A citation-based method for searching scientific literature

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
Times Cited: 125







List of co-cited articles
1052 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
87

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
80

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
55

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
53

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
45

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
167
44

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
52

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
39

Congenital stationary night blindness with negative electroretinogram. A new classification.
Y Miyake, K Yagasaki, M Horiguchi, Y Kawase, T Kanda. Arch Ophthalmol 1986
351
37

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
37

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
36

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
39

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
35

[Analysis of the human electroretinogram].
G SCHUBERT, H BORNSCHEIN. Ophthalmologica 1952
226
32

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
34

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
126
27

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
26

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
39


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
23

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
32

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
22

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
22

TRPM1: a vertebrate TRP channel responsible for retinal ON bipolar function.
Chieko Koike, Tomohiro Numata, Hiroshi Ueda, Yasuo Mori, Takahisa Furukawa. Cell Calcium 2010
61
34

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
21


Autoantibodies in melanoma-associated retinopathy target TRPM1 cation channels of retinal ON bipolar cells.
Anuradha Dhingra, Marie E Fina, Adam Neinstein, David J Ramsey, Ying Xu, Gerald A Fishman, Kenneth R Alexander, Haohua Qian, Neal S Peachey, Ronald G Gregg,[...]. J Neurosci 2011
48
39

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
18

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
25

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
18

Identification of autoantibodies against TRPM1 in patients with paraneoplastic retinopathy associated with ON bipolar cell dysfunction.
Mineo Kondo, Rikako Sanuki, Shinji Ueno, Yuji Nishizawa, Naozumi Hashimoto, Hiroshi Ohguro, Shuichi Yamamoto, Shigeki Machida, Hiroko Terasaki, Grazyna Adamus,[...]. PLoS One 2011
62
27

Light response of retinal ON bipolar cells requires a specific splice variant of Galpha(o).
Anuradha Dhingra, Meisheng Jiang, Tian-Li Wang, Arkady Lyubarsky, Andrey Savchenko, Tehilla Bar-Yehuda, Peter Sterling, Lutz Birnbaumer, Noga Vardi. J Neurosci 2002
93
16

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
31

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
44

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
14



Transient receptor potential melastatin 1 (TRPM1) is an ion-conducting plasma membrane channel inhibited by zinc ions.
Sachar Lambert, Anna Drews, Oleksandr Rizun, Thomas F J Wagner, Annette Lis, Stefanie Mannebach, Sandra Plant, Melanie Portz, Marcel Meissner, Stephan E Philipp,[...]. J Biol Chem 2011
53
24

Localization of nyctalopin in the mammalian retina.
Catherine W Morgans, Gaoying Ren, Lakshmi Akileswaran. Eur J Neurosci 2006
56
23

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
22

Down-regulation of the novel gene melastatin correlates with potential for melanoma metastasis.
L M Duncan, J Deeds, J Hunter, J Shao, L M Holmgren, E A Woolf, R I Tepper, A W Shyjan. Cancer Res 1998
293
12

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
25

G-protein-mediated inhibition of the Trp channel TRPM1 requires the Gβγ dimer.
Yin Shen, Melissa Ann F Rampino, Reed C Carroll, Scott Nawy. Proc Natl Acad Sci U S A 2012
53
22

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
11

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
36


Calcium homeostasis in human melanocytes: role of transient receptor potential melastatin 1 (TRPM1) and its regulation by ultraviolet light.
Sulochana Devi, Rajendra Kedlaya, Nityanand Maddodi, Kumar M R Bhat, Craig S Weber, Hector Valdivia, Vijayasaradhi Setaluri. Am J Physiol Cell Physiol 2009
63
17

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
22

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

Ultrastructural localization and expression of TRPM1 in the human retina.
Jan Klooster, Joyce Blokker, Jacoline B Ten Brink, Unga Unmehopa, Kees Fluiter, Arthur A B Bergen, Maarten Kamermans. Invest Ophthalmol Vis Sci 2011
23
47


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.