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Page 1
Exploring the Genetic Risk of Childhood Daytime Urinary Incontinence: A Genome-Wide Association Study.
Breinbjerg A, Jørgensen CS, Walters GB, Grove J, Als TD, Kamperis K, Stéfansdóttir L, Thirstrup JP, Borg B, Albiñana C, Vilhjálmsson BJ, Eðvarðsson VÖ, Stefánsson H, Mortensen PB, Agerbo E, Werge T, Børglum A, Demontis D, Stefánsson K, Rittig S, Christensen JH. Breinbjerg A, et al. Among authors: edvardsson vo. J Urol. 2024 Dec;212(6):851-861. doi: 10.1097/JU.0000000000004187. Epub 2024 Aug 2. J Urol. 2024. PMID: 39093873
Identification of genetic loci associated with nocturnal enuresis: a genome-wide association study.
Jørgensen CS, Horsdal HT, Rajagopal VM, Grove J, Als TD, Kamperis K, Nyegaard M, Walters GB, Eðvarðsson VÖ, Stefánsson H, Nordentoft M, Hougaard DM, Werge T, Mors O, Mortensen PB, Agerbo E, Rittig S, Stefánsson K, Børglum AD, Demontis D, Christensen JH. Jørgensen CS, et al. Among authors: edvardsson vo. Lancet Child Adolesc Health. 2021 Mar;5(3):201-209. doi: 10.1016/S2352-4642(20)30350-3. Epub 2021 Jan 15. Lancet Child Adolesc Health. 2021. PMID: 33453761
Familiality of kidney stone disease in Iceland.
Edvardsson VO, Palsson R, Indridason OS, Thorvaldsson S, Stefansson K. Edvardsson VO, et al. Scand J Urol Nephrol. 2009;43(5):420-4. doi: 10.3109/00365590903151479. Scand J Urol Nephrol. 2009. PMID: 19921989
Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density.
Thorleifsson G, Holm H, Edvardsson V, Walters GB, Styrkarsdottir U, Gudbjartsson DF, Sulem P, Halldorsson BV, de Vegt F, d'Ancona FC, den Heijer M, Franzson L, Christiansen C, Alexandersen P, Rafnar T, Kristjansson K, Sigurdsson G, Kiemeney LA, Bodvarsson M, Indridason OS, Palsson R, Kong A, Thorsteinsdottir U, Stefansson K. Thorleifsson G, et al. Nat Genet. 2009 Aug;41(8):926-30. doi: 10.1038/ng.404. Epub 2009 Jun 28. Nat Genet. 2009. PMID: 19561606
Common and rare variants associated with kidney stones and biochemical traits.
Oddsson A, Sulem P, Helgason H, Edvardsson VO, Thorleifsson G, Sveinbjörnsson G, Haraldsdottir E, Eyjolfsson GI, Sigurdardottir O, Olafsson I, Masson G, Holm H, Gudbjartsson DF, Thorsteinsdottir U, Indridason OS, Palsson R, Stefansson K. Oddsson A, et al. Among authors: edvardsson vo. Nat Commun. 2015 Aug 14;6:7975. doi: 10.1038/ncomms8975. Nat Commun. 2015. PMID: 26272126 Free PMC article.
Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiency.
Runolfsdottir HL, Sayer JA, Indridason OS, Edvardsson VO, Jensson BO, Arnadottir GA, Gudjonsson SA, Fridriksdottir R, Katrinardottir H, Gudbjartsson D, Thorsteinsdottir U, Sulem P, Stefansson K, Palsson R. Runolfsdottir HL, et al. Among authors: edvardsson vo. Eur J Hum Genet. 2021 Jul;29(7):1061-1070. doi: 10.1038/s41431-020-00805-6. Epub 2021 Mar 11. Eur J Hum Genet. 2021. PMID: 33707627 Free PMC article.
Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases.
Gudbjartsson DF, Holm H, Indridason OS, Thorleifsson G, Edvardsson V, Sulem P, de Vegt F, d'Ancona FC, den Heijer M, Wetzels JF, Franzson L, Rafnar T, Kristjansson K, Bjornsdottir US, Eyjolfsson GI, Kiemeney LA, Kong A, Palsson R, Thorsteinsdottir U, Stefansson K. Gudbjartsson DF, et al. PLoS Genet. 2010 Jul 29;6(7):e1001039. doi: 10.1371/journal.pgen.1001039. PLoS Genet. 2010. PMID: 20686651 Free PMC article.
Sequence variants associating with urinary biomarkers.
Benonisdottir S, Kristjansson RP, Oddsson A, Steinthorsdottir V, Mikaelsdottir E, Kehr B, Jensson BO, Arnadottir GA, Sulem G, Sveinbjornsson G, Kristmundsdottir S, Ivarsdottir EV, Tragante V, Gunnarsson B, Runolfsdottir HL, Arthur JG, Deaton AM, Eyjolfsson GI, Davidsson OB, Asselbergs FW, Hreidarsson AB, Rafnar T, Thorleifsson G, Edvardsson V, Sigurdsson G, Helgadottir A, Halldorsson BV, Masson G, Holm H, Onundarson PT, Indridason OS, Benediktsson R, Palsson R, Gudbjartsson DF, Olafsson I, Thorsteinsdottir U, Sulem P, Stefansson K. Benonisdottir S, et al. Hum Mol Genet. 2019 Apr 1;28(7):1199-1211. doi: 10.1093/hmg/ddy409. Hum Mol Genet. 2019. PMID: 30476138 Free PMC article.
49 results