English Curriculum vitae_KU

CV for Claus Børsting

Curriculum vitae

Name Claus BørstingBirthday and place 27.05.1967 in Copenhagen, DenmarkFamily Married. Father to one daughter, born 31.12.2007.

1984-1986 Gymnasium education (mathematics and physics)1986-1987 Military serviceFeb. 1994 Cand. Scient (Institute of Molecular Biologi, University of

Odense)Title; Yeast acyl-CoA binding protein (ACBP)

Nov. 1998-Apr. 2000 Postdoctoral position at the Department of Biochemistry and Molecular Biology at the Albany Medical Center, Albany, New York, USA

Apr. 1999 Ph.D. (Institute of Molecular Biologi, University of Odense)Title; The role of acyl-CoA binding protein in acyl-CoA metabolism in the yeast Saccharomyces cerevisiae.

Jan. 2001-May 2004 Forensic Geneticist at the Section of Forensic Genetics, Department of Forensic Medicine, University of Copenhagen, Denmark

June 2004-May 2007 Assistant Professor at the Section of Forensic Genetics, Department of Forensic Medicine, University of Copenhagen, Denmark

June 2007-Feb. 2010 Forensic Geneticist at the Section of Forensic Genetics, Department of Forensic Medicine, University of Copenhagen, Denmark

Mar. 2010- Senior Advisor at the Section of Forensic Genetics, Department of Forensic Medicine, University of Copenhagen, Denmark

Teaching experience;Introduction to forensic medicine (PhD course, 2011)Introduction to forensic genetics (PhD course, 2012)Introduction to forensic medicine (PhD course, 2013)Co-supervisor of 2 Bachelor students, 9 Master students and 5 PhD students.

List of publications;

1. Knudsen J., Færgeman N.J., Skøtt H., Hummel R., Børsting C., Rose T.M., Andersen J.S., Højrup P., Roepstorff P. and Kristiansen K. Yeast acyl-CoA-binding protein: acyl-CoA-binding affinity and effect on intracellular acyl-CoA pool size (1994) Biochem. J. 302, 479-485.

2. Schjerling C.K., Hummel R., Hansen J.K., Børsting C., Mikkelsen J.M., Kristiansen K. and Knudsen J. Disruption of the gene encoding the acyl-CoA-binding protein (ACB1) perturbs acyl-CoA metabolism in Saccharomyces cerevisiae (1996) J. Biol. Chem. 271, 22514-22521.

3. Børsting C., Hummel R., Schultz E.R., Rose T.M., Pedersen M.B., Knudsen J. and Kristiansen K. Saccharomyces carlsbergensis contains two functional genes encoding the acyl-CoA-binding protein, one similar to the ACB1 gene from S.

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cerevisiae and one identical to the ACB1 gene from S. monacensis (1997) Yeast 13, 1409-1421.

4. Børsting C. Yeast ACB1 DNA sequences (1997), EMBL accession numbers Y08687, Y08688, Y08689 and Y08690.

5. Zhiying Z., Tong F., Færgeman N.J., Børsting C., Black P.N. and DiRusso C.C. Vectorial acylation in Saccharomyces cerevisiae (2003) J. Biol. Chem. 278, 16414-16422.

6. Sanchez J.J., Børsting C., Hallenberg C., Buchard A., Hernandez A. and Morling N. Genotyping of 35 Y chromosome SNPs by multiplex PCR and minisequencing (2003) Forensic Sci. Int., 137, 74-84.

7. Sanchez J.J., Brión M., Parson W., Blanco-Verea A., Børsting C., Lareu M., Niederstätter A., Oberacher H., Morling M. and Carrecedo A. Duplications of the Y-chromosome specific loci P25 and 92R7 and forensic implications (2004) Forensic Sci. Int., 140, 241-250.

8. Børsting C., Sanchez J.J. and Morling N. Multiplex PCR, amplicon size and hybridization efficiency on the NanoChip electronic microarray (2004) Int. J. Leg. Med., 118, 75-82.

