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



E Matsunaga, K Shiota. Teratology 1977
Times Cited: 236




List of shared articles



Times cited

Cyclopia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research.
Iêda M Orioli, Emmanuelle Amar, Marian K Bakker, Eva Bermejo-Sánchez, Fabrizio Bianchi, Mark A Canfield, Maurizio Clementi, Adolfo Correa, Melinda Csáky-Szunyogh, Marcia L Feldkamp,[...]. Am J Med Genet C Semin Med Genet 2011
14

Embryogenesis of holoprosencephaly.
Kohei Shiota, Shigehito Yamada, Munekazu Komada, Makoto Ishibashi. Am J Med Genet A 2007
19

Early pathogenesis of holoprosencephaly.
Kohei Shiota, Shigehito Yamada. Am J Med Genet C Semin Med Genet 2010
19

Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly.
Erich Roessler, Wuhong Pei, Maia V Ouspenskaia, Jayaprakash D Karkera, Jorge Ivan Veléz, Sharmilla Banerjee-Basu, Gretchen Gibney, Philip J Lupo, Laura E Mitchell, Jeffrey A Towbin,[...]. Mol Genet Metab 2009
49


Beneficial effect of supplemental lipoic acid on diabetes-induced pregnancy loss in the mouse.
Rengasamy Padmanabhan, Shafiullah Mohamed, Sarabjit Singh. Ann N Y Acad Sci 2006
13

Embryonic holoprosencephaly: pathology and phenotypic variability.
Shigehito Yamada. Congenit Anom (Kyoto) 2006
9

Nationwide epidemiological survey of holoprosencephaly in Japan.
Yuichi Abe, Ryuichiro Araki, Hisanori Sobajima, Masanori Tamura, Tetsuya Kunikata, Akira Ohtake, Hideo Yamanouchi. Pediatr Int 2020
0

Holoprosencephaly.
Jin S Hahn. Handb Clin Neurol 2008
2

Fetal midline anomalies: Diagnosis and counselling part 2: Septal anomalies.
Martina Leombroni, Asma Khalil, Marco Liberati, Francesco D'Antonio. Eur J Paediatr Neurol 2018
3

Holoprosencephaly in an 8.5-week triploidy gestation.
Benjamin D Solomon, Lorraine Potocki, Calvin E Oyer, Maximilian Muenke. Clin Dysmorphol 2009
1

Epidemiology of holoprosencephaly: Prevalence and risk factors.
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet C Semin Med Genet 2010
62

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


Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly.
Erich Roessler, Maia V Ouspenskaia, Jayaprakash D Karkera, Jorge I Vélez, Amy Kantipong, Felicitas Lacbawan, Peter Bowers, John W Belmont, Jeffrey A Towbin, Elizabeth Goldmuntz,[...]. Am J Hum Genet 2008
101