A citation-based method for searching scientific literature

C Li, M Cheng, H Yang, N S Peachey, M I Naash. Optom Vis Sci 2001
Times Cited: 67







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



Times Cited
  Times     Co-cited
Similarity


Structure-function analysis of rods and cones in juvenile, adult, and aged C57bl/6 and Balb/c mice.
Jeffrey Gresh, Patrice W Goletz, Rosalie K Crouch, Baerbel Rohrer. Vis Neurosci 2003
107
41

Cone-based vision in the aging mouse.
Gary A Williams, Gerald H Jacobs. Vision Res 2007
35
48


Age-related deterioration of rod vision in mice.
Alexander V Kolesnikov, Jie Fan, Rosalie K Crouch, Vladimir J Kefalov. J Neurosci 2010
56
23

Preservation of retinal structure in aged pigmented mice.
R A Trachimowicz, L J Fisher, J W Hinds. Neurobiol Aging 1981
29
37


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
13

The major cell populations of the mouse retina.
C J Jeon, E Strettoi, R H Masland. J Neurosci 1998
884
13

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
506
11

A naturally occurring mouse model of X-linked congenital stationary night blindness.
M T Pardue, M A McCall, M M LaVail, R G Gregg, N S Peachey. Invest Ophthalmol Vis Sci 1998
126
10

The effect of peripherin/rds haploinsufficiency on rod and cone photoreceptors.
T Cheng, N S Peachey, S Li, Y Goto, Y Cao, M I Naash. J Neurosci 1997
82
10


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
727
8

Augmented rod bipolar cell function in partial receptor loss: an ERG study in P23H rhodopsin transgenic and aging normal rats.
T S Aleman, M M LaVail, R Montemayor, G Ying, M M Maguire, A M Laties, S G Jacobson, A V Cideciyan. Vision Res 2001
79
8

The murine cone photoreceptor: a single cone type expresses both S and M opsins with retinal spatial patterning.
M L Applebury, M P Antoch, L C Baxter, L L Chun, J D Falk, F Farhangfar, K Kage, M G Krzystolik, L A Lyass, J T Robbins. Neuron 2000
394
8


Temporal properties of the mouse cone electroretinogram.
Vivek R Krishna, Kenneth R Alexander, Neal S Peachey. J Neurophysiol 2002
58
10

Lipofuscin accumulation, abnormal electrophysiology, and photoreceptor degeneration in mutant ELOVL4 transgenic mice: a model for macular degeneration.
G Karan, C Lillo, Z Yang, D J Cameron, K G Locke, Y Zhao, S Thirumalaichary, C Li, D G Birch, H R Vollmer-Snarr,[...]. Proc Natl Acad Sci U S A 2005
132
8


Age-dependent remodelling of retinal circuitry.
E Terzibasi, M Calamusa, E Novelli, L Domenici, E Strettoi, A Cellerino. Neurobiol Aging 2009
44
13

The ageing photoreceptor.
Alexander Cunea, Glen Jeffery. Vis Neurosci 2007
36
16

Death by color: differential cone loss in the aging mouse retina.
Alexander Cunea, Michael B Powner, Glen Jeffery. Neurobiol Aging 2014
22
27


Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis.
G Clarke, A F Goldberg, D Vidgen, L Collins, L Ploder, L Schwarz, L L Molday, J Rossant, A Szél, R S Molday,[...]. Nat Genet 2000
123
7


Morphological, physiological, and biochemical changes in rhodopsin knockout mice.
J Lem, N V Krasnoperova, P D Calvert, B Kosaras, D A Cameron, M Nicolò, C L Makino, R L Sidman. Proc Natl Acad Sci U S A 1999
313
7

Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.
Z M Ahmed, S Riazuddin, S L Bernstein, Z Ahmed, S Khan, A J Griffith, R J Morell, T B Friedman, S Riazuddin, E R Wilcox. Am J Hum Genet 2001
282
7