9. Mengel-Jørgensen J., Sanchez J.J., Børsting C., Kirpekar F. and Morling N. MALDI-TOF mass spectrometric detection of multiplex single base extended primers - a study of 17 Y-chromosome SNPs (2004) Anal. Chem., 76, 6039-6045.

10. Mengel-Jørgensen J., Sanchez J.J., Børsting C., Kirpekar F. and Morling N. Multiplex Y chromosome SNP genotyping using MALDI-TOF mass spectrometry. Prog. For. Genetics 10, International Congress Series 1261 (2004), 15-17. Proceedings of the 20’th congress of the International Society of Forensic Genetics (France, September 2003).

11. Sanchez JJ, Hernandez A., Børsting C., Mamely I., Zurita A. and Morling N. SNP and STR Y chromosome markers in the Canary island population. Prog. For. Genetics 10, International Congress Series 1261 (2004), 328-330. Proceedings of the 20’th congress of the International Society of Forensic Genetics (France, September 2003).

12. Sanchez JJ, Børsting C., Hernandez A., Mengel-Jørgensen J. and Morling N. Y chromosome SNP haplogroups in Danes, Greenlanders and Somalis. Prog. For. Genetics 10, International Congress Series 1261 (2004), 347-349. Proceedings of the 20’th congress of the International Society of Forensic Genetics (France, September 2003).

13. Børsting C., Sanchez J.J. and Morling N. In Forensic DNA Typing Protocols - SNP typing on the NanoChip electronic microarray. Angel Carracedo (Ed.). Methods in Molecular Biology series. Humana Press, Totowa, USA. Vol. 297 (2005), Chapter 11: 155-168.

14. Sanchez J.J., Børsting C. and Morling N. In Forensic DNA Typing Protocols - Typing of Y chromosome SNPs with multiplex PCR methods. Angel Carracedo (Ed.). Methods in Molecular Biology series. Humana Press, Totowa, USA. Vol. 297 (2005), Chapter 15: 209-228.

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15. Sanchez J.J., Hallenberg C., Børsting C., Hernandez A. and Morling N. Predominant E3b1 cluster lineages in Somali Y chromosomes (2005) Eur. J. Hum. Genet., 13, 856-866.

16. Mengel-Jørgensen J., Sanchez J.J., Børsting C., Kirpekar F. and Morling N. Typing of multiple SNPs using ribonuclease cleavage of DNA/RNA chimeric single base extension primers and detection by MALDI-TOF mass spectrometry (2005) Anal. Chem., 77, 5229-5235.

17. Brión M., Sanchez J.J., Balogh K., Thacker C., Blanco-Verea A., Børsting C., Stradmann-Bellinghausen B., Bogus M., Syndercombe-Court D., Schneider P.M., Carracedo A., and Morling N. Introduction of a SNP-based “Major Y-chromosome haplogroup typing kit” suitable for predicting the geographical origin of male lineages. Electrophoresis (2005), 26, 4411-4420.

18. Sanchez J.J., Phillips C., Børsting C., Balogh K., Bogus M., Fondevilla M., Harrison C.D., Musgrave-Brown E., Salas A., Syndercombe-Court D., Schneider P.M., Carracedo A. and Morling N. A multiplex assay with 52 single nucleotide polymorphisms for human identification. Electrophoresis (2006), 27, 1713-1724.

19. Sanchez JJ, Phillips C, Børsting C, Bogus M, Carracedo A, Syndercombe Court D, Fondevilla M, Harrison CD, Morling N, Balogh K, and Schneider PM. Development of a multiplex PCR assay with 52 autosomal SNPs. Prog. For. Genetics 11, International Congress Series 1288 (2006), 67-69. Proceedings of the 21’st congress of the International Society of Forensic Genetics (Portugal, September 2005).

