A citation-based method for searching scientific literature

Dyonne T Hartong, Eliot L Berson, Thaddeus P Dryja. Lancet 2006
Times Cited: 1891







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



Times Cited
  Times     Co-cited
Similarity


Non-syndromic retinitis pigmentosa.
Sanne K Verbakel, Ramon A C van Huet, Camiel J F Boon, Anneke I den Hollander, Rob W J Collin, Caroline C W Klaver, Carel B Hoyng, Ronald Roepman, B Jeroen Klevering. Prog Retin Eye Res 2018
215
16

Retinitis pigmentosa.
Christian Hamel. Orphanet J Rare Dis 2006
468
14

Genes and mutations causing retinitis pigmentosa.
S P Daiger, L S Sullivan, S J Bowne. Clin Genet 2013
312
12

Efficacy and safety of voretigene neparvovec (AAV2-hRPE65v2) in patients with RPE65-mediated inherited retinal dystrophy: a randomised, controlled, open-label, phase 3 trial.
Stephen Russell, Jean Bennett, Jennifer A Wellman, Daniel C Chung, Zi-Fan Yu, Amy Tillman, Janet Wittes, Julie Pappas, Okan Elci, Sarah McCague,[...]. Lancet 2017
588
11

Retinitis pigmentosa: genes and disease mechanisms.
Stefano Ferrari, Enzo Di Iorio, Vanessa Barbaro, Diego Ponzin, Francesco S Sorrentino, Francesco Parmeggiani. Curr Genomics 2011
279
10

Antioxidants reduce cone cell death in a model of retinitis pigmentosa.
Keiichi Komeima, Brian S Rogers, Lili Lu, Peter A Campochiaro. Proc Natl Acad Sci U S A 2006
293
8

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
778
8

Molecular genetics and emerging therapies for retinitis pigmentosa: Basic research and clinical perspectives.
Marina França Dias, Kwangsic Joo, Jessica A Kemp, Silvia Ligório Fialho, Armando da Silva Cunha, Se Joon Woo, Young Jik Kwon. Prog Retin Eye Res 2018
147
8

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
7

Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease.
Keren J Carss, Gavin Arno, Marie Erwood, Jonathan Stephens, Alba Sanchis-Juan, Sarah Hull, Karyn Megy, Detelina Grozeva, Eleanor Dewhurst, Samantha Malka,[...]. Am J Hum Genet 2017
191
7


Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.
T P Dryja, T L McGee, L B Hahn, G S Cowley, J E Olsson, E Reichel, M A Sandberg, E L Berson. N Engl J Med 1990
337
7

Vessel density analysis in patients with retinitis pigmentosa by means of optical coherence tomography angiography.
Maurizio Battaglia Parodi, Maria Vittoria Cicinelli, Alessandro Rabiolo, Luisa Pierro, Marco Gagliardi, Gianluigi Bolognesi, Francesco Bandello. Br J Ophthalmol 2017
74
8

Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat.
P M D'Cruz, D Yasumura, J Weir, M T Matthes, H Abderrahim, M M LaVail, D Vollrath. Hum Mol Genet 2000
655
6

Increasing the yield in targeted next-generation sequencing by implicating CNV analysis, non-coding exons and the overall variant load: the example of retinal dystrophies.
Tobias Eisenberger, Christine Neuhaus, Arif O Khan, Christian Decker, Markus N Preising, Christoph Friedburg, Anika Bieg, Martin Gliem, Peter Charbel Issa, Frank G Holz,[...]. PLoS One 2013
148
6

The molecular and cellular basis of rhodopsin retinitis pigmentosa reveals potential strategies for therapy.
Dimitra Athanasiou, Monica Aguila, James Bellingham, Wenwen Li, Caroline McCulley, Philip J Reeves, Michael E Cheetham. Prog Retin Eye Res 2018
111
6

