A citation-based method for searching scientific literature

M Urioste, E Valcarcel, M A Gomez, I Pinel, R Garcia de León, A Diaz de Bustamante, R Tebar, M L Martinez-Frias. Am J Med Genet 1988
Times Cited: 29



S Ong, A Tonks, E R Woodward, M P Wyldes, M D Kilby. Prenat Diagn 2007
Times Cited: 30




List of shared articles



Times cited

Risk factors for nonsyndromic holoprosencephaly: a Manitoba case-control study.
Simone S Vaz, Bernard Chodirker, Chitra Prasad, Jamie A Seabrook, Albert E Chudley, Asuri N Prasad. Am J Med Genet A 2012
10

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

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

Clinical epidemiologic study of holoprosencephaly in South America.
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet A 2007
36

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