A citation-based method for searching scientific literature

Adam M Dubis, Robert F Cooper, Jonathan Aboshiha, Christopher S Langlo, Venki Sundaram, Benjamin Liu, Frederick Collison, Gerald A Fishman, Anthony T Moore, Andrew R Webster, Alfredo Dubra, Joseph Carroll, Michel Michaelides. Invest Ophthalmol Vis Sci 2014
Times Cited: 54







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



Times Cited
  Times     Co-cited
Similarity


In vivo imaging of human cone photoreceptor inner segments.
Drew Scoles, Yusufu N Sulai, Christopher S Langlo, Gerald A Fishman, Christine A Curcio, Joseph Carroll, Alfredo Dubra. Invest Ophthalmol Vis Sci 2014
228
64

Photoreceptor structure and function in patients with congenital achromatopsia.
Mohamed A Genead, Gerald A Fishman, Jungtae Rha, Adam M Dubis, Daniela Maria O Bonci, Alfredo Dubra, Edwin M Stone, Maureen Neitz, Joseph Carroll. Invest Ophthalmol Vis Sci 2011
119
57

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
55

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
44

A prospective longitudinal study of retinal structure and function in achromatopsia.
Jonathan Aboshiha, Adam M Dubis, Jill Cowing, Rachel T A Fahy, Venki Sundaram, James W Bainbridge, Robin R Ali, Alfredo Dubra, Marko Nardini, Andrew R Webster,[...]. Invest Ophthalmol Vis Sci 2014
53
43

Human photoreceptor topography.
C A Curcio, K R Sloan, R E Kalina, A E Hendrickson. J Comp Neurol 1990
40

Noninvasive imaging of the human rod photoreceptor mosaic using a confocal adaptive optics scanning ophthalmoscope.
Alfredo Dubra, Yusufu Sulai, Jennifer L Norris, Robert F Cooper, Adam M Dubis, David R Williams, Joseph Carroll. Biomed Opt Express 2011
215
38

Reflective afocal broadband adaptive optics scanning ophthalmoscope.
Alfredo Dubra, Yusufu Sulai. Biomed Opt Express 2011
210
38

A nonsense mutation in PDE6H causes autosomal-recessive incomplete achromatopsia.
Susanne Kohl, Frauke Coppieters, Françoise Meire, Simone Schaich, Susanne Roosing, Christina Brennenstuhl, Sylvia Bolz, Maria M van Genderen, Frans C C Riemslag, Robert Lukowski,[...]. Am J Hum Genet 2012
109
37

Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsia.
Susanne Kohl, Britta Baumann, Thomas Rosenberg, Ulrich Kellner, Birgit Lorenz, Maria Vadalà, Samuel G Jacobson, Bernd Wissinger. Am J Hum Genet 2002
191
37

In vivo imaging of the photoreceptor mosaic of a rod monochromat.
Joseph Carroll, Stacey S Choi, David R Williams. Vision Res 2008
60
35

Progressive loss of cones in achromatopsia: an imaging study using spectral-domain optical coherence tomography.
Alberta A H J Thiadens, Ville Somervuo, L Ingeborgh van den Born, Susanne Roosing, Mary J van Schooneveld, Robert W A M Kuijpers, Norka van Moll-Ramirez, Frans P M Cremers, Carel B Hoyng, Caroline C W Klaver. Invest Ophthalmol Vis Sci 2010
118
35

Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia.
Susanne Kohl, Ditta Zobor, Wei-Chieh Chiang, Nicole Weisschuh, Jennifer Staller, Irene Gonzalez Menendez, Stanley Chang, Susanne C Beck, Marina Garcia Garrido, Vithiyanjali Sothilingam,[...]. Nat Genet 2015
131
35

Reliability and Repeatability of Cone Density Measurements in Patients with Congenital Achromatopsia.
Mortada A Abozaid, Christopher S Langlo, Adam M Dubis, Michel Michaelides, Sergey Tarima, Joseph Carroll. Adv Exp Med Biol 2016
33
54

CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia.
Susanne Kohl, Balazs Varsanyi, Gesine Abadin Antunes, Britta Baumann, Carel B Hoyng, Herbert Jägle, Thomas Rosenberg, Ulrich Kellner, Birgit Lorenz, Roberto Salati,[...]. Eur J Hum Genet 2005
173
29

High-resolution in vivo imaging in achromatopsia.
Mervyn G Thomas, Anil Kumar, Susanne Kohl, Frank A Proudlock, Irene Gottlob. Ophthalmology 2011
91
29

REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA.
Christopher S Langlo, Laura R Erker, Maria Parker, Emily J Patterson, Brian P Higgins, Phyllis Summerfelt, Moataz M Razeen, Frederick T Collison, Gerald A Fishman, Christine N Kay,[...]. Retina 2017
40
40

Longitudinal study of cone photoreceptors during retinal degeneration and in response to ciliary neurotrophic factor treatment.
Katherine E Talcott, Kavitha Ratnam, Sanna M Sundquist, Anna S Lucero, Brandon J Lujan, Weng Tao, Travis C Porco, Austin Roorda, Jacque L Duncan. Invest Ophthalmol Vis Sci 2011
188
27

Relationship between foveal cone specialization and pit morphology in albinism.
Melissa A Wilk, John T McAllister, Robert F Cooper, Adam M Dubis, Teresa N Patitucci, Phyllis Summerfelt, Jennifer L Anderson, Kimberly E Stepien, Deborah M Costakos, Thomas B Connor,[...]. Invest Ophthalmol Vis Sci 2014
100
27

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
50

Long-term and age-dependent restoration of visual function in a mouse model of CNGB3-associated achromatopsia following gene therapy.
Livia S Carvalho, Jianhua Xu, Rachael A Pearson, Alexander J Smith, James W Bainbridge, Lynsie M Morris, Steven J Fliesler, Xi-Qin Ding, Robin R Ali. Hum Mol Genet 2011
124
25


Genetic etiology and clinical consequences of complete and incomplete achromatopsia.
Alberta A H J Thiadens, Niki W R Slingerland, Susanne Roosing, Mary J van Schooneveld, Janneke J C van Lith-Verhoeven, Norka van Moll-Ramirez, L Ingeborgh van den Born, Carel B Hoyng, Frans P M Cremers, Caroline C W Klaver. Ophthalmology 2009
85
25

Early signs of longitudinal progressive cone photoreceptor degeneration in achromatopsia.
Mervyn George Thomas, Rebecca Jane McLean, Susanne Kohl, Viral Sheth, Irene Gottlob. Br J Ophthalmol 2012
53
26

The cone dysfunction syndromes.
Jonathan Aboshiha, Adam M Dubis, Joseph Carroll, Alison J Hardcastle, Michel Michaelides. Br J Ophthalmol 2016
79
25

Repeatability of in vivo parafoveal cone density and spacing measurements.
Robert Garrioch, Christopher Langlo, Adam M Dubis, Robert F Cooper, Alfredo Dubra, Joseph Carroll. Optom Vis Sci 2012
116
25

Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel.
S Kohl, T Marx, I Giddings, H Jägle, S G Jacobson, E Apfelstedt-Sylla, E Zrenner, L T Sharpe, B Wissinger. Nat Genet 1998
263
24

CNGA3 mutations in hereditary cone photoreceptor disorders.
B Wissinger, D Gamer, H Jägle, R Giorda, T Marx, S Mayer, S Tippmann, M Broghammer, B Jurklies, T Rosenberg,[...]. Am J Hum Genet 2001
227
24

High-resolution imaging with adaptive optics in patients with inherited retinal degeneration.
Jacque L Duncan, Yuhua Zhang, Jarel Gandhi, Chiaki Nakanishi, Mohammad Othman, Kari E H Branham, Anand Swaroop, Austin Roorda. Invest Ophthalmol Vis Sci 2007
198
24

Achromatopsia: clinical features, molecular genetics, animal models and therapeutic options.
Nashila Hirji, Jonathan Aboshiha, Michalis Georgiou, James Bainbridge, Michel Michaelides. Ophthalmic Genet 2018
60
24

Gene therapy rescues cone function in congenital achromatopsia.
András M Komáromy, John J Alexander, Jessica S Rowlan, Monique M Garcia, Vince A Chiodo, Asli Kaya, Jacqueline C Tanaka, Gregory M Acland, William W Hauswirth, Gustavo D Aguirre. Hum Mol Genet 2010
181
22

The cone dysfunction syndromes.
M Michaelides, D M Hunt, A T Moore. Br J Ophthalmol 2004
159
22

A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene.
Bo Chang, Tanja Grau, Susann Dangel, Ron Hurd, Bernhard Jurklies, E Cumhur Sener, Sten Andreasson, Helene Dollfus, Britta Baumann, Sylvia Bolz,[...]. Proc Natl Acad Sci U S A 2009
141
22

The effect of cone opsin mutations on retinal structure and the integrity of the photoreceptor mosaic.
Joseph Carroll, Alfredo Dubra, Jessica C Gardner, Liliana Mizrahi-Meissonnier, Robert F Cooper, Adam M Dubis, Rick Nordgren, Mohamed Genead, Thomas B Connor, Kimberly E Stepien,[...]. Invest Ophthalmol Vis Sci 2012
64
22

