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Genome-wide linkage analysis with clustered SNP markers.
Selmer KK, Brandal K, Olstad OK, Birkenes B, Undlien DE, Egeland T. Selmer KK, et al. Among authors: egeland t. J Biomol Screen. 2009 Jan;14(1):92-6. doi: 10.1177/1087057108327327. J Biomol Screen. 2009. PMID: 19171925
Parental SCN1A mutation mosaicism in familial Dravet syndrome.
Selmer KK, Eriksson AS, Brandal K, Egeland T, Tallaksen C, Undlien DE. Selmer KK, et al. Among authors: egeland t. Clin Genet. 2009 Oct;76(4):398-403. doi: 10.1111/j.1399-0004.2009.01208.x. Epub 2009 Aug 10. Clin Genet. 2009. PMID: 19673951
A TLR2 polymorphism is associated with type 1 diabetes and allergic asthma.
Bjørnvold M, Munthe-Kaas MC, Egeland T, Joner G, Dahl-Jørgensen K, Njølstad PR, Akselsen HE, Gervin K, Carlsen KC, Carlsen KH, Undlien DE. Bjørnvold M, et al. Among authors: egeland t. Genes Immun. 2009 Mar;10(2):181-7. doi: 10.1038/gene.2008.100. Epub 2009 Jan 15. Genes Immun. 2009. PMID: 19148143
X-linked congenital adrenal hypoplasia with hypogonadotropic hypogonadism caused by an inversion disrupting a conserved noncoding element upstream of the NR0B1 (DAX1) gene.
Skinningsrud B, Husebye ES, Gilfillan GD, Frengen E, Erichsen A, Gervin K, Ormerod E, Egeland T, Undlien DE. Skinningsrud B, et al. Among authors: egeland t. J Clin Endocrinol Metab. 2009 Oct;94(10):4086-93. doi: 10.1210/jc.2009-0923. Epub 2009 Sep 22. J Clin Endocrinol Metab. 2009. PMID: 19773398
262 results