Treatment of retinitis pigmentosa due to MERTK mutations by ocular subretinal injection of adeno-associated virus gene vector: results of a phase I trial.
Nicola G Ghazi, Emad B Abboud, Sawsan R Nowilaty, Hisham Alkuraya, Abdulrahman Alhommadi, Huimin Cai, Rui Hou, Wen-Tao Deng, Sanford L Boye, Abdulrahman Almaghamsi,[...]. Hum Genet 2016
126
6


Histopathology of the human retina in retinitis pigmentosa.
A H Milam, Z Y Li, R N Fariss. Prog Retin Eye Res 1998
439
5

Retinal hemodynamics in retinitis pigmentosa.
J E Grunwald, A M Maguire, J Dupont. Am J Ophthalmol 1996
104
5

Genotype-phenotype correlation and mutation spectrum in a large cohort of patients with inherited retinal dystrophy revealed by next-generation sequencing.
Xiu-Feng Huang, Fang Huang, Kun-Chao Wu, Juan Wu, Jie Chen, Chi-Pui Pang, Fan Lu, Jia Qu, Zi-Bing Jin. Genet Med 2015
115
5

Macular abnormalities in Italian patients with retinitis pigmentosa.
Francesco Testa, Settimio Rossi, Raffaella Colucci, Beatrice Gallo, Valentina Di Iorio, Michele della Corte, Claudio Azzolini, Paolo Melillo, Francesca Simonelli. Br J Ophthalmol 2014
45
11

Global prevalence of age-related macular degeneration and disease burden projection for 2020 and 2040: a systematic review and meta-analysis.
Wan Ling Wong, Xinyi Su, Xiang Li, Chui Ming G Cheung, Ronald Klein, Ching-Yu Cheng, Tien Yin Wong. Lancet Glob Health 2014
5

Autologous Induced Stem-Cell-Derived Retinal Cells for Macular Degeneration.
Michiko Mandai, Akira Watanabe, Yasuo Kurimoto, Yasuhiko Hirami, Chikako Morinaga, Takashi Daimon, Masashi Fujihara, Hiroshi Akimaru, Noriko Sakai, Yumiko Shibata,[...]. N Engl J Med 2017
588
5

Prevalence of retinitis pigmentosa in Maine.
C H Bunker, E L Berson, W C Bromley, R P Hayes, T H Roderick. Am J Ophthalmol 1984
312
5

Glia-neuron interactions in the mammalian retina.
Elena Vecino, F David Rodriguez, Noelia Ruzafa, Xandra Pereiro, Sansar C Sharma. Prog Retin Eye Res 2016
302
5

G protein-coupled receptor rhodopsin.
Krzysztof Palczewski. Annu Rev Biochem 2006
469
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
97
5

Correction of the retinal dystrophy phenotype of the RCS rat by viral gene transfer of Mertk.
D Vollrath, W Feng, J L Duncan, D Yasumura, P M D'Cruz, A Chappelow, M T Matthes, M A Kay, M M LaVail. Proc Natl Acad Sci U S A 2001
221
5

Worldwide carrier frequency and genetic prevalence of autosomal recessive inherited retinal diseases.
Mor Hanany, Carlo Rivolta, Dror Sharon. Proc Natl Acad Sci U S A 2020
45
11

Genetic Basis of Inherited Retinal Disease in a Molecularly Characterized Cohort of More Than 3000 Families from the United Kingdom.
Nikolas Pontikos, Gavin Arno, Neringa Jurkute, Elena Schiff, Rola Ba-Abbad, Samantha Malka, Ainoa Gimenez, Michalis Georgiou, Genevieve Wright, Monica Armengol,[...]. Ophthalmology 2020
38
13

Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa.
A Gal, Y Li, D A Thompson, J Weir, U Orth, S G Jacobson, E Apfelstedt-Sylla, D Vollrath. Nat Genet 2000
491
5