The relationship between opsin overexpression and photoreceptor degeneration.
E Tan, Q Wang, A B Quiambao, X Xu, N M Qtaishat, N S Peachey, J Lem, S J Fliesler, D R Pepperberg, M I Naash,[...]. Invest Ophthalmol Vis Sci 2001
131
7


Simulation of human autosomal dominant retinitis pigmentosa in transgenic mice expressing a mutated murine opsin gene.
M I Naash, J G Hollyfield, M R al-Ubaidi, W Baehr. Proc Natl Acad Sci U S A 1993
162
7


Genetic inactivation of an inwardly rectifying potassium channel (Kir4.1 subunit) in mice: phenotypic impact in retina.
P Kofuji, P Ceelen, K R Zahs, L W Surbeck, H A Lester, E A Newman. J Neurosci 2000
325
7



Morphological and functional abnormalities in the inner retina of the rd/rd mouse.
Enrica Strettoi, Vittorio Porciatti, Benedetto Falsini, Vincenzo Pignatelli, Chiara Rossi. J Neurosci 2002
227
7

A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy.
K Zhang, M Kniazeva, M Han, W Li, Z Yu, Z Yang, Y Li, M L Metzker, R Allikmets, D J Zack,[...]. Nat Genet 2001
324
7


Dendrites of rod bipolar cells sprout in normal aging retina.
Lauren C Liets, Kasra Eliasieh, Deborah A van der List, Leo M Chalupa. Proc Natl Acad Sci U S A 2006
68
7


Age- and sex-related differences in contrast sensitivity in C57BL/6 mice.
Bart van Alphen, Beerend H J Winkelman, Maarten A Frens. Invest Ophthalmol Vis Sci 2009
41
12

Aging of the human photoreceptor mosaic: evidence for selective vulnerability of rods in central retina.
C A Curcio, C L Millican, K A Allen, R E Kalina. Invest Ophthalmol Vis Sci 1993
456
7

Retinal organization in the retinal degeneration 10 (rd10) mutant mouse: a morphological and ERG study.
Claudia Gargini, Eva Terzibasi, Francesca Mazzoni, Enrica Strettoi. J Comp Neurol 2007
331
7

The development of the rod photoresponse from dark-adapted rats.
A B Fulton, R M Hansen, O Findl. Invest Ophthalmol Vis Sci 1995
61
6

Modifications of retinal neurons in a mouse model of retinitis pigmentosa.
E Strettoi, V Pignatelli. Proc Natl Acad Sci U S A 2000
230
5

Constitutive "light" adaptation in rods from G90D rhodopsin: a mechanism for human congenital nightblindness without rod cell loss.
P A Sieving, M L Fowler, R A Bush, S Machida, P D Calvert, D G Green, C L Makino, C L McHenry. J Neurosci 2001
64
6

Defective myosin VIIA gene responsible for Usher syndrome type 1B.
D Weil, S Blanchard, J Kaplan, P Guilford, F Gibson, J Walsh, P Mburu, A Varela, J Levilliers, M D Weston. Nature 1995
696
5

Analysis of ERG a-wave amplification and kinetics in terms of the G-protein cascade of phototransduction.
M E Breton, A W Schueller, T D Lamb, E N Pugh. Invest Ophthalmol Vis Sci 1994
190
5

Role of the beta(2) subunit of voltage-dependent calcium channels in the retinal outer plexiform layer.
Sherry L Ball, Patricia A Powers, Hee-Sup Shin, Catherine W Morgans, Neal S Peachey, Ronald G Gregg. Invest Ophthalmol Vis Sci 2002
145
5

Specific deficit of the ON response in visual transmission by targeted disruption of the mGluR6 gene.
M Masu, H Iwakabe, Y Tagawa, T Miyoshi, M Yamashita, Y Fukuda, H Sasaki, K Hiroi, Y Nakamura, R Shigemoto. Cell 1995
364
5

The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene.
K N Alagramam, C L Murcia, H Y Kwon, K S Pawlowski, C G Wright, R P Woychik. Nat Genet 2001
232
5


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.