A citation-based method for searching scientific literature

Takahisa Furukawa, Akiko Ueno, Yoshihiro Omori. Cell Mol Life Sci 2020
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


Arf-like Protein 3 (ARL3) Regulates Protein Trafficking and Ciliogenesis in Mouse Photoreceptors.
Christin Hanke-Gogokhia, Zhijian Wu, Cecilia D Gerstner, Jeanne M Frederick, Houbin Zhang, Wolfgang Baehr. J Biol Chem 2016
64
33

Crumbs homologue 1 is required for maintenance of photoreceptor cell polarization and adhesion during light exposure.
Serge A van de Pavert, Albena Kantardzhieva, Anna Malysheva, Jan Meuleman, Inge Versteeg, Christiaan Levelt, Jan Klooster, Sylvia Geiger, Mathias W Seeliger, Penny Rashbass,[...]. J Cell Sci 2004
182
33


Rod disc renewal occurs by evagination of the ciliary plasma membrane that makes cadherin-based contacts with the inner segment.
Thomas Burgoyne, Ingrid P Meschede, Jemima J Burden, Maryse Bailly, Miguel C Seabra, Clare E Futter. Proc Natl Acad Sci U S A 2015
57
33

Photoreceptor discs form through peripherin-dependent suppression of ciliary ectosome release.
Raquel Y Salinas, Jillian N Pearring, Jin-Dong Ding, William J Spencer, Ying Hao, Vadim Y Arshavsky. J Cell Biol 2017
59
33

Deletion of PrBP/delta impedes transport of GRK1 and PDE6 catalytic subunits to photoreceptor outer segments.
H Zhang, S Li, T Doan, F Rieke, P B Detwiler, J M Frederick, W Baehr. Proc Natl Acad Sci U S A 2007
131
33

Subunit stoichiometry of the CNG channel of rod photoreceptors.
Dietmar Weitz, Nicole Ficek, Elisabeth Kremmer, Paul J Bauer, U Benjamin Kaupp. Neuron 2002
124
33

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
33


Essential role of Ca2+-binding protein 4, a Cav1.4 channel regulator, in photoreceptor synaptic function.
Françoise Haeseleer, Yoshikazu Imanishi, Tadao Maeda, Daniel E Possin, Akiko Maeda, Amy Lee, Fred Rieke, Krzysztof Palczewski. Nat Neurosci 2004
217
33

The intraflagellar transport protein, IFT88, is essential for vertebrate photoreceptor assembly and maintenance.
Gregory J Pazour, Sheila A Baker, James A Deane, Douglas G Cole, Bethany L Dickert, Joel L Rosenbaum, George B Witman, Joseph C Besharse. J Cell Biol 2002
358
33

Interaction and colocalization of CaBP4 and Unc119 (MRG4) in photoreceptors.
Françoise Haeseleer. Invest Ophthalmol Vis Sci 2008
29
33

BBSome function is required for both the morphogenesis and maintenance of the photoreceptor outer segment.
Ying Hsu, Janelle E Garrison, Gunhee Kim, Addison R Schmitz, Charles C Searby, Qihong Zhang, Poppy Datta, Darryl Y Nishimura, Seongjin Seo, Val C Sheffield. PLoS Genet 2017
30
33

Progressive Rod-Cone Degeneration (PRCD) Protein Requires N-Terminal S-Acylation and Rhodopsin Binding for Photoreceptor Outer Segment Localization and Maintaining Intracellular Stability.
William J Spencer, Jillian N Pearring, Raquel Y Salinas, David R Loiselle, Nikolai P Skiba, Vadim Y Arshavsky. Biochemistry 2016
20
33

Three-dimensional architecture of the rod sensory cilium and its disruption in retinal neurodegeneration.
Jared C Gilliam, Juan T Chang, Ivette M Sandoval, Youwen Zhang, Tiansen Li, Steven J Pittler, Wah Chiu, Theodore G Wensel. Cell 2012
104
33

ARL3 regulates trafficking of prenylated phototransduction proteins to the rod outer segment.
Zachary C Wright, Ratnesh K Singh, Ryan Alpino, Andrew F X Goldberg, Maxim Sokolov, Visvanathan Ramamurthy. Hum Mol Genet 2016
30
33

IFT20 is required for opsin trafficking and photoreceptor outer segment development.
Brian T Keady, Yun Zheng Le, Gregory J Pazour. Mol Biol Cell 2011
85
33


Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome.
Vincent Cantagrel, Jennifer L Silhavy, Stephanie L Bielas, Dominika Swistun, Sarah E Marsh, Julien Y Bertrand, Sophie Audollent, Tania Attié-Bitach, Kenton R Holden, William B Dobyns,[...]. Am J Hum Genet 2008
247
33


Heterotrimeric kinesin-2 (KIF3) mediates transition zone and axoneme formation of mouse photoreceptors.
Li Jiang, Yuxiao Wei, Cecinio C Ronquillo, Robert E Marc, Bradley K Yoder, Jeanne M Frederick, Wolfgang Baehr. J Biol Chem 2015
35
33

