A citation-based method for searching scientific literature

Alberto Auricchio, Ivana Trapani, Rando Allikmets. Cold Spring Harb Perspect Med 2015
Times Cited: 20







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



Times Cited
  Times     Co-cited
Similarity


A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy.
R Allikmets, N Singh, H Sun, N F Shroyer, A Hutchinson, A Chidambaram, B Gerrard, L Baird, D Stauffer, A Peiffer,[...]. Nat Genet 1997
991
30

Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR.
F P Cremers, D J van de Pol, M van Driel, A I den Hollander, F J van Haren, N V Knoers, N Tijmes, A A Bergen, K Rohrschneider, A Blankenagel,[...]. Hum Mol Genet 1998
434
25

ABCA4 is an N-retinylidene-phosphatidylethanolamine and phosphatidylethanolamine importer.
Faraz Quazi, Stepan Lenevich, Robert S Molday. Nat Commun 2012
156
25

Gene therapy for Stargardt disease associated with ABCA4 gene.
Zongchao Han, Shannon M Conley, Muna I Naash. Adv Exp Med Biol 2014
49
25

Visual acuity loss and clinical observations in a large series of patients with Stargardt disease.
Ygal Rotenstreich, Gerald A Fishman, Robert J Anderson. Ophthalmology 2003
149
25

Stargardt disease: clinical features, molecular genetics, animal models and therapeutic options.
Preena Tanna, Rupert W Strauss, Kaoru Fujinami, Michel Michaelides. Br J Ophthalmol 2017
152
25



Clinical and molecular characteristics of childhood-onset Stargardt disease.
Kaoru Fujinami, Jana Zernant, Ravinder K Chana, Genevieve A Wright, Kazushige Tsunoda, Yoko Ozawa, Kazuo Tsubota, Anthony G Robson, Graham E Holder, Rando Allikmets,[...]. Ophthalmology 2015
98
20

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
720
20

Embryonic stem cell trials for macular degeneration: a preliminary report.
Steven D Schwartz, Jean-Pierre Hubschman, Gad Heilwell, Valentina Franco-Cardenas, Carolyn K Pan, Rosaleen M Ostrick, Edmund Mickunas, Roger Gay, Irina Klimanskaya, Robert Lanza. Lancet 2012
892
20

Analysis of the ABCA4 genomic locus in Stargardt disease.
Jana Zernant, Yajing Angela Xie, Carmen Ayuso, Rosa Riveiro-Alvarez, Miguel-Angel Lopez-Martinez, Francesca Simonelli, Francesco Testa, Michael B Gorin, Samuel P Strom, Mette Bertelsen,[...]. Hum Mol Genet 2014
87
20

Novel therapeutics for Stargardt disease.
Louise J Lu, Ji Liu, Ron A Adelman. Graefes Arch Clin Exp Ophthalmol 2017
34
20

Clinical and genetic characteristics of late-onset Stargardt's disease.
Sarah C Westeneng-van Haaften, Camiel J F Boon, Frans P M Cremers, Lies H Hoefsloot, Anneke I den Hollander, Carel B Hoyng. Ophthalmology 2012
113
15

In vivo fluorescence of the ocular fundus exhibits retinal pigment epithelium lipofuscin characteristics.
F C Delori, C K Dorey, G Staurenghi, O Arend, D G Goger, J J Weiter. Invest Ophthalmol Vis Sci 1995
725
15

Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration.
R Allikmets, N F Shroyer, N Singh, J M Seddon, R A Lewis, P S Bernstein, A Peiffer, N A Zabriskie, Y Li, A Hutchinson,[...]. Science 1997
682
15

Complement system dysregulation and inflammation in the retinal pigment epithelium of a mouse model for Stargardt macular degeneration.
Roxana A Radu, Jane Hu, Quan Yuan, Darcy L Welch, Jacob Makshanoff, Marcia Lloyd, Stephen McMullen, Gabriel H Travis, Dean Bok. J Biol Chem 2011
108
15

