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249 results
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Possible role of mtDNA mutations in sudden infant death.
Opdal SH, Vege A, Egeland T, Musse MA, Rognum TO. Opdal SH, et al. Among authors: egeland t. Pediatr Neurol. 2002 Jul;27(1):23-9. doi: 10.1016/s0887-8994(02)00384-3. Pediatr Neurol. 2002. PMID: 12160969
A statistical framework for the interpretation of mtDNA mixtures: forensic and medical applications.
Egeland T, Salas A. Egeland T, et al. PLoS One. 2011;6(10):e26723. doi: 10.1371/journal.pone.0026723. Epub 2011 Oct 28. PLoS One. 2011. PMID: 22053205 Free PMC article.
Mixtures with relatives: a pedigree perspective.
Egeland T, Dørum G, Vigeland MD, Sheehan NA. Egeland T, et al. Forensic Sci Int Genet. 2014 May;10:49-54. doi: 10.1016/j.fsigen.2014.01.007. Epub 2014 Jan 31. Forensic Sci Int Genet. 2014. PMID: 24572837
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome.
Gilfillan GD, Selmer KK, Roxrud I, Smith R, Kyllerman M, Eiklid K, Kroken M, Mattingsdal M, Egeland T, Stenmark H, Sjøholm H, Server A, Samuelsson L, Christianson A, Tarpey P, Whibley A, Stratton MR, Futreal PA, Teague J, Edkins S, Gecz J, Turner G, Raymond FL, Schwartz C, Stevenson RE, Undlien DE, Strømme P. Gilfillan GD, et al. Among authors: egeland t. Am J Hum Genet. 2008 Apr;82(4):1003-10. doi: 10.1016/j.ajhg.2008.01.013. Epub 2008 Mar 13. Am J Hum Genet. 2008. PMID: 18342287 Free PMC article.
T cell-specific T-box transcription factor haplotype is associated with allergic asthma in children.
Munthe-Kaas MC, Carlsen KH, Håland G, Devulapalli CS, Gervin K, Egeland T, Carlsen KL, Undlien D. Munthe-Kaas MC, et al. Among authors: egeland t. J Allergy Clin Immunol. 2008 Jan;121(1):51-6. doi: 10.1016/j.jaci.2007.07.068. Epub 2007 Oct 18. J Allergy Clin Immunol. 2008. PMID: 17949803
Y-chromosome variation in a Norwegian population sample.
Dupuy BM, Andreassen R, Flønes AG, Tomassen K, Egeland T, Brion M, Carracedo A, Olaisen B. Dupuy BM, et al. Among authors: egeland t. Forensic Sci Int. 2001 Apr 1;117(3):163-73. doi: 10.1016/s0379-0738(00)00397-2. Forensic Sci Int. 2001. PMID: 11248446
Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease.
Skinningsrud B, Husebye ES, Gervin K, Løvås K, Blomhoff A, Wolff AB, Kemp EH, Egeland T, Undlien DE. Skinningsrud B, et al. Among authors: egeland t. Eur J Hum Genet. 2008 Aug;16(8):977-82. doi: 10.1038/ejhg.2008.33. Epub 2008 Feb 27. Eur J Hum Genet. 2008. PMID: 18301444
Using object oriented bayesian networks to model linkage, linkage disequilibrium and mutations between STR markers.
Kling D, Egeland T, Mostad P. Kling D, et al. Among authors: egeland t. PLoS One. 2012;7(9):e43873. doi: 10.1371/journal.pone.0043873. Epub 2012 Sep 11. PLoS One. 2012. PMID: 22984448 Free PMC article.
The influence of patient characteristics, disease variables, and HLA alleles on the development of radiographically evident sacroiliitis in juvenile idiopathic arthritis.
Flatø B, Smerdel A, Johnston V, Lien G, Dale K, Vinje O, Egeland T, Sørskaar D, Førre Ø. Flatø B, et al. Among authors: egeland t. Arthritis Rheum. 2002 Apr;46(4):986-94. doi: 10.1002/art.10146. Arthritis Rheum. 2002. PMID: 11953976
Structured incorporation of prior information in relationship identification problems.
Sheehan NA, Egeland T. Sheehan NA, et al. Among authors: egeland t. Ann Hum Genet. 2007 Jul;71(Pt 4):501-18. doi: 10.1111/j.1469-1809.2006.00345.x. Epub 2007 Jan 18. Ann Hum Genet. 2007. PMID: 17233753
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