The guanine nucleotide exchange factor Arf-like protein 13b is essential for assembly of the mouse photoreceptor transition zone and outer segment.
Christin Hanke-Gogokhia, Zhijian Wu, Ali Sharif, Hussein Yazigi, Jeanne M Frederick, Wolfgang Baehr. J Biol Chem 2017
18
33

Discs of mammalian rod photoreceptors form through the membrane evagination mechanism.
Jin-Dong Ding, Raquel Y Salinas, Vadim Y Arshavsky. J Cell Biol 2015
61
33

Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy.
Takaaki Hayashi, Katsuhiro Hosono, Kentaro Kurata, Satoshi Katagiri, Kei Mizobuchi, Shinji Ueno, Mineo Kondo, Tadashi Nakano, Yoshihiro Hotta. Doc Ophthalmol 2020
9
33

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
33

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
33

[Analysis of the human electroretinogram].
G SCHUBERT, H BORNSCHEIN. Ophthalmologica 1952
223
33

Congenital stationary night blindness with negative electroretinogram. A new classification.
Y Miyake, K Yagasaki, M Horiguchi, Y Kawase, T Kanda. Arch Ophthalmol 1986
348
33

Novel homozygous CLN3 missense variant in isolated retinal dystrophy: A case report and electron microscopic findings.
Kei Mizobuchi, Takaaki Hayashi, Kazutoshi Yoshitake, Kaoru Fujinami, Toshiaki Tachibana, Kazushige Tsunoda, Takeshi Iwata, Tadashi Nakano. Mol Genet Genomic Med 2020
11
33


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
33

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
33

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
33

ISCEV Standard for full-field clinical electroretinography (2015 update).
Daphne L McCulloch, Michael F Marmor, Mitchell G Brigell, Ruth Hamilton, Graham E Holder, Radouil Tzekov, Michael Bach. Doc Ophthalmol 2015
802
33

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
33

RDH5-Related Fundus Albipunctatus in a Large Japanese Cohort.
Satoshi Katagiri, Takaaki Hayashi, Masaki Nakamura, Kei Mizobuchi, Tamaki Gekka, Shiori Komori, Shinji Ueno, Hiroko Terasaki, Hiroyuki Sakuramoto, Kazuki Kuniyoshi,[...]. Invest Ophthalmol Vis Sci 2020
8
33

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
33

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
33

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
33

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
33

Electroretinographic abnormalities associated with pregabalin: a case report.
Wakana Ninomiya, Kei Mizobuchi, Takaaki Hayashi, Sachiyo Okude, Satoshi Katagiri, Akiko Kubo, Nami Masuhara, Tadashi Nakano. Doc Ophthalmol 2020
9
33

Whole exome analysis identifies frequent CNGA1 mutations in Japanese population with autosomal recessive retinitis pigmentosa.
Satoshi Katagiri, Masakazu Akahori, Yuri Sergeev, Kazutoshi Yoshitake, Kazuho Ikeo, Masaaki Furuno, Takaaki Hayashi, Mineo Kondo, Shinji Ueno, Kazushige Tsunoda,[...]. PLoS One 2014
42
33

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
33


Mapping of genetic modifiers of Nr2e3 rd7/rd7 that suppress retinal degeneration and restore blue cone cells to normal quantity.
Neena B Haider, Weidong Zhang, Ron Hurd, Akihiro Ikeda, Arne M Nystuen, Jürgen K Naggert, Patsy M Nishina. Mamm Genome 2008
23
16

Retinal degeneration mutants in the mouse.
B Chang, N L Hawes, R E Hurd, M T Davisson, S Nusinowitz, J R Heckenlively. Vision Res 2002
556
16

Protein misfolding and the pathogenesis of ABCA4-associated retinal degenerations.
Ning Zhang, Yaroslav Tsybovsky, Alexander V Kolesnikov, Malgorzata Rozanowska, Malgorzata Swider, Sharon B Schwartz, Edwin M Stone, Grazyna Palczewska, Akiko Maeda, Vladimir J Kefalov,[...]. Hum Mol Genet 2015
48
16

Phenotypic analysis of mice expressing exclusively apolipoprotein B48 or apolipoprotein B100.
R V Farese, M M Véniant, C M Cham, L M Flynn, V Pierotti, J F Loring, M Traber, S Ruland, R S Stokowski, D Huszar,[...]. Proc Natl Acad Sci U S A 1996
110
16

Essential roles of mitochondrial biogenesis regulator Nrf1 in retinal development and homeostasis.
Takae Kiyama, Ching-Kang Chen, Steven W Wang, Ping Pan, Zhenlin Ju, Jing Wang, Shinako Takada, William H Klein, Chai-An Mao. Mol Neurodegener 2018
29
16

Dicer inactivation leads to progressive functional and structural degeneration of the mouse retina.
Devid Damiani, John J Alexander, Jason R O'Rourke, Mike McManus, Ashutosh P Jadhav, Constance L Cepko, William W Hauswirth, Brian D Harfe, Enrica Strettoi. J Neurosci 2008
169
16


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.