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122 results

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Page 1
Modelling the contribution of family history and variation in single nucleotide polymorphisms to risk of schizophrenia: a Danish national birth cohort-based study.
Agerbo E, Mortensen PB, Wiuf C, Pedersen MS, McGrath J, Hollegaard MV, Nørgaard-Pedersen B, Hougaard DM, Mors O, Pedersen CB. Agerbo E, et al. Among authors: wiuf c. Schizophr Res. 2012 Feb;134(2-3):246-52. doi: 10.1016/j.schres.2011.10.025. Epub 2011 Nov 22. Schizophr Res. 2012. PMID: 22108675
Genome-wide scans using archived neonatal dried blood spot samples.
Hollegaard MV, Grauholm J, Børglum A, Nyegaard M, Nørgaard-Pedersen B, Ørntoft T, Mortensen PB, Wiuf C, Mors O, Didriksen M, Thorsen P, Hougaard DM. Hollegaard MV, et al. Among authors: wiuf c. BMC Genomics. 2009 Jul 4;10:297. doi: 10.1186/1471-2164-10-297. BMC Genomics. 2009. PMID: 19575812 Free PMC article.
Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci.
Børglum AD, Demontis D, Grove J, Pallesen J, Hollegaard MV, Pedersen CB, Hedemand A, Mattheisen M; GROUP investigators10; Uitterlinden A, Nyegaard M, Ørntoft T, Wiuf C, Didriksen M, Nordentoft M, Nöthen MM, Rietschel M, Ophoff RA, Cichon S, Yolken RH, Hougaard DM, Mortensen PB, Mors O. Børglum AD, et al. Among authors: wiuf c. Mol Psychiatry. 2014 Mar;19(3):325-33. doi: 10.1038/mp.2013.2. Epub 2013 Jan 29. Mol Psychiatry. 2014. PMID: 23358160 Free PMC article.
Common variants at VRK2 and TCF4 conferring risk of schizophrenia.
Steinberg S, de Jong S; Irish Schizophrenia Genomics Consortium; Andreassen OA, Werge T, Børglum AD, Mors O, Mortensen PB, Gustafsson O, Costas J, Pietiläinen OP, Demontis D, Papiol S, Huttenlocher J, Mattheisen M, Breuer R, Vassos E, Giegling I, Fraser G, Walker N, Tuulio-Henriksson A, Suvisaari J, Lönnqvist J, Paunio T, Agartz I, Melle I, Djurovic S, Strengman E; GROUP; Jürgens G, Glenthøj B, Terenius L, Hougaard DM, Ørntoft T, Wiuf C, Didriksen M, Hollegaard MV, Nordentoft M, van Winkel R, Kenis G, Abramova L, Kaleda V, Arrojo M, Sanjuán J, Arango C, Sperling S, Rossner M, Ribolsi M, Magni V, Siracusano A, Christiansen C, Kiemeney LA, Veldink J, van den Berg L, Ingason A, Muglia P, Murray R, Nöthen MM, Sigurdsson E, Petursson H, Thorsteinsdottir U, Kong A, Rubino IA, De Hert M, Réthelyi JM, Bitter I, Jönsson EG, Golimbet V, Carracedo A, Ehrenreich H, Craddock N, Owen MJ, O'Donovan MC; Wellcome Trust Case Control Consortium 2; Ruggeri M, Tosato S, Peltonen L, Ophoff RA, Collier DA, St Clair D, Rietschel M, Cichon S, Stefansson H, Rujescu D, Stefansson K. Steinberg S, et al. Among authors: wiuf c. Hum Mol Genet. 2011 Oct 15;20(20):4076-81. doi: 10.1093/hmg/ddr325. Epub 2011 Jul 26. Hum Mol Genet. 2011. PMID: 21791550 Free PMC article.
Short tandem repeats and genetic variation.
Madsen BE, Villesen P, Wiuf C. Madsen BE, et al. Among authors: wiuf c. Methods Mol Biol. 2010;628:297-306. doi: 10.1007/978-1-60327-367-1_16. Methods Mol Biol. 2010. PMID: 20238088
A periodic pattern of SNPs in the human genome.
Madsen BE, Villesen P, Wiuf C. Madsen BE, et al. Among authors: wiuf c. Genome Res. 2007 Oct;17(10):1414-9. doi: 10.1101/gr.6223207. Epub 2007 Aug 2. Genome Res. 2007. PMID: 17673700 Free PMC article.
Conflicting results in SNP genotype assessment.
Hansen LL, Madsen BE, Pedersen K, Wiuf C. Hansen LL, et al. Among authors: wiuf c. Biotechniques. 2007 Dec;43(6):756, 758, 760 passim. doi: 10.2144/000112675. Biotechniques. 2007. PMID: 18251251 Free article. Clinical Trial.
122 results