A citation-based method for searching scientific literature

Dyonne T Hartong, Eliot L Berson, Thaddeus P Dryja. Lancet 2006
Times Cited: 1693







List of co-cited articles
831 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
179
16

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
14

Retinitis pigmentosa.
Christian Hamel. Orphanet J Rare Dis 2006
403
13

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
692
11

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
510
11

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
125
10

Genes and mutations causing retinitis pigmentosa.
S P Daiger, L S Sullivan, S J Bowne. Clin Genet 2013
291
10

Retinitis pigmentosa: genes and disease mechanisms.
Stefano Ferrari, Enzo Di Iorio, Vanessa Barbaro, Diego Ponzin, Francesco S Sorrentino, Francesco Parmeggiani. Curr Genomics 2011
248
9

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
90
10

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
174
8

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
108
8

Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy.
Hugo F Mendes, Jacqueline van der Spuy, J Paul Chapple, Michael E Cheetham. Trends Mol Med 2005
241
7

The molecular basis of human retinal and vitreoretinal diseases.
Wolfgang Berger, Barbara Kloeckener-Gruissem, John Neidhardt. Prog Retin Eye Res 2010
299
7


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
96
6

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
69
8

Rod-derived cone viability factor promotes cone survival by stimulating aerobic glycolysis.
Najate Aït-Ali, Ram Fridlich, Géraldine Millet-Puel, Emmanuelle Clérin, François Delalande, Céline Jaillard, Frédéric Blond, Ludivine Perrocheau, Sacha Reichman, Leah C Byrne,[...]. Cell 2015
157
6

Prevalence of cystoid macular oedema, epiretinal membrane and cataract in retinitis pigmentosa.
Gerald Liew, Stacey Strong, Patrick Bradley, Philip Severn, Anthony T Moore, Andrew R Webster, Paul Mitchell, Annette Kifley, Michel Michaelides. Br J Ophthalmol 2019
13
46

Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic Cups.
David A Parfitt, Amelia Lane, Conor M Ramsden, Amanda-Jayne F Carr, Peter M Munro, Katarina Jovanovic, Nele Schwarz, Naheed Kanuga, Manickam N Muthiah, Sarah Hull,[...]. Cell Stem Cell 2016
146
6

Generation of three-dimensional retinal tissue with functional photoreceptors from human iPSCs.
Xiufeng Zhong, Christian Gutierrez, Tian Xue, Christopher Hampton, M Natalia Vergara, Li-Hui Cao, Ann Peters, Tea Soon Park, Elias T Zambidis, Jason S Meyer,[...]. Nat Commun 2014
374
6

MutationTaster2: mutation prediction for the deep-sequencing age.
Jana Marie Schwarz, David N Cooper, Markus Schuelke, Dominik Seelow. Nat Methods 2014
6

Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing.
Yan Xu, Liping Guan, Tao Shen, Jianguo Zhang, Xueshan Xiao, Hui Jiang, Shiqiang Li, Jianhua Yang, Xiaoyun Jia, Ye Yin,[...]. Hum Genet 2014
97
6

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
272
6

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
6

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
126
6

Five-Year Safety and Performance Results from the Argus II Retinal Prosthesis System Clinical Trial.
Lyndon da Cruz, Jessy D Dorn, Mark S Humayun, Gislin Dagnelie, James Handa, Pierre-Olivier Barale, José-Alain Sahel, Paulo E Stanga, Farhad Hafezi, Avinoam B Safran,[...]. Ophthalmology 2016
139
5

Leber congenital amaurosis: genes, proteins and disease mechanisms.
Anneke I den Hollander, Ronald Roepman, Robert K Koenekoop, Frans P M Cremers. Prog Retin Eye Res 2008
483
5


EYS mutation update: In silico assessment of 271 reported and 26 novel variants in patients with retinitis pigmentosa.
Muriël Messchaert, Lonneke Haer-Wigman, Muhammad I Khan, Frans P M Cremers, Rob W J Collin. Hum Mutat 2018
15
33

