A citation-based method for searching scientific literature

Rebecca R Bellone, Samantha A Brooks, Lynne Sandmeyer, Barbara A Murphy, George Forsyth, Sheila Archer, Ernest Bailey, Bruce Grahn. Genetics 2008
Times Cited: 103







List of co-cited articles
1044 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
45

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
155
43

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
151
41

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
195
40

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
121
40

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
121
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
189
33

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
286
29


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
72
30

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
234
21

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
20

Melastatin expression and prognosis in cutaneous malignant melanoma.
L M Duncan, J Deeds, F E Cronin, M Donovan, A J Sober, M Kauffman, J J McCarthy. J Clin Oncol 2001
156
19

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
19

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
19

Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses.
Rebecca R Bellone, George Forsyth, Tosso Leeb, Sheila Archer, Snaevar Sigurdsson, Freyja Imsland, Evan Mauceli, Martina Engensteiner, Ernest Bailey, Lynne Sandmeyer,[...]. Brief Funct Genomics 2010
30
63

Regulation of melastatin, a TRP-related protein, through interaction with a cytoplasmic isoform.
X Z Xu, F Moebius, D L Gill, C Montell. Proc Natl Acad Sci U S A 2001
158
18

Congenital stationary night blindness with negative electroretinogram. A new classification.
Y Miyake, K Yagasaki, M Horiguchi, Y Kawase, T Kanda. Arch Ophthalmol 1986
348
18

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
156
17


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
66
25

Transcriptional regulation of the melanoma prognostic marker melastatin (TRPM1) by MITF in melanocytes and melanoma.
Arlo J Miller, Jinyan Du, Sheldon Rowan, Christine L Hershey, Hans R Widlund, David E Fisher. Cancer Res 2004
153
16

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
17

TRPM1: a vertebrate TRP channel responsible for retinal ON bipolar function.
Chieko Koike, Tomohiro Numata, Hiroshi Ueda, Yasuo Mori, Takahisa Furukawa. Cell Calcium 2010
58
27

Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse.
Rebecca R Bellone, Heather Holl, Vijayasaradhi Setaluri, Sulochana Devi, Nityanand Maddodi, Sheila Archer, Lynne Sandmeyer, Arne Ludwig, Daniel Foerster, Melanie Pruvost,[...]. PLoS One 2013
58
27

Identification of molecular markers of bipolar cells in the murine retina.
Douglas S Kim, Sarah E Ross, Jeffrey M Trimarchi, John Aach, Michael E Greenberg, Constance L Cepko. J Comp Neurol 2008
86
17

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
60
25

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
348
14

Congenital stationary night blindness: an animal model.
D A Witzel, E L Smith, R D Wilson, G D Aguirre. Invest Ophthalmol Vis Sci 1978
45
31

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
183
14

Congenital stationary night blindness is associated with the leopard complex in the Miniature Horse.
Lynne S Sandmeyer, Rebecca R Bellone, Sheila Archer, Bianca S Bauer, Janelle Nelson, George Forsyth, Bruce H Grahn. Vet Ophthalmol 2012
19
68


Human melastatin 1 (TRPM1) is regulated by MITF and produces multiple polypeptide isoforms in melanocytes and melanoma.
Song Zhiqi, Mohammad H Soltani, Kumar Megur R Bhat, Namrata Sangha, Dong Fang, John J Hunter, Vijayasaradhi Setaluri. Melanoma Res 2004
51
23

TRP channels as cellular sensors.
David E Clapham. Nature 2003
12

Chromosomal localization and genomic characterization of the mouse melastatin gene (Mlsn1).
J J Hunter, J Shao, J S Smutko, B J Dussault, D L Nagle, E A Woolf, L M Holmgren, K J Moore, A W Shyjan. Genomics 1998
79
15

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
69
17

TRP channels.
Kartik Venkatachalam, Craig Montell. Annu Rev Biochem 2007
12

An introduction to TRP channels.
I Scott Ramsey, Markus Delling, David E Clapham. Annu Rev Physiol 2006
11


The capsaicin receptor: a heat-activated ion channel in the pain pathway.
M J Caterina, M A Schumacher, M Tominaga, T A Rosen, J D Levine, D Julius. Nature 1997
11

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
61
18

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
87
12

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
88
12

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
121
10


Transient receptor potential cation channels in disease.
Bernd Nilius, Grzegorz Owsianik, Thomas Voets, John A Peters. Physiol Rev 2007
968
10

[Analysis of the human electroretinogram].
G SCHUBERT, H BORNSCHEIN. Ophthalmologica 1952
223
10

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
47
21

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
90
11

ADP-ribose gating of the calcium-permeable LTRPC2 channel revealed by Nudix motif homology.
A L Perraud, A Fleig, C A Dunn, L A Bagley, P Launay, C Schmitz, A J Stokes, Q Zhu, M J Bessman, R Penner,[...]. Nature 2001
682
9


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.