A citation-based method for searching scientific literature

G SCHUBERT, H BORNSCHEIN. Ophthalmologica 1952
Times Cited: 227







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



Times Cited
  Times     Co-cited
Similarity


Evidence for genetic heterogeneity in X-linked congenital stationary night blindness.
K M Boycott, W G Pearce, M A Musarella, R G Weleber, T A Maybaum, D G Birch, Y Miyake, R S Young, N T Bech-Hansen. Am J Hum Genet 1998
36
27


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
128
10

Characteristic ERG-flicker anomaly in incomplete congenital stationary night blindness.
Y Miyake, M Horiguchi, I Ota, N Shiroyama. Invest Ophthalmol Vis Sci 1987
74
13


Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness.
S Yamamoto, K C Sippel, E L Berson, T P Dryja. Nat Genet 1997
189
10


Retinal and optic disc atrophy associated with a CACNA1F mutation in a Japanese family.
Makoto Nakamura, Sei Ito, Chang-Hua Piao, Hiroko Terasaki, Yozo Miyake. Arch Ophthalmol 2003
27
37

Photopic abnormalities in congenital stationary nightblindness.
A E Krill, D Martin. Invest Ophthalmol 1971
54
16

Rod and cone function in the Nougaret form of stationary night blindness.
M A Sandberg, B S Pawlyk, J Dan, B Arnaud, T P Dryja, E L Berson. Arch Ophthalmol 1998
24
37


Variable expressivity in X-linked congenital stationary night blindness.
W G Pearce, M Reedyk, S G Coupland. Can J Ophthalmol 1990
43
20


Developmentally regulated postsynaptic localization of a metabotropic glutamate receptor in rat rod bipolar cells.
A Nomura, R Shigemoto, Y Nakamura, N Okamoto, N Mizuno, S Nakanishi. Cell 1994
356
9

Identification and functional characterization of a novel rhodopsin mutation associated with autosomal dominant CSNB.
Christina Zeitz, Alecia K Gross, Dorothee Leifert, Barbara Kloeckener-Gruissem, Suzanne D McAlear, Johannes Lemke, John Neidhardt, Wolfgang Berger. Invest Ophthalmol Vis Sci 2008
42
21

Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB).
Marion Neuillé, Said El Shamieh, Elise Orhan, Christelle Michiels, Aline Antonio, Marie-Elise Lancelot, Christel Condroyer, Kinga Bujakowska, Olivier Poch, José-Alain Sahel,[...]. PLoS One 2014
36
25


A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants.
K M Boycott, T A Maybaum, M J Naylor, R G Weleber, J Robitaille, Y Miyake, A A Bergen, M E Pierpont, W G Pearce, N T Bech-Hansen. Hum Genet 2001
66
12

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
25

Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina.
Fiona Mansergh, Noelle C Orton, John P Vessey, Melanie R Lalonde, William K Stell, Francois Tremblay, Steven Barnes, Derrick E Rancourt, N Torben Bech-Hansen. Hum Mol Genet 2005
190
8

Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2.
Carolyn I Hope, Dianne M Sharp, Ariana Hemara-Wahanui, Jennifer I Sissingh, Patricia Lundon, Ed A Mitchell, Marion A Maw, Gillian M Clover. Clin Exp Ophthalmol 2005
58
13

The light response of ON bipolar neurons requires G[alpha]o.
A Dhingra, A Lyubarsky, M Jiang, E N Pugh, L Birnbaumer, P Sterling, N Vardi. J Neurosci 2000
158
8

Localization of nyctalopin in the mammalian retina.
Catherine W Morgans, Gaoying Ren, Lakshmi Akileswaran. Eur J Neurosci 2006
56
14


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
8

Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses.
Dennis M Maddox, Kirstan A Vessey, Gary L Yarbrough, Brandon M Invergo, Donald R Cantrell, Samsoon Inayat, Victoria Balannik, Wanda L Hicks, Norman L Hawes, Shannon Byers,[...]. J Physiol 2008
50
16

Essential role of Ca2+-binding protein 4, a Cav1.4 channel regulator, in photoreceptor synaptic function.
Françoise Haeseleer, Yoshikazu Imanishi, Tadao Maeda, Daniel E Possin, Akiko Maeda, Amy Lee, Fred Rieke, Krzysztof Palczewski. Nat Neurosci 2004
218
8