Identification and characterization of rod-derived cone viability factor.
Thierry Léveillard, Saddek Mohand-Saïd, Olivier Lorentz, David Hicks, Anne-Claire Fintz, Emmanuelle Clérin, Manuel Simonutti, Valérie Forster, Nükhet Cavusoglu, Frédéric Chalmel,[...]. Nat Genet 2004
262
5

Two-Step Reactivation of Dormant Cones in Retinitis Pigmentosa.
Wei Wang, Sang Joon Lee, Patrick A Scott, Xiaoqin Lu, Douglas Emery, Yongqin Liu, Toshihiko Ezashi, Michael R Roberts, Jason W Ross, Henry J Kaplan,[...]. Cell Rep 2016
44
11

An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients.
Crystel Bonnet, Zied Riahi, Sandra Chantot-Bastaraud, Luce Smagghe, Mélanie Letexier, Charles Marcaillou, Gaëlle M Lefèvre, Jean-Pierre Hardelin, Aziz El-Amraoui, Amrit Singh-Estivalet,[...]. Eur J Hum Genet 2016
44
11

Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations in PDE6A and PDE6B.
Samer Khateb, Marco Nassisi, Kinga M Bujakowska, Cécile Méjécase, Christel Condroyer, Aline Antonio, Marine Foussard, Vanessa Démontant, Saddek Mohand-Saïd, José-Alain Sahel,[...]. JAMA Ophthalmol 2019
10
50

Retinitis Pigmentosa with EYS Mutations Is the Most Prevalent Inherited Retinal Dystrophy in Japanese Populations.
Yuuki Arai, Akiko Maeda, Yasuhiko Hirami, Chie Ishigami, Shinji Kosugi, Michiko Mandai, Yasuo Kurimoto, Masayo Takahashi. J Ophthalmol 2015
34
14

Gene Correction Reverses Ciliopathy and Photoreceptor Loss in iPSC-Derived Retinal Organoids from Retinitis Pigmentosa Patients.
Wen-Li Deng, Mei-Ling Gao, Xin-Lan Lei, Ji-Neng Lv, Huan Zhao, Kai-Wen He, Xi-Xi Xia, Ling-Yun Li, Yu-Chen Chen, Yan-Ping Li,[...]. Stem Cell Reports 2018
72
6

Stepwise differentiation of pluripotent stem cells into retinal cells.
Fumitaka Osakada, Hanako Ikeda, Yoshiki Sasai, Masayo Takahashi. Nat Protoc 2009
178
5

Self-formation of optic cups and storable stratified neural retina from human ESCs.
Tokushige Nakano, Satoshi Ando, Nozomu Takata, Masako Kawada, Keiko Muguruma, Kiyotoshi Sekiguchi, Koichi Saito, Shigenobu Yonemura, Mototsugu Eiraku, Yoshiki Sasai. Cell Stem Cell 2012
683
5


Histopathology of the human retina in retinitis pigmentosa.
A H Milam, Z Y Li, R N Fariss. Prog Retin Eye Res 1998
387
5

Effect of gene therapy on visual function in Leber's congenital amaurosis.
James W B Bainbridge, Alexander J Smith, Susie S Barker, Scott Robbie, Robert Henderson, Kamaljit Balaggan, Ananth Viswanathan, Graham E Holder, Andrew Stockman, Nick Tyler,[...]. N Engl J Med 2008
5

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
5

Disrupted alternative splicing for genes implicated in splicing and ciliogenesis causes PRPF31 retinitis pigmentosa.
Adriana Buskin, Lili Zhu, Valeria Chichagova, Basudha Basu, Sina Mozaffari-Jovin, David Dolan, Alastair Droop, Joseph Collin, Revital Bronstein, Sudeep Mehrotra,[...]. Nat Commun 2018
52
9




Development of a gene-editing approach to restore vision loss in Leber congenital amaurosis type 10.
Morgan L Maeder, Michael Stefanidakis, Christopher J Wilson, Reshica Baral, Luis Alberto Barrera, George S Bounoutas, David Bumcrot, Hoson Chao, Dawn M Ciulla, Jennifer A DaSilva,[...]. Nat Med 2019
157
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
44
11

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
61
8

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
539
5

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
565
5


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.