A citation-based method for searching scientific literature

Yan Cao, Ikuo Masuho, Haruhisa Okawa, Keqiang Xie, Junko Asami, Paul J Kammermeier, Dennis M Maddox, Takahisa Furukawa, Takayoshi Inoue, Alapakkam P Sampath, Kirill A Martemyanov. J Neurosci 2009
Times Cited: 66







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



Times Cited
  Times     Co-cited
Similarity



Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix.
O Ibraghimov-Beskrovnaya, J M Ervasti, C J Leveille, C A Slaughter, S W Sernett, K P Campbell. Nature 1992
1

Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness.
Ajoy Vincent, Isabelle Audo, Erika Tavares, Jason T Maynes, Anupreet Tumber, Thomas Wright, Shuning Li, Christelle Michiels, Christel Condroyer, Heather MacDonald,[...]. Am J Hum Genet 2016
28
3


Differential association of syntrophin pairs with the dystrophin complex.
M F Peters, M E Adams, S C Froehner. J Cell Biol 1997
210
1

Plexin-a4 mediates axon-repulsive activities of both secreted and transmembrane semaphorins and plays roles in nerve fiber guidance.
Fumikazu Suto, Keisuke Ito, Masato Uemura, Masayuki Shimizu, Yutaka Shinkawa, Makoto Sanbo, Tomoyasu Shinoda, Miu Tsuboi, Seiji Takashima, Takeshi Yagi,[...]. J Neurosci 2005
159
1

How to make a synaptic ribbon: RIBEYE deletion abolishes ribbons in retinal synapses and disrupts neurotransmitter release.
Stephan Maxeiner, Fujun Luo, Alison Tan, Frank Schmitz, Thomas C Südhof. EMBO J 2016
63
1


Role of the mouse retinal photoreceptor ribbon synapse in visual motion processing for optokinetic responses.
Yuko Sugita, Fumiyuki Araki, Taro Chaya, Kenji Kawano, Takahisa Furukawa, Kenichiro Miura. PLoS One 2015
6
16

Accelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndrome.
Jonathan M Cordeiro, Mark Marieb, Ryan Pfeiffer, Kirstine Calloe, Elena Burashnikov, Charles Antzelevitch. J Mol Cell Cardiol 2009
69
1


Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death.
Charles Antzelevitch, Guido D Pollevick, Jonathan M Cordeiro, Oscar Casis, Michael C Sanguinetti, Yoshiyasu Aizawa, Alejandra Guerchicoff, Ryan Pfeiffer, Antonio Oliva, Bernd Wollnik,[...]. Circulation 2007
590
1

Cbln1 is a ligand for an orphan glutamate receptor delta2, a bidirectional synapse organizer.
Keiko Matsuda, Eriko Miura, Taisuke Miyazaki, Wataru Kakegawa, Kyoichi Emi, Sakae Narumi, Yugo Fukazawa, Aya Ito-Ishida, Tetsuro Kondo, Ryuichi Shigemoto,[...]. Science 2010
226
1



Cast: a novel protein of the cytomatrix at the active zone of synapses that forms a ternary complex with RIM1 and munc13-1.
Toshihisa Ohtsuka, Etsuko Takao-Rikitsu, Eiji Inoue, Marie Inoue, Masakazu Takeuchi, Kaho Matsubara, Maki Deguchi-Tawarada, Keiko Satoh, Koji Morimoto, Hiroyuki Nakanishi,[...]. J Cell Biol 2002
214
1

Structural basis for integration of GluD receptors within synaptic organizer complexes.
Jonathan Elegheert, Wataru Kakegawa, Jordan E Clay, Natalie F Shanks, Ester Behiels, Keiko Matsuda, Kazuhisa Kohda, Eriko Miura, Maxim Rossmann, Nikolaos Mitakidis,[...]. Science 2016
76
1


Imaging an optogenetic pH sensor reveals that protons mediate lateral inhibition in the retina.
Tzu-Ming Wang, Lars C Holzhausen, Richard H Kramer. Nat Neurosci 2014
62
1

Homozygous dystroglycan mutation associated with a novel muscle-eye-brain disease-like phenotype with multicystic leucodystrophy.
Tobias Geis, Klaus Marquard, Tanja Rödl, Christof Reihle, Sophie Schirmer, Thekla von Kalle, Antje Bornemann, Ute Hehr, Markus Blankenburg. Neurogenetics 2013
41
2

A novel large in-frame deletion within the CACNA1F gene associates with a cone-rod dystrophy 3-like phenotype.
Jan Hauke, Andrea Schild, Antje Neugebauer, Alexandra Lappa, Julia Fricke, Sascha Fauser, Stefanie Rösler, Andrea Pannes, Dirk Zarrinnam, Janine Altmüller,[...]. PLoS One 2013
21
4

Versatile functional roles of horizontal cells in the retinal circuit.
Taro Chaya, Akihiro Matsumoto, Yuko Sugita, Satoshi Watanabe, Ryusuke Kuwahara, Masao Tachibana, Takahisa Furukawa. Sci Rep 2017
14
7

Transsynaptic Modulation of Kainate Receptor Functions by C1q-like Proteins.
Keiko Matsuda, Timotheus Budisantoso, Nikolaos Mitakidis, Yuki Sugaya, Eriko Miura, Wataru Kakegawa, Miwako Yamasaki, Kohtarou Konno, Motokazu Uchigashima, Manabu Abe,[...]. Neuron 2016
89
1


Muscular dystrophies and the dystrophin-glycoprotein complex.
V Straub, K P Campbell. Curr Opin Neurol 1997
305
1

