488 nanometers from childhood on in patients with early-onset severe retinal dystrophy associated with mutations in RPE65.
Birgit Lorenz, Bettina Wabbels, Erika Wegscheider, Christian P Hamel, Wolfgang Drexler, Markus N Preising. Ophthalmology 2004
105
15

Retinal structure and function in achromatopsia: implications for gene therapy.
Venki Sundaram, Caroline Wilde, Jonathan Aboshiha, Jill Cowing, Colin Han, Christopher S Langlo, Ravinder Chana, Alice E Davidson, Panagiotis I Sergouniotis, James W Bainbridge,[...]. Ophthalmology 2014
117
15

Fine central macular dots associated with childhood-onset Stargardt Disease.
Kaoru Fujinami, Ravjit Singh, Joseph Carroll, Jana Zernant, Rando Allikmets, Michel Michaelides, Anthony T Moore. Acta Ophthalmol 2014
11
36


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.