A citation-based method for searching scientific literature

Charles B Wright, Micah A Chrenek, Wei Feng, Shannon E Getz, Todd Duncan, Machelle T Pardue, Yue Feng, T Michael Redmond, Jeffrey H Boatright, John M Nickerson. Invest Ophthalmol Vis Sci 2014
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


Independent visual threshold measurements in the two eyes of freely moving rats and mice using a virtual-reality optokinetic system.
R M Douglas, N M Alam, B D Silver, T J McGill, W W Tschetter, G T Prusky. Vis Neurosci 2005
271
45

Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).
Ji-Jing Pang, Bo Chang, Norman L Hawes, Ronald E Hurd, Muriel T Davisson, Jie Li, Syed M Noorwez, Ritu Malhotra, J Hugh McDowell, Shalesh Kaushal,[...]. Mol Vis 2005
160
36

Rpe65 is the retinoid isomerase in bovine retinal pigment epithelium.
Minghao Jin, Songhua Li, Walid N Moghrabi, Hui Sun, Gabriel H Travis. Cell 2005
327
36

Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle.
T M Redmond, S Yu, E Lee, D Bok, D Hamasaki, N Chen, P Goletz, J X Ma, R K Crouch, K Pfeifer. Nat Genet 1998
730
36

R91W mutation in Rpe65 leads to milder early-onset retinal dystrophy due to the generation of low levels of 11-cis-retinal.
Marijana Samardzija, Johannes von Lintig, Naoyuki Tanimoto, Vitus Oberhauser, Markus Thiersch, Charlotte E Remé, Mathias Seeliger, Christian Grimm, Andreas Wenzel. Hum Mol Genet 2008
74
36

Complementation test of Rpe65 knockout and tvrm148.
Charles B Wright, Micah A Chrenek, Stephanie L Foster, Todd Duncan, T Michael Redmond, Machelle T Pardue, Jeffrey H Boatright, John M Nickerson. Invest Ophthalmol Vis Sci 2013
9
44

Rapid quantification of adult and developing mouse spatial vision using a virtual optomotor system.
Glen T Prusky, Nazia M Alam, Steven Beekman, Robert M Douglas. Invest Ophthalmol Vis Sci 2004
510
36

Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy.
S M Gu, D A Thompson, C R Srikumari, B Lorenz, U Finckh, A Nicoletti, K R Murthy, M Rathmann, G Kumaramanickavel, M J Denton,[...]. Nat Genet 1997
490
27

A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement.
Sara J Bowne, Marian M Humphries, Lori S Sullivan, Paul F Kenna, Lawrence C S Tam, Anna S Kiang, Matthew Campbell, George M Weinstock, Daniel C Koboldt, Li Ding,[...]. Eur J Hum Genet 2011
101
27

Mouse model resources for vision research.
Jungyeon Won, Lan Ying Shi, Wanda Hicks, Jieping Wang, Ronald Hurd, Jürgen K Naggert, Bo Chang, Patsy M Nishina. J Ophthalmol 2011
58
27

Mutation of key residues of RPE65 abolishes its enzymatic role as isomerohydrolase in the visual cycle.
T Michael Redmond, Eugenia Poliakov, Shirley Yu, Jen-Yue Tsai, Zhongjian Lu, Susan Gentleman. Proc Natl Acad Sci U S A 2005
300
27

RPE65 is the isomerohydrolase in the retinoid visual cycle.
Gennadiy Moiseyev, Ying Chen, Yusuke Takahashi, Bill X Wu, Jian-Xing Ma. Proc Natl Acad Sci U S A 2005
377
27

Early visual deficits in streptozotocin-induced diabetic long evans rats.
Moe H Aung, Moon K Kim, Darin E Olson, Peter M Thule, Machelle T Pardue. Invest Ophthalmol Vis Sci 2013
91
27

Dark adaptation and the retinoid cycle of vision.
T D Lamb, E N Pugh. Prog Retin Eye Res 2004
449
27

Mutations of the opsin gene (Y102H and I307N) lead to light-induced degeneration of photoreceptors and constitutive activation of phototransduction in mice.
Ewa Budzynski, Alecia K Gross, Suzanne D McAlear, Neal S Peachey, Meera Shukla, Feng He, Malia Edwards, Jungyeon Won, Wanda L Hicks, Theodore G Wensel,[...]. J Biol Chem 2010
28
27