Perspective on genes and mutations causing retinitis pigmentosa.
Stephen P Daiger, Sara J Bowne, Lori S Sullivan. Arch Ophthalmol 2007
304
5

Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease.
Edwin M Stone, Jeaneen L Andorf, S Scott Whitmore, Adam P DeLuca, Joseph C Giacalone, Luan M Streb, Terry A Braun, Robert F Mullins, Todd E Scheetz, Val C Sheffield,[...]. Ophthalmology 2017
148
5

Efficacy, Safety, and Durability of Voretigene Neparvovec-rzyl in RPE65 Mutation-Associated Inherited Retinal Dystrophy: Results of Phase 1 and 3 Trials.
Albert M Maguire, Stephen Russell, Jennifer A Wellman, Daniel C Chung, Zi-Fan Yu, Amy Tillman, Janet Wittes, Julie Pappas, Okan Elci, Kathleen A Marshall,[...]. Ophthalmology 2019
100
5

Initial results from a first-in-human gene therapy trial on X-linked retinitis pigmentosa caused by mutations in RPGR.
Jasmina Cehajic-Kapetanovic, Kanmin Xue, Cristina Martinez-Fernandez de la Camara, Anika Nanda, Alexandra Davies, Laura J Wood, Anna Paola Salvetti, M Dominik Fischer, James W Aylward, Alun R Barnard,[...]. Nat Med 2020
70
7

Retinal degeneration and local oxygen metabolism.
Dao-Yi Yu, Stephen J Cringle. Exp Eye Res 2005
212
4

Retinitis pigmentosa.
R A Pagon. Surv Ophthalmol 1988
196
4

Long-term effect of gene therapy on Leber's congenital amaurosis.
James W B Bainbridge, Manjit S Mehat, Venki Sundaram, Scott J Robbie, Susie E Barker, Caterina Ripamonti, Anastasios Georgiadis, Freya M Mowat, Stuart G Beattie, Peter J Gardner,[...]. N Engl J Med 2015
417
4

Retinal blood flow velocity measured by retinal function imaging in retinitis pigmentosa.
Sven C Beutelspacher, Nermin Serbecic, Hila Barash, Zvia Burgansky-Eliash, Amiram Grinvald, Hermann Krastel, Jost B Jonas. Graefes Arch Clin Exp Ophthalmol 2011
52
7

Retinal vessel oxygen saturation and its correlation with structural changes in retinitis pigmentosa.
Cengiz Türksever, Christophe Valmaggia, Selim Orgül, Daniel F Schorderet, Josef Flammer, Margarita G Todorova. Acta Ophthalmol 2014
39
10


Retinal vessel oxygen saturation and vessel diameter in retinitis pigmentosa.
Thor Eysteinsson, Sveinn H Hardarson, David Bragason, Einar Stefánsson. Acta Ophthalmol 2014
53
7

Retinitis pigmentosa.
S Merin, E Auerbach. Surv Ophthalmol 1976
77
5

Vascular atrophy in the retinal degenerative rd mouse.
J C Blanks, L V Johnson. J Comp Neurol 1986
65
6

Metabolic and functional changes in retinitis pigmentosa: comparing retinal vessel oximetry to full-field electroretinography, electrooculogram and multifocal electroretinography.
Margarita G Todorova, Cengiz Türksever, Andreas Schötzau, Daniel F Schorderet, Christophe Valmaggia. Acta Ophthalmol 2016
21
19

Optical coherence tomography angiography in patients with retinitis pigmentosa who have normal visual acuity.
Seiji Takagi, Yasuhiko Hirami, Masayo Takahashi, Masashi Fujihara, Michiko Mandai, Chisato Miyakoshi, Goji Tomita, Yasuo Kurimoto. Acta Ophthalmol 2018
15
26

Age-related macular degeneration.
Paul Mitchell, Gerald Liew, Bamini Gopinath, Tien Y Wong. Lancet 2018
314
4

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
62
6


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.