Fumihiro Sata
Department of Public Heath
Hokkaido University Graduate School of Medicine
Sapporo
Japan
Name/email consistency: high
- Functional maternal catechol-O-methyltransferase polymorphism and fetal growth restriction. Sata, F., Yamada, H., Suzuki, K., Saijo, Y., Yamada, T., Minakami, H., Kishi, R. Pharmacogenet. Genomics (2006)
- Caffeine intake, CYP1A2 polymorphism and the risk of recurrent pregnancy loss. Sata, F., Yamada, H., Suzuki, K., Saijo, Y., Kato, E.H., Morikawa, M., Minakami, H., Kishi, R. Mol. Hum. Reprod. (2005)
- Glutathione S-transferase M1 and T1 polymorphisms and the risk of recurrent pregnancy loss. Sata, F., Yamada, H., Kondo, T., Gong, Y., Tozaki, S., Kobashi, G., Kato, E.H., Fujimoto, S., Kishi, R. Mol. Hum. Reprod. (2003)
- A polymorphism in the CYP17 gene relates to the risk of recurrent pregnancy loss. Sata, F., Yamada, H., Yamada, A., Kato, E.H., Kataoka, S., Saijo, Y., Kondo, T., Tamaki, J., Minakami, H., Kishi, R. Mol. Hum. Reprod. (2003)