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Browsing by Author "Kiemeney, L.A.L.M."
Now showing items 1-50 of 614
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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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Systematic analyses of regulatory variants in DNase I hypersensitive sites identified two novel lung cancer susceptibility loci Dai, J.; Li, Z.; Amos, C.I.; Hung, R.J.; Tardon, A.; Andrew, A.S.; Chen, C; Christiani, D.C.; Albanes, D.; ; et al.2019, Article / Letter to editor (Carcinogenesis, vol. 40, iss. 3, (2019), pp. 432-440)
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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.C. 't; Galesloot, T.E.; Leeuw, C. de; ; et al.2019, Article / Letter to editor (Nature Genetics, vol. 51, iss. 2, (2019), pp. 245-257)
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Mendelian Randomization and mediation analysis of leukocyte telomere length and risk of lung and head and neck cancers Kachuri, L.; Saarela, O.; Bojesen, S.E.; Smith, G.; Liu, G.; Landi, M.T.; Caporaso, N.E.; Christiani, D.C.; Johansson, M.; Panico, S.; et al.2019, Article / Letter to editor (International Journal of Epidemiology, vol. 48, iss. 3, (2019), pp. 751-766)
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Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene ; Ludwig, K.U.; Welzenbach, J.; Ishorst, N.; Thonissen, M.; Galesloot, T.E.; Ongkosuwito, E.M.; ; Aldhorae, K.; Rojas-Martinez, A.; et al.2019, Article / Letter to editor (Genes, vol. 10, iss. 12, (2019), article E1023)
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A potential role for the STXBP5-AS1 gene in adult ADHD symptoms ; Groffen, A.J.; Spijker, S.; Ouwens, K.G.; Klein, M.; Vojinovic, D.; Galesloot, T.E.; ; ; ; et al.2019, Article / Letter to editor (Behavior Genetics, vol. 49, iss. 3, (2019), pp. 270-285)
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Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations Putte, R. van de; ; Reutter, H.; ; ; Brosens, E.; Broens, P.; Homberg, M.; Ludwig, M.; Jenetzky, E.; et al.2019, Article / Letter to editor (PLoS One, vol. 14, iss. 5, (2019), article e0217477)
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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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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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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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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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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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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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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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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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Now showing items 1-50 of 614
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