A citation-based method for searching scientific literature

Zhiwei Shi, Drew Jervis, Philip E B Nickerson, Robert L Chow. J Comp Neurol 2012
Times Cited: 17







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



Times Cited
  Times     Co-cited
Similarity


Control of late off-center cone bipolar cell differentiation and visual signaling by the homeobox gene Vsx1.
Robert L Chow, Bela Volgyi, Rachel K Szilard, David Ng, Colin McKerlie, Stewart A Bloomfield, David G Birch, Roderick R McInnes. Proc Natl Acad Sci U S A 2004
115
64

Vsx1 regulates terminal differentiation of type 7 ON bipolar cells.
Zhiwei Shi, Stuart Trenholm, Minyan Zhu, Sarah Buddingh, Erin N Star, Gautam B Awatramani, Robert L Chow. J Neurosci 2011
33
64

Regulation of retinal cone bipolar cell differentiation and photopic vision by the CVC homeobox gene Vsx1.
Akihira Ohtoshi, Steven W Wang, Hidetaka Maeda, Shannon M Saszik, Laura J Frishman, William H Klein, Richard R Behringer. Curr Biol 2004
77
58

Vsx1, a rapidly evolving paired-like homeobox gene expressed in cone bipolar cells.
R L Chow, B Snow, J Novak, J Looser, C Freund, D Vidgen, L Ploder, R R McInnes. Mech Dev 2001
77
52

Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation.
M Burmeister, J Novak, M Y Liang, S Basu, L Ploder, N L Hawes, D Vidgen, F Hoover, D Goldman, V I Kalnins,[...]. Nat Genet 1996
410
47

Cone contacts, mosaics, and territories of bipolar cells in the mouse retina.
Heinz Wässle, Christian Puller, Frank Müller, Silke Haverkamp. J Neurosci 2009
279
29


Types of bipolar cells in the mouse retina.
Krishna K Ghosh, Sascha Bujan, Silke Haverkamp, Andreas Feigenspan, Heinz Wässle. J Comp Neurol 2004
285
29

Requirement for Bhlhb5 in the specification of amacrine and cone bipolar subtypes in mouse retina.
Liang Feng, Xiaoling Xie, Pushkar S Joshi, Zhiyong Yang, Koji Shibasaki, Robert L Chow, Lin Gan. Development 2006
103
29

Negative regulation of Vsx1 by its paralog Chx10/Vsx2 is conserved in the vertebrate retina.
Anna M Clark, Sanghee Yun, Eric S Veien, Yuan Y Wu, Robert L Chow, Richard I Dorsky, Edward M Levine. Brain Res 2008
48
29

The Iroquois homeobox gene, Irx5, is required for retinal cone bipolar cell development.
Chi Wa Cheng, Robert L Chow, Mélanie Lebel, Rui Sakuma, Helen Oi-Lam Cheung, Vijitha Thanabalasingham, Xiaoyun Zhang, Benoit G Bruneau, David G Birch, Chi-chung Hui,[...]. Dev Biol 2005
68
29

VSX1: a gene for posterior polymorphous dystrophy and keratoconus.
Elise Héon, Alex Greenberg, Kelly K Kopp, David Rootman, Andrea L Vincent, Gail Billingsley, Megan Priston, Kimberley M Dorval, Robert L Chow, Roderick R McInnes,[...]. Hum Mol Genet 2002
205
29

Genetic control of circuit function: Vsx1 and Irx5 transcription factors regulate contrast adaptation in the mouse retina.
Daniel Kerschensteiner, Haiquan Liu, Chi Wa Cheng, Jay Demas, Shuk Han Cheng, Chi-chung Hui, Robert L Chow, Rachel O L Wong. J Neurosci 2008
32
23

Immunocytochemical description of five bipolar cell types of the mouse retina.
Silke Haverkamp, Krishna K Ghosh, Arlene A Hirano, Heinz Wässle. J Comp Neurol 2003
169
23

The transcription factor Bhlhb4 is required for rod bipolar cell maturation.
Debra E Bramblett, Mark E Pennesi, Samuel M Wu, Ming-Jer Tsai. Neuron 2004
78
23


Transcriptional activity of the paired-like homeodomain proteins CHX10 and VSX1.
Kimberley M Dorval, Brian P Bobechko, K Farid Ahmad, Rod Bremner. J Biol Chem 2005
43
17



Chx10 is required to block photoreceptor differentiation but is dispensable for progenitor proliferation in the postnatal retina.
Izzy Livne-Bar, Marek Pacal, Melissa C Cheung, Mark Hankin, Judy Trogadis, Danian Chen, Kimberley M Dorval, Rod Bremner. Proc Natl Acad Sci U S A 2006
69
17


Mutational screening of VSX1 in keratoconus patients from the European population.
D P Dash, S George, D O'Prey, D Burns, S Nabili, U Donnelly, A E Hughes, G Silvestri, J Jackson, D Frazer,[...]. Eye (Lond) 2010
54
17

Three VSX1 gene mutations, L159M, R166W, and H244R, are not associated with keratoconus.
Yongming G Tang, Yoana Picornell, Xiaowen Su, Xiaohui Li, Huiying Yang, Yaron S Rabinowitz. Cornea 2008
54
17

