A citation-based method for searching scientific literature

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
Times Cited: 215







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



Times Cited
  Times     Co-cited
Similarity


Retinitis pigmentosa.
Dyonne T Hartong, Eliot L Berson, Thaddeus P Dryja. Lancet 2006
34

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
18

Retinitis pigmentosa.
Christian Hamel. Orphanet J Rare Dis 2006
468
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
16

Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions.
Neruban Kumaran, Anthony T Moore, Richard G Weleber, Michel Michaelides. Br J Ophthalmol 2017
108
13

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
12

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
11

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
11

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
11

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
15

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
9

Progressive cone and cone-rod dystrophies: clinical features, molecular genetics and prospects for therapy.
Jasdeep S Gill, Michalis Georgiou, Angelos Kalitzeos, Anthony T Moore, Michel Michaelides. Br J Ophthalmol 2019
48
16


Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect.
Artur V Cideciyan, Samuel G Jacobson, Arlene V Drack, Allen C Ho, Jason Charng, Alexandra V Garafalo, Alejandro J Roman, Alexander Sumaroka, Ian C Han, Maria D Hochstedler,[...]. Nat Med 2019
102
8

Next-generation sequencing identifies unexpected genotype-phenotype correlations in patients with retinitis pigmentosa.
Johannes Birtel, Martin Gliem, Elisabeth Mangold, Philipp L Müller, Frank G Holz, Christine Neuhaus, Steffen Lenzner, Diana Zahnleiter, Christian Betz, Tobias Eisenberger,[...]. PLoS One 2018
35
22

Retinitis pigmentosa.
R A Pagon. Surv Ophthalmol 1988
196
8

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
7

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
518
7

Emerging therapies for inherited retinal degeneration.
Hendrik P N Scholl, Rupert W Strauss, Mandeep S Singh, Deniz Dalkara, Botond Roska, Serge Picaud, José-Alain Sahel. Sci Transl Med 2016
107
7

Clinical course, genetic etiology, and visual outcome in cone and cone-rod dystrophy.
Alberta A H J Thiadens, T My Lan Phan, Renate C Zekveld-Vroon, Bart P Leroy, L Ingeborgh van den Born, Carel B Hoyng, Caroline C W Klaver, Susanne Roosing, Jan-Willem R Pott, Mary J van Schooneveld,[...]. Ophthalmology 2012
81
8

Safety and efficacy of gene transfer for Leber's congenital amaurosis.
Albert M Maguire, Francesca Simonelli, Eric A Pierce, Edward N Pugh, Federico Mingozzi, Jeannette Bennicelli, Sandro Banfi, Kathleen A Marshall, Francesco Testa, Enrico M Surace,[...]. N Engl J Med 2008
7

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
7

Retinal gene therapy in patients with choroideremia: initial findings from a phase 1/2 clinical trial.
Robert E MacLaren, Markus Groppe, Alun R Barnard, Charles L Cottriall, Tanya Tolmachova, Len Seymour, K Reed Clark, Matthew J During, Frans P M Cremers, Graeme C M Black,[...]. Lancet 2014
497
7

Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa.
R Vervoort, A Lennon, A C Bird, B Tulloch, R Axton, M G Miano, A Meindl, T Meitinger, A Ciccodicola, A F Wright. Nat Genet 2000
312
7

Progress in treating inherited retinal diseases: Early subretinal gene therapy clinical trials and candidates for future initiatives.
Alexandra V Garafalo, Artur V Cideciyan, Elise Héon, Rebecca Sheplock, Alexander Pearson, Caberry WeiYang Yu, Alexander Sumaroka, Gustavo D Aguirre, Samuel G Jacobson. Prog Retin Eye Res 2020
50
14



Inherited Retinal Degenerations: Current Landscape and Knowledge Gaps.
Jacque L Duncan, Eric A Pierce, Amy M Laster, Stephen P Daiger, David G Birch, John D Ash, Alessandro Iannaccone, John G Flannery, José A Sahel, Donald J Zack,[...].  2018
64
9

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
416
6

Human embryonic stem cell-derived retinal pigment epithelium in patients with age-related macular degeneration and Stargardt's macular dystrophy: follow-up of two open-label phase 1/2 studies.
Steven D Schwartz, Carl D Regillo, Byron L Lam, Dean Eliott, Philip J Rosenfeld, Ninel Z Gregori, Jean-Pierre Hubschman, Janet L Davis, Gad Heilwell, Marc Spirn,[...]. Lancet 2015
662
6

Genes and mutations causing retinitis pigmentosa.
S P Daiger, L S Sullivan, S J Bowne. Clin Genet 2013
312
6

Retinitis pigmentosa: genes and disease mechanisms.
Stefano Ferrari, Enzo Di Iorio, Vanessa Barbaro, Diego Ponzin, Francesco S Sorrentino, Francesco Parmeggiani. Curr Genomics 2011
279
6

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
196
6

Beneficial effects on vision in patients undergoing retinal gene therapy for choroideremia.
Kanmin Xue, Jasleen K Jolly, Alun R Barnard, Anna Rudenko, Anna P Salvetti, Maria I Patrício, Thomas L Edwards, Markus Groppe, Harry O Orlans, Tanya Tolmachova,[...]. Nat Med 2018
74
8

Visual Acuity after Retinal Gene Therapy for Choroideremia.
Thomas L Edwards, Jasleen K Jolly, Markus Groppe, Alun R Barnard, Charles L Cottriall, Tanya Tolmachova, Graeme C Black, Andrew R Webster, Andrew J Lotery, Graham E Holder,[...]. N Engl J Med 2016
138
6

Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait.
Alan F Wright, Christina F Chakarova, Mai M Abd El-Aziz, Shomi S Bhattacharya. Nat Rev Genet 2010
389
6

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
15


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
6

Retinal organization in the retinal degeneration 10 (rd10) mutant mouse: a morphological and ERG study.
Claudia Gargini, Eva Terzibasi, Francesca Mazzoni, Enrica Strettoi. J Comp Neurol 2007
331
5

The mechanism of cone cell death in Retinitis Pigmentosa.
Peter A Campochiaro, Tahreem A Mir. Prog Retin Eye Res 2018
114
5

Cone rod dystrophies.
Christian P Hamel. Orphanet J Rare Dis 2007
265
5

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
258
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

Stargardt disease: clinical features, molecular genetics, animal models and therapeutic options.
Preena Tanna, Rupert W Strauss, Kaoru Fujinami, Michel Michaelides. Br J Ophthalmol 2017
134
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

Long-term safety of human retinal progenitor cell transplantation in retinitis pigmentosa patients.
Yong Liu, Shao Jun Chen, Shi Ying Li, Ling Hui Qu, Xiao Hong Meng, Yi Wang, Hai Wei Xu, Zhi Qing Liang, Zheng Qin Yin. Stem Cell Res Ther 2017
35
14

AAV-mediated gene therapy for retinal degeneration in the rd10 mouse containing a recessive PDEbeta mutation.
Ji-Jing Pang, Sanford L Boye, Ashok Kumar, Astra Dinculescu, Wentao Deng, Jie Li, Qiuhong Li, Asha Rani, Thomas C Foster, Bo Chang,[...]. Invest Ophthalmol Vis Sci 2008
103
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
66
7



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.