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Items: 16

1.

Introduction of the Python script STRinNGS for analysis of STR regions in FASTQ or BAM files and expansion of the Danish STR sequence database to 11 STRs.

Friis SL, Buchard A, Rockenbauer E, Børsting C, Morling N.

Forensic Sci Int Genet. 2016 Mar;21:68-75. doi: 10.1016/j.fsigen.2015.12.006. Epub 2015 Dec 12.

PMID:
26722765
2.

Second generation sequencing of three STRs D3S1358, D12S391 and D21S11 in Danes and a new nomenclature for sequenced STR alleles.

Gelardi C, Rockenbauer E, Dalsgaard S, Børsting C, Morling N.

Forensic Sci Int Genet. 2014 Sep;12:38-41. doi: 10.1016/j.fsigen.2014.04.016. Epub 2014 May 10.

PMID:
24893347
3.

Non-uniform phenotyping of D12S391 resolved by second generation sequencing.

Dalsgaard S, Rockenbauer E, Buchard A, Mogensen HS, Frank-Hansen R, Børsting C, Morling N.

Forensic Sci Int Genet. 2014 Jan;8(1):195-9. doi: 10.1016/j.fsigen.2013.09.008. Epub 2013 Oct 1.

PMID:
24315608
4.

Characterization of mutations and sequence variants in the D21S11 locus by next generation sequencing.

Rockenbauer E, Hansen S, Mikkelsen M, Børsting C, Morling N.

Forensic Sci Int Genet. 2014 Jan;8(1):68-72. doi: 10.1016/j.fsigen.2013.06.011. Epub 2013 Sep 7.

PMID:
24315591
5.

Forensic and phylogeographic characterisation of mtDNA lineages from Somalia.

Mikkelsen M, Fendt L, Röck AW, Zimmermann B, Rockenbauer E, Hansen AJ, Parson W, Morling N.

Int J Legal Med. 2012 Jul;126(4):573-9. doi: 10.1007/s00414-012-0694-6. Epub 2012 Apr 14.

PMID:
22527188
6.

Typing of 30 insertion/deletions in Danes using the first commercial indel kit--Mentype® DIPplex.

Friis SL, Børsting C, Rockenbauer E, Poulsen L, Fredslund SF, Tomas C, Morling N.

Forensic Sci Int Genet. 2012 Mar;6(2):e72-4. doi: 10.1016/j.fsigen.2011.08.002. Epub 2011 Sep 7.

PMID:
21903497
7.

High-throughput sequencing of core STR loci for forensic genetic investigations using the Roche Genome Sequencer FLX platform.

Fordyce SL, Ávila-Arcos MC, Rockenbauer E, Børsting C, Frank-Hansen R, Petersen FT, Willerslev E, Hansen AJ, Morling N, Gilbert MT.

Biotechniques. 2011 Aug;51(2):127-33. doi: 10.2144/000113721.

8.

Frequencies of 33 coding region mitochondrial SNPs in a Danish and a Turkish population.

Mikkelsen M, Rockenbauer E, Demir H, Børsting C, Morling N.

Forensic Sci Int Genet. 2011 Nov;5(5):559-60. doi: 10.1016/j.fsigen.2010.08.001. Epub 2010 Aug 30. No abstract available.

PMID:
20801092
9.

Typing of 49 autosomal SNPs by SNaPshot in the Slovenian population.

Drobnic K, Børsting C, Rockenbauer E, Tomas C, Morling N.

Forensic Sci Int Genet. 2010 Oct;4(5):e125-7. doi: 10.1016/j.fsigen.2010.01.014. Epub 2010 Mar 1.

PMID:
20457083
10.

Validation of a single nucleotide polymorphism (SNP) typing assay with 49 SNPs for forensic genetic testing in a laboratory accredited according to the ISO 17025 standard.

Børsting C, Rockenbauer E, Morling N.

Forensic Sci Int Genet. 2009 Dec;4(1):34-42. doi: 10.1016/j.fsigen.2009.04.004. Epub 2009 May 7.

PMID:
19948332
11.

Identification of new loci controlling collagen-induced arthritis in mouse using a partial advanced intercross and congenic strains.

Popovic M, Ahlqvist E, Rockenbauer E, Bockermann R, Holmdahl R.

Scand J Immunol. 2008 Oct;68(4):405-13. doi: 10.1111/j.1365-3083.2008.02151.x.

12.

Linkage disequilibrium mapping of a breast cancer susceptibility locus near RAI/PPP1R13L/iASPP.

Nexø BA, Vogel U, Olsen A, Nyegaard M, Bukowy Z, Rockenbauer E, Zhang X, Koca C, Mains M, Hansen B, Hedemand A, Kjeldgaard A, Laska MJ, Raaschou-Nielsen O, Cold S, Overvad K, Tjønneland A, Bolund L, Børglum AD.

BMC Med Genet. 2008 Jun 27;9:56. doi: 10.1186/1471-2350-9-56.

13.

SNP genotyping using microsphere-linked PNA and flow cytometric detection.

Rockenbauer E, Petersen K, Vogel U, Bolund L, Kølvraa S, Nielsen KV, Nexø BA.

Cytometry A. 2005 Apr;64(2):80-6.

14.

Short PNA molecular beacons for real-time PCR allelic discrimination of single nucleotide polymorphisms.

Petersen K, Vogel U, Rockenbauer E, Nielsen KV, Kølvraa S, Bolund L, Nexø B.

Mol Cell Probes. 2004 Apr;18(2):117-22.

PMID:
15051121
15.

Multiple single nucleotide polymorphisms on human chromosome 19q13.2-3 associate with risk of Basal cell carcinoma.

Yin J, Rockenbauer E, Hedayati M, Jacobsen NR, Vogel U, Grossman L, Bolund L, Nexø BA.

Cancer Epidemiol Biomarkers Prev. 2002 Nov;11(11):1449-53.

16.

Association of chromosome 19q13.2-3 haplotypes with basal cell carcinoma: tentative delineation of an involved region using data for single nucleotide polymorphisms in two cohorts.

Rockenbauer E, Bendixen MH, Bukowy Z, Yin J, Jacobsen NR, Hedayati M, Vogel U, Grossman L, Bolund L, Nexø BA.

Carcinogenesis. 2002 Jul;23(7):1149-53.

PMID:
12117772

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