A citation-based method for searching scientific literature

Rehan M Hussain, Thomas A Ciulla, Audina M Berrocal, Ninel Z Gregori, Harry W Flynn, Byron L Lam. Expert Opin Biol Ther 2018
Times Cited: 22







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



Times Cited
  Times     Co-cited
Similarity


Stargardt disease: clinical features, molecular genetics, animal models and therapeutic options.
Preena Tanna, Rupert W Strauss, Kaoru Fujinami, Michel Michaelides. Br J Ophthalmol 2017
137
45

Emixustat Hydrochloride for Geographic Atrophy Secondary to Age-Related Macular Degeneration: A Randomized Clinical Trial.
Philip J Rosenfeld, Pravin U Dugel, Frank G Holz, Jeffrey S Heier, Joel A Pearlman, Roger L Novack, Karl G Csaky, John M Koester, Jeffrey K Gregory, Ryo Kubota. Ophthalmology 2018
59
27

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
50
27

Novel therapeutics for Stargardt disease.
Louise J Lu, Ji Liu, Ron A Adelman. Graefes Arch Clin Exp Ophthalmol 2017
33
27

Progression of Stargardt Disease as Determined by Fundus Autofluorescence in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 9).
Rupert W Strauss, Beatriz Muñoz, Alexander Ho, Anamika Jha, Michel Michaelides, Artur V Cideciyan, Isabelle Audo, David G Birch, Amir H Hariri, Muneeswar G Nittala,[...]. JAMA Ophthalmol 2017
46
22

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
70
22

The Natural History of the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Studies: Design and Baseline Characteristics: ProgStar Report No. 1.
Rupert W Strauss, Alex Ho, Beatriz Muñoz, Artur V Cideciyan, José-Alain Sahel, Janet S Sunness, David G Birch, Paul S Bernstein, Michel Michaelides, Elias I Traboulsi,[...]. Ophthalmology 2016
87
18

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
966
18

Visual Acuity Change Over 24 Months and Its Association With Foveal Phenotype and Genotype in Individuals With Stargardt Disease: ProgStar Study Report No. 10.
Xiangrong Kong, Kaoru Fujinami, Rupert W Strauss, Beatriz Munoz, Sheila K West, Artur V Cideciyan, Michel Michaelides, Mohamed Ahmed, Ann-Margret Ervin, Etienne Schönbach,[...]. JAMA Ophthalmol 2018
27
18

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
674
18

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
82
18

Clinical and molecular analysis of Stargardt disease with preserved foveal structure and function.
Kaoru Fujinami, Panagiotis I Sergouniotis, Alice E Davidson, Genevieve Wright, Ravinder K Chana, Kazushige Tsunoda, Kazuo Tsubota, Catherine A Egan, Anthony G Robson, Anthony T Moore,[...]. Am J Ophthalmol 2013
71
18

Pharmacotherapy of retinal disease with visual cycle modulators.
Rehan M Hussain, Ninel Z Gregori, Thomas A Ciulla, Byron L Lam. Expert Opin Pharmacother 2018
18
22

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
110
18

Investigation of oral fenretinide for treatment of geographic atrophy in age-related macular degeneration.
Nathan L Mata, Jay B Lichter, Roger Vogel, Yun Han, Tam V Bui, Lawrence J Singerman. Retina 2013
96
18

Transplantation of Human Embryonic Stem Cell-Derived Retinal Pigment Epithelial Cells in Macular Degeneration.
Manjit S Mehat, Venki Sundaram, Caterina Ripamonti, Anthony G Robson, Alexander J Smith, Shyamanga Borooah, Martha Robinson, Adam N Rosenthal, William Innes, Richard G Weleber,[...]. Ophthalmology 2018
81
13


COMPARISON OF MANUAL AND SEMIAUTOMATED FUNDUS AUTOFLUORESCENCE ANALYSIS OF MACULAR ATROPHY IN STARGARDT DISEASE PHENOTYPE.
Laura Kuehlewein, Amir H Hariri, Alexander Ho, Laurie Dustin, Yulia Wolfson, Rupert W Strauss, Hendrik P N Scholl, SriniVas R Sadda. Retina 2016
40
13

