A citation-based method for searching scientific literature

T Nagai, J Aruga, O Minowa, T Sugimoto, Y Ohno, T Noda, K Mikoshiba. Proc Natl Acad Sci U S A 2000
Times Cited: 178







List of co-cited articles
1006 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired.
S A Brown, D Warburton, L Y Brown, C Y Yu, E R Roeder, S Stengel-Rutkowski, R C Hennekam, M Muenke. Nat Genet 1998
365
46

The expression of the mouse Zic1, Zic2, and Zic3 gene suggests an essential role for Zic genes in body pattern formation.
T Nagai, J Aruga, S Takada, T Günther, R Spörle, K Schughart, K Mikoshiba. Dev Biol 1997
266
35

The role of Zic genes in neural development.
Jun Aruga. Mol Cell Neurosci 2004
187
28

Zic2 is required for neural crest formation and hindbrain patterning during mouse development.
Paul Elms, Pam Siggers, Diane Napper, Andy Greenfield, Ruth Arkell. Dev Biol 2003
81
33

Zic2-associated holoprosencephaly is caused by a transient defect in the organizer region during gastrulation.
Nicholas Warr, Nicola Powles-Glover, Anna Chappell, Joan Robson, Dominic Norris, Ruth M Arkell. Hum Mol Genet 2008
68
39


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
25

Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination.
L Y Brown, S Odent, V David, M Blayau, C Dubourg, C Apacik, M A Delgado, B D Hall, J F Reynolds, A Sommer,[...]. Hum Mol Genet 2001
137
25

Mouse Zic5 deficiency results in neural tube defects and hypoplasia of cephalic neural crest derivatives.
Takashi Inoue, Minoru Hatayama, Takahide Tohmonda, Shigeyoshi Itohara, Jun Aruga, Katsuhiko Mikoshiba. Dev Biol 2004
76
28

The ZIC gene family in development and disease.
I Grinberg, K J Millen. Clin Genet 2005
107
21


Zic2 patterns binocular vision by specifying the uncrossed retinal projection.
Eloísa Herrera, Lucia Brown, Jun Aruga, Rivka A Rachel, Gül Dolen, Katsuhiko Mikoshiba, Stephen Brown, Carol A Mason. Cell 2003
181
18

Overlapping and distinct expression domains of Zic2 and Zic3 during mouse gastrulation.
Paul Elms, Andrew Scurry, Jennifer Davies, Catherine Willoughby, Terry Hacker, Debora Bogani, Ruth Arkell. Gene Expr Patterns 2004
50
34

The mouse zic gene family. Homologues of the Drosophila pair-rule gene odd-paired.
J Aruga, T Nagai, T Tokuyama, Y Hayashizaki, Y Okazaki, V M Chapman, K Mikoshiba. J Biol Chem 1996
170
17

Zic1 promotes the expansion of dorsal neural progenitors in spinal cord by inhibiting neuronal differentiation.
Jun Aruga, Takahide Tohmonda, Shunsaku Homma, Katsuhiko Mikoshiba. Dev Biol 2002
103
17

Zic2 controls cerebellar development in cooperation with Zic1.
Jun Aruga, Takashi Inoue, Jun Hoshino, Katsuhiko Mikoshiba. J Neurosci 2002
101
17

A wide-range phylogenetic analysis of Zic proteins: implications for correlations between protein structure conservation and body plan complexity.
Jun Aruga, Akiko Kamiya, Hirokazu Takahashi, Takahiko J Fujimi, Yuri Shimizu, Keiko Ohkawa, Shigenobu Yazawa, Yoshihiko Umesono, Hideki Noguchi, Takashi Shimizu,[...]. Genomics 2006
60
28

Holoprosencephaly: clinical, anatomic, and molecular dimensions.
M Michael Cohen. Birth Defects Res A Clin Mol Teratol 2006
138
17

A complex syndrome of left-right axis, central nervous system and axial skeleton defects in Zic3 mutant mice.
Smita M Purandare, Stephanie M Ware, Kin Ming Kwan, Marinella Gebbia, Maria Teresa Bassi, Jian Min Deng, Hannes Vogel, Richard R Behringer, John W Belmont, Brett Casey. Development 2002
123
16

Physical and functional interactions between Zic and Gli proteins.
Y Koyabu, K Nakata, K Mizugishi, J Aruga, K Mikoshiba. J Biol Chem 2001
148
16

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.
E Roessler, E Belloni, K Gaudenz, P Jay, P Berta, S W Scherer, L C Tsui, M Muenke. Nat Genet 1996
841
16

Central roles of the roof plate in telencephalic development and holoprosencephaly.
Xun Cheng, Ching-mei Hsu, D Spencer Currle, Jia Sheng Hu, A James Barkovich, Edwin S Monuki. J Neurosci 2006
80
20

Zic2 and Zic3 synergistically control neurulation and segmentation of paraxial mesoderm in mouse embryo.
Takashi Inoue, Maya Ota, Katsuhiko Mikoshiba, Jun Aruga. Dev Biol 2007
44
36

Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
221
16

Transcription factor Zic2 inhibits Wnt/β-catenin protein signaling.
Rasoul Pourebrahim, Rob Houtmeyers, Stephen Ghogomu, Sylvie Janssens, Aurore Thelie, Hong Thi Tran, Tobias Langenberg, Kris Vleminckx, Eric Bellefroid, Jean-Jacques Cassiman,[...]. J Biol Chem 2011
61
26

Myogenic repressor I-mfa interferes with the function of Zic family proteins.
Kiyomi Mizugishi, Minoru Hatayama, Takahide Tohmonda, Miyuki Ogawa, Takashi Inoue, Katsuhiko Mikoshiba, Jun Aruga. Biochem Biophys Res Commun 2004
41
36

Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination.
K W Gripp, D Wotton, M C Edwards, E Roessler, L Ades, P Meinecke, A Richieri-Costa, E H Zackai, J Massagué, M Muenke,[...]. Nat Genet 2000
300
15

Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals.
Benjamin D Solomon, Felicitas Lacbawan, Sandra Mercier, Nancy J Clegg, Mauricio R Delgado, Kenneth Rosenbaum, Christèle Dubourg, Veronique David, Ann Haskins Olney, Lars-Erik Wehner,[...]. J Med Genet 2010
57
26

Immunolocalization of Zic2 expression in the developing mouse forebrain.
Lúcia Y Brown, Andreas H Kottmann, Stephen Brown. Gene Expr Patterns 2003
43
32

The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.
L Nanni, J E Ming, M Bocian, K Steinhaus, D W Bianchi, C Die-Smulders, A Giannotti, K Imaizumi, K L Jones, M D Campo,[...]. Hum Mol Genet 1999
258
14


Mutations in the BMP pathway in mice support the existence of two molecular classes of holoprosencephaly.
Marie Fernandes, Grigoriy Gutin, Heather Alcorn, Susan K McConnell, Jean M Hébert. Development 2007
73
17

A deletion encompassing Zic3 in bent tail, a mouse model for X-linked neural tube defects.
R Klootwijk, B Franke, C E van der Zee, R T de Boer, W Wilms, F A Hol, E C Mariman. Hum Mol Genet 2000
57
21

Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations.
Christèle Dubourg, Leïla Lazaro, Laurent Pasquier, Claude Bendavid, Martine Blayau, Franck Le Duff, Marie-Renée Durou, Sylvie Odent, Véronique David. Hum Mutat 2004
115
12

Mouse Zic1 is involved in cerebellar development.
J Aruga, O Minowa, H Yaginuma, J Kuno, T Nagai, T Noda, K Mikoshiba. J Neurosci 1998
149
12

Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation.
Inessa Grinberg, Hope Northrup, Holly Ardinger, Chitra Prasad, William B Dobyns, Kathleen J Millen. Nat Genet 2004
137
12

The full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanism.
Erich Roessler, Felicitas Lacbawan, Christèle Dubourg, Aimee Paulussen, Jos Herbergs, Ute Hehr, Claude Bendavid, Nan Zhou, Maia Ouspenskaia, Sherri Bale,[...]. Hum Mutat 2009
49
24

Xenopus Zic family and its role in neural and neural crest development.
K Nakata, T Nagai, J Aruga, K Mikoshiba. Mech Dev 1998
135
11

Xenopus Zic3, a primary regulator both in neural and neural crest development.
K Nakata, T Nagai, J Aruga, K Mikoshiba. Proc Natl Acad Sci U S A 1997
208
11

Zic1 regulates the patterning of vertebral arches in cooperation with Gli3.
J Aruga, K Mizugishi, H Koseki, K Imai, R Balling, T Noda, K Mikoshiba. Mech Dev 1999
63
17

Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly.
Jeffrey E Ming, Michelle E Kaupas, Erich Roessler, Han G Brunner, Mahin Golabi, Mustafa Tekin, Robert F Stratton, Eva Sujansky, Sherri J Bale, Maximilian Muenke. Hum Genet 2002
158
11

Middle interhemispheric fusion: an unusual variant of holoprosencephaly.
A J Barkovich, D J Quint. AJNR Am J Neuroradiol 1993
110
11


Genetics of ventral forebrain development and holoprosencephaly.
M Muenke, P A Beachy. Curr Opin Genet Dev 2000
197
11


Dose-dependent functions of Fgf8 in regulating telencephalic patterning centers.
Elaine E Storm, Sonia Garel, Ugo Borello, Jean M Hebert, Salvador Martinez, Susan K McConnell, Gail R Martin, John L R Rubenstein. Development 2006
263
11

Early steps in the development of the forebrain.
Stephen W Wilson, Corinne Houart. Dev Cell 2004
299
11

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
D E Wallis, E Roessler, U Hehr, L Nanni, T Wiltshire, A Richieri-Costa, G Gillessen-Kaesbach, E H Zackai, J Rommens, M Muenke. Nat Genet 1999
283
11

The X-linked mouse mutation Bent tail is associated with a deletion of the Zic3 locus.
T Carrel, S M Purandare, W Harrison, F Elder, T Fox, B Casey, G E Herman. Hum Mol Genet 2000
41
24



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.