Further insights into GPR179: expression, localization, and associated pathogenic mechanisms leading to complete congenital stationary night blindness.
Elise Orhan, Laurent Prézeau, Said El Shamieh, Kinga M Bujakowska, Christelle Michiels, Yvrick Zagar, Claire Vol, Shomi S Bhattacharya, José-Alain Sahel, Florian Sennlaub,[...]. Invest Ophthalmol Vis Sci 2013
16
50

Localization of CSNBX (CSNB4) between the retinitis pigmentosa loci RP2 and RP3 on proximal Xp.
A J Hardcastle, Z K David-Gray, M Jay, A C Bird, S S Bhattacharya. Invest Ophthalmol Vis Sci 1997
16
43


The photopic electroretinogram in congenital stationary night blindness with myopia.
P Lachapelle, J M Little, R C Polomeno. Invest Ophthalmol Vis Sci 1983
115
7



X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene.
R Jalkanen, M Mäntyjärvi, R Tobias, J Isosomppi, E-M Sankila, T Alitalo, N T Bech-Hansen. J Med Genet 2006
58
12


TRPM1 forms ion channels associated with melanin content in melanocytes.
Elena Oancea, Joris Vriens, Sebastian Brauchi, Janice Jun, Igor Splawski, David E Clapham. Sci Signal 2009
127
7

Effects of presynaptic mutations on a postsynaptic Cacna1s calcium channel colocalized with mGluR6 at mouse photoreceptor ribbon synapses.
Dana Specht, Shu-Biao Wu, Paul Turner, Peter Dearden, Frank Koentgen, Uwe Wolfrum, Marion Maw, Johann Helmut Brandstätter, Susanne tom Dieck. Invest Ophthalmol Vis Sci 2009
77
9

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
12

Structural and functional abnormalities of retinal ribbon synapses due to Cacna2d4 mutation.
Katharina A Wycisk, Birgit Budde, Silke Feil, Sergej Skosyrski, Francesca Buzzi, John Neidhardt, Esther Glaus, Peter Nürnberg, Klaus Ruether, Wolfgang Berger. Invest Ophthalmol Vis Sci 2006
91
7

Generation, identification and functional characterization of the nob4 mutation of Grm6 in the mouse.
Lawrence H Pinto, Martha H Vitaterna, Kazuhiro Shimomura, Sandra M Siepka, Victoria Balannik, Erin L McDearmon, Chiaki Omura, Stephen Lumayag, Brandon M Invergo, Brett Glawe,[...]. Vis Neurosci 2007
50
14

Gbeta5 is required for normal light responses and morphology of retinal ON-bipolar cells.
Anjali Rao, Rebecca Dallman, Scott Henderson, Ching-Kang Chen. J Neurosci 2007
80
8

Identification of the gene and the mutation responsible for the mouse nob phenotype.
Ronald G Gregg, Suparna Mukhopadhyay, Sophie I Candille, Sherry L Ball, Machelle T Pardue, Maureen A McCall, Neal S Peachey. Invest Ophthalmol Vis Sci 2003
85
8


Dysregulation of Ca(v)1.4 channels disrupts the maturation of photoreceptor synaptic ribbons in congenital stationary night blindness type 2.
Xiaoni Liu, Vasily Kerov, Françoise Haeseleer, Anurima Majumder, Nikolai Artemyev, Sheila A Baker, Amy Lee. Channels (Austin) 2013
66
10

A truncated form of rod photoreceptor PDE6 β-subunit causes autosomal dominant congenital stationary night blindness by interfering with the inhibitory activity of the γ-subunit.
Gaël Manes, Pallavi Cheguru, Anurima Majumder, Béatrice Bocquet, Audrey Sénéchal, Nikolai O Artemyev, Christian P Hamel, Philippe Brabet. PLoS One 2014
15
46

LRIT3 is essential to localize TRPM1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation.
Marion Neuillé, Catherine W Morgans, Yan Cao, Elise Orhan, Christelle Michiels, José-Alain Sahel, Isabelle Audo, Robert M Duvoisin, Kirill A Martemyanov, Christina Zeitz. Eur J Neurosci 2015
28
25

Paraneoplastic night blindness with malignant melanoma.
E L Berson, S Lessell. Am J Ophthalmol 1988
128
6


The leucine-rich repeat: a versatile binding motif.
B Kobe, J Deisenhofer. Trends Biochem Sci 1994
939
6

Congenital stationary nightblindness.
R E Carr. Trans Am Ophthalmol Soc 1974
57
10


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.