The association between headache and Val158Met polymorphism in the catechol–O–methyltransferase gene: the HUNT Study

por Hagen, K., Pettersen, E., Stovner, L. J., Skorpen, F., Zwart, J.-A.
Publicado 2006

A low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2)

por Roten, L.T., Fenstad, M.H., Forsmo, S., Johnson, M.P., Moses, E.K., Austgulen, R., Skorpen, F.
Publicado 2011

Is there a genetic cause for cancer cachexia? – a clinical validation study in 1797 patients

por Solheim, T S, Fayers, P M, Fladvad, T, Tan, B, Skorpen, F, Fearon, K, Baracos, V E, Klepstad, P, Strasser, F, Kaasa, S
Publicado 2011