Supernormal vision and high-resolution retinal imaging through adaptive optics.
J Liang, D R Williams, D T Miller. J Opt Soc Am A Opt Image Sci Vis 1997
748
22

Adaptive optics scanning laser ophthalmoscopy.
Austin Roorda, Fernando Romero-Borja, William Donnelly Iii, Hope Queener, Thomas Hebert, Melanie Campbell. Opt Express 2002
534
22

Spatial and temporal variation of rod photoreceptor reflectance in the human retina.
Robert F Cooper, Adam M Dubis, Ashavini Pavaskar, Jungtae Rha, Alfredo Dubra, Joseph Carroll. Biomed Opt Express 2011
70
22

Adaptive optics microperimetry and OCT images show preserved function and recovery of cone visibility in macular telangiectasia type 2 retinal lesions.
Qinyun Wang, William S Tuten, Brandon J Lujan, Jennifer Holland, Paul S Bernstein, Steven D Schwartz, Jacque L Duncan, Austin Roorda. Invest Ophthalmol Vis Sci 2015
64
22

Normal Perceptual Sensitivity Arising From Weakly Reflective Cone Photoreceptors.
Kady S Bruce, Wolf M Harmening, Bradley R Langston, William S Tuten, Austin Roorda, Lawrence C Sincich. Invest Ophthalmol Vis Sci 2015
49
24

Evaluating Descriptive Metrics of the Human Cone Mosaic.
Robert F Cooper, Melissa A Wilk, Sergey Tarima, Joseph Carroll. Invest Ophthalmol Vis Sci 2016
70
22

Longitudinal Assessment of Retinal Structure in Achromatopsia Patients With Long-Term Follow-up.
Nashila Hirji, Michalis Georgiou, Angelos Kalitzeos, James W Bainbridge, Neruban Kumaran, Jonathan Aboshiha, Joseph Carroll, Michel Michaelides. Invest Ophthalmol Vis Sci 2018
26
46

Restoration of cone vision in the CNGA3-/- mouse model of congenital complete lack of cone photoreceptor function.
Stylianos Michalakis, Regine Mühlfriedel, Naoyuki Tanimoto, Vidhyasankar Krishnamoorthy, Susanne Koch, M Dominik Fischer, Elvir Becirovic, Lin Bai, Gesine Huber, Susanne C Beck,[...]. Mol Ther 2010
141
20

Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the alpha subunit of cone transducin (GNAT2).
I A Aligianis, T Forshew, S Johnson, M Michaelides, C A Johnson, R C Trembath, D M Hunt, A T Moore, E R Maher. J Med Genet 2002
92
20

Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21.
S Kohl, B Baumann, M Broghammer, H Jägle, P Sieving, U Kellner, R Spegal, M Anastasi, E Zrenner, L T Sharpe,[...]. Hum Mol Genet 2000
228
20

AAV-mediated cone rescue in a naturally occurring mouse model of CNGA3-achromatopsia.
Ji-jing Pang, Wen-Tao Deng, Xufeng Dai, Bo Lei, Drew Everhart, Yumiko Umino, Jie Li, Keqing Zhang, Song Mao, Sanford L Boye,[...]. PLoS One 2012
93
20

Adaptive optics ophthalmoscopy.
Austin Roorda, Jacque L Duncan. Annu Rev Vis Sci 2015
85
20

Assessing Photoreceptor Structure in Retinitis Pigmentosa and Usher Syndrome.
Lynn W Sun, Ryan D Johnson, Christopher S Langlo, Robert F Cooper, Moataz M Razeen, Madia C Russillo, Alfredo Dubra, Thomas B Connor, Dennis P Han, Mark E Pennesi,[...]. Invest Ophthalmol Vis Sci 2016
64
20

Human cone visual pigment deletions spare sufficient photoreceptors to warrant gene therapy.
Artur V Cideciyan, Robert B Hufnagel, Joseph Carroll, Alexander Sumaroka, Xunda Luo, Sharon B Schwartz, Alfredo Dubra, Megan Land, Michel Michaelides, Jessica C Gardner,[...]. Hum Gene Ther 2013
79
18


High-resolution images of retinal structure in patients with choroideremia.
Reema Syed, Sanna M Sundquist, Kavitha Ratnam, Shiri Zayit-Soudry, Yuhua Zhang, J Brooks Crawford, Ian M MacDonald, Pooja Godara, Jungtae Rha, Joseph Carroll,[...]. Invest Ophthalmol Vis Sci 2013
75
18


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.