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Browsing by Author Jonasdottir, A.

Full Text	Issue Date	Title	Author(s)
	2011	Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption	Sulem, P.; Gudbjartsson, D.F.; Geller, F.; Prokopenko, I.; Feenstra, B., et al
	2011	Identification of low-frequency variants associated with gout and serum uric acid levels	Sulem, P.; Gudbjartsson, D.F.; Walters, G.B.; Helgadottir, H.T.; Helgason, A., et al
	2011	Mutations in BRIP1 confer high risk of ovarian cancer	Rafnar, T.; Gudbjartsson, D.F.; Sulem, P.; Jonasdottir, A.; Sigurdsson, A., et al
	2011	A rare variant in MYH6 is associated with high risk of sick sinus syndrome	Holm, H.; Gudbjartsson, D.F.; Sulem, P.; Masson, G.; Helgadottir, H.T., et al
	2011	A germline variant in the TP53 polyadenylation signal confers cancer susceptibility	Stacey, S.N.; Sulem, P.; Jonasdottir, A.; Masson, G.; Gudmundsson, J., et al
	2010	Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm.	Gretarsdottir, S.; Baas, A.F.; Thorleifsson, G.; Holm, H.; Heijer, M. den, et al
	2010	Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locus.	Stacey, S.N.; Sulem, P.; Zanon, C.; Gudjonsson, S.A.; Thorleifsson, G., et al
	2009	Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche.	Sulem, P.; Gudbjartsson, D.F.; Rafnar, T.; Holm, H.; Olafsdottir, E.J., et al