20. Brión M, Sanchez JJ, Balogh K, Thacker C, Blanco-Verea A, Børsting C, Stradmann-Bellinghausen B, Bogus M, Syndercombe Court D, Schneider PM, Carracedo A, and Morling N. Analysis of 29 Y-chromosome SNPs in a single multiplex useful to predict the geographic origin of male lineages. Prog. For. Genetics 11, International Congress Series 1288 (2006), 13-15. Proceedings of the 21’st congress of the International Society of Forensic Genetics (Portugal, September 2005).

21. Børsting C, Sanchez JJ, Birk AH, Bruun HQ, Hallenberg C, Hansen AJ, Hansen HE, Simonsen BT, and Morling N. Comparison of paternity indices based on typing of 15 STRs, 7 VNTRs, and 52 SNPs in 50 Danish mother-child-father trios. Prog. For. Genetics 11, International Congress Series 1288 (2006), 436-438. Proceedings of the 21’st congress of the International Society of Forensic Genetics (Portugal, September 2005).

22. Balogh K, Børsting C, Sánchez Diz P, Thacker C, Syndercombe Court D, Carracedo A, Morling N, and Schneider PM. Application of Whole Genome Amplification for forensic analysis. Prog. For. Genetics 11, International Congress Series 1288 (2006), 725-727. Proceedings of the 21’st congress of the International Society of Forensic Genetics (Portugal, September 2005).

23. Thacker C, Balogh K, Børsting C, Sánchez Diz P, Carracedo A, Morling N, Schneider PM, and Syndercombe Court D. The effect of Whole Genome Amplification on samples originating from more than one donor. Prog. For. Genetics 11, International Congress Series 1288 (2006), 722-724. Proceedings of the 21’st congress of the International Society of Forensic Genetics (Portugal, September 2005).

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24. Børsting C and Morling N. Multiple Displacement Amplification of blood and saliva samples placed on FTA cards. Prog. For. Genetics 11, International Congress Series 1288 (2006), 716-718. Proceedings of the 21’st congress of the International Society of Forensic Genetics (Portugal, September 2005).

25. Hansen AJ, Simonsen BT, Børsting C, Hallenberg C and Morling N. Semi-automatic preparation of biological database samples for STR and SNP typing. Prog. For. Genetics 11, International Congress Series 1288 (2006), 663-665. Proceedings of the 21’st congress of the International Society of Forensic Genetics (Portugal, September 2005).

26. Mengel-From J, Eiberg H, Børsting C, and Morling N. Hair colour in Danish families: Genetic screening of 15 SNPs in the MC1R gene by analysis of a multiplexed SBE reaction using capillary electrophoresis or MALDI-TOF MS. Prog. For. Genetics 11, International Congress Series 1288 (2006), 55-57. Proceedings of the 21’st congress of the International Society of Forensic Genetics (Portugal, September 2005).

27. Sanchez J.J., Monaghon G., Børsting C., Morling N. and Gaspar H.B. Carrier frequency of a non-sense mutation in the adenosine deaminase (ADA) gene implies a high incidence of ADA deficient severe combined immunodeficiency (SCID) in Somalia and a single, common haplotype indicates common ancestry. Ann. Hum. Genet. (2007), 71, 336-347.

28. Børsting C., Sanchez J.J., and Morling N. In PCR - Forensic genetic DNA typing with PCR-based methods. Simon Hughes and Adrian Moody (Ed.). Method Express series (2007). Scion Publishing Ltd., Bloxham, UK. Chapter 8, 123-142.

29. Sanchez J.J., Børsting C. and Morling N. In PCR - Large PCR multiplexes with special reference to forensic single nucleotide polymorphism typing. Simon Hughes and Adrian Moody (Ed.). Method Express series (2007). Scion Publishing Ltd., Bloxham, UK. Chapter 9, 143-158.

30. Gilbert M.T.P., Sanchez J.J., Haselkorn T., Jewell L.D., Lucas S.B., Van Marck E., Børsting C., Morling N., and Worobey M. Multiplex PCR with minisequencing as an effective high-throughput SNP typing method for formalin fixed tissue. Electrophoresis (2007), 28, 2361-2367.

