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



Erich Roessler, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
Times Cited: 155




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

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

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

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: a survey of the entity, with embryology and fetal imaging.
Thomas C Winter, Anne M Kennedy, Paula J Woodward. Radiographics 2015
42