A citation-based method for searching scientific literature

I Matsuo, S Kuratani, C Kimura, N Takeda, S Aizawa. Genes Dev 1995
Times Cited: 561







List of co-cited articles
1069 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
42


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
20

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
17

The homeobox gene Otx2 in development and disease.
Francis Beby, Thomas Lamonerie. Exp Eye Res 2013
78
20

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
17


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
16

Nested expression domains of four homeobox genes in developing rostral brain.
A Simeone, D Acampora, M Gulisano, A Stornaiuolo, E Boncinelli. Nature 1992
688
11

Genetic modifiers of otocephalic phenotypes in Otx2 heterozygous mutant mice.
Takuichiro Hide, Jun Hatakeyama, Chiharu Kimura-Yoshida, E Tian, Naoki Takeda, Yukitaka Ushio, Toshihiko Shiroishi, Shinichi Aizawa, Isao Matsuo. Development 2002
51
19

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
9

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
9

A novel dominant negative mutation of OTX2 associated with combined pituitary hormone deficiency.
Daniel Diaczok, Christopher Romero, Janice Zunich, Ian Marshall, Sally Radovick. J Clin Endocrinol Metab 2008
77
11

Temporal and spatial delineation of mouse Otx2 functions by conditional self-knockout.
Nicolas Fossat, Gilles Chatelain, Gilbert Brun, Thomas Lamonerie. EMBO Rep 2006
43
20

OTX2 mutations contribute to the otocephaly-dysgnathia complex.
Nicolas Chassaing, Susanna Sorrentino, Erica E Davis, Dominique Martin-Coignard, Anthony Iacovelli, William Paznekas, Bryn D Webb, Ona Faye-Petersen, Férechté Encha-Razavi, Leopoldine Lequeux,[...]. J Med Genet 2012
40
22

The Rx homeobox gene is essential for vertebrate eye development.
P H Mathers, A Grinberg, K A Mahon, M Jamrich. Nature 1997
541
9

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse.
M T Dattani, J P Martinez-Barbera, P Q Thomas, J M Brickman, R Gupta, I L Mårtensson, H Toresson, M Fox, J K Wales, P C Hindmarsh,[...]. Nat Genet 1998
499
9


OTX2 loss of function mutation causes anophthalmia and combined pituitary hormone deficiency with a small anterior and ectopic posterior pituitary.
Toshihiro Tajima, Akira Ohtake, Masaya Hoshino, Shin Amemiya, Nozomu Sasaki, Katsura Ishizu, Kenji Fujieda. J Clin Endocrinol Metab 2009
62
12

A role for Gbx2 in repression of Otx2 and positioning the mid/hindbrain organizer.
S Millet, K Campbell, D J Epstein, K Losos, E Harris, A L Joyner. Nature 1999
226
8

Six3 repression of Wnt signaling in the anterior neuroectoderm is essential for vertebrate forebrain development.
Oleg V Lagutin, Changqi C Zhu, Daisuke Kobayashi, Jacek Topczewski, Kenji Shimamura, Luis Puelles, Helen R C Russell, Peter J McKinnon, Lilianna Solnica-Krezel, Guillermo Oliver. Genes Dev 2003
346
8


Interaction between Otx2 and Gbx2 defines the organizing center for the optic tectum.
T Katahira, T Sato, S Sugiyama, T Okafuji, I Araki, J Funahashi, H Nakamura. Mech Dev 2000
115
7

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
7

A novel loss-of-function mutation in OTX2 in a patient with anophthalmia and isolated growth hormone deficiency.
Liat Ashkenazi-Hoffnung, Yael Lebenthal, Alexander W Wyatt, Nicola K Ragge, Sumito Dateki, Maki Fukami, Tsutomu Ogata, Moshe Phillip, Galia Gat-Yablonski. Hum Genet 2010
31
22


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
417
7


Heterozygous orthodenticle homeobox 2 mutations are associated with variable pituitary phenotype.
Sumito Dateki, Kitaro Kosaka, Kosei Hasegawa, Hiroyuki Tanaka, Noriyuki Azuma, Susumu Yokoya, Koji Muroya, Masanori Adachi, Toshihiro Tajima, Katsuaki Motomura,[...]. J Clin Endocrinol Metab 2010
74
9

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
14

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
7


Visceral endoderm mediates forebrain development by suppressing posteriorizing signals.
C Kimura, K Yoshinaga, E Tian, M Suzuki, S Aizawa, I Matsuo. Dev Biol 2000
170
6

Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways.
Preeti Bakrania, Maria Efthymiou, Johannes C Klein, Alison Salt, David J Bunyan, Alex Wyatt, Chris P Ponting, Angela Martin, Steven Williams, Victoria Lindley,[...]. Am J Hum Genet 2008
185
6

OTX2 directly activates cell cycle genes and inhibits differentiation in medulloblastoma cells.
Jens Bunt, Nancy E Hasselt, Danny A Zwijnenburg, Mohamed Hamdi, Jan Koster, Rogier Versteeg, Marcel Kool. Int J Cancer 2012
59
10

The Xenopus homologue of Otx2 is a maternal homeobox gene that demarcates and specifies anterior body regions.
M Pannese, C Polo, M Andreazzoli, R Vignali, B Kablar, G Barsacchi, E Boncinelli. Development 1995
379
6

Mutations in the human RAX homeobox gene in a patient with anophthalmia and sclerocornea.
Vera A Voronina, Elena A Kozhemyakina, Christina M O'Kernick, Natan D Kahn, Sharon L Wenger, John V Linberg, Adele S Schneider, Peter H Mathers. Hum Mol Genet 2004
149
6

Mouse small eye results from mutations in a paired-like homeobox-containing gene.
R E Hill, J Favor, B L Hogan, C C Ton, G F Saunders, I M Hanson, J Prosser, T Jordan, N D Hastie, V van Heyningen. Nature 1991
6

Lhx2, a LIM homeobox gene, is required for eye, forebrain, and definitive erythrocyte development.
F D Porter, J Drago, Y Xu, S S Cheema, C Wassif, S P Huang, E Lee, A Grinberg, J S Massalas, D Bodine,[...]. Development 1997
361
6

Specification of the vertebrate eye by a network of eye field transcription factors.
Michael E Zuber, Gaia Gestri, Andrea S Viczian, Giuseppina Barsacchi, William A Harris. Development 2003
342
6

Specification of the anterior hindbrain and establishment of a normal mid/hindbrain organizer is dependent on Gbx2 gene function.
K M Wassarman, M Lewandoski, K Campbell, A L Joyner, J L Rubenstein, S Martinez, G R Martin. Development 1997
289
6



Early eye development in vertebrates.
R L Chow, R A Lang. Annu Rev Cell Dev Biol 2001
451
6

Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function.
C Chiang, Y Litingtung, E Lee, K E Young, J L Corden, H Westphal, P A Beachy. Nature 1996
6

Deletion of OTX2 in neural ectoderm delays anterior pituitary development.
Amanda H Mortensen, Vanessa Schade, Thomas Lamonerie, Sally A Camper. Hum Mol Genet 2015
30
20

Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling.
Stuart M Chambers, Christopher A Fasano, Eirini P Papapetrou, Mark Tomishima, Michel Sadelain, Lorenz Studer. Nat Biotechnol 2009
5

Regulation of Otx2 expression and its functions in mouse forebrain and midbrain.
Daisuke Kurokawa, Hiroshi Kiyonari, Rika Nakayama, Chiharu Kimura-Yoshida, Isao Matsuo, Shinichi Aizawa. Development 2004
77
6


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
13


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.