Incidence of Atrophic Lesions in Stargardt Disease in the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Study: Report No. 5.
Rupert W Strauss, Beatriz Muñoz, Alex Ho, Anamika Jha, Michel Michaelides, Saddek Mohand-Said, Artur V Cideciyan, David Birch, Amir H Hariri, Muneeswar G Nittala,[...]. JAMA Ophthalmol 2017
33
13

Dark Atrophy: An Optical Coherence Tomography Angiography Study.
Marco Pellegrini, Alessandra Acquistapace, Marta Oldani, Matteo Giuseppe Cereda, Andrea Giani, Mariano Cozzi, Giovanni Staurenghi. Ophthalmology 2016
46
13

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
44
13

Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy.
Kamron N Khan, Melissa Kasilian, Omar A R Mahroo, Preena Tanna, Angelos Kalitzeos, Anthony G Robson, Kazushige Tsunoda, Takeshi Iwata, Anthony T Moore, Kaoru Fujinami,[...]. Ophthalmology 2018
28
13

Macular Sensitivity Measured With Microperimetry in Stargardt Disease in the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Study: Report No. 7.
Etienne M Schönbach, Yulia Wolfson, Rupert W Strauss, Mohamed A Ibrahim, Xiangrong Kong, Beatriz Muñoz, David G Birch, Artur V Cideciyan, Gesa-Astrid Hahn, Muneeswar Nittala,[...]. JAMA Ophthalmol 2017
39
13

In Silico Functional Meta-Analysis of 5,962 ABCA4 Variants in 3,928 Retinal Dystrophy Cases.
Stéphanie S Cornelis, Nathalie M Bax, Jana Zernant, Rando Allikmets, Lars G Fritsche, Johan T den Dunnen, Muhammad Ajmal, Carel B Hoyng, Frans P M Cremers. Hum Mutat 2017
69
13

Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides.
Riccardo Sangermano, Alejandro Garanto, Mubeen Khan, Esmee H Runhart, Miriam Bauwens, Nathalie M Bax, L Ingeborgh van den Born, Muhammad Imran Khan, Stéphanie S Cornelis, Joke B G M Verheij,[...]. Genet Med 2019
65
13

Genotyping microarray (gene chip) for the ABCR (ABCA4) gene.
K Jaakson, J Zernant, M Külm, A Hutchinson, N Tonisson, D Glavac, M Ravnik-Glavac, M Hawlina, M R Meltzer, R C Caruso,[...]. Hum Mutat 2003
180
13

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
106
13

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
13

Frequent hypomorphic alleles account for a significant fraction of ABCA4 disease and distinguish it from age-related macular degeneration.
Jana Zernant, Winston Lee, Frederick T Collison, Gerald A Fishman, Yuri V Sergeev, Kaspar Schuerch, Janet R Sparrow, Stephen H Tsang, Rando Allikmets. J Med Genet 2017
78
13

An augmented ABCA4 screen targeting noncoding regions reveals a deep intronic founder variant in Belgian Stargardt patients.
Miriam Bauwens, Julie De Zaeytijd, Nicole Weisschuh, Susanne Kohl, Françoise Meire, Karin Dahan, Fanny Depasse, Sarah De Jaegere, Thomy De Ravel, Marjan De Rademaeker,[...]. Hum Mutat 2015
47
13

ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders: novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variants.
Miriam Bauwens, Alejandro Garanto, Riccardo Sangermano, Sarah Naessens, Nicole Weisschuh, Julie De Zaeytijd, Mubeen Khan, Françoise Sadler, Irina Balikova, Caroline Van Cauwenbergh,[...]. Genet Med 2019
45
13

Correlations among near-infrared and short-wavelength autofluorescence and spectral-domain optical coherence tomography in recessive Stargardt disease.
Tobias Duncker, Marcela Marsiglia, Winston Lee, Jana Zernant, Stephen H Tsang, Rando Allikmets, Vivienne C Greenstein, Janet R Sparrow. Invest Ophthalmol Vis Sci 2014
60
13

Expanding the Mutation Spectrum in ABCA4: Sixty Novel Disease Causing Variants and Their Associated Phenotype in a Large French Stargardt Cohort.
Marco Nassisi, Saddek Mohand-Saïd, Claire-Marie Dhaenens, Fiona Boyard, Vanessa Démontant, Camille Andrieu, Aline Antonio, Christel Condroyer, Marine Foussard, Cécile Méjécase,[...]. Int J Mol Sci 2018
12
25

