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



Wei Zhang, Jong-Sun Kang, Francesca Cole, Min-Jeong Yi, Robert S Krauss. Dev Cell 2006
Times Cited: 189




List of shared articles



Times cited

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

Murine models of holoprosencephaly.
Karen A Schachter, Robert S Krauss. Curr Top Dev Biol 2008
36

CDON gene contributes to pituitary stalk interruption syndrome associated with unilateral facial and abducens nerve palsy.
Monika Obara-Moszyńska, Bartłomiej Budny, Małgorzata Kałużna, Katarzyna Zawadzka, Aleksander Jamsheer, Anna Rohde, Marek Ruchała, Katarzyna Ziemnicka, Marek Niedziela. J Appl Genet 2021
0

Mutations in CDON, encoding a hedgehog receptor, result in holoprosencephaly and defective interactions with other hedgehog receptors.
Gyu-Un Bae, Sabina Domené, Erich Roessler, Karen Schachter, Jong-Sun Kang, Maximilian Muenke, Robert S Krauss. Am J Hum Genet 2011
90

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

Boc modifies the holoprosencephaly spectrum of Cdo mutant mice.
Wei Zhang, Mingi Hong, Gyu-un Bae, Jong-Sun Kang, Robert S Krauss. Dis Model Mech 2011
47

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