31. Enevold A., Alifrangis M., Sanchez J.J., Carneiro I., Roper C., Børsting C., Lusingu J., Vestergaard L.S., Lemnge M.M., Morling N., Riley E., and Drakeley C. Associations between +-thalassaemia and Plasmodium Falciparum malaria infection in North-Eastern Tanzania. J. Infect. Dis. (2007), 196, 451-459.

32. Børsting C., Sanchez J.J., and Morling N. In Molecular Forensics - Application of SNPs in forensic caseworks. Ralph Rapley and David Whitehouse (Ed.). John Wiley & sons Ltd., Hobroken, USA. Chapter 6 (2007), 91-103.

33. Musgrave-Brown E., Ballard D., Balogh K., Bender K., Berger B., Bogus M., Børsting

C., Brion M., Fondevila M., Harrison C., Oguzturun C., Parson W., Phillips C., Proff C., Ramos-Luis E., Sanchez J.J., Diz P.S., Rey B., Stradmann-Bellinghausen B., Thacker

C., Carracedo A., Morling N., Scheithauer R., Schneider P.M. and Court D.S. Forensic validation of the SNPforID 52-plex assay. Forensic Sci. Int. Genet. (2007), 1, 186-190.

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34. Parson W., Fendt L., Ballard D., Børsting C., Brinkmann B., Carrecedo A., Carvalho M., Coble M.D., Real F.C., Desmyter S., Dupuy B.M., Harrison C., Hohoff C., Just R., Krämer T., Morling N., Salas A., Schmitter H., Schneider P.M., Sonntag M., Valone P.M. and Brandstätter A. Identification of west Eurasian mitochondrial haplogroups by mtDNA SNP screening: Results of the 2006-2007 EDNAP collaborative exercise. Forensic Sci. Int. Genet. (2008), 2, 61-68.

35. Sanchez J.J., Børsting C., Balogh K., Berger B., Bogus M., Butler J.M., Carrecedo A., Court D.S., Dixon L.A., Eichmann C., Fondevila M., Gill P., Harrison C.D., Hohoff C., Huel R., Ludes B., Parson W., Parsons T.J., Petkovski E., Phillips C., Schmitter H., Schneider P.M., Vallone P.M. and Morling N. Forensic typing of autosomal SNPs with a 29 SNP-multiplex – results of a collaborative EDNAP exercise. Forensic Sci. Int. Genet. (2008), 2, 176-183.

36. Børsting C., Sanchez J.J., Hansen H.E., Hansen A.J., Bruun H.Q. and Morling N. Performance of the SNPforID 52 SNP-plex assay in paternity testing. Forensic Sci. Int. Genet. (2008), 2, 292-300.

37. Stangegaard M., Tomas C., Hansen A.J., Frank-Hansen R., Børsting C. and Morling N. Biomek®-3000 and GenPlex SNP genotyping in forensic genetics. JALA (2008), 13, 297-303.

38. Mengel-From J., Børsting C., Sanchez J.J., Eiberg H. and Morling N. Determination of cis/trans phase of variations in the MC1R gene with allele specific PCR and single base extension. Electrophoresis (2008), 29, 4780-4787.

39. Tomas C., Stangegaard M., Børsting C., Hansen A.J. and Morling N. Typing of 48 autosomal SNPs and amelogenin with GenPlex SNP genotyping system in forensic genetics. Forensic Sci. Int. Genet. (2008), 3, 1-6.

40. Wächter A, Mengel-From J, Børsting C and Morling N. A 50 SNP-plex mass spectrometry assay for human identification. Prog. For. Genetics 12, Forensic Sci. Int. Genet. Suppl. 1 (2008), 487-489. Proceedings of the 22’nd congress of the International Society of Forensic Genetics (Denmark, August 2007).

