A citation-based method for searching scientific literature

Marion Neuillé, Yan Cao, Romain Caplette, Debbie Guerrero-Given, Connon Thomas, Naomi Kamasawa, José-Alain Sahel, Christian P Hamel, Isabelle Audo, Serge Picaud, Kirill A Martemyanov, Christina Zeitz. Invest Ophthalmol Vis Sci 2017
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


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
26
90

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
91
72


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
35
72

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
63

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
62
63

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
13
63

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
63
54

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
184
54

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
235
54

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
54

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
366
54

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
189
45


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
45

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
49
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
166
45

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
45

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
200
45


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
189
36

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
36

A missense mutation in Grm6 reduces but does not eliminate mGluR6 expression or rod depolarizing bipolar cell function.
Neal S Peachey, Nazarul Hasan, Bernard FitzMaurice, Samantha Burrill, Gobinda Pangeni, Son Yong Karst, Laura Reinholdt, Melissa L Berry, Marge Strobel, Ronald G Gregg,[...]. J Neurophysiol 2017
7
57

Lrit1, a Retinal Transmembrane Protein, Regulates Selective Synapse Formation in Cone Photoreceptor Cells and Visual Acuity.
Akiko Ueno, Yoshihiro Omori, Yuko Sugita, Satoshi Watanabe, Taro Chaya, Takashi Kozuka, Tetsuo Kon, Satoyo Yoshida, Kenji Matsushita, Ryusuke Kuwahara,[...]. Cell Rep 2018
19
36

Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness.
Miranda L Scalabrino, Sanford L Boye, Kathryn M H Fransen, Jennifer M Noel, Frank M Dyka, Seok Hong Min, Qing Ruan, Charles N De Leeuw, Elizabeth M Simpson, Ronald G Gregg,[...]. Hum Mol Genet 2015
38
36

Intermolecular Interaction between Anchoring Subunits Specify Subcellular Targeting and Function of RGS Proteins in Retina ON-Bipolar Neurons.
Ignacio Sarria, Cesare Orlandi, Maureen A McCall, Ronald G Gregg, Kirill A Martemyanov. J Neurosci 2016
11
36

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
65
36

[Analysis of the human electroretinogram].
G SCHUBERT, H BORNSCHEIN. Ophthalmologica 1952
223
36

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
123
36

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
40

Congenital stationary night blindness with negative electroretinogram. A new classification.
Y Miyake, K Yagasaki, M Horiguchi, Y Kawase, T Kanda. Arch Ophthalmol 1986
348
36

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
142
36


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
194
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
105
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
156
36

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
153
36

TRPM1: a vertebrate TRP channel responsible for retinal ON bipolar function.
Chieko Koike, Tomohiro Numata, Hiroshi Ueda, Yasuo Mori, Takahisa Furukawa. Cell Calcium 2010
60
27

Cone contacts, mosaics, and territories of bipolar cells in the mouse retina.
Heinz Wässle, Christian Puller, Frank Müller, Silke Haverkamp. J Neurosci 2009
283
27

Presynaptic dystroglycan-pikachurin complex regulates the proper synaptic connection between retinal photoreceptor and bipolar cells.
Yoshihiro Omori, Fumiyuki Araki, Taro Chaya, Naoko Kajimura, Shoichi Irie, Koji Terada, Yuki Muranishi, Toshinori Tsujii, Shinji Ueno, Toshiyuki Koyasu,[...]. J Neurosci 2012
57
27

Synaptogenesis in the photoreceptor terminal of the mouse retina.
J C Blanks, A M Adinolfi, R N Lolley. J Comp Neurol 1974
179
27

The presynaptic active zone protein bassoon is essential for photoreceptor ribbon synapse formation in the retina.
Oliver Dick, Susanne tom Dieck, Wilko Detlef Altrock, Josef Ammermüller, Reto Weiler, Craig Curtis Garner, Eckart Dieter Gundelfinger, Johann Helmut Brandstätter. Neuron 2003
305
27

Structure and function of ribbon synapses.
Peter Sterling, Gary Matthews. Trends Neurosci 2005
216
27

Elfn1 recruits presynaptic mGluR7 in trans and its loss results in seizures.
Naoko H Tomioka, Hiroki Yasuda, Hiroyuki Miyamoto, Minoru Hatayama, Naoko Morimura, Yoshifumi Matsumoto, Toshimitsu Suzuki, Maya Odagawa, Yuri S Odaka, Yoshimi Iwayama,[...]. Nat Commun 2014
56
27

CACNA1S expression in mouse retina: Novel isoforms and antibody cross-reactivity with GPR179.
Nazarul Hasan, Thomas A Ray, Ronald G Gregg. Vis Neurosci 2016
16
27

LRIT1 Modulates Adaptive Changes in Synaptic Communication of Cone Photoreceptors.
Ignacio Sarria, Yan Cao, Yuchen Wang, Norianne T Ingram, Cesare Orlandi, Naomi Kamasawa, Alexander V Kolesnikov, Johan Pahlberg, Vladimir J Kefalov, Alapakkam P Sampath,[...]. Cell Rep 2018
12
27

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
27

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
367
27

Role of the beta(2) subunit of voltage-dependent calcium channels in the retinal outer plexiform layer.
Sherry L Ball, Patricia A Powers, Hee-Sup Shin, Catherine W Morgans, Neal S Peachey, Ronald G Gregg. Invest Ophthalmol Vis Sci 2002
145
27

NGL-2 regulates pathway-specific neurite growth and lamination, synapse formation, and signal transmission in the retina.
Florentina Soto, Kelly L Watkins, Robert E Johnson, Frank Schottler, Daniel Kerschensteiner. J Neurosci 2013
46
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.