A citation-based method for searching scientific literature

M F Marmor, A B Fulton, G E Holder, Y Miyake, M Brigell, M Bach. Doc Ophthalmol 2009
Times Cited: 767







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



Times Cited
  Times     Co-cited
Similarity


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
862
26

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
12

ISCEV standard for clinical multifocal electroretinography (mfERG) (2011 edition).
Donald C Hood, Michael Bach, Mitchell Brigell, David Keating, Mineo Kondo, Jonathan S Lyons, Michael F Marmor, Daphne L McCulloch, Anja M Palmowski-Wolfe. Doc Ophthalmol 2012
397
11

Retinitis pigmentosa.
Dyonne T Hartong, Eliot L Berson, Thaddeus P Dryja. Lancet 2006
11

ISCEV standard for clinical pattern electroretinography (PERG): 2012 update.
Michael Bach, Mitchell G Brigell, Marko Hawlina, Graham E Holder, Mary A Johnson, Daphne L McCulloch, Thomas Meigen, Suresh Viswanathan. Doc Ophthalmol 2013
287
9

Retinitis pigmentosa.
Christian Hamel. Orphanet J Rare Dis 2006
502
7

Spectral-domain optical coherence tomography measures of outer segment layer progression in patients with X-linked retinitis pigmentosa.
David G Birch, Kirsten G Locke, Yuquan Wen, Kelly I Locke, Dennis R Hoffman, Donald C Hood. JAMA Ophthalmol 2013
122
6

Correlation between macular volume and focal macular electroretinogram in patients with retinitis pigmentosa.
Tadasu Sugita, Mineo Kondo, Chang-Hua Piao, Yasuki Ito, Hiroko Terasaki. Invest Ophthalmol Vis Sci 2008
43
13

The cone dysfunction syndromes.
M Michaelides, D M Hunt, A T Moore. Br J Ophthalmol 2004
157
5

Detailed phenotypic and genotypic characterization of bietti crystalline dystrophy.
Stephanie Halford, Gerald Liew, Donna S Mackay, Panagiotis I Sergouniotis, Richard Holt, Suzanne Broadgate, Emanuela V Volpi, Louise Ocaka, Anthony G Robson, Graham E Holder,[...]. Ophthalmology 2014
49
10

A comparison of progressive loss of the ellipsoid zone (EZ) band in autosomal dominant and x-linked retinitis pigmentosa.
Cindy X Cai, Kirsten G Locke, Rithambara Ramachandran, David G Birch, Donald C Hood. Invest Ophthalmol Vis Sci 2014
66
7

ISCEV Standard for clinical electro-oculography (2017 update).
Paul A Constable, Michael Bach, Laura J Frishman, Brett G Jeffrey, Anthony G Robson. Doc Ophthalmol 2017
52
9

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
108
5

Clinical and Genetic Evaluation of a Cohort of Pediatric Patients with Severe Inherited Retinal Dystrophies.
Valentina Di Iorio, Marianthi Karali, Raffaella Brunetti-Pierri, Mariaelena Filippelli, Giuseppina Di Fruscio, Mariateresa Pizzo, Margherita Mutarelli, Vincenzo Nigro, Francesco Testa, Sandro Banfi,[...]. Genes (Basel) 2017
18
27

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
12

Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2.
Anren Li, Xiaodong Jiao, Francis L Munier, Daniel F Schorderet, Wenliang Yao, Fumino Iwata, Mutsuko Hayakawa, Atsushi Kanai, Muh Shy Chen, Richard Alan Lewis,[...]. Am J Hum Genet 2004
172
4

PRPF mutations are associated with generalized defects in spliceosome formation and pre-mRNA splicing in patients with retinitis pigmentosa.
Goranka Tanackovic, Adriana Ransijn, Philippe Thibault, Sherif Abou Elela, Roscoe Klinck, Eliot L Berson, Benoit Chabot, Carlo Rivolta. Hum Mol Genet 2011
78
5

Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing.
Nicole Weisschuh, Anja K Mayer, Tim M Strom, Susanne Kohl, Nicola Glöckle, Max Schubach, Sten Andreasson, Antje Bernd, David G Birch, Christian P Hamel,[...]. PLoS One 2016
70
5