41. Rockenbauer E, Mikkelsen M, Børsting C, Sørensen E, Rasmussen M and Morling N. A mitochondrial DNA SNP multiplex assigning Caucasians into 32 haplo- and subhaplogroups. Prog. For. Genetics 12, Forensic Sci. Int. Genet. Suppl. 1 (2008), 287-289. Proceedings of the 22’nd congress of the International Society of Forensic Genetics (Denmark, August 2007).

42. Tomàs C, Sanchez JJ, Castro JA, Børsting C, and Morling N. Utility of X-chromosome SNPs in forensic science. Prog. For. Genetics 12, Forensic Sci. Int. Genet. Suppl. 1 (2008), 528-530. Proceedings of the 22’nd congress of the International Society of Forensic Genetics (Denmark, August 2007).

43. Børsting C., Rockenbauer E. and Morling N. 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. Forensic Sci. Int. Genet. (2009), 4, 34-42.

44. Olsen AN, Christensen LC, Nielsen SJ, Hallenberg C, Frank-Hansen R, Simonsen BT, Børsting C, Madsen TM, Stangegaard M, Dalsgaard S, Hansen AJ, and Morling N. Customizing a commercial laboratory management system for a forensic laboratory. Prog. For. Genetics 13, Forensic Sci. Int. Genet. Suppl. 2 (2009), 77-

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79. Proceedings of the 23’rd congress of the International Society of Forensic Genetics (Argentina, September 2009).

45. Rockenbauer E, Børsting C, Stangegaard M, Frank-Hansen R and Morling N. Successful STR and SNP typing of FTA-card samples with low amounts of DNA after DNA extraction using a Qiagen BioRobot® EZ1. Prog. For. Genetics 13, Forensic Sci. Int. Genet. Suppl. 2 (2009), 83-84. Proceedings of the 23’rd congress of the International Society of Forensic Genetics (Argentina, September 2009).

46. Tomas C, Stangegaard M, Børsting C, Smidt H, Frisk S, Schneider P, Carracedo A, Jacobsen S, Lindblom B, Bär W, Bastisch I, Westen T, Syndercombe D, Prinz M, Vallone PM, Fang R, Coble MD, Eisenberg A, Hansen AJ and Morling N. SNP typing of forensic samples with the GenPlex™ HID System: A collaborative study. Prog. For. Genetics 13, Forensic Sci. Int. Genet. Suppl. 2 (2009), 508-509. Proceedings of the 23’rd congress of the International Society of Forensic Genetics (Argentina, September 2009).

47. Mengel-From J., Børsting C., Sanchez J.J., Eiberg H. and Morling N. Associations between human eye colour variations and variations in the MATP, OCA2 and HERC2 genes. Forensic Sci. Int. Genet. (2010), 4, 323-328.

48. Drobnic K., Børsting C., Rockenbauer E., Tomas C. and Morling N. Typing of 49 autosomal SNPs by SNaPshot® in the Slovenian population. Forensic Sci. Int. Genet. (2010), 4, e125-e127.

49. Tomas C., Sanchez J.J., Castro J.A., Børsting C. and Morling N. Forensic usefulness of a 25 X-chromosome SNP marker set. Transfusion (2010), 50, 2258-2265.

50. Børsting C. and Morling N. Mutations and/or relatives? Six case work examples where 49 autosomal SNPs were used as supplementary markers. Forensic Sci. Int. Genet. (2011), 5, 236-241.

51. Børsting C., Tomas C. and Morling N. SNP typing of the reference materials SRM 2391b 1-10, K562, XY1, XX74, and 007 with the SNPforID multiplex. Forensic Sci. Int. Genet. (2011), 5, e81-e82.

52. Poulsen L., Børsting C., Tomas C., González-Andrade F., Lopez-Pulles R., González-Solórzano J. and Morling N. Typing of Amerindian Kichwas and Mestizos from Ecuador with the SNPforID multiplex. Forensic Sci. Int. Genet. (2011) 5, e105-e107.

