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Browsing by Author "Kiemeney, L.A.L.M."
Now showing items 1-50 of 591
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Functional Analysis and Fine Mapping of the 9p22.2 Ovarian Cancer Susceptibility Locus Buckley, Melissa A.; Woods, N.; Tyrer, J.P.; Mendoza-Fandino, Gustavo; Lawrenson, Kate; Hazelett, D.J.; ; ; ; ; et al.2019, Article / Letter to editor (Cancer Research, vol. 79, iss. 3, (2019), pp. 467-481)
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Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences Linner, Richard Karlsson; Biroli, Pietro; Kong, E.; Meddens, Fleur W.; Wedow, R.; Fontana, M.A.; Hoen, P.A. 't; Galesloot, T.E.; Leeuw, Christiaan de; ; et al.2019, Article / Letter to editor (Nature Genetics, vol. 51, iss. 2, (2019), pp. 245-+)
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Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition Mikropoulos, Christos; Selkirk, C.; Saya, Sibel; Bancroft, Elizabeth; Vertosick, Emily; Dadaev, Tokhir; ; ; ; Zelst-Stams, W.A. van; et al.2018, Article / Letter to editor (British Journal of Cancer, vol. 118, iss. 2, (2018), pp. 266-276)
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Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity Turcot, V.; Lu, Y.; Highland, H.M.; Schurmann, C.; Justice, A.E.; Fine, R.S.; Corominas-Galbany, J.; ; ; Galesloot, T.E.; et al.2018, Article / Letter to editor (Nature Genetics, vol. 50, iss. 1, (2018), pp. 26-41)
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A Genetic Polymorphism in CTLA-4 Is Associated with Overall Survival in Sunitinib-Treated Patients with Clear Cell Metastatic Renal Cell Carcinoma Liu, Xiaoyan; Swen, J.J.; Diekstra, M.H.M.; Boven, Epie; Castellano, D.; Gelderblom, Hans; ; ; ; Rini, Brian I.; et al.2018, Article / Letter to editor (Clinical Cancer Research, vol. 24, iss. 10, (2018), pp. 2350-2356)
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Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals Lee, J.J.; Wedow, R.; Okbay, A.; Kong, E.; Maghzian, O.; Zacher, M.; Galesloot, T.E.; ; ; Benjamin, D.J.; et al.2018, Article / Letter to editor (Nature Genetics, vol. 50, iss. 8, (2018), pp. 1112-1121)
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Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility Earp, M.; Tyrer, J.P.; Winham, S.J.; Lin, H.Y.; Chornokur, G.; Dennis, J.; ; ; ; ; et al.2018, Article / Letter to editor (PLoS One, vol. 13, iss. 7, (2018), article e0197561)
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rs495139 in the TYMS-ENOSF1 Region and Risk of Ovarian Carcinoma of Mucinous Histology Kelemen, L.E.; Earp, M.; Fridley, B.L.; Chenevix-Trench, G.; Fasching, P.A.; Beckmann, M.W.; Ekici, A.B.; Hein, A.; Lambrechts, D.; Lambrechts, S.; et al.2018, Article / Letter to editor (International Journal of Molecular Sciences, vol. 19, iss. 9, (2018), article E2473)
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Association of BRCA2 K3326* With Small Cell Lung Cancer and Squamous Cell Cancer of the Skin Rafnar, T.; Sigurjonsdottir, G.R.; Stacey, S.N.; Halldorsson, G.; Sulem, P.; Pardo, L.M.; Helgason, H.; Sigurdsson, S.T.; Gudjonsson, T.; Tryggvadottir, L.; et al.2018, Article / Letter to editor (Journal of the National Cancer Institute, vol. 110, iss. 9, (2018), pp. 967-974)
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Role of the Complement System in Chronic Central Serous Chorioretinopathy A Genome-Wide Association Study Schellevis, R.L.; Dijk, E.H.C. van; Breukink, M.B.; Altay, L.; Bakker, B.; Koeleman, Bobby P. C.; ; ; ; ; et al.2018, Article / Letter to editor (Jama Ophthalmology, vol. 136, iss. 10, (2018), pp. 1128-1136)
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Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation Teumer, A.; Chaker, L.; Groeneweg, Stefan; Li, Yong; Munno, Celia Di; Barbieri, C.; Galesloot, T.E.; ; ; Visser, T.J.; et al.2018, Article / Letter to editor (Nature Communications, vol. 9, (2018), article 4455)
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GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes Franceschini, N.; Giambartolomei, Claudia; Vries, P.S. de; Finan, Chris; Bis, J.C.; Huntley, R.P.; ; ; Galesloot, T.E.; Casas, J.P.; et al.2018, Article / Letter to editor (Nature Communications, vol. 9, (2018), article 5141)