Comprehensive molecular diagnosis of a large cohort of Japanese retinitis pigmentosa and Usher syndrome patients by next-generation sequencing.
Maho Oishi, Akio Oishi, Norimoto Gotoh, Ken Ogino, Koichiro Higasa, Kei Iida, Yukiko Makiyama, Satoshi Morooka, Fumihiko Matsuda, Nagahisa Yoshimura. Invest Ophthalmol Vis Sci 2014
104
4

A pilot study of Fourier-domain optical coherence tomography of retinal dystrophy patients.
Jennifer I Lim, Ou Tan, Amani A Fawzi, J Jill Hopkins, John H Gil-Flamer, David Huang. Am J Ophthalmol 2008
72
5

Ultra-high resolution optical coherence tomography assessment of photoreceptors in retinitis pigmentosa and related diseases.
Andre J Witkin, Tony H Ko, James G Fujimoto, Annie Chan, Wolfgang Drexler, Joel S Schuman, Elias Reichel, Jay S Duker. Am J Ophthalmol 2006
118
4

Thickness of receptor and post-receptor retinal layers in patients with retinitis pigmentosa measured with frequency-domain optical coherence tomography.
Donald C Hood, Christine E Lin, Margot A Lazow, Kirsten G Locke, Xian Zhang, David G Birch. Invest Ophthalmol Vis Sci 2009
153
4

CLINICAL PRESENTATION AND DISEASE COURSE OF USHER SYNDROME BECAUSE OF MUTATIONS IN MYO7A OR USH2A.
Francesco Testa, Paolo Melillo, Crystel Bonnet, Vincenzo Marcelli, Antonella de Benedictis, Raffaella Colucci, Beatrice Gallo, Anne Kurtenbach, Settimio Rossi, Elio Marciano,[...]. Retina 2017
20
20

Visual Acuity Loss and Associated Risk Factors in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 2).
Xiangrong Kong, Rupert W Strauss, Michel Michaelides, Artur V Cideciyan, José-Alain Sahel, Beatriz Muñoz, Sheila West, Hendrik P N Scholl. Ophthalmology 2016
48
8

Method for deriving visual field boundaries from OCT scans of patients with retinitis pigmentosa.
Donald C Hood, Rithambara Ramachandran, Karen Holopigian, Margot Lazow, David G Birch, Vivienne C Greenstein. Biomed Opt Express 2011
62
6

Pattern ERG correlates of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity.
Anthony G Robson, Ahmed El-Amir, Claire Bailey, Catherine A Egan, Frederick W Fitzke, Andrew R Webster, Alan C Bird, Graham E Holder. Invest Ophthalmol Vis Sci 2003
86
4

ISCEV standard for clinical pattern electroretinography--2007 update.
Graham E Holder, Mitchell G Brigell, Marko Hawlina, Thomas Meigen, Vaegan, Michael Bach. Doc Ophthalmol 2007
142
4

ISCEV guide to visual electrodiagnostic procedures.
Anthony G Robson, Josefin Nilsson, Shiying Li, Subhadra Jalali, Anne B Fulton, Alma Patrizia Tormene, Graham E Holder, Scott E Brodie. Doc Ophthalmol 2018
126
4

The association between visual acuity and central retinal thickness in retinitis pigmentosa.
Michael A Sandberg, Robert J Brockhurst, Alexander R Gaudio, Eliot L Berson. Invest Ophthalmol Vis Sci 2005
156
4

Histopathology of the human retina in retinitis pigmentosa.
A H Milam, Z Y Li, R N Fariss. Prog Retin Eye Res 1998
454
4

Report from the NEI/FDA Ophthalmic Clinical Trial Design and Endpoints Symposium.
Karl G Csaky, Elaine A Richman, Frederick L Ferris. Invest Ophthalmol Vis Sci 2008
159
4

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
44
6

Electroretinograms in patients with achromatopsia.
S Andréasson, K Tornqvist. Acta Ophthalmol (Copenh) 1991
37
8

ISCEV standard for clinical visual evoked potentials: (2016 update).
J Vernon Odom, Michael Bach, Mitchell Brigell, Graham E Holder, Daphne L McCulloch, Atsushi Mizota, Alma Patrizia Tormene. Doc Ophthalmol 2016
260
3


