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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 1
1993 3
1994 3
1995 4
1997 4
1998 4
1999 3
2000 4
2001 6
2002 3
2003 7
2004 9
2005 5
2006 3
2007 6
2008 9
2009 13
2010 5
2011 6
2012 8
2013 2
2016 4
2017 1
2018 1
2019 3
2024 1

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107 results

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Page 1
[Individual genome sequencing].
Undlien DE. Undlien DE. Tidsskr Nor Laegeforen. 2012 Feb 7;132(3):264. doi: 10.4045/tidsskr.11.1490. Tidsskr Nor Laegeforen. 2012. PMID: 22314723 Free article. Norwegian. No abstract available.
[Molecular diagnostics in diabetes mellitus].
Bjørkhaug L, Johansson S, Raeder H, Thorsby PM, Undlien DE, Søvik O, Molven A, Sagen JV, Njølstad PR. Bjørkhaug L, et al. Among authors: undlien de. Tidsskr Nor Laegeforen. 2005 Nov 3;125(21):2968-72. Tidsskr Nor Laegeforen. 2005. PMID: 16276383 Free article. Review. Norwegian.
Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease.
Aslaksen S, Methlie P, Vigeland MD, Jøssang DE, Wolff AB, Sheng Y, Oftedal BE, Skinningsrud B, Undlien DE, Selmer KK, Husebye ES, Bratland E. Aslaksen S, et al. Among authors: undlien de. Front Endocrinol (Lausanne). 2019 Sep 27;10:648. doi: 10.3389/fendo.2019.00648. eCollection 2019. Front Endocrinol (Lausanne). 2019. PMID: 31611844 Free PMC article.
Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF.
Filges I, Bruder E, Brandal K, Meier S, Undlien DE, Waage TR, Hoesli I, Schubach M, de Beer T, Sheng Y, Hoeller S, Schulzke S, Røsby O, Miny P, Tercanli S, Oppedal T, Meyer P, Selmer KK, Strømme P. Filges I, et al. Among authors: undlien de. Hum Mutat. 2016 Apr;37(4):359-63. doi: 10.1002/humu.22960. Epub 2016 Feb 9. Hum Mutat. 2016. PMID: 26820108
Limitations and possibilities of low cell number ChIP-seq.
Gilfillan GD, Hughes T, Sheng Y, Hjorthaug HS, Straub T, Gervin K, Harris JR, Undlien DE, Lyle R. Gilfillan GD, et al. Among authors: undlien de. BMC Genomics. 2012 Nov 21;13:645. doi: 10.1186/1471-2164-13-645. BMC Genomics. 2012. PMID: 23171294 Free PMC article.
Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's disease.
Aslaksen S, Wolff AB, Vigeland MD, Breivik L, Sheng Y, Oftedal BE, Artaza H, Skinningsrud B, Undlien DE, Selmer KK, Husebye ES, Bratland E. Aslaksen S, et al. Among authors: undlien de. J Transl Autoimmun. 2019 May 28;1:100005. doi: 10.1016/j.jtauto.2019.100005. eCollection 2019 Apr. J Transl Autoimmun. 2019. PMID: 32743495 Free PMC article.
107 results