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Browsing by Author Gulcher, J.R.
Showing results 1 to 19 of 19
| Full Text | Issue Date | Title | Author(s) | | 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 |
| 2010 | Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. | Thorgeirsson, T.E.; Gudbjartsson, D.F.; Surakka, I.; Vink, J.M.; Amin, N., 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 |
| 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 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 | 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 | Common variants conferring risk of schizophrenia. | Stefansson, H.; Ophoff, R.A.; Steinberg, S.; Andreassen, O.A.; Cichon, S., 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 | 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 | Large recurrent microdeletions associated with schizophrenia. | Stefansson, H.; Rujescu, D.; Cichon, S.; Pietilainen, O.P.H.; Ingason, A., 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 | 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 | 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 |
| 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 | 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 | 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 |
Showing results 1 to 19 of 19
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