53. Fordyce S.L., Arcos M.C.A, Rockenbauer E., Børsting C., Willerslev E., Frank-Hansen R., Hansen A.J., Morling N. and Gilbert M.T.P. High-throughput sequencing of core STR loci used for forensic genetic investigations using the Roche Genome Sequencer FLX platform. Biotechniques (2011) 51, 127-133.

54. Tomas C., Axler-DiPerte G., Budimlija Z.M., Børsting C., Coble M.D., Decker A.E., Eisenberg A., Fang R., Fondevila M., Fredslund S.F., Gonzalez S., Hansen A.J., Hoff-Olsen P., Haas C., Kohler P., Kriegel A.K., Lindblom B., Manohar F., Maroñas O., Mogensen H.S., Neureuther K., Nilsson H., Scheible M.K., Schneider P.M., Sonntag M.L., Stangegaard M., Syndercombe-Court D., Thacker C.R., Vallone P.M., Westen A.A. and Morling N. Autosomal SNP typing of forensic samples with the GenPlex™ HID System: Results of a collaborative study. Forensic Sci. Int. Genet. (2011) 5, 369-375.

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55. Mikkelsen M., Rockenbauer E., Demir H., Børsting C. and Morling N. Frequencies of 33 coding region mitochondrial SNPs in a Danish and Turkish population. Forensic Sci. Int. Genet. (2011) 5, 559-560.

56. Stangegaard M, Ferrero-Miliani L, Børsting C, Frank-Hansen R, Hansen AJ, Morling N. Repeated Extraction of DNA From The Same FTA Card. Prog. For. Genetics 14, Forensic Sci. Int. Genet. Suppl. 3 (2011), e345-e346. Proceedings of the 24’nd congress of the International Society of Forensic Genetics (Austria, September 2011).

57. Andersen JD, Johansen P, Petersen B, Børsting C, Morling N. Genetic variants and skin colour in Danes. Prog. For. Genetics 14, Forensic Sci. Int. Genet. Suppl. 3 (2011), e153-e154. Proceedings of the 24’th congress of the International Society of Forensic Genetics (Austria, September 2011).

58. Andersen JD, Mogensen HS, Johansen P, Børsting C, Morling N. Eye colour and SNPs in Danes. Prog. For. Genetics 14, Forensic Sci. Int. Genet. Suppl. 3 (2011), e151-e152. Proceedings of the 24’th congress of the International Society of Forensic Genetics (Austria, September 2011).

59. Poulsen L, Børsting C, Morling N. Implementation of the SNPforID multiplex on the Sequenom® MassARRAY® analyzer 4 system. Prog. For. Genetics 14, Forensic Sci. Int. Genet. Suppl. 3 (2011), e496-e497. Proceedings of the 24’th congress of the International Society of Forensic Genetics (Austria, September 2011).

60. Rockenbauer E, Holgersson MB, Fordyce SL, Avila Arcos MC, Børsting C, Frank-Hansen R, Hansen AJ, Willerslev E, Gilbert MTP and Morling N. Next generation sequencing of microvariant/“off-ladder” alleles of core STR loci using the Roche Genome Sequencer Junior System. Prog. For. Genetics 14, Forensic Sci. Int. Genet. Suppl. 3 (2011), e204-e205. Proceedings of the 24’th congress of the International Society of Forensic Genetics (Austria, September 2011).

61. Stene M, Buchard A, Børsting C, Morling N. Validation of the AmpFlSTR® Identifiler® Direct PCR Amplification kit in a laboratory accreditated according to the ISO17025 standard. Prog. For. Genetics 14, Forensic Sci. Int. Genet. Suppl. 3 (2011), e165-e166. Proceedings of the 24’th congress of the International Society of Forensic Genetics (Austria, September 2011).

