DSpace at RU >

Browsing by Author Thorleifsson, G.

Full Text	Issue Date	Title	Author(s)
	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
	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	Large-scale gene-centric analysis identifies novel variants for coronary artery disease	Butterworth, A.S.; Braund, P.S.; Hardwick, R.J.; Saleheen, D.; Peden, J.F., et al
	2011	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Chambers, J.C.; Zhang, W.; Sehmi, J.; Li, X.; Wass, M.N., et al
	2011	Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus	Jacquemont, S.; Reymond, A.; Zufferey, F.; Harewood, L.; Walters, R.G., et al
	2011	Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1	Bown, M.J.; Jones, G.T.; Harrison, S.C.; Wright, B.J.; Bumpstead, S., 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
	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	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
	2010	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Lango Allen, H.; Estrada, K.; Lettre, G.; Berndt, S.I.; Weedon, M.N., et al
	2010	Association of variants at UMOD with chronic kidney disease and kidney stones : role of age and comorbid diseases	Gudbjartsson, D.F.; Holm, H.; Indridason, O.S.; Thorleifsson, G.; Edvardsson, V., et al
	2010	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Speliotes, E.K.; Willer, C.J.; Berndt, S.I.; Monda, K.L.; Thorleifsson, G., 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
	2009	Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density.	Thorleifsson, G.; Holm, H.; Edvardsson, V.; Walters, G.B.; Styrkarsdottir, U., 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
	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 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	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Thorleifsson, G.; Walters, G.B.; Gudbjartsson, D.F.; Steinthorsdottir, V.; Sulem, P., et al
	2008	The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm.	Helgadottir, A.; Thorleifsson, G.; Magnusson, K.P.; Gretarsdottir, S.; Steinthorsdottir, V., 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	Many sequence variants affecting diversity of adult human height.	Gudbjartsson, D.F.; Walters, G.B.; Thorleifsson, G.; Stefansson, H.; Halldorsson, B.V., 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 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	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
	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	Genetic determinants of hair, eye and skin pigmentation in Europeans.	Sulem, P.; Gudbjartsson, D.F.; Stacey, S.N.; Helgason, A.; Rafnar, T., et al