A citation-based method for searching scientific literature

Venki Sundaram, Caroline Wilde, Jonathan Aboshiha, Jill Cowing, Colin Han, Christopher S Langlo, Ravinder Chana, Alice E Davidson, Panagiotis I Sergouniotis, James W Bainbridge, Robin R Ali, Alfredo Dubra, Gary Rubin, Andrew R Webster, Anthony T Moore, Marko Nardini, Joseph Carroll, Michel Michaelides. Ophthalmology 2014
Times Cited: 113







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



Times Cited
  Times     Co-cited
Similarity


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
116
43

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
71

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
36

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
107
30

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
66
45

Genotype-dependent variability in residual cone structure in achromatopsia: toward developing metrics for assessing cone health.
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,[...]. Invest Ophthalmol Vis Sci 2014
53
54

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
52

High-resolution in vivo imaging in achromatopsia.
Mervyn G Thomas, Anil Kumar, Susanne Kohl, Frank A Proudlock, Irene Gottlob. Ophthalmology 2011
90
30

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
127
27

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
188
26

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
170
25

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
223
25

Achromatopsia: clinical features, molecular genetics, animal models and therapeutic options.
Nashila Hirji, Jonathan Aboshiha, Michalis Georgiou, James Bainbridge, Michel Michaelides. Ophthalmic Genet 2018
58
43

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
28

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
261
23

Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders.
Alberta A H J Thiadens, Anneke I den Hollander, Susanne Roosing, Sander B Nabuurs, Renate C Zekveld-Vroon, Rob W J Collin, Elfride De Baere, Robert K Koenekoop, Mary J van Schooneveld, Tim M Strom,[...]. Am J Hum Genet 2009
150
23

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
139
23

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
180
22

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
226
22

The cone dysfunction syndromes.
Jonathan Aboshiha, Adam M Dubis, Joseph Carroll, Alison J Hardcastle, Michel Michaelides. Br J Ophthalmol 2016
78
28

The cone dysfunction syndromes.
M Michaelides, D M Hunt, A T Moore. Br J Ophthalmol 2004
158
21

Human photoreceptor topography.
C A Curcio, K R Sloan, R E Kalina, A E Hendrickson. J Comp Neurol 1990
19

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
223
19

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
19

The Clinical Phenotype of CNGA3-Related Achromatopsia: Pretreatment Characterization in Preparation of a Gene Replacement Therapy Trial.
Ditta Zobor, Annette Werner, Franco Stanzial, Francesco Benedicenti, Günther Rudolph, Ulrich Kellner, Christian Hamel, Sten Andréasson, Gergely Zobor, Torsten Strasser,[...]. Invest Ophthalmol Vis Sci 2017
31
61

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
73

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
19

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
18

CNGB3 achromatopsia with progressive loss of residual cone function and impaired rod-mediated function.
Naheed Wali Khan, Bernd Wissinger, Susanne Kohl, Paul A Sieving. Invest Ophthalmol Vis Sci 2007
70
24

Spectral-domain optical coherence tomography staging and autofluorescence imaging in achromatopsia.
Jonathan P Greenberg, Jerome Sherman, Sandrine A Zweifel, Royce W S Chen, Tobias Duncker, Susanne Kohl, Britta Baumann, Bernd Wissinger, Lawrence A Yannuzzi, Stephen H Tsang. JAMA Ophthalmol 2014
46
36

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
28
60

Genetic basis of total colourblindness among the Pingelapese islanders.
O H Sundin, J M Yang, Y Li, D Zhu, J N Hurd, T N Mitchell, E D Silva, I H Maumenee. Nat Genet 2000
163
16

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

Diagnostic fundus autofluorescence patterns in achromatopsia.
Abigail T Fahim, Naheed W Khan, Sarwar Zahid, Ira H Schachar, Kari Branham, Susanne Kohl, Bernd Wissinger, Victor M Elner, John R Heckenlively, Thiran Jayasundera. Am J Ophthalmol 2013
32
46

In vivo imaging of the photoreceptor mosaic of a rod monochromat.
Joseph Carroll, Stacey S Choi, David R Williams. Vision Res 2008
60
25

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
213
15


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
901
15

Genetics and Disease Expression in the CNGA3 Form of Achromatopsia: Steps on the Path to Gene Therapy.
Lina Zelinger, Artur V Cideciyan, Susanne Kohl, Sharon B Schwartz, Ada Rosenmann, Dalia Eli, Alexander Sumaroka, Alejandro J Roman, Xunda Luo, Cassondra Brown,[...]. Ophthalmology 2015
45
31


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
96
14

Restoration of cone vision in a mouse model of achromatopsia.
John J Alexander, Yumiko Umino, Drew Everhart, Bo Chang, Seok H Min, Qiuhong Li, Adrian M Timmers, Norman L Hawes, Ji-Jing Pang, Robert B Barlow,[...]. Nat Med 2007
165
13

Achromatopsia caused by novel mutations in both CNGA3 and CNGB3.
S Johnson, M Michaelides, I A Aligianis, J R Ainsworth, J D Mollon, E R Maher, A T Moore, D M Hunt. J Med Genet 2004
85
15

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
90
14

Structural grading of foveal hypoplasia using spectral-domain optical coherence tomography a predictor of visual acuity?
Mervyn G Thomas, Anil Kumar, Sarim Mohammad, Frank A Proudlock, Elizabeth C Engle, Caroline Andrews, Wai-Man Chan, Shery Thomas, Irene Gottlob. Ophthalmology 2011
235
13

Retinal morphology of patients with achromatopsia during early childhood: implications for gene therapy.
Paul Yang, Keith V Michaels, Robert J Courtney, Yuquan Wen, Daniel A Greninger, Leah Reznick, Daniel J Karr, Lorri B Wilson, Richard G Weleber, Mark E Pennesi. JAMA Ophthalmol 2014
26
50

Reflective afocal broadband adaptive optics scanning ophthalmoscope.
Alfredo Dubra, Yusufu Sulai. Biomed Opt Express 2011
206
13

CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients.
Anja K Mayer, Caroline Van Cauwenbergh, Christine Rother, Britta Baumann, Peggy Reuter, Elfride De Baere, Bernd Wissinger, Susanne Kohl. Hum Mutat 2017
34
38

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
26
50

Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases.
Koji M Nishiguchi, Michael A Sandberg, Nasim Gorji, Eliot L Berson, Thaddeus P Dryja. Hum Mutat 2005
101
12


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.