H244R VSX1 is associated with selective cone ON bipolar cell dysfunction and macular degeneration in a PPCD family.
Sophie Valleix, Brigitte Nedelec, Florence Rigaudiere, Paul Dighiero, Yves Pouliquen, Gilles Renard, Jean-François Le Gargasson, Marc Delpech. Invest Ophthalmol Vis Sci 2006
29
17

Keratoconus associated with posterior polymorphous dystrophy.
S J Bechara, H E Grossniklaus, G O Waring, J A Wells. Am J Ophthalmol 1991
29
17

Familial segregation of a VSX1 mutation adds a new dimension to its role in the causation of keratoconus.
Preeti Paliwal, Radhika Tandon, Divya Dube, Punit Kaur, Arundhati Sharma. Mol Vis 2011
26
17

No VSX1 gene mutations associated with keratoconus.
Anthony J Aldave, Vivek S Yellore, Andrew K Salem, Gina L Yoo, Sylvia A Rayner, Huiying Yang, George Y Tang, Yoana Piconell, Yaron S Rabinowitz. Invest Ophthalmol Vis Sci 2006
76
17

A novel VSX1 mutation identified in an individual with keratoconus in India.
Preeti Paliwal, Anuradha Singh, Radhika Tandon, Jeevan S Titiyal, Arundhati Sharma. Mol Vis 2009
34
17


Screening the visual system homeobox 1 gene in keratoconus and posterior polymorphous dystrophy cohorts identifies a novel variant.
Andrea L Vincent, Charlotte Jordan, Leo Sheck, Rachel Niederer, Dipika V Patel, Charles N J McGhee. Mol Vis 2013
14
21

VSX1 mutational analysis in a series of Italian patients affected by keratoconus: detection of a novel mutation.
Luigi Bisceglia, Marilena Ciaschetti, Patrizia De Bonis, Pablo Alberto Perafan Campo, Costantina Pizzicoli, Costanza Scala, Michele Grifa, Pio Ciavarella, Nicola Delle Noci, Filippo Vaira,[...]. Invest Ophthalmol Vis Sci 2005
93
17

Molecular analysis of the VSX1 gene in familial keratoconus.
Petra Liskova, Neil D Ebenezer, Pirro G Hysi, Rhian Gwilliam, Mohamed F El-Ashry, Lalitha C Moodaley, Scott Hau, Michael Twa, Stephen J Tuft, Shomi S Bhatacharya. Mol Vis 2007
41
17

VSX1 gene analysis in keratoconus.
Mukesh Tanwar, Manoj Kumar, Bhagabat Nayak, Dhananjay Pathak, Namrata Sharma, Jeewan S Titiyal, Rima Dada. Mol Vis 2010
41
17

VSX1 gene variants are associated with keratoconus in unrelated Korean patients.
Jee-Won Mok, Sun-Jin Baek, Choun-Ki Joo. J Hum Genet 2008
53
17


Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus.
Samira Saee-Rad, Hassan Hashemi, Mohammad Miraftab, Mohammad Reza Noori-Daloii, Morteza Hashemzadeh Chaleshtori, Reza Raoofian, Fatemeh Jafari, Wayne Greene, Ghasem Fakhraie, Farhad Rezvan,[...]. Mol Vis 2011
50
17

The D144E substitution in the VSX1 gene: a non-pathogenic variant or a disease causing mutation?
Pras Eran, Abu Almogit, Zadok David, Haike Reznik Wolf, Garzozi Hana, Barkana Yaniv, Pras Elon, Avni Isaac. Ophthalmic Genet 2008
51
17

A regulatory network involving Foxn4, Mash1 and delta-like 4/Notch1 generates V2a and V2b spinal interneurons from a common progenitor pool.
Marta G Del Barrio, Raquel Taveira-Marques, Yuko Muroyama, Dong-In Yuk, Shengguo Li, Mary Wines-Samuelson, Jie Shen, Hazel K Smith, Mengqing Xiang, David Rowitch,[...]. Development 2007
84
17



Regulation of retinal interneuron subtype identity by the Iroquois homeobox gene Irx6.
Erin N Star, Minyan Zhu, Zhiwei Shi, Haiquan Liu, Mohammad Pashmforoush, Yves Sauve, Benoit G Bruneau, Robert L Chow. Development 2012
18
17

Islet-1 controls the differentiation of retinal bipolar and cholinergic amacrine cells.
Yasser Elshatory, Drew Everhart, Min Deng, Xiaoling Xie, Robert B Barlow, Lin Gan. J Neurosci 2007
135
17

Ggamma13 colocalizes with gustducin in taste receptor cells and mediates IP3 responses to bitter denatonium.
L Huang, Y G Shanker, J Dubauskaite, J Z Zheng, W Yan, S Rosenzweig, A I Spielman, M Max, R F Margolskee. Nat Neurosci 1999
241
11

Iroquois transcription factors recognize a unique motif to mediate transcriptional repression in vivo.
Aphrodite Bilioni, Gavin Craig, Caroline Hill, Helen McNeill. Proc Natl Acad Sci U S A 2005
45
11

The fundamental plan of the retina.
R H Masland. Nat Neurosci 2001
628
11

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
87
11

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10.
E Ferda Percin, L A Ploder, J J Yu, K Arici, D J Horsford, A Rutherford, B Bapat, D W Cox, A M Duncan, V I Kalnins,[...]. Nat Genet 2000
207
11


Immunocytochemical analysis of the mouse retina.
S Haverkamp, H Wässle. J Comp Neurol 2000
563
11



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.