A citation-based method for searching scientific literature

Marion Neuillé, Said El Shamieh, Elise Orhan, Christelle Michiels, Aline Antonio, Marie-Elise Lancelot, Christel Condroyer, Kinga Bujakowska, Olivier Poch, José-Alain Sahel, Isabelle Audo, Christina Zeitz. PLoS One 2014
Times Cited: 36







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



Times Cited
  Times     Co-cited
Similarity


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
66

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
63

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
58

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
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
200
52

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
64

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
89
47

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
47


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
44

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
168
44

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
239
41

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
72
38

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
148
38


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
36

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
163
36

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
36

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
33

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
33

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
33

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
35

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
33

Congenital stationary night blindness with negative electroretinogram. A new classification.
Y Miyake, K Yagasaki, M Horiguchi, Y Kawase, T Kanda. Arch Ophthalmol 1986
352
33

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
33

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
30

Retina-specific GTPase accelerator RGS11/G beta 5S/R9AP is a constitutive heterotrimer selectively targeted to mGluR6 in ON-bipolar neurons.
Yan Cao, Ikuo Masuho, Haruhisa Okawa, Keqiang Xie, Junko Asami, Paul J Kammermeier, Dennis M Maddox, Takahisa Furukawa, Takayoshi Inoue, Alapakkam P Sampath,[...]. J Neurosci 2009
67
30


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
127
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
27

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
27

Presynaptic Expression of LRIT3 Transsynaptically Organizes the Postsynaptic Glutamate Signaling Complex Containing TRPM1.
Nazarul Hasan, Gobinda Pangeni, Catherine A Cobb, Thomas A Ray, Emily R Nettesheim, Kristina J Ertel, Daniel M Lipinski, Maureen A McCall, Ronald G Gregg. Cell Rep 2019
16
62

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
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
356
25


[Analysis of the human electroretinogram].
G SCHUBERT, H BORNSCHEIN. Ophthalmologica 1952
227
25

Mechanism for Selective Synaptic Wiring of Rod Photoreceptors into the Retinal Circuitry and Its Role in Vision.
Yan Cao, Ignacio Sarria, Katherine E Fehlhaber, Naomi Kamasawa, Cesare Orlandi, Kiely N James, Jennifer L Hazen, Matthew R Gardner, Michael Farzan, Amy Lee,[...]. Neuron 2015
66
25

LRIT3 Differentially Affects Connectivity and Synaptic Transmission of Cones to ON- and OFF-Bipolar Cells.
Marion Neuillé, Yan Cao, Romain Caplette, Debbie Guerrero-Given, Connon Thomas, Naomi Kamasawa, José-Alain Sahel, Christian P Hamel, Isabelle Audo, Serge Picaud,[...]. Invest Ophthalmol Vis Sci 2017
12
75

Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation.
Shigeru Sato, Yoshihiro Omori, Kimiko Katoh, Mineo Kondo, Motoi Kanagawa, Kentaro Miyata, Kazuo Funabiki, Toshiyuki Koyasu, Naoko Kajimura, Tomomitsu Miyoshi,[...]. Nat Neurosci 2008
192
22

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
371
22

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
22

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
347
22

Gβ3 is required for normal light ON responses and synaptic maintenance.
Anuradha Dhingra, Hariharasubramanian Ramakrishnan, Adam Neinstein, Marie E Fina, Ying Xu, Jian Li, Daniel C Chung, Arkady Lyubarsky, Noga Vardi. J Neurosci 2012
43
22

Identification of a new mutant allele, Grm6(nob7), for complete congenital stationary night blindness.
Haohua Qian, Rui Ji, Ronald G Gregg, Neal S Peachey. Vis Neurosci 2015
10
80

Types of bipolar cells in the mouse retina.
Krishna K Ghosh, Sascha Bujan, Silke Haverkamp, Andreas Feigenspan, Heinz Wässle. J Comp Neurol 2004
290
19

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
19

Localization of nyctalopin in the mammalian retina.
Catherine W Morgans, Gaoying Ren, Lakshmi Akileswaran. Eur J Neurosci 2006
56
19

The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses.
Bo Chang, John R Heckenlively, Philippa R Bayley, Nicholas C Brecha, Muriel T Davisson, Norm L Hawes, Arlene A Hirano, Ronald E Hurd, Akihiro Ikeda, Britt A Johnson,[...]. Vis Neurosci 2006
162
16

Nyctalopin is essential for synaptic transmission in the cone dominated zebrafish retina.
Ronja Bahadori, Oliver Biehlmaier, Christina Zeitz, Thomas Labhart, Yuri V Makhankov, Ursula Forster, Matthias Gesemann, Wolfgang Berger, Stephan C F Neuhauss. Eur J Neurosci 2006
22
27


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.