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Epidemiology of Bladder Cancer: A Systematic Review and Contemporary Update of Risk Factors in 2018 Cumberbatch, M.G.K.; Jubber, I.; Black, P.C.; Esperto, F.; Figueroa, J.D.; Kamat, A.M.; ; Lotan, Y.; Pang, K.; Silverman, D.T.; et al.2018, Article / Letter to editor (European Urology, vol. 74, iss. 6, (2018), pp. 784-795)
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Genetic modifiers of radon-induced lung cancer risk: a genome-wide interaction study in former uranium miners Rosenberger, A.; Hung, R.J.; Christiani, D.C.; Caporaso, N.E.; Liu, G.; Bojesen, S.E.; Marchand, L. Le; Haiman, C.A.; Albanes, D.; Aldrich, M.C.; et al.2018, Article / Letter to editor (International Archives of Occupational and Environmental Health, vol. 91, iss. 8, (2018), pp. 937-950)
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Exploring the role of low-frequency and rare exonic variants in alcohol and tobacco use Marees, A.T.; Hammerschlag, A.R.; Bastarache, L.; Kluiver, H. de; Vorspan, F.; ; Smit, D.J.A.; Denys, D.; Gamazon, E.R.; Li-Gao, R.; et al.2018, Article / Letter to editor (Drug and Alcohol Dependence, vol. 188, (2018), pp. 94-101)
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Identification and replication of the interplay of four genetic high-risk variants for urinary bladder cancer Selinski, S.; Blaszkewicz, M.; Ickstadt, K.; Gerullis, H.; Otto, T.; Roth, E.; Volkert, F.; Ovsiannikov, D.; Moormann, O.; Banfi, G.; et al.2017, Article / Letter to editor (Carcinogenesis, vol. 38, iss. 12, (2017), pp. 1167-1179)
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Meta-analysis of five genome-wide association studies identifies multiple new loci associated with testicular germ cell tumor Wang, Z.; McGlynn, K.A.; Rajpert- de Meyts, E.; Bishop, D.T.; Chung, C.C.; Dalgaard, M.D.; Greene, M.H.; Gupta, R; Grotmol, T.; Haugen, T.B.; et al.2017, Article / Letter to editor (Nature Genetics, vol. 49, iss. 7, (2017), pp. 1141-1147)
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A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease. Bjornsson, E.; Halldorsson, G.; Helgadottir, A.; Gylfason, A; Kehr, B.; Jonasdottir, A.; Sigurdsson, A.; Oddsson, A.; Thorleifsson, G.; Magnusson, O.T.; et al.2017, Article / Letter to editor (Human Molecular Genetics, vol. 26, iss. 12, (2017), pp. 2364-2376)
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Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis Styrkarsdottir, U.; Helgason, H.; Sigurdsson, A.; Norddahl, G.L.; Agustsdottir, A.B.; Reynard, L.N.; Villalvilla, A.; Halldorsson, G.H.; Jonasdottir, A.; Magnusdottir, A.; et al.2017, Article / Letter to editor (Nature Genetics, vol. 49, iss. 5, (2017), pp. 801-805)
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Description of the EuroTARGET cohort: A European collaborative project on TArgeted therapy in renal cell cancer-GEnetic- and tumor-related biomarkers for response and toxicity ; ; Oskarsdottir, A.; Maurits, JSF; Diekstra, M.H.M.; Ambert, V.; Cambon-Thomsen, A.; Castellano, D.; Fritsch, A.; Garcia Donas, J.; et al.2017, Article / Letter to editor (Urologic Oncology-Seminars and Original Investigations, vol. 35, iss. 8, (2017), pp. 529.e9-529.e16)
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A genome-wide association study yields five novel thyroid cancer risk loci Gudmundsson, J.; Thorleifsson, G.; Sigurdsson, J.K.; Stefansdottir, L.; Jonasson, J.G.; Gudjonsson, S.A.; Gudbjartsson, D.F.; Masson, G.; Johannsdottir, H.; Halldorsson, G.H.; et al.2017, Article / Letter to editor (Nature Communications, vol. 8, (2017), pp. 14517)
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Sequence variant at 4q25 near PITX2 associates with appendicitis Kristjansson, R.P.; Benonisdottir, S.; Oddsson, A.; Galesloot, T.E.; Thorleifsson, G.; ; Davidsson, O.B.; Jonsson, S.; Arnadottir, G.A.; Jensson, B.O.; et al.2017, Article / Letter to editor (Scientific Reports, vol. 7, iss. 1, (2017), article 3119)
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Population Modeling Integrating Pharmacokinetics, Pharmacodynamics, Pharmacogenetics, and Clinical Outcome in Patients With Sunitinib-Treated Cancer Diekstra, M.H.M.; Fritsch, A.; Kanefendt, F.; Swen, J.J.; Moes, D.; Sorgel, F.; Kinzig, M.; Stelzer, C.; Schindele, D.; Gauler, T.; et al.2017, Article / Letter to editor (Cpt Pharmacometrics and Systems Pharmacology, vol. 6, iss. 9, (2017), pp. 604-613)
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Now showing items 1-50 of 591
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