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Browsing by Author Stacey, S.N.

Full Text	Issue Date	Title	Author(s)
	2012	A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer	Gudmundsson, J.; Sulem, P.; Gudbjartsson, D.F.; Masson, G.; Agnarsson, B.A., et al
	2012	Discovery of common variants associated with low TSH levels and thyroid cancer risk.	Gudmundsson, J.; Sulem, P.; Gudbjartsson, D.F.; Jonasson, J.G.; Masson, G., et al
	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	European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene	Rafnar, T.; Vermeulen, H.H.M.; Sulem, P.; Thorleifsson, G.; Aben, K.K.H., et al
	2011	Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk	Rafnar, T.; Sulem, P.; Besenbacher, S.; Gudbjartsson, D.F.; Zanon, C., 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 germline variant in the TP53 polyadenylation signal confers cancer susceptibility	Stacey, S.N.; Sulem, P.; Jonasdottir, A.; Masson, G.; Gudmundsson, J., 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
	2010	Genetic correction of PSA values using sequence variants associated with PSA levels.	Gudmundsson, J.; Besenbacher, S.; Sulem, P.; Gudbjartsson, D.F.; Olafsson, I., et al
	2010	A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer.	Kiemeney, L.A.L.M.; Sulem, P.; Besenbacher, S.; Vermeulen, S.; Sigurdsson, A., et al
	2009	New common variants affecting susceptibility to basal cell carcinoma.	Stacey, S.N.; Sulem, P.; Masson, G.; Gudjonsson, S.A.; Thorleifsson, G., et al
	2009	Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility.	Gudmundsson, J.; Sulem, P.; Gudbjartsson, D.F.; Blondal, T.; Gylfason, A., 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
	2009	Sequence variants at the TERT-CLPTM1L locus associate with many cancer types.	Rafnar, T.; Sulem, P.; Stacey, S.N.; Geller, F.; Gudmundsson, J., et al
	2008	ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma.	Gudbjartsson, D.F.; Sulem, P.; Stacey, S.N.; Goldstein, A.M.; Rafnar, T., et al
	2008	Two newly identified genetic determinants of pigmentation in Europeans.	Sulem, P.; Gudbjartsson, D.F.; Stacey, S.N.; Helgason, A.; Rafnar, T., et al
	2008	A variant associated with nicotine dependence, lung cancer and peripheral arterial disease.	Thorgeirsson, T.E.; Geller, F.; Sulem, P.; Rafnar, T.; Wiste, A., et al
	2008	Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer.	Gudmundsson, J.; Sulem, P.; Rafnar, T.; Bergthorsson, J.T.; Manolescu, A., et al
	2008	Sequence variant on 8q24 confers susceptibility to urinary bladder cancer.	Kiemeney, L.A.L.M.; Thorlacius, S.; Sulem, P.; Geller, F.; Aben, K.K.H., et al
	2008	Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer.	Stacey, S.N.; Manolescu, A.; Sulem, P.; Thorlacius, S.; Gudjonsson, S.A., et al
	2007	Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.	Gudmundsson, J.; Sulem, P.; Manolescu, A.; Amundadottir, L.T.; Gudbjartsson, D.F., et al
	2007	Genetic determinants of hair, eye and skin pigmentation in Europeans.	Sulem, P.; Gudbjartsson, D.F.; Stacey, S.N.; Helgason, A.; Rafnar, T., et al
	2007	Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes.	Gudmundsson, J.; Sulem, P.; Steinthorsdottir, V.; Bergthorsson, J.T.; Thorleifsson, G., et al
	2007	Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer.	Stacey, S.N.; Manolescu, A.; Sulem, P.; Rafnar, T.; Gudmundsson, J., et al