A citation-based method for searching scientific literature

Michael Housset, Alexander Samuel, Mohamed Ettaiche, Alexis Bemelmans, Francis Béby, Nathalie Billon, Thomas Lamonerie. J Neurosci 2013
Times Cited: 45







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



Times Cited
  Times     Co-cited
Similarity


Otx2 gene deletion in adult mouse retina induces rapid RPE dystrophy and slow photoreceptor degeneration.
Francis Béby, Michael Housset, Nicolas Fossat, Coralie Le Greneur, Frédéric Flamant, Pierre Godement, Thomas Lamonerie. PLoS One 2010
36
50

Otx2 homeobox gene controls retinal photoreceptor cell fate and pineal gland development.
Akihiro Nishida, Akiko Furukawa, Chieko Koike, Yasuo Tano, Shinichi Aizawa, Isao Matsuo, Takahisa Furukawa. Nat Neurosci 2003
412
35


OTX2 activates the molecular network underlying retina pigment epithelium differentiation.
Juan Ramón Martínez-Morales, Vincent Dolez, Isabel Rodrigo, Raffaella Zaccarini, Laurence Leconte, Paola Bovolenta, Simon Saule. J Biol Chem 2003
126
28

Otx genes are required for tissue specification in the developing eye.
J R Martinez-Morales, M Signore, D Acampora, A Simeone, P Bovolenta. Development 2001
187
26

Functional roles of Otx2 transcription factor in postnatal mouse retinal development.
Chieko Koike, Akihiro Nishida, Shinji Ueno, Hiromitsu Saito, Rikako Sanuki, Shigeru Sato, Akiko Furukawa, Shinichi Aizawa, Isao Matsuo, Noboru Suzuki,[...]. Mol Cell Biol 2007
133
24

Experience-dependent transfer of Otx2 homeoprotein into the visual cortex activates postnatal plasticity.
Sayaka Sugiyama, Ariel A Di Nardo, Shinichi Aizawa, Isao Matsuo, Michel Volovitch, Alain Prochiantz, Takao K Hensch. Cell 2008
323
20

An essential role for RAX homeoprotein and NOTCH-HES signaling in Otx2 expression in embryonic retinal photoreceptor cell fate determination.
Yuki Muranishi, Koji Terada, Tatsuya Inoue, Kimiko Katoh, Toshinori Tsujii, Rikako Sanuki, Daisuke Kurokawa, Shinichi Aizawa, Yasuhiro Tamaki, Takahisa Furukawa. J Neurosci 2011
80
17

A regulatory loop involving PAX6, MITF, and WNT signaling controls retinal pigment epithelium development.
Kapil Bharti, Melanie Gasper, Jingxing Ou, Martha Brucato, Katharina Clore-Gronenborn, James Pickel, Heinz Arnheiter. PLoS Genet 2012
89
15

Alternative promoter use in eye development: the complex role and regulation of the transcription factor MITF.
Kapil Bharti, Wenfang Liu, Tamas Csermely, Stefano Bertuzzi, Heinz Arnheiter. Development 2008
98
15

Otx2 promotes the survival of damaged adult retinal ganglion cells and protects against excitotoxic loss of visual acuity in vivo.
Raoul Torero Ibad, Jinguen Rheey, Sarah Mrejen, Valérie Forster, Serge Picaud, Alain Prochiantz, Kenneth L Moya. J Neurosci 2011
35
20


Otx2 ChIP-seq reveals unique and redundant functions in the mature mouse retina.
Alexander Samuel, Michael Housset, Bruno Fant, Thomas Lamonerie. PLoS One 2014
36
19

The homeobox gene Otx2 in development and disease.
Francis Beby, Thomas Lamonerie. Exp Eye Res 2013
78
15

Eye development: a view from the retina pigmented epithelium.
Juan Ramón Martínez-Morales, Isabel Rodrigo, Paola Bovolenta. Bioessays 2004
173
13

Implication of OTX2 in pigment epithelium determination and neural retina differentiation.
P Bovolenta, A Mallamaci, P Briata, G Corte, E Boncinelli. J Neurosci 1997
122
13

