A citation-based method for searching scientific literature

Jun Aruga, Hiroo Ogura, Fumihiro Shutoh, Miyuki Ogawa, Barbara Franke, Soichi Nagao, Katsuhiko Mikoshiba. Eur J Neurosci 2004
Times Cited: 15







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



Times Cited
  Times     Co-cited
Similarity


The ZIC gene family in development and disease.
I Grinberg, K J Millen. Clin Genet 2005
107
40

X-linked situs abnormalities result from mutations in ZIC3.
M Gebbia, G B Ferrero, G Pilia, M T Bassi, A Aylsworth, M Penman-Splitt, L M Bird, J S Bamforth, J Burn, D Schlessinger,[...]. Nat Genet 1997
303
40

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
136
33

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
33

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
265
33

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
26

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
26

Zic2 regulates the kinetics of neurulation.
T Nagai, J Aruga, O Minowa, T Sugimoto, Y Ohno, T Noda, K Mikoshiba. Proc Natl Acad Sci U S A 2000
177
26

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
124
26

The role of Zic genes in neural development.
Jun Aruga. Mol Cell Neurosci 2004
186
26

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
74
26

Zic2 controls cerebellar development in cooperation with Zic1.
Jun Aruga, Takashi Inoue, Jun Hoshino, Katsuhiko Mikoshiba. J Neurosci 2002
101
26


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
26

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
43
26

Dandy-Walker malformation: prenatal diagnosis and prognosis.
O Klein, A Pierre-Kahn, N Boddaert, D Parisot, F Brunelle. Childs Nerv Syst 2003
107
20

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
20

Analysis of the embryonic phenotype of Bent tail, a mouse model for X-linked neural tube defects.
Barbara Franke, Riko Klootwijk, Johan W M Hekking, Roelie T de Boer, Hans J ten Donkelaar, Edwin C M Mariman, Henny W M van Straaten. Anat Embryol (Berl) 2003
9
33

Physical and functional interactions between Zic and Gli proteins.
Y Koyabu, K Nakata, K Mizugishi, J Aruga, K Mikoshiba. J Biol Chem 2001
146
20

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
20

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
59
20


Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia.
G Zanni, Y Saillour, M Nagara, P Billuart, L Castelnau, C Moraine, L Faivre, E Bertini, A Durr, A Guichet,[...]. Neurology 2005
68
20

X-linked nonprogressive congenital cerebellar hypoplasia: clinical description and mapping to chromosome Xq.
S N Illarioshkin, H Tanaka, E D Markova, N N Nikolskaya, I A Ivanova-Smolenskaya, S Tsuji. Ann Neurol 1996
31
20

A spinocerebellar degeneration with X-linked inheritance.
P J Spira, J G McLeod, W A Evans. Brain 1979
32
20

Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes.
Guy Froyen, Hilde Van Esch, Marijke Bauters, Karen Hollanders, Suzanna G M Frints, Joris R Vermeesch, Koen Devriendt, Jean-Pierre Fryns, Peter Marynen. Hum Mutat 2007
138
20

Non-progressive congenital ataxias.
M Steinlin. Brain Dev 1998
44
20

Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation.
P Billuart, T Bienvenu, N Ronce, V des Portes, M C Vinet, R Zemni, H Roest Crollius, A Carrié, F Fauchereau, M Cherry,[...]. Nature 1998
336
20

Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A).
R Allikmets, W H Raskind, A Hutchinson, N D Schueck, M Dean, D M Koeller. Hum Mol Genet 1999
288
20

X linked severe mental retardation, craniofacial dysmorphology, epilepsy, ophthalmoplegia, and cerebellar atrophy in a large South African kindred is localised to Xq24-q27.
A L Christianson, R E Stevenson, C H van der Meyden, J Pelser, F W Theron, P L van Rensburg, M Chandler, C E Schwartz. J Med Genet 1999
72
20


Prenatal sonographic diagnosis of vermal agenesis.
S Blazer, M Berant, P O Sujov, E Z Zimmer, M Bronshtein. Prenat Diagn 1997
12
16

MRI of the fetal posterior fossa.
Catherine Adamsbaum, Marie Laure Moutard, Christine André, Valérie Merzoug, Solène Ferey, Marie Pierre Quéré, Fanny Lewin, Catherine Fallet-Bianco. Pediatr Radiol 2005
119
13



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
13

Wnt-3a regulates somite and tailbud formation in the mouse embryo.
S Takada, K L Stark, M J Shea, G Vassileva, J A McMahon, A P McMahon. Genes Dev 1994
626
13

"Bent-Tail," A Dominant, Sex-Linked Mutation in the Mouse.
E D Garber. Proc Natl Acad Sci U S A 1952
32
13

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
80
13

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
49
13

The role of ZIC3 in vertebrate development.
G E Herman, H M El-Hodiri. Cytogenet Genome Res 2002
22
13


Closure of the cerebellar vermis: evaluation with second trimester US.
B Bromley, A S Nadel, S Pauker, J A Estroff, B R Benacerraf. Radiology 1994
99
13


Rotation of the vermis as a cause of enlarged cisterna magna on prenatal imaging.
Y Zalel, Y Gilboa, L Gabis, L Ben-Sira, C Hoffman, Y Wiener, R Achiron. Ultrasound Obstet Gynecol 2006
34
13


Dandy-Walker malformation complex: correlation between ultrasonographic diagnosis and postmortem neuropathology.
Joanna J Phillips, Barry S Mahony, Joseph R Siebert, Tasneem Lalani, Corinne L Fligner, Raj P Kapur. Obstet Gynecol 2006
26
13

A different approach to cysts of the posterior fossa.
Marvin D Nelson, Karima Maher, Floyd H Gilles. Pediatr Radiol 2004
63
13

Sonographic detection of inferior vermian agenesis in Dandy-Walker malformations: prognostic implications.
M C Chang, S A Russell, P W Callen, R A Filly, R B Goldstein. Radiology 1994
40
13

Morphogenetic and cellular movements that shape the mouse cerebellum; insights from genetic fate mapping.
Sema K Sgaier, Sandrine Millet, Melissa P Villanueva, Frada Berenshteyn, Christian Song, Alexandra L Joyner. Neuron 2005
122
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.