A citation-based method for searching scientific literature

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
Times Cited: 167







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



Times Cited
  Times     Co-cited
Similarity


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
108
49

TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.
Isabelle Audo, Susanne Kohl, Bart P Leroy, Francis L Munier, Xavier Guillonneau, Saddek Mohand-Saïd, Kinga Bujakowska, Emeline F Nandrot, Birgit Lorenz, Markus Preising,[...]. Am J Hum Genet 2009
161
48

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
N T Bech-Hansen, M J Naylor, T A Maybaum, R L Sparkes, B Koop, D G Birch, A A Bergen, C F Prinsen, R C Polomeno, A Gal,[...]. Nat Genet 2000
237
46

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
146
43

Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.
Zheng Li, Panagiotis I Sergouniotis, Michel Michaelides, Donna S Mackay, Genevieve A Wright, Sophie Devery, Anthony T Moore, Graham E Holder, Anthony G Robson, Andrew R Webster. Am J Hum Genet 2009
125
40

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
C M Pusch, C Zeitz, O Brandau, K Pesch, H Achatz, S Feil, C Scharfe, J Maurer, F K Jacobi, A Pinckers,[...]. Nat Genet 2000
186
40

Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness.
Isabelle Audo, Kinga Bujakowska, Elise Orhan, Charlotte M Poloschek, Sabine Defoort-Dhellemmes, Isabelle Drumare, Susanne Kohl, Tien D Luu, Odile Lecompte, Eberhart Zrenner,[...]. Am J Hum Genet 2012
88
44

GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.
Neal S Peachey, Thomas A Ray, Ralph Florijn, Lucy B Rowe, Trijntje Sjoerdsma, Susana Contreras-Alcantara, Kenkichi Baba, Gianluca Tosini, Nikita Pozdeyev, P Michael Iuvone,[...]. Am J Hum Genet 2012
94
40

Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness.
Christina Zeitz, Samuel G Jacobson, Christian P Hamel, Kinga Bujakowska, Marion Neuillé, Elise Orhan, Xavier Zanlonghi, Marie-Elise Lancelot, Christelle Michiels, Sharon B Schwartz,[...]. Am J Hum Genet 2013
89
40

Congenital stationary night blindness with negative electroretinogram. A new classification.
Y Miyake, K Yagasaki, M Horiguchi, Y Kawase, T Kanda. Arch Ophthalmol 1986
351
35

TRPM1 is a component of the retinal ON bipolar cell transduction channel in the mGluR6 cascade.
Chieko Koike, Takehisa Obara, Yoshitsugu Uriu, Tomohiro Numata, Rikako Sanuki, Kentarou Miyata, Toshiyuki Koyasu, Shinji Ueno, Kazuo Funabiki, Akiko Tani,[...]. Proc Natl Acad Sci U S A 2010
199
35

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
369
34

TRPM1 is required for the depolarizing light response in retinal ON-bipolar cells.
Catherine W Morgans, Jianmei Zhang, Brett G Jeffrey, Steve M Nelson, Neal S Burke, Robert M Duvoisin, R Lane Brown. Proc Natl Acad Sci U S A 2009
203
34

[Analysis of the human electroretinogram].
G SCHUBERT, H BORNSCHEIN. Ophthalmologica 1952
226
33


Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness.
Christina Zeitz, Barbara Kloeckener-Gruissem, Ursula Forster, Susanne Kohl, István Magyar, Bernd Wissinger, Gábor Mátyás, François-Xavier Borruat, Daniel F Schorderet, Eberhart Zrenner,[...]. Am J Hum Genet 2006
122
26

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.
T M Strom, G Nyakatura, E Apfelstedt-Sylla, H Hellebrand, B Lorenz, B H Weber, K Wutz, N Gutwillinger, K Rüther, B Drescher,[...]. Nat Genet 1998
346
22

Nyctalopin expression in retinal bipolar cells restores visual function in a mouse model of complete X-linked congenital stationary night blindness.
Ronald G Gregg, Maarten Kamermans, Jan Klooster, Peter D Lukasiewicz, Neal S Peachey, Kirstan A Vessey, Maureen A McCall. J Neurophysiol 2007
71
30

Night blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein trafficking.
Christina Zeitz, Ursula Forster, John Neidhardt, Silke Feil, Stefan Kälin, Dorothee Leifert, Peter J Flor, Wolfgang Berger. Hum Mutat 2007
47
44

A transient receptor potential-like channel mediates synaptic transmission in rod bipolar cells.
Yin Shen, J Alexander Heimel, Maarten Kamermans, Neal S Peachey, Ronald G Gregg, Scott Nawy. J Neurosci 2009
154
21

Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
N T Bech-Hansen, M J Naylor, T A Maybaum, W G Pearce, B Koop, G A Fishman, M Mets, M A Musarella, K M Boycott. Nat Genet 1998
369
20