Adult human RPE can be activated into a multipotent stem cell that produces mesenchymal derivatives.
Enrique Salero, Timothy A Blenkinsop, Barbara Corneo, Ashley Harris, David Rabin, Jeffrey H Stern, Sally Temple. Cell Stem Cell 2012
162
13


Mouse Otx2 functions in the formation and patterning of rostral head.
I Matsuo, S Kuratani, C Kimura, N Takeda, S Aizawa. Genes Dev 1995
561
13

Forebrain and midbrain regions are deleted in Otx2-/- mutants due to a defective anterior neuroectoderm specification during gastrulation.
D Acampora, S Mazan, Y Lallemand, V Avantaggiato, M Maury, A Simeone, P Brûlet. Development 1995
527
13

Heterozygous mutations of OTX2 cause severe ocular malformations.
Nicola K Ragge, Alison G Brown, Charlotte M Poloschek, Birgit Lorenz, R Alex Henderson, Michael P Clarke, Isabelle Russell-Eggitt, Alistair Fielder, Dianne Gerrelli, Juan Pedro Martinez-Barbera,[...]. Am J Hum Genet 2005
216
13

Otx2 binding to perineuronal nets persistently regulates plasticity in the mature visual cortex.
Marine Beurdeley, Julien Spatazza, Henry H C Lee, Sayaka Sugiyama, Clémence Bernard, Ariel A Di Nardo, Takao K Hensch, Alain Prochiantz. J Neurosci 2012
235
13

A new GFP-tagged line reveals unexpected Otx2 protein localization in retinal photoreceptors.
Nicolas Fossat, Coralie Le Greneur, Francis Béby, Stéphane Vincent, Pierre Godement, Gilles Chatelain, Thomas Lamonerie. BMC Dev Biol 2007
46
13

Nrl is required for rod photoreceptor development.
A J Mears, M Kondo, P K Swain, Y Takada, R A Bush, T L Saunders, P A Sieving, A Swaroop. Nat Genet 2001
671
13

Transcriptional regulation of rod photoreceptor homeostasis revealed by in vivo NRL targetome analysis.
Hong Hao, Douglas S Kim, Bernward Klocke, Kory R Johnson, Kairong Cui, Norimoto Gotoh, Chongzhi Zang, Janina Gregorski, Linn Gieser, Weiqun Peng,[...]. PLoS Genet 2012
75
13

Directed differentiation of human embryonic stem cells into functional retinal pigment epithelium cells.
Maria Idelson, Ruslana Alper, Alexey Obolensky, Etti Ben-Shushan, Itzhak Hemo, Nurit Yachimovich-Cohen, Hanita Khaner, Yoav Smith, Ofer Wiser, Michal Gropp,[...]. Cell Stem Cell 2009
303
13

Graded Otx2 activities demonstrate dose-sensitive eye and retina phenotypes.
Clémence Bernard, Hyoung-Tai Kim, Raoul Torero Ibad, Eun Jung Lee, Manuel Simonutti, Serge Picaud, Dario Acampora, Antonio Simeone, Ariel A Di Nardo, Alain Prochiantz,[...]. Hum Mol Genet 2014
25
24


Microphthalmia-associated transcription factor (MITF) promotes differentiation of human retinal pigment epithelium (RPE) by regulating microRNAs-204/211 expression.
Jeffrey Adijanto, John J Castorino, Zi-Xuan Wang, Arvydas Maminishkis, Gerald B Grunwald, Nancy J Philp. J Biol Chem 2012
74
11

Molecular dissection reveals decreased activity and not dominant negative effect in human OTX2 mutants.
Gilles Chatelain, Nicolas Fossat, Gilbert Brun, Thomas Lamonerie. J Mol Med (Berl) 2006
45
11

A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunction.
Robert H Henderson, Kathleen A Williamson, Joanna S Kennedy, Andrew R Webster, Graham E Holder, Anthony G Robson, David R FitzPatrick, Veronica van Heyningen, Anthony T Moore. Mol Vis 2009
47
11

CRX ChIP-seq reveals the cis-regulatory architecture of mouse photoreceptors.
Joseph C Corbo, Karen A Lawrence, Marcus Karlstetter, Connie A Myers, Musa Abdelaziz, William Dirkes, Karin Weigelt, Martin Seifert, Vladimir Benes, Lars G Fritsche,[...]. Genome Res 2010
135
11

Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa.
A Gal, Y Li, D A Thompson, J Weir, U Orth, S G Jacobson, E Apfelstedt-Sylla, D Vollrath. Nat Genet 2000
503
11

Embryonic stem cell trials for macular degeneration: a preliminary report.
Steven D Schwartz, Jean-Pierre Hubschman, Gad Heilwell, Valentina Franco-Cardenas, Carolyn K Pan, Rosaleen M Ostrick, Edmund Mickunas, Roger Gay, Irina Klimanskaya, Robert Lanza. Lancet 2012
885
11

Transcription factor SOX9 plays a key role in the regulation of visual cycle gene expression in the retinal pigment epithelium.
Tomohiro Masuda, Karl Wahlin, Jun Wan, Jianfei Hu, Julien Maruotti, Xue Yang, Jared Iacovelli, Natalie Wolkow, Ralf Kist, Joshua L Dunaief,[...]. J Biol Chem 2014
31
16

Temporal and spatial delineation of mouse Otx2 functions by conditional self-knockout.
Nicolas Fossat, Gilles Chatelain, Gilbert Brun, Thomas Lamonerie. EMBO Rep 2006
43
11

Activated monocytes resist elimination by retinal pigment epithelium and downregulate their OTX2 expression via TNF-α.
Thibaud Mathis, Michael Housset, Chiara Eandi, Fanny Beguier, Sara Touhami, Sacha Reichman, Sebastien Augustin, Pauline Gondouin, José-Alain Sahel, Laurent Kodjikian,[...]. Aging Cell 2017
26
19


The other pigment cell: specification and development of the pigmented epithelium of the vertebrate eye.
Kapil Bharti, Minh-Thanh T Nguyen, Susan Skuntz, Stefano Bertuzzi, Heinz Arnheiter. Pigment Cell Res 2006
144
8

Transdifferentiation of the retina into pigmented cells in ocular retardation mice defines a new function of the homeodomain gene Chx10.
Sheldon Rowan, C-M Amy Chen, Tracy L Young, David E Fisher, Constance L Cepko. Development 2004
120
8


Lhx2 links the intrinsic and extrinsic factors that control optic cup formation.
Sanghee Yun, Yukio Saijoh, Karla E Hirokawa, Daniel Kopinke, L Charles Murtaugh, Edwin S Monuki, Edward M Levine. Development 2009
62
8

Retinal degeneration triggered by inactivation of PTEN in the retinal pigment epithelium.
Jin Woo Kim, Kyung Hwa Kang, Patrick Burrola, Tak W Mak, Greg Lemke. Genes Dev 2008
56
8

Analysis of transcriptional regulatory pathways of photoreceptor genes by expression profiling of the Otx2-deficient retina.
Yoshihiro Omori, Kimiko Katoh, Shigeru Sato, Yuki Muranishi, Taro Chaya, Akishi Onishi, Takashi Minami, Takashi Fujikado, Takahisa Furukawa. PLoS One 2011
49
8

Novel heterozygous OTX2 mutations and whole gene deletions in anophthalmia, microphthalmia and coloboma.
Alexander Wyatt, Preeti Bakrania, David J Bunyan, Robert J Osborne, John A Crolla, Alison Salt, Carmen Ayuso, Ruth Newbury-Ecob, Y Abou-Rayyah, J Richard O Collin,[...]. Hum Mutat 2008
78
8

OTX2 microphthalmia syndrome: four novel mutations and delineation of a phenotype.
K F Schilter, A Schneider, T Bardakjian, J-F Soucy, R C Tyler, L M Reis, E V Semina. Clin Genet 2011
71
8

BEST1 expression in the retinal pigment epithelium is modulated by OTX family members.
Noriko Esumi, Shu Kachi, Laszlo Hackler, Tomohiro Masuda, Zhiyong Yang, Peter A Campochiaro, Donald J Zack. Hum Mol Genet 2009
36
11


Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes.
S Chen, Q L Wang, Z Nie, H Sun, G Lennon, N G Copeland, D J Gilbert, N A Jenkins, D J Zack. Neuron 1997
549
8

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
401
8


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.