Synaptic transmission from horizontal cells to cones is impaired by loss of connexin hemichannels.
Lauw J Klaassen, Ziyi Sun, Marvin N Steijaert, Petra Bolte, Iris Fahrenfort, Trijntje Sjoerdsma, Jan Klooster, Yvonne Claassen, Colleen R Shields, Huub M M Ten Eikelder,[...]. PLoS Biol 2011
69
1

Hemichannel-mediated inhibition in the outer retina.
M Kamermans, I Fahrenfort, K Schultz, U Janssen-Bienhold, T Sjoerdsma, R Weiler. Science 2001
282
1

X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene.
R Jalkanen, M Mäntyjärvi, R Tobias, J Isosomppi, E-M Sankila, T Alitalo, N T Bech-Hansen. J Med Genet 2006
58
1

Ultrastructure of the distal retina of the adult zebrafish, Danio rerio.
R Tarboush, G B Chapman, V P Connaughton. Tissue Cell 2012
20
5

Early steps in the assembly of photoreceptor ribbon synapses in the mouse retina: the involvement of precursor spheres.
Hanna Regus-Leidig, Susanne Tom Dieck, Dana Specht, Lars Meyer, Johann Helmut Brandstätter. J Comp Neurol 2009
78
1

Differential role for synaptojanin 1 in rod and cone photoreceptors.
Lars C Holzhausen, Alaron A Lewis, Kimberly K Cheong, Susan E Brockerhoff. J Comp Neurol 2009
26
3

A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants.
K M Boycott, T A Maybaum, M J Naylor, R G Weleber, J Robitaille, Y Miyake, A A Bergen, M E Pierpont, W G Pearce, N T Bech-Hansen. Hum Genet 2001
66
1

Homeostatic plasticity in neural development.
Nai-Wen Tien, Daniel Kerschensteiner. Neural Dev 2018
30
3


Balancing plasticity/stability across brain development.
Anne E Takesian, Takao K Hensch. Prog Brain Res 2013
269
1

Viral-mediated RdCVF and RdCVFL expression protects cone and rod photoreceptors in retinal degeneration.
Leah C Byrne, Deniz Dalkara, Gabriel Luna, Steven K Fisher, Emmanuelle Clérin, Jose-Alain Sahel, Thierry Léveillard, John G Flannery. J Clin Invest 2015
102
1

The accessory optic system.
J I Simpson. Annu Rev Neurosci 1984
413
1

Partial Cone Loss Triggers Synapse-Specific Remodeling and Spatial Receptive Field Rearrangements in a Mature Retinal Circuit.
Rachel A Care, David B Kastner, Irina De la Huerta, Simon Pan, Atrey Khoche, Luca Della Santina, Clare Gamlin, Chad Santo Tomas, Jenita Ngo, Allen Chen,[...]. Cell Rep 2019
10
10

Retinal Remodeling and Metabolic Alterations in Human AMD.
Bryan W Jones, Rebecca L Pfeiffer, William D Ferrell, Carl B Watt, James Tucker, Robert E Marc. Front Cell Neurosci 2016
36
2

DSCAM-mediated control of dendritic and axonal arbor outgrowth enforces tiling and inhibits synaptic plasticity.
Aaron B Simmons, Samuel J Bloomsburg, Joshua M Sukeena, Calvin J Miller, Yohaniz Ortega-Burgos, Bart G Borghuis, Peter G Fuerst. Proc Natl Acad Sci U S A 2017
16
6

Molecular Classification and Comparative Taxonomics of Foveal and Peripheral Cells in Primate Retina.
Yi-Rong Peng, Karthik Shekhar, Wenjun Yan, Dustin Herrmann, Anna Sappington, Gregory S Bryman, Tavé van Zyl, Michael Tri H Do, Aviv Regev, Joshua R Sanes. Cell 2019
137
1

Control of Synaptic Specificity by Establishing a Relative Preference for Synaptic Partners.
Chundi Xu, Emma Theisen, Ryan Maloney, Jing Peng, Ivan Santiago, Clarence Yapp, Zachary Werkhoven, Elijah Rumbaut, Bryan Shum, Dorota Tarnogorska,[...]. Neuron 2019
15
6

Prevalence and causes of visual impairment and blindness among 9980 Scandinavian adults: the Copenhagen City Eye Study.
Helena Buch, Troels Vinding, Morten La Cour, Merete Appleyard, Gorm B Jensen, Niels Vesti Nielsen. Ophthalmology 2004
249
1

Spatiotemporally Asymmetric Excitation Supports Mammalian Retinal Motion Sensitivity.
Akihiro Matsumoto, Kevin L Briggman, Keisuke Yonehara. Curr Biol 2019
16
6

Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait.
Alan F Wright, Christina F Chakarova, Mai M Abd El-Aziz, Shomi S Bhattacharya. Nat Rev Genet 2010
393
1

Cone structure imaged with adaptive optics scanning laser ophthalmoscopy in eyes with nonneovascular age-related macular degeneration.
Shiri Zayit-Soudry, Jacque L Duncan, Reema Syed, Moreno Menghini, Austin J Roorda. Invest Ophthalmol Vis Sci 2013
49
2

AMIGO2 Scales Dendrite Arbors in the Retina.
Florentina Soto, Nai-Wen Tien, Anurag Goel, Lei Zhao, Philip A Ruzycki, Daniel Kerschensteiner. Cell Rep 2019
6
16



Fiji: an open-source platform for biological-image analysis.
Johannes Schindelin, Ignacio Arganda-Carreras, Erwin Frise, Verena Kaynig, Mark Longair, Tobias Pietzsch, Stephan Preibisch, Curtis Rueden, Stephan Saalfeld, Benjamin Schmid,[...]. Nat Methods 2012
1


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.