Clinical biochemical and pathologic correlations in Bietti's crystalline dystrophy.
M I Kaiser-Kupfer, C C Chan, T C Markello, M A Crawford, R C Caruso, K G Csaky, J Guo, W A Gahl. Am J Ophthalmol 1994
98
3

Clinical and genetic features in Italian Bietti crystalline dystrophy patients.
Settimio Rossi, Francesco Testa, Anren Li, Fulya Yaylacioğlu, Carlo Gesualdo, J Fielding Hejtmancik, Francesca Simonelli. Br J Ophthalmol 2013
31
9

The molecular basis of human retinal and vitreoretinal diseases.
Wolfgang Berger, Barbara Kloeckener-Gruissem, John Neidhardt. Prog Retin Eye Res 2010
348
3

Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families.
Caroline Van Cauwenbergh, Frauke Coppieters, Dimitri Roels, Sarah De Jaegere, Helena Flipts, Julie De Zaeytijd, Sophie Walraedt, Charlotte Claes, Erik Fransen, Guy Van Camp,[...]. PLoS One 2017
35
8

Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families.
Lori S Sullivan, Sara J Bowne, David G Birch, Dianna Hughbanks-Wheaton, John R Heckenlively, Richard Alan Lewis, Charles A Garcia, Richard S Ruiz, Susan H Blanton, Hope Northrup,[...]. Invest Ophthalmol Vis Sci 2006
206
3

Panel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies.
Nicola Glöckle, Susanne Kohl, Julia Mohr, Tim Scheurenbrand, Andrea Sprecher, Nicole Weisschuh, Antje Bernd, Günther Rudolph, Max Schubach, Charlotte Poloschek,[...]. Eur J Hum Genet 2014
190
3

Two novel mutations in the EYS gene are possible major causes of autosomal recessive retinitis pigmentosa in the Japanese population.
Katsuhiro Hosono, Chie Ishigami, Masayo Takahashi, Dong Ho Park, Yasuhiko Hirami, Hiroshi Nakanishi, Shinji Ueno, Tadashi Yokoi, Akiko Hikoya, Taichi Fujita,[...]. PLoS One 2012
65
4

Good epidemiologic practice in retinitis pigmentosa: from phenotyping to biobanking.
Marzio Chizzolini, Alessandro Galan, Elisabeth Milan, Adolfo Sebastiani, Ciro Costagliola, Francesco Parmeggiani. Curr Genomics 2011
83
3

Expression of PRPF31 mRNA in patients with autosomal dominant retinitis pigmentosa: a molecular clue for incomplete penetrance?
Eranga N Vithana, Leen Abu-Safieh, Lucia Pelosini, Elizabeth Winchester, Dan Hornan, Alan C Bird, David M Hunt, Stephen A Bustin, Shomi S Bhattacharya. Invest Ophthalmol Vis Sci 2003
99
3

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
3

Normal central retinal function and structure preserved in retinitis pigmentosa.
Samuel G Jacobson, Alejandro J Roman, Tomas S Aleman, Alexander Sumaroka, Waldo Herrera, Elizabeth A M Windsor, Lori A Atkinson, Sharon B Schwartz, Janet D Steinberg, Artur V Cideciyan. Invest Ophthalmol Vis Sci 2010
68
4

Optical Coherence Tomography of Retinal Degeneration in Royal College of Surgeons Rats and Its Correlation with Morphology and Electroretinography.
Kobu Adachi, Shizuka Takahashi, Kodai Yamauchi, Natsuki Mounai, Reiko Tanabu, Mitsuru Nakazawa. PLoS One 2016
25
12

Automated segmentation of outer retinal layers in macular OCT images of patients with retinitis pigmentosa.
Qi Yang, Charles A Reisman, Kinpui Chan, Rithambara Ramachandran, Ali Raza, Donald C Hood. Biomed Opt Express 2011
42
7

Evaluation of choroidal thickness in retinitis pigmentosa using enhanced depth imaging optical coherence tomography.
Dilsher S Dhoot, Siya Huo, Alex Yuan, David Xu, Sunil Srivistava, Justis P Ehlers, Elias Traboulsi, Peter K Kaiser. Br J Ophthalmol 2013
95
3



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.