A citation-based method for searching scientific literature

A Martínez-Mir, E Paloma, R Allikmets, C Ayuso, T del Rio, M Dean, L Vilageliu, R Gonzàlez-Duarte, S Balcells. Nat Genet 1998
Times Cited: 329







List of co-cited articles
1000 articles co-cited >1



Times Cited
  Times     Co-cited
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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
80

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
422
73

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
231
44

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
250
36

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
677
34

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
33

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
201
33


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
32

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
29

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
235
29

Variation of clinical expression in patients with Stargardt dystrophy and sequence variations in the ABCR gene.
G A Fishman, E M Stone, S Grover, D J Derlacki, H L Haines, R R Hockey. Arch Ophthalmol 1999
160
26

G1961E mutant allele in the Stargardt disease gene ABCA4 causes bull's eye maculopathy.
Wener Cella, Vivienne C Greenstein, Jana Zernant-Rajang, Theodore R Smith, Gaetano Barile, Rando Allikmets, Stephen H Tsang. Exp Eye Res 2009
68
35

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
92
25

An analysis of allelic variation in the ABCA4 gene.
A R Webster, E Héon, A J Lotery, K Vandenburgh, T L Casavant, K T Oh, G Beck, G A Fishman, B L Lam, A Levin,[...]. Invest Ophthalmol Vis Sci 2001
161
23

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
103
23


ABCA4 disease progression and a proposed strategy for gene therapy.
Artur V Cideciyan, Malgorzata Swider, Tomas S Aleman, Yaroslav Tsybovsky, Sharon B Schwartz, Elizabeth A M Windsor, Alejandro J Roman, Alexander Sumaroka, Janet D Steinberg, Samuel G Jacobson,[...]. Hum Mol Genet 2009
128
22


ABCA4 is an N-retinylidene-phosphatidylethanolamine and phosphatidylethanolamine importer.
Faraz Quazi, Stepan Lenevich, Robert S Molday. Nat Commun 2012
144
21

Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 gene.
Tomas R Burke, Gerald A Fishman, Jana Zernant, Carl Schubert, Stephen H Tsang, R Theodore Smith, Radha Ayyagari, Robert K Koenekoop, Allison Umfress, Maria Laura Ciccarelli,[...]. Invest Ophthalmol Vis Sci 2012
57
36

ABCA4 gene sequence variations in patients with autosomal recessive cone-rod dystrophy.
Gerald A Fishman, Edwin M Stone, David A Eliason, Chris M Taylor, Martin Lindeman, Deborah J Derlacki. Arch Ophthalmol 2003
76
26


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
21



Visual function in patients with cone-rod dystrophy (CRD) associated with mutations in the ABCA4(ABCR) gene.
D G Birch, A Y Peters, K L Locke, R Spencer, C F Megarity, G H Travis. Exp Eye Res 2001
50
34


Mutations in ABCR (ABCA4) in patients with Stargardt macular degeneration or cone-rod degeneration.
C E Briggs, D Rucinski, P J Rosenfeld, T Hirose, E L Berson, T P Dryja. Invest Ophthalmol Vis Sci 2001
99
16

ABCR unites what ophthalmologists divide(s)
M A van Driel, A Maugeri, B J Klevering, C B Hoyng, F P Cremers. Ophthalmic Genet 1998
94
17

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
16

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
144
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
106
15


ABCA4 mutations causing mislocalization are found frequently in patients with severe retinal dystrophies.
Wojciech Wiszniewski, Charles M Zaremba, Alexander N Yatsenko, Milan Jamrich, Theodore G Wensel, Richard Alan Lewis, James R Lupski. Hum Mol Genet 2005
65
21

Genotype-phenotype correlation in Italian families with Stargardt disease.
Francesca Simonelli, Francesco Testa, Jana Zernant, Anna Nesti, Settimio Rossi, Rando Allikmets, Ernesto Rinaldi. Ophthalmic Res 2005
37
37

RPE lipofuscin and its role in retinal pathobiology.
Janet R Sparrow, Mike Boulton. Exp Eye Res 2005
412
14

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
14

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
48
29

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
17

ISCEV Standard for full-field clinical electroretinography (2008 update).
M F Marmor, A B Fulton, G E Holder, Y Miyake, M Brigell, M Bach. Doc Ophthalmol 2009
759
13

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
44
29

Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone-rod dystrophy and retinitis pigmentosa.
B Jeroen Klevering, Suzanne Yzer, Klaus Rohrschneider, Marijke Zonneveld, Rando Allikmets, L Ingeborgh van den Born, Alessandra Maugeri, Carel B Hoyng, Frans P M Cremers. Eur J Hum Genet 2004
80
16

Correction of the disease phenotype in the mouse model of Stargardt disease by lentiviral gene therapy.
J Kong, S-R Kim, K Binley, I Pata, K Doi, J Mannik, J Zernant-Rajang, O Kan, S Iqball, S Naylor,[...]. Gene Ther 2008
144
13


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
187
13

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
127
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
18


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.