Analysis of the ABCA4 gene by next-generation sequencing.
Jana Zernant, Carl Schubert, Kate M Im, Tomas Burke, Carolyn M Brown, Gerald A Fishman, Stephen H Tsang, Peter Gouras, Michael Dean, Rando Allikmets. Invest Ophthalmol Vis Sci 2011
111
13

Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus.
N Lois, G E Holder, C Bunce, F W Fitzke, A C Bird. Arch Ophthalmol 2001
203
13


Progression of Stargardt Disease as Determined by Fundus Autofluorescence Over a 12-Month Period: ProgStar Report No. 11.
Rupert W Strauss, Xiangrong Kong, Alexander Ho, Anamika Jha, Sheila West, Michael Ip, Paul S Bernstein, David G Birch, Artur V Cideciyan, Michel Michaelides,[...]. JAMA Ophthalmol 2019
28
13

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
91
13

A longitudinal study of Stargardt disease: quantitative assessment of fundus autofluorescence, progression, and genotype correlations.
Kaoru Fujinami, Noemi Lois, Rajarshi Mukherjee, Vikki A McBain, Kazushige Tsunoda, Kazuo Tsubota, Edwin M Stone, Fred W Fitzke, Catey Bunce, Anthony T Moore,[...]. Invest Ophthalmol Vis Sci 2013
81
13

Gene therapy for Stargardt disease associated with ABCA4 gene.
Zongchao Han, Shannon M Conley, Muna I Naash. Adv Exp Med Biol 2014
46
13

Identification and characterization of a non-retinoid ligand for retinol-binding protein 4 which lowers serum retinol-binding protein 4 levels in vivo.
Alykhan Motani, Zhulun Wang, Marion Conn, Karen Siegler, Ying Zhang, Qingxiang Liu, Sheree Johnstone, Haoda Xu, Steve Thibault, Yingcai Wang,[...]. J Biol Chem 2009
54
13

Early-onset stargardt disease: phenotypic and genotypic characteristics.
Stanley Lambertus, Ramon A C van Huet, Nathalie M Bax, Lies H Hoefsloot, Frans P M Cremers, Camiel J F Boon, B Jeroen Klevering, Carel B Hoyng. Ophthalmology 2015
70
13

Towards Treatment of Stargardt Disease: Workshop Organized and Sponsored by the Foundation Fighting Blindness.
Avery E Sears, Paul S Bernstein, Artur V Cideciyan, Carel Hoyng, Peter Charbel Issa, Krzysztof Palczewski, Philip J Rosenfeld, SriniVas Sadda, Ulrich Schraermeyer, Janet R Sparrow,[...]. Transl Vis Sci Technol 2017
30
13

Primary amines protect against retinal degeneration in mouse models of retinopathies.
Akiko Maeda, Marcin Golczak, Yu Chen, Kiichiro Okano, Hideo Kohno, Satomi Shiose, Kaede Ishikawa, William Harte, Grazyna Palczewska, Tadao Maeda,[...]. Nat Chem Biol 2011
105
13

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
68
13

Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations.
Frans P M Cremers, Winston Lee, Rob W J Collin, Rando Allikmets. Prog Retin Eye Res 2020
53
13

Reductions in serum vitamin A arrest accumulation of toxic retinal fluorophores: a potential therapy for treatment of lipofuscin-based retinal diseases.
Roxana A Radu, Yun Han, Tam V Bui, Steven Nusinowitz, Dean Bok, Jay Lichter, Ken Widder, Gabriel H Travis, Nathan L Mata. Invest Ophthalmol Vis Sci 2005
159
13

A bioengineered retinal pigment epithelial monolayer for advanced, dry age-related macular degeneration.
Amir H Kashani, Jane S Lebkowski, Firas M Rahhal, Robert L Avery, Hani Salehi-Had, Wei Dang, Chih-Min Lin, Debbie Mitra, Danhong Zhu, Biju B Thomas,[...]. Sci Transl Med 2018
131
9


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
9


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.