Quantitative fundus autofluorescence in recessive Stargardt disease.
Tomas R Burke, Tobias Duncker, Russell L Woods, Jonathan P Greenberg, Jana Zernant, Stephen H Tsang, R Theodore Smith, Rando Allikmets, Janet R Sparrow, François C Delori. Invest Ophthalmol Vis Sci 2014
120
15

Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophy.
A Maugeri, B J Klevering, K Rohrschneider, A Blankenagel, H G Brunner, A F Deutman, C B Hoyng, F P Cremers. Am J Hum Genet 2000
238
15

Accelerated accumulation of lipofuscin pigments in the RPE of a mouse model for ABCA4-mediated retinal dystrophies following Vitamin A supplementation.
Roxana A Radu, Quan Yuan, Jane Hu, Jennifer H Peng, Marcia Lloyd, Steven Nusinowitz, Dean Bok, Gabriel H Travis. Invest Ophthalmol Vis Sci 2008
120
15

Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy.
Francesco Testa, Settimio Rossi, Andrea Sodi, Ilaria Passerini, Valentina Di Iorio, Michele Della Corte, Sandro Banfi, Enrico Maria Surace, Ugo Menchini, Alberto Auricchio,[...]. Invest Ophthalmol Vis Sci 2012
52
15

Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus.
N Lois, G E Holder, C Bunce, F W Fitzke, A C Bird. Arch Ophthalmol 2001
213
15

A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlations.
Kaoru Fujinami, Noemi Lois, Alice E Davidson, Donna S Mackay, Chris R Hogg, Edwin M Stone, Kazushige Tsunoda, Kazuo Tsubota, Catey Bunce, Anthony G Robson,[...]. Am J Ophthalmol 2013
83
15


Embryonic stem cell lines derived from human blastocysts.
J A Thomson, J Itskovitz-Eldor, S S Shapiro, M A Waknitz, J J Swiergiel, V S Marshall, J M Jones. Science 1998
15

Induced pluripotent stem cell lines derived from human somatic cells.
Junying Yu, Maxim A Vodyanik, Kim Smuga-Otto, Jessica Antosiewicz-Bourget, Jennifer L Frane, Shulan Tian, Jeff Nie, Gudrun A Jonsdottir, Victor Ruotti, Ron Stewart,[...]. Science 2007
15

Clinical characteristics and current therapies for inherited retinal degenerations.
José-Alain Sahel, Katia Marazova, Isabelle Audo. Cold Spring Harb Perspect Med 2014
92
15

Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease.
Terry A Braun, Robert F Mullins, Alex H Wagner, Jeaneen L Andorf, Rebecca M Johnston, Benjamin B Bakall, Adam P Deluca, Gerald A Fishman, Byron L Lam, Richard G Weleber,[...]. Hum Mol Genet 2013
117
15

Rescue of the Stargardt phenotype in Abca4 knockout mice through inhibition of vitamin A dimerization.
Peter Charbel Issa, Alun R Barnard, Philipp Herrmann, Ilyas Washington, Robert E MacLaren. Proc Natl Acad Sci U S A 2015
76
15

A1120, a nonretinoid RBP4 antagonist, inhibits formation of cytotoxic bisretinoids in the animal model of enhanced retinal lipofuscinogenesis.
Nicoleta Dobri, Qiong Qin, Jian Kong, Kazunori Yamamoto, Zhao Liu, Gennadiy Moiseyev, Jian-Xing Ma, Rando Allikmets, Janet R Sparrow, Konstantin Petrukhin. Invest Ophthalmol Vis Sci 2013
55
15


Effective delivery of large genes to the retina by dual AAV vectors.
Ivana Trapani, Pasqualina Colella, Andrea Sommella, Carolina Iodice, Giulia Cesi, Sonia de Simone, Elena Marrocco, Settimio Rossi, Massimo Giunti, Arpad Palfi,[...]. EMBO Mol Med 2014
141
15

