A citation-based method for searching scientific literature

Faraz Quazi, Stepan Lenevich, Robert S Molday. Nat Commun 2012
Times Cited: 153







List of co-cited articles
1491 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
983
35



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
431
21

Structure of the Human Lipid Exporter ABCA1.
Hongwu Qian, Xin Zhao, Pingping Cao, Jianlin Lei, Nieng Yan, Xin Gong. Cell 2017
138
20


Stargardt disease: clinical features, molecular genetics, animal models and therapeutic options.
Preena Tanna, Rupert W Strauss, Kaoru Fujinami, Michel Michaelides. Br J Ophthalmol 2017
148
19




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
236
16

Crystal structure of the human sterol transporter ABCG5/ABCG8.
Jyh-Yeuan Lee, Lisa N Kinch, Dominika M Borek, Jin Wang, Junmei Wang, Ina L Urbatsch, Xiao-Song Xie, Nikolai V Grishin, Jonathan C Cohen, Zbyszek Otwinowski,[...]. Nature 2016
164
16


Structure of a bacterial multidrug ABC transporter.
Roger J P Dawson, Kaspar P Locher. Nature 2006
951
15

Molecular organization and ATP-induced conformational changes of ABCA4, the photoreceptor-specific ABC transporter.
Yaroslav Tsybovsky, Tivadar Orban, Robert S Molday, Derek Taylor, Krzysztof Palczewski. Structure 2013
43
34

Retinopathy in mice induced by disrupted all-trans-retinal clearance.
Akiko Maeda, Tadao Maeda, Marcin Golczak, Krzysztof Palczewski. J Biol Chem 2008
205
15

Structure and mechanism of an active lipid-linked oligosaccharide flippase.
Camilo Perez, Sabina Gerber, Jérémy Boilevin, Monika Bucher, Tamis Darbre, Markus Aebi, Jean-Louis Reymond, Kaspar P Locher. Nature 2015
143
14

N965S is a common ABCA4 variant in Stargardt-related retinopathies in the Danish population.
Thomas Rosenberg, Flemming Klie, Peter Garred, Marianne Schwartz. Mol Vis 2007
47
29



Protein misfolding and the pathogenesis of ABCA4-associated retinal degenerations.
Ning Zhang, Yaroslav Tsybovsky, Alexander V Kolesnikov, Malgorzata Rozanowska, Malgorzata Swider, Sharon B Schwartz, Edwin M Stone, Grazyna Palczewska, Akiko Maeda, Vladimir J Kefalov,[...]. Hum Mol Genet 2015
52
26

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
88
15


A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration.
A Rivera, K White, H Stöhr, K Steiner, N Hemmrich, T Grimm, B Jurklies, B Lorenz, H P Scholl, E Apfelstedt-Sylla,[...]. Am J Hum Genet 2000
255
13


Correlating the Expression and Functional Activity of ABCA4 Disease Variants With the Phenotype of Patients With Stargardt Disease.
Fabian Garces, Kailun Jiang, Laurie L Molday, Heidi Stöhr, Bernhard H Weber, Christopher J Lyons, David Maberley, Robert S Molday. Invest Ophthalmol Vis Sci 2018
30
43

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
111
12

Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt disease.
R A Lewis, N F Shroyer, N Singh, R Allikmets, A Hutchinson, Y Li, J R Lupski, M Leppert, M Dean. Am J Hum Genet 1999
239
12


Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR.
A Martínez-Mir, E Paloma, R Allikmets, C Ayuso, T del Rio, M Dean, L Vilageliu, R Gonzàlez-Duarte, S Balcells. Nat Genet 1998
333
12

RPE lipofuscin and its role in retinal pathobiology.
Janet R Sparrow, Mike Boulton. Exp Eye Res 2005
422
12


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
76
15

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
70
17

ATP binding to the motor domain from an ABC transporter drives formation of a nucleotide sandwich dimer.
Paul C Smith, Nathan Karpowich, Linda Millen, Jonathan E Moody, Jane Rosen, Philip J Thomas, John F Hunt. Mol Cell 2002
645
11

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
112
11


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
681
11


The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt disease.
A Maugeri, M A van Driel, D J van de Pol, B J Klevering, F J van Haren, N Tijmes, A A Bergen, K Rohrschneider, A Blankenagel, A J Pinckers,[...]. Am J Hum Genet 1999
207
11


Screening of ABCA4 Gene in a Chinese Cohort With Stargardt Disease or Cone-Rod Dystrophy With a Report on 85 Novel Mutations.
Feng Jiang, Zhe Pan, Ke Xu, Lu Tian, Yue Xie, Xiaohui Zhang, Jieqiong Chen, Bing Dong, Yang Li. Invest Ophthalmol Vis Sci 2016
37
29

Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus.
N Lois, G E Holder, C Bunce, F W Fitzke, A C Bird. Arch Ophthalmol 2001
207
11

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
72
15

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
85
12

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
74
14

Expression of ABCA4 in the retinal pigment epithelium and its implications for Stargardt macular degeneration.
Tamara L Lenis, Jane Hu, Sze Yin Ng, Zhichun Jiang, Shanta Sarfare, Marcia B Lloyd, Nicholas J Esposito, William Samuel, Cynthia Jaworski, Dean Bok,[...]. Proc Natl Acad Sci U S A 2018
45
24

Crystal structure of the multidrug transporter P-glycoprotein from Caenorhabditis elegans.
Mi Sun Jin, Michael L Oldham, Qiuju Zhang, Jue Chen. Nature 2012
326
10

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
108
10

Genetic and clinical analysis of ABCA4-associated disease in African American patients.
Jana Zernant, Frederick T Collison, Winston Lee, Gerald A Fishman, Kalev Noupuu, Bo Yuan, Carolyn Cai, James R Lupski, Lawrence A Yannuzzi, Stephen H Tsang,[...]. Hum Mutat 2014
32
31


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.