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A computerised method for calculating the probability of pedigrees from genetic data.
Egeland T, Mostad PF, Olaisen B. Egeland T, et al. Sci Justice. 1997 Oct-Dec;37(4):269-74. doi: 10.1016/S1355-0306(97)72202-0. Sci Justice. 1997. PMID: 9519542 No abstract available.
Extraction of DNA from decomposed human tissue. An evaluation of five extraction methods for short tandem repeat typing.
Hoff-Olsen P, Mevåg B, Staalstrøm E, Hovde B, Egeland T, Olaisen B. Hoff-Olsen P, et al. Forensic Sci Int. 1999 Nov 8;105(3):171-83. doi: 10.1016/s0379-0738(99)00128-0. Forensic Sci Int. 1999. PMID: 10643651
Inferring the most likely geographical origin of mtDNA sequence profiles.
Egeland T, Bøvelstad HM, Storvik GO, Salas A. Egeland T, et al. Ann Hum Genet. 2004 Sep;68(Pt 5):461-71. doi: 10.1046/j.1529-8817.2004.00109.x. Ann Hum Genet. 2004. PMID: 15469423
Genetic screening of Scandinavian families with febrile seizures and epilepsy or GEFS+.
Selmer KK, Egeland T, Solaas MH, Nakken KO, Kjeldsen MJ, Friis ML, Brandal K, Corey LA, Undlien DE. Selmer KK, et al. Acta Neurol Scand. 2008 Apr;117(4):289-92. doi: 10.1111/j.1600-0404.2007.00941.x. Epub 2007 Oct 10. Acta Neurol Scand. 2008. PMID: 17927801
PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia.
Stray-Pedersen A, Backe PH, Sorte HS, Mørkrid L, Chokshi NY, Erichsen HC, Gambin T, Elgstøen KB, Bjørås M, Wlodarski MW, Krüger M, Jhangiani SN, Muzny DM, Patel A, Raymond KM, Sasa GS, Krance RA, Martinez CA, Abraham SM, Speckmann C, Ehl S, Hall P, Forbes LR, Merckoll E, Westvik J, Nishimura G, Rustad CF, Abrahamsen TG, Rønnestad A, Osnes LT, Egeland T, Rødningen OK, Beck CR; Baylor-Johns Hopkins Center for Mendelian Genomics, Boerwinkle EA, Gibbs RA, Lupski JR, Orange JS, Lausch E, Hanson IC. Stray-Pedersen A, et al. Am J Hum Genet. 2014 Jul 3;95(1):96-107. doi: 10.1016/j.ajhg.2014.05.007. Epub 2014 Jun 12. Am J Hum Genet. 2014. PMID: 24931394 Free PMC article.
We identified three unrelated children with recurrent infections, congenital leukopenia including neutropenia, B and T cell lymphopenia, and progression to bone marrow failure. ...
We identified three unrelated children with recurrent infections, congenital leukopenia including neutropenia, B and T cell lymphopen …
HLA Dr-Dq haplotypes and the TNFA-308 polymorphism: associations with asthma and allergy.
Munthe-Kaas MC, Carlsen KL, Carlsen KH, Egeland T, Håland G, Devulapalli CS, Akselsen H, Undlien D. Munthe-Kaas MC, et al. Allergy. 2007 Sep;62(9):991-8. doi: 10.1111/j.1398-9995.2007.01377.x. Allergy. 2007. PMID: 17686102
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. Genes Immun. 2009 Mar;10(2):181-7. doi: 10.1038/gene.2008.100. Epub 2009 Jan 15. Genes Immun. 2009. PMID: 19148143
Both T1D and allergic asthma were significantly associated with the TLR2 rs3804100 T allele and further associated with the haplotype including this SNP, possibly representing a susceptibility locus common for the two diseases. ...
Both T1D and allergic asthma were significantly associated with the TLR2 rs3804100 T allele and further associated with the haplotype …
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