62. Børsting C, Hjort BB, Morling N. SNP typing of crime case samples with the SNPforID multiplex assay. Prog. For. Genetics 14, Forensic Sci. Int. Genet. Suppl. 3 (2011), e99-e100. Proceedings of the 24’th congress of the International Society of Forensic Genetics (Austria, September 2011).

63. Tomas C., Børsting C. and Morling N. In DNA electrophoresis protocols for forensic genetics - Capillary electrophoresis of a 48-plex autosomal SNP GenPlex assay for human individualization and paternity testing, A. Alonso (Ed.). Methods in Molecular Biology series. Humana Press, New Jersey, USA. Vol. 830 (2012), Chapter 6, 73-86.

64. Børsting C., Tomas C. and Morling N. In DNA electrophoresis protocols for forensic genetics - Typing of 49 Autosomal SNPs by Single Base Extention and Capillary Electrophoresis for Forensic Genetic Testing, A. Alonso (Ed.). Methods in

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Molecular Biology series. Humana Press, New Jersey, USA. Vol. 830 (2012), Chapter 7, 87-108.

65. Børsting C and Morling N. Re-investigations of six unusual paternity cases by typing of autosomal single nucleotide polymorphisms. Transfusion (2012) 52, 425-430.

66. Friis S.L., Børsting C., Poulsen L., Fredslund S.F., Tomas C. and Morling N. Typing of 30 insertion/deletions in Danes using the first commercial Indel kit. Forensic Sci. Int. Genet. (2012) 6, e72-e74.

67. Børsting C., Mikkelsen M. and Morling N. Kinship Analysis with Diallelic SNPs– Experiences with the SNPforID multiplex in an ISO17025 accredited laboratory. Transfus. Med. Hemother. (2012) 39, 195-201.

68. Stangegaard M., Meijer P., Børsting C., Hansen A.J., Morling N. Biomek 3000: The workhorse in an automated accredited forensic genetic laboratory. JALA (2012) 17, 378-386.

69. Børsting C. and Morling N. Single nucleotide polymorphisms. In: Siegel J.A. and Pekka S. (Eds.) Encyclopedia of Forensic Sciences 2nd Edition (2013). Elsevier, Maryland, USA. Chapter 42, 233-238.

70. Tomas C., Diez I.E., Moncada E., Børsting C., and Morling N. Analysis of 49 autosomal SNPs in an Iraqi population. Forensic Sci. Int. Genet. (2013) 7, 198-199.

71. Hvilsom C., Frandsen P., Børsting C., Carlsen F., Sallé B., Simonsen B.T., Siegismund H.R. Understanding geographic origins and history of admixture among chimpanzees in European zoos, with implications for future breeding programmes. Heredity (2013) 110, 586-593.

72. Børsting C., Mogensen H.S., Morling N. Forensic genetic SNP typing of low-template DNA and highly degraded DNA from crime case samples. Forensic Sci. Int. Genet. (2013) 7, 345-352.

73. Sharafi Farzad M., Tomas C., Børsting C., Zeinali Z., Malekdoost M., Zeinali S. and Morling N. Analysis of 49 autosomal SNPs in three ethnic groups from Iran: Persians, Lurs and Kurds. Forensic Sci. Int. Genet. (2013), 7, 471-473.

74. Stangegaard M., Børsting C., Ferrero-Miliani L., Frank-Hansen R., Poulsen L., Hansen A.J., Morling N. Evaluation of four automated protocols for extraction of DNA from FTA cards. JALA (2013), 18, 404-410.

75. Johansen P., Andersen J.D., Børsting C., Morling N. Evaluation of the iPLEX® Sample ID Plus Panel designed for the Sequenom MassARRAY® system. A SNP typing assay developed for human identification and sample tracking based on the SNPforID panel. Forensic Sci. Int. Genet. (2013) 7, 482-487.

76. Andersen J.D., Johansen P., Harder S., Christoffersen S.R., Delgado M.C., Sørensen E., Ullum H., Henriksen S.T., Nielsen M.M., Dahl A.