A role for nyctalopin, a small leucine-rich repeat protein, in localizing the TRP melastatin 1 channel to retinal depolarizing bipolar cell dendrites.
Jillian N Pearring, Pasano Bojang, Yin Shen, Chieko Koike, Takahisa Furukawa, Scott Nawy, Ronald G Gregg. J Neurosci 2011
64
31


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
762
17

A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness.
S Amer Riazuddin, Amber Shahzadi, Christina Zeitz, Zubair M Ahmed, Radha Ayyagari, Venkata R M Chavali, Virgilio G Ponferrada, Isabelle Audo, Christelle Michiels, Marie-Elise Lancelot,[...]. Am J Hum Genet 2010
48
35

TRPM1 mutations are associated with the complete form of congenital stationary night blindness.
Makoto Nakamura, Rikako Sanuki, Tetsuhiro R Yasuma, Akishi Onishi, Koji M Nishiguchi, Chieko Koike, Mikiko Kadowaki, Mineo Kondo, Yozo Miyake, Takahisa Furukawa. Mol Vis 2010
74
22

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
17


The negative ERG: clinical phenotypes and disease mechanisms of inner retinal dysfunction.
Isabelle Audo, Anthony G Robson, Graham E Holder, Anthony T Moore. Surv Ophthalmol 2008
91
17

Genotype and phenotype of 101 dutch patients with congenital stationary night blindness.
Mieke M C Bijveld, Ralph J Florijn, Arthur A B Bergen, L Ingeborgh van den Born, Maarten Kamermans, Liesbeth Prick, Frans C C Riemslag, Mary J van Schooneveld, Astrid M L Kappers, Maria M van Genderen. Ophthalmology 2013
57
28

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
32

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
44


Localization of nyctalopin in the mammalian retina.
Catherine W Morgans, Gaoying Ren, Lakshmi Akileswaran. Eur J Neurosci 2006
56
26

TRPM1: the endpoint of the mGluR6 signal transduction cascade in retinal ON-bipolar cells.
Catherine W Morgans, Ronald Lane Brown, Robert M Duvoisin. Bioessays 2010
68
22

Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation.
Neal S Peachey, Jillian N Pearring, Pasano Bojang, Matthew E Hirschtritt, Gwen Sturgill-Short, Thomas A Ray, Takahisa Furukawa, Chieko Koike, Andrew F X Goldberg, Yin Shen,[...]. J Neurophysiol 2012
34
41


Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy.
Katharina Agnes Wycisk, Christina Zeitz, Silke Feil, Mariana Wittmer, Ursula Forster, John Neidhardt, Bernd Wissinger, Eberhart Zrenner, Robert Wilke, Susanne Kohl,[...]. Am J Hum Genet 2006
105
13

A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 gene.
Panagiotis I Sergouniotis, Anthony G Robson, Zheng Li, Sophie Devery, Graham E Holder, Anthony T Moore, Andrew R Webster. Acta Ophthalmol 2012
24
54


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
13

Genotyping microarray for CSNB-associated genes.
Christina Zeitz, Stephan Labs, Birgit Lorenz, Ursula Forster, Janne Uksti, Hester Y Kroes, Elfride De Baere, Bart P Leroy, Frans P M Cremers, Mariana Wittmer,[...]. Invest Ophthalmol Vis Sci 2009
30
40

GPR179 is required for high sensitivity of the mGluR6 signaling cascade in depolarizing bipolar cells.
Thomas A Ray, Kathryn M Heath, Nazarul Hasan, Jennifer M Noel, Ivy S Samuels, Kirill A Martemyanov, Neal S Peachey, Maureen A McCall, Ronald G Gregg. J Neurosci 2014
42
28


Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus).
Rebecca R Bellone, Samantha A Brooks, Lynne Sandmeyer, Barbara A Murphy, George Forsyth, Sheila Archer, Ernest Bailey, Bruce Grahn. Genetics 2008
106
11

GPR158/179 regulate G protein signaling by controlling localization and activity of the RGS7 complexes.
Cesare Orlandi, Ekaterina Posokhova, Ikuo Masuho, Thomas A Ray, Nazarul Hasan, Ronald G Gregg, Kirill A Martemyanov. J Cell Biol 2012
67
16

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
13

Regulators of G protein signaling RGS7 and RGS11 determine the onset of the light response in ON bipolar neurons.
Yan Cao, Johan Pahlberg, Ignacio Sarria, Naomi Kamasawa, Alapakkam P Sampath, Kirill A Martemyanov. Proc Natl Acad Sci U S A 2012
58
18

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
127
11

GNAT1 associated with autosomal recessive congenital stationary night blindness.
Muhammad Asif Naeem, Venkata R M Chavali, Shahbaz Ali, Muhammad Iqbal, Saima Riazuddin, Shaheen N Khan, Tayyab Husnain, Paul A Sieving, Radha Ayyagari, Sheikh Riazuddin,[...]. Invest Ophthalmol Vis Sci 2012
44
25


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.