A citation-based method for searching scientific literature

Shigehito Yamada, Chigako Uwabe, Shingo Fujii, Kohei Shiota. Birth Defects Res A Clin Mol Teratol 2004
Times Cited: 63







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



Times Cited
  Times     Co-cited
Similarity





Teratogenesis of holoprosencephaly.
M Michael Cohen, Kohei Shiota. Am J Med Genet 2002
131
19


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
840
15

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
15



Holoprosencephaly: clinical, anatomic, and molecular dimensions.
M Michael Cohen. Birth Defects Res A Clin Mol Teratol 2006
139
14

Cdo functions at multiple points in the Sonic Hedgehog pathway, and Cdo-deficient mice accurately model human holoprosencephaly.
Wei Zhang, Jong-Sun Kang, Francesca Cole, Min-Jeong Yi, Robert S Krauss. Dev Cell 2006
190
12

Imaging of a large collection of human embryo using a super-parallel MR microscope.
Yoshimasa Matsuda, Shinya Ono, Yosuke Otake, Shinya Handa, Katsumi Kose, Tomoyuki Haishi, Shigeto Yamada, Chikako Uwabe, Kohei Shiota. Magn Reson Med Sci 2007
25
32

Super-parallel MR microscope.
Yoshimasa Matsuda, Shin Utsuzawa, Takeaki Kurimoto, Tomoyuki Haishi, Yukako Yamazaki, Katsumi Kose, Izumi Anno, Mitsuhiro Marutani. Magn Reson Med 2003
41
17




The middle interhemispheric variant of holoprosencephaly.
Erin M Simon, Robert F Hevner, Joseph D Pinter, Nancy J Clegg, Mauricio Delgado, Stephen L Kinsman, Jin S Hahn, A James Barkovich. AJNR Am J Neuroradiol 2002
96
11


Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
222
11

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
179
9

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly.
E Belloni, M Muenke, E Roessler, G Traverso, J Siegel-Bartelt, A Frumkin, H F Mitchell, H Donis-Keller, C Helms, A V Hing,[...]. Nat Genet 1996
487
9

Magnetic resonance microscopy of embryos.
B R Smith, E Linney, D S Huff, G A Johnson. Comput Med Imaging Graph 1996
47
12

Development of a 1.0 T MR microscope using a Nd-Fe-B permanent magnet.
T Haishi, T Uematsu, Y Matsuda, K Kose. Magn Reson Imaging 2001
50
12

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
9

Middle interhemispheric fusion: an unusual variant of holoprosencephaly.
A J Barkovich, D J Quint. AJNR Am J Neuroradiol 1993
110
9

Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: searching for population variations.
Emanuele Leoncini, Giovanni Baranello, Iêda M Orioli, Göran Annerén, Marian Bakker, Fabrizio Bianchi, Carol Bower, Mark A Canfield, Eduardo E Castilla, Guido Cocchi,[...]. Birth Defects Res A Clin Mol Teratol 2008
64
9

The molecular genetics of holoprosencephaly.
Erich Roessler, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
155
9

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
138
7

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
7

The cell surface membrane proteins Cdo and Boc are components and targets of the Hedgehog signaling pathway and feedback network in mice.
Toyoaki Tenzen, Benjamin L Allen, Francesca Cole, Jong-Sun Kang, Robert S Krauss, Andrew P McMahon. Dev Cell 2006
265
7

Middle interhemispheric variant of holoprosencephaly: a distinct cliniconeuroradiologic subtype.
A J Lewis, E M Simon, A J Barkovich, N J Clegg, M R Delgado, E Levey, J S Hahn. Neurology 2002
64
7



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
7

Graphic and movie illustrations of human prenatal development and their application to embryological education based on the human embryo specimens in the Kyoto collection.
Shigehito Yamada, Chigako Uwabe, Tomoko Nakatsu-Komatsu, Yutaka Minekura, Masaji Iwakura, Tamaki Motoki, Kazuhiko Nishimiya, Masaaki Iiyama, Koh Kakusho, Michihiko Minoh,[...]. Dev Dyn 2006
26
19


Assessment of the deep gray nuclei in holoprosencephaly.
E M Simon, R Hevner, J D Pinter, N J Clegg, V S Miller, S L Kinsman, J S Hahn, A J Barkovich. AJNR Am J Neuroradiol 2000
66
7

Holoprosencephaly: new models, new insights.
Robert S Krauss. Expert Rev Mol Med 2007
40
12

Neuroanatomy of holoprosencephaly as predictor of function: beyond the face predicting the brain.
L L Plawner, M R Delgado, V S Miller, E B Levey, S L Kinsman, A J Barkovich, E M Simon, N J Clegg, V T Sweet, E E Stashinko,[...]. Neurology 2002
63
7

Visualization of human prenatal development by magnetic resonance imaging (MRI).
Kohei Shiota, Shigehito Yamada, Tomoko Nakatsu-Komatsu, Chigako Uwabe, Katsumi Kose, Yoshimasa Matsuda, Tomoyuki Haishi, Shinobu Mizuta, Tetsuya Matsuda. Am J Med Genet A 2007
21
23

MR microscopy of chick embryo vasculature.
B R Smith, E L Effmann, G A Johnson. J Magn Reson Imaging 1992
28
17

Magnetic resonance microscopy of chick embryos in ovo.
E L Effmann, G A Johnson, B R Smith, G A Talbott, G Cofer. Teratology 1988
28
17

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
6

Holoprosencephaly: birth data, benetic and demographic analyses of 30 families.
E Roach, W Demyer, P M Conneally, C Palmer, A D Merritt. Birth Defects Orig Artic Ser 1975
106
6

Holoprosencephaly survival and performance.
M Barr, M M Cohen. Am J Med Genet 1999
62
6

Rapid high resolution three dimensional reconstruction of embryos with episcopic fluorescence image capture.
Julie Rosenthal, Vipul Mangal, Diana Walker, Michael Bennett, Tim J Mohun, Cecilia W Lo. Birth Defects Res C Embryo Today 2004
65
6

The mammalian twisted gastrulation gene functions in foregut and craniofacial development.
Anna Petryk, Ryan M Anderson, Michael P Jarcho, Irina Leaf, Cathy S Carlson, John Klingensmith, William Shawlot, Michael B O'Connor. Dev Biol 2004
87
6


Developmental roles and clinical significance of hedgehog signaling.
Andrew P McMahon, Philip W Ingham, Clifford J Tabin. Curr Top Dev Biol 2003
660
6



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.