The ATP-binding cassette transporter ABCA4: structural and functional properties and role in retinal disease.
Yaroslav Tsybovsky, Robert S Molday, Krzysztof Palczewski. Adv Exp Med Biol 2010
116
15

The molecular basis of human retinal and vitreoretinal diseases.
Wolfgang Berger, Barbara Kloeckener-Gruissem, John Neidhardt. Prog Retin Eye Res 2010
353
15

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
15

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
15

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
15

Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort-Impact of Selected Deep Intronic Variants and Common SNPs.
Heidi L Schulz, Felix Grassmann, Ulrich Kellner, Georg Spital, Klaus Rüther, Herbert Jägle, Karsten Hufendiek, Philipp Rating, Cord Huchzermeyer, Maria J Baier,[...]. Invest Ophthalmol Vis Sci 2017
76
15

A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity.
Martin Jinek, Krzysztof Chylinski, Ines Fonfara, Michael Hauer, Jennifer A Doudna, Emmanuelle Charpentier. Science 2012
15

Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequence.
Artur V Cideciyan, Tomas S Aleman, Malgorzata Swider, Sharon B Schwartz, Janet D Steinberg, Alexander J Brucker, Albert M Maguire, Jean Bennett, Edwin M Stone, Samuel G Jacobson. Hum Mol Genet 2004
196
10

Isolation and one-step preparation of A2E and iso-A2E, fluorophores from human retinal pigment epithelium.
C A Parish, M Hashimoto, K Nakanishi, J Dillon, J Sparrow. Proc Natl Acad Sci U S A 1998
357
10

Rpe65 Leu450Met variant is associated with reduced levels of the retinal pigment epithelium lipofuscin fluorophores A2E and iso-A2E.
So Ra Kim, Nathan Fishkin, Jian Kong, Koji Nakanishi, Rando Allikmets, Janet R Sparrow. Proc Natl Acad Sci U S A 2004
110
10

The spectrum of retinal phenotypes caused by mutations in the ABCA4 gene.
B Jeroen Klevering, August F Deutman, Alessandra Maugeri, Frans P M Cremers, Carel B Hoyng. Graefes Arch Clin Exp Ophthalmol 2005
95
10

ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathy.
M Michaelides, L L Chen, M A Brantley, J L Andorf, E M Isaak, S A Jenkins, G E Holder, A C Bird, E M Stone, A R Webster. Br J Ophthalmol 2007
60
10

Spectrum of ABCR gene mutations in autosomal recessive macular dystrophies.
J M Rozet, S Gerber, E Souied, I Perrault, S Châtelin, I Ghazi, C Leowski, J L Dufier, A Munnich, J Kaplan. Eur J Hum Genet 1998
128
10

Predicting functional effect of human missense mutations using PolyPhen-2.
Ivan Adzhubei, Daniel M Jordan, Shamil R Sunyaev. Curr Protoc Hum Genet 2013
10

Allelic variation in ABCR associated with Stargardt disease but not age-related macular degeneration.
E M Stone, A R Webster, K Vandenburgh, L M Streb, R R Hockey, A J Lotery, V C Sheffield. Nat Genet 1998
159
10


Fundus autofluorescence in the Abca4(-/-) mouse model of Stargardt disease--correlation with accumulation of A2E, retinal function, and histology.
Peter Charbel Issa, Alun R Barnard, Mandeep S Singh, Emma Carter, Zhichun Jiang, Roxana A Radu, Ulrich Schraermeyer, Robert E MacLaren. Invest Ophthalmol Vis Sci 2013
69
10

In vivo measurement of lipofuscin in Stargardt's disease--Fundus flavimaculatus.
F C Delori, G Staurenghi, O Arend, C K Dorey, D G Goger, J J Weiter. Invest Ophthalmol Vis Sci 1995
196
10


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.