A citation-based method for searching scientific literature

Hendrik P N Scholl, Dorothea Besch, Reinhard Vonthein, Bernhard H F Weber, Eckart Apfelstedt-Sylla. Invest Ophthalmol Vis Sci 2002
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


Rod pathways: the importance of seeing nothing.
L T Sharpe, A Stockman. Trends Neurosci 1999
156
40

Convergence and segregation of the multiple rod pathways in mammalian retina.
Béla Völgyi, Michael R Deans, David L Paul, Stewart A Bloomfield. J Neurosci 2004
124
40

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
79
40

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
947
30


Histopathology and immunocytochemistry of the neurosensory retina in fundus flavimaculatus.
C D Birnbach, M Järveläinen, D E Possin, A H Milam. Ophthalmology 1994
159
30

Two signals in the human rod visual system: a model based on electrophysiological data.
A Stockman, L T Sharpe, K Rüther, K Nordby. Vis Neurosci 1995
43
30

In vivo studies of signaling in rod pathways of the mouse using the electroretinogram.
J G Robson, H Maeda, S M Saszik, L J Frishman. Vision Res 2004
68
30

Parallel processing in the mammalian retina.
Heinz Wässle. Nat Rev Neurosci 2004
660
30

Clinical electrophysiology of two rod pathways: normative values and clinical application.
H P Scholl, H Langrová, B H Weber, E Zrenner, E Apfelstedt-Sylla. Graefes Arch Clin Exp Ophthalmol 2001
18
30


Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene.
H P Scholl, H Langrová, C M Pusch, B Wissinger, E Zrenner, E Apfelstedt-Sylla. Invest Ophthalmol Vis Sci 2001
31
30

Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.
Christina Zeitz, Maria van Genderen, John Neidhardt, Ulrich F O Luhmann, Frank Hoeben, Ursula Forster, Katharina Wycisk, Gábor Mátyás, Carel B Hoyng, Frans Riemslag,[...]. Invest Ophthalmol Vis Sci 2005
103
30

Rod vision: pathways and processing in the mammalian retina.
S A Bloomfield, R F Dacheux. Prog Retin Eye Res 2001
231
30

Slow and fast pathways in the human rod visual system: electrophysiology and psychophysics.
A Stockman, L T Sharpe, E Zrenner, K Nordby. J Opt Soc Am A 1991
45
30

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
41
30

[Fundus flavimaculatus].
A Franceschetti, J François. Arch Ophtalmol Rev Gen Ophtalmol 1965
56
20

Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus.
N Lois, G E Holder, C Bunce, F W Fitzke, A C Bird. Arch Ophthalmol 2001
200
20

Fundus flavimaculatus and Stargardt's disease.
O B Hadden, J D Gass. Am J Ophthalmol 1976
86
20



The dark choroid in posterior retinal dystrophies.
G Fish, R Grey, K S Sehmi, A C Bird. Br J Ophthalmol 1981
64
20


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
49
20

A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p.
K L Anderson, L Baird, R A Lewis, A C Chinault, B Otterud, M Leppert, J R Lupski. Am J Hum Genet 1995
42
20

Fundus flavimaculatus. A clinical classification.
G A Fishman. Arch Ophthalmol 1976
149
20

Flicker electroretinograms: a systems analytic approach.
J V Odom, D Reits, N Burgers, F C Riemslag. Optom Vis Sci 1992
41
20




Dual rod pathways in complete achromatopsia.
K Rüther, L T Sharpe, E Zrenner. Ger J Ophthalmol 1994
6
33

Rod photoreceptors detect rapid flicker.
J D Conner, D I MacLeod. Science 1977
75
20

Into the twilight zone: the complexities of mesopic vision and luminous efficiency.
Andrew Stockman, Lindsay T Sharpe. Ophthalmic Physiol Opt 2006
108
20

The spectral properties of the two rod pathways.
L T Sharpe, C C Fach, A Stockman. Vision Res 1993
13
20

Mutations in TRPM1 are a common cause of complete congenital stationary night blindness.
Maria M van Genderen, Mieke M C Bijveld, Yvonne B Claassen, Ralph J Florijn, Jillian N Pearring, Francoise M Meire, Maureen A McCall, Frans C C Riemslag, Ronald G Gregg, Arthur A B Bergen,[...]. Am J Hum Genet 2009
141
20

A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder.
Karin W Littink, Maria M van Genderen, Rob W J Collin, Susanne Roosing, Arjan P M de Brouwer, Frans C C Riemslag, Hanka Venselaar, Alberta A H J Thiadens, Carel B Hoyng, Klaus Rohrschneider,[...]. Invest Ophthalmol Vis Sci 2009
57
20

Controlling the gain of rod-mediated signals in the Mammalian retina.
Felice A Dunn, Thuy Doan, Alapakkam P Sampath, Fred Rieke. J Neurosci 2006
127
20

Improved electrode for electroretinography.
W W Dawson, G L Trick, C A Litzkow. Invest Ophthalmol Vis Sci 1979
295
20

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
749
20

Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6.
Thaddeus P Dryja, Terri L McGee, Eliot L Berson, Gerald A Fishman, Michael A Sandberg, Kenneth R Alexander, Deborah J Derlacki, Aruna S Rajagopalan. Proc Natl Acad Sci U S A 2005
163
20

Rods cancel cones in flicker.
D I MacLeod. Nature 1972
90
20

An extended 15 Hz ERG protocol (1): the contributions of primary and secondary rod pathways and the cone pathway.
Mieke M C Bijveld, Astrid M L Kappers, Frans C C Riemslag, Frank P Hoeben, Anne C L Vrijling, Maria M van Genderen. Doc Ophthalmol 2011
8
25

Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene.
Qingjiong Zhang, Fareeha Zulfiqar, Xueshan Xiao, S Amer Riazuddin, Zahoor Ahmad, Raphael Caruso, Ian MacDonald, Paul Sieving, Sheikh Riazuddin, J Fielding Hejtmancik. Hum Genet 2007
78
20

Retinitis pigmentosa.
Dyonne T Hartong, Eliot L Berson, Thaddeus P Dryja. Lancet 2006
20

A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration.
M A Maw, D Corbeil, J Koch, A Hellwig, J C Wilson-Wheeler, R J Bridges, G Kumaramanickavel, S John, D Nancarrow, K Röper,[...]. Hum Mol Genet 2000
208
20

Retinopathy in mice induced by disrupted all-trans-retinal clearance.
Akiko Maeda, Tadao Maeda, Marcin Golczak, Krzysztof Palczewski. J Biol Chem 2008
193
20

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
103
20

A new locus for autosomal dominant stargardt-like disease maps to chromosome 4.
M Kniazeva, M F Chiang, B Morgan, A L Anduze, D J Zack, M Han, K Zhang. Am J Hum Genet 1999
66
20

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
249
20

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
100
20


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.