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Browsing by Author "Kiemeney, L.A.L.M."
Now showing items 1-50 of 640
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The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis Xie, J; Liu, L.; Mladkova, N.; Li, Yifu; Ren, H.; Wang, W.; Cui, Z.; Lin, L.; Hu, X.; Yu, X; et al.2020, Article / Letter to editor (Nature Communications, vol. 11, iss. 1, (2020), article 1600)
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Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing ; ; Zayats, T.; Rivero, O.; Ziegler, G.C.; Pauper, M.; ; ; ; ; et al.2020, Article / Letter to editor (Molecular Psychiatry, vol. 25, iss. 9, (2020), pp. 2047-2057)
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GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer Zhou, W.; Brumpton, Ben; Kabil, Omer; Gudmundsson, J.; Thorleifsson, G.; Weinstock, Josh; ; ; ; ; et al.2020, Article / Letter to editor (Nature Communications, vol. 11, iss. 1, (2020), article 3981)
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Papillary urothelial neoplasm of low malignant potential (PUN-LMP): Still a meaningful histo-pathological grade category for Ta, noninvasive bladder tumors in 2019? Hentschel, Anouk E.; Rhijn, B.W. van; Bruendl, Johannes; Comperat, Eva M.; Plass, K.; Rodriguez, Oscar; Runneboom, W.; ; Heijden, A.G. van der; ; et al.2020, Article / Letter to editor (Urologic Oncology-Seminars and Original Investigations, vol. 38, iss. 5, (2020), pp. 440-448)
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Assessing thyroid cancer risk using polygenic risk scores Liyanarachchi, S.; Gudmundsson, J.; Ferkingstad, Egil; He, H.; Jonasson, J.G.; Tragante, V.; ; ; ; Stefansson, Kari; et al.2020, Article / Letter to editor (Proceedings of the National Academy of Sciences USA, vol. 117, iss. 11, (2020), pp. 5997-6002)
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Contribution of Intellectual Disability-Related Genes to ADHD Risk and to Locomotor Activity in Drosophila ; ; Rens, A.B. van; Demontis, Ditte; Borglum, Anders D.; ; Castells Nobau, A.; ; ; ; et al.2020, Article / Letter to editor (American Journal of Psychiatry, vol. 177, iss. 6, (2020), pp. 526-536)
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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.; ; ; Leeuw, C. de; ; et al.2019, Article / Letter to editor (Nature Genetics, vol. 51, iss. 2, (2019), pp. 245-257)
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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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A potential role for the STXBP5-AS1 gene in adult ADHD symptoms ; Groffen, A.J.; Spijker, S.; Ouwens, K.G.; ; Vojinovic, D.; ; ; ; ; et al.2019, Article / Letter to editor (Behavior Genetics, vol. 49, iss. 3, (2019), pp. 270-285)
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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.; ; ; ; Aldhorae, K.; Rojas-Martinez, A.; et al.2019, Article / Letter to editor (Genes, vol. 10, iss. 12, (2019), article E1023)
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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 ; ; 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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Now showing items 1-50 of 640
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