Insights into the pathogenesis of dominant retinitis pigmentosa associated with a D477G mutation in RPE65.
Elliot H Choi, Susie Suh, Christopher L Sander, Christian J Ortiz Hernandez, Elizabeth R Bulman, Nimesh Khadka, Zhiqian Dong, Wuxian Shi, Krzysztof Palczewski, Philip D Kiser. Hum Mol Genet 2018
16
27

Retinal degeneration mutants in the mouse.
B Chang, N L Hawes, R E Hurd, M T Davisson, S Nusinowitz, J R Heckenlively. Vision Res 2002
556
27

Non-syndromic retinitis pigmentosa.
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
233
27

Importance of membrane structural integrity for RPE65 retinoid isomerization activity.
Marcin Golczak, Philip D Kiser, David T Lodowski, Akiko Maeda, Krzysztof Palczewski. J Biol Chem 2010
48
18

Identification of a novel palmitylation site essential for membrane association and isomerohydrolase activity of RPE65.
Yusuke Takahashi, Gennadiy Moiseyev, Zsolt Ablonczy, Ying Chen, Rosalie K Crouch, Jian-Xing Ma. J Biol Chem 2009
27
18

Negative charge of the glutamic acid 417 residue is crucial for isomerohydrolase activity of RPE65.
Olga Nikolaeva, Yusuke Takahashi, Gennadiy Moiseyev, Jian-Xing Ma. Biochem Biophys Res Commun 2010
10
20

Crystal structure of native RPE65, the retinoid isomerase of the visual cycle.
Philip D Kiser, Marcin Golczak, David T Lodowski, Mark R Chance, Krzysztof Palczewski. Proc Natl Acad Sci U S A 2009
103
18

Fatty acid transport protein 4 (FATP4) prevents light-induced degeneration of cone and rod photoreceptors by inhibiting RPE65 isomerase.
Songhua Li, Jungsoo Lee, Yongdong Zhou, William C Gordon, James M Hill, Nicolas G Bazan, Jeffrey H Miner, Minghao Jin. J Neurosci 2013
26
18

Mutations in RPE65 cause Leber's congenital amaurosis.
F Marlhens, C Bareil, J M Griffoin, E Zrenner, P Amalric, C Eliaou, S Y Liu, E Harris, T M Redmond, B Arnaud,[...]. Nat Genet 1997
487
18

The role of interphotoreceptor retinoid-binding protein on the translocation of visual retinoids and function of cone photoreceptors.
Minghao Jin, Songhua Li, Steven Nusinowitz, Marcia Lloyd, Jane Hu, Roxana A Radu, Dean Bok, Gabriel H Travis. J Neurosci 2009
67
18

Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration.
D A Thompson, P Gyürüs, L L Fleischer, E L Bingham, C L McHenry, E Apfelstedt-Sylla, E Zrenner, B Lorenz, J E Richards, S G Jacobson,[...]. Invest Ophthalmol Vis Sci 2000
184
18

Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis.
H Morimura, G A Fishman, S A Grover, A B Fulton, E L Berson, T P Dryja. Proc Natl Acad Sci U S A 1998
344
18


Purified RPE65 shows isomerohydrolase activity after reassociation with a phospholipid membrane.
Olga Nikolaeva, Yusuke Takahashi, Gennadiy Moiseyev, Jian-Xing Ma. FEBS J 2009
31
18

Retinyl esters are the substrate for isomerohydrolase.
Gennadiy Moiseyev, Rosalie K Crouch, Patrice Goletz, John Oatis, T Michael Redmond, Jian-xing Ma. Biochemistry 2003
99
18


Role of LRAT on the retinoid isomerase activity and membrane association of Rpe65.
Minghao Jin, Quan Yuan, Songhua Li, Gabriel H Travis. J Biol Chem 2007
36
18

Structure of RPE65 isomerase in a lipidic matrix reveals roles for phospholipids and iron in catalysis.
Philip D Kiser, Erik R Farquhar, Wuxian Shi, Xuewu Sui, Mark R Chance, Krzysztof Palczewski. Proc Natl Acad Sci U S A 2012
47
18

Proteasome overload is a common stress factor in multiple forms of inherited retinal degeneration.
Ekaterina S Lobanova, Stella Finkelstein, Nikolai P Skiba, Vadim Y Arshavsky. Proc Natl Acad Sci U S A 2013
66
18

Dopamine deficiency contributes to early visual dysfunction in a rodent model of type 1 diabetes.
Moe H Aung, Han Na Park, Moon K Han, Tracy S Obertone, Jane Abey, Fazila Aseem, Peter M Thule, P Michael Iuvone, Machelle T Pardue. J Neurosci 2014
79
18


Generation, characterization, and molecular cloning of the Noerg-1 mutation of rhodopsin in the mouse.
Lawrence H Pinto, Martha H Vitaterna, Kazuhiro Shimomura, Sandra M Siepka, Erin L McDearmon, Deborah Fenner, Stephen L Lumayag, Chiaki Omura, Anne W Andrews, Matthew Baker,[...]. Vis Neurosci 2005
17
18

Light-activated channels targeted to ON bipolar cells restore visual function in retinal degeneration.
Pamela S Lagali, David Balya, Gautam B Awatramani, Thomas A Münch, Douglas S Kim, Volker Busskamp, Constance L Cepko, Botond Roska. Nat Neurosci 2008
342
18

The optomotor response: a robust first-line visual screening method for mice.
Jellali Abdeljalil, Meziane Hamid, Ouagazzal Abdel-Mouttalib, Rousseau Stéphane, Romand Raymond, Auwerx Johan, Sahel José, Chambon Pierre, Picaud Serge. Vision Res 2005
76
18

Congenital stationary night blindness in mice - a tale of two Cacna1f mutants.
N Lodha, S Bonfield, N C Orton, C J Doering, J E McRory, S C Mema, R Rehak, Y Sauvé, R Tobias, W K Stell,[...]. Adv Exp Med Biol 2010
25
18

Increased susceptibility to light damage in an arrestin knockout mouse model of Oguchi disease (stationary night blindness)
J Chen, M I Simon, M T Matthes, D Yasumura, M M LaVail. Invest Ophthalmol Vis Sci 1999
139
18

A mouse M-opsin monochromat: retinal cone photoreceptors have increased M-opsin expression when S-opsin is knocked out.
Lauren L Daniele, Christine Insinna, Rebecca Chance, Jinhua Wang, Sergei S Nikonov, Edward N Pugh. Vision Res 2011
30
18


Diseases caused by defects in the visual cycle: retinoids as potential therapeutic agents.
Gabriel H Travis, Marcin Golczak, Alexander R Moise, Krzysztof Palczewski. Annu Rev Pharmacol Toxicol 2007
283
18

edgeR: a Bioconductor package for differential expression analysis of digital gene expression data.
Mark D Robinson, Davis J McCarthy, Gordon K Smyth. Bioinformatics 2010
18

Retinopathy in mice induced by disrupted all-trans-retinal clearance.
Akiko Maeda, Tadao Maeda, Marcin Golczak, Krzysztof Palczewski. J Biol Chem 2008
200
18

Retinal light damage: mechanisms and protection.
Daniel T Organisciak, Dana K Vaughan. Prog Retin Eye Res 2010
325
18

The Rd8 mutation of the Crb1 gene is present in vendor lines of C57BL/6N mice and embryonic stem cells, and confounds ocular induced mutant phenotypes.
Mary J Mattapallil, Eric F Wawrousek, Chi-Chao Chan, Hui Zhao, Jayeeta Roychoudhury, Thomas A Ferguson, Rachel R Caspi. Invest Ophthalmol Vis Sci 2012
442
18

Involvement of all-trans-retinal in acute light-induced retinopathy of mice.
Akiko Maeda, Tadao Maeda, Marcin Golczak, Steven Chou, Amar Desai, Charles L Hoppel, Shigemi Matsuyama, Krzysztof Palczewski. J Biol Chem 2009
172
18

Melatonin modulates visual function and cell viability in the mouse retina via the MT1 melatonin receptor.
Kenkichi Baba, Nikita Pozdeyev, Francesca Mazzoni, Susana Contreras-Alcantara, Cuimei Liu, Manami Kasamatsu, Theresa Martinez-Merlos, Enrica Strettoi, P Michael Iuvone, Gianluca Tosini. Proc Natl Acad Sci U S A 2009
90
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.