Identification of protein altering variants influencing preeclampsia risk

Status	Finished
Effective start/end date	1/01/13 → 30/06/16

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Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes
Melton, P. E., Johnson, M. P., Gokhale-Agashe, D., Rea, A. J., Ariff, A., Cadby, G., Peralta, J. M., Mcnab, T. J., Allcock, R. J., Abraham, L. J., Blangero, J., Brennecke, S. P. & Moses, E. K., May 2019, In: Journal of Hypertension. 37, 5, p. 997-1011 15 p.
Research output: Contribution to journal › Article › peer-review
24 Citations (Scopus)
Preeclampsia does not share common risk alleles in 9p21 with coronary artery disease and type 2 diabetes
Kaartokallio, T., Lokki, A. I., Peterson, H., Kivinen, K., Hiltunen, L., Salmela, E., Lappalainen, T., Maanselkä, P., Heino, S., Knuutila, S., Sayed, A., Poston, L., Brennecke, S. P., Johnson, M. P., Morgan, L., Moses, E., Kere, J. & Laivuori, H., 3 Jul 2016, In: Annals of Medicine. 48, 5, p. 330-336 7 p.
Research output: Contribution to journal › Article › peer-review
2 Citations (Scopus)