Publications Åsa Johansson
Selected publications:
- Akerblom, A., Eriksson, N., Wallentin, L., Siegbahn, A., Barratt, B.J., Becker, R.C., Budaj, A., Himmelmann, A., Husted, S., Storey, R.F., Johansson, A., and James, S.K., Polymorphism of the cystatin C gene in patients with acute coronary syndromes: Results from the PLATelet inhibition and patient Outcomes study. Am Heart J, 2014, 168(1).
- Besingi, W. and Johansson, A., Smoke-related DNA methylation changes in the etiology of human disease. Hum Mol Genet, 2014, 23(9).
- Enroth, S., Johansson, A., Enroth, S.B., and Gyllensten, U., Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. Nat Commun, 2014, 5.
- Wood, A.R., et al., Defining the role of common variation in the genomic and biological architecture of adult human height. Nat Genet, 2014.
- Deloukas, P., et al., Large-scale association analysis identifies new risk loci for coronary artery disease. Nat Genet, 2013, 45(1).
- Johansson, A., Enroth, S., and Gyllensten, U., Continuous Aging of the Human DNA Methylome Throughout the Human Lifespan. PLoS One, 2013, 8(6).
- Johansson, A., Enroth, S., Palmblad, M., Deelder, A.M., Bergquist, J., and Gyllensten, U., Identification of genetic variants influencing the human plasma proteome. Proc Natl Acad Sci U S A, 2013, 110(12).
- Lian, I.A., Langaas, M., Moses, E., and Johansson, A., Differential gene expression at the maternal-fetal interface in preeclampsia is influenced by gestational age. PLoS One, 2013, 8(7).
- Ameur, A., Enroth, S., Johansson, A., Zaboli, G., Igl, W., Johansson, A.C., Rivas, M.A., Daly, M.J., Schmitz, G., Hicks, A.A., Meitinger, T., Feuk, L., van Duijn, C., Oostra, B., Pramstaller, P.P., et al., Genetic adaptation of fatty-acid metabolism: a human-specific haplotype increasing the biosynthesis of long-chain omega-3 and omega-6 fatty acids. Am J Hum Genet, 2012, 90(5).
- Johansson, A., Loset, M., Mundal, S.B., Johnson, M.P., Freed, K.A., Fenstad, M.H., Moses, E.K., Austgulen, R., and Blangero, J., Partial correlation network analyses to detect altered gene interactions in human disease: using preeclampsia as a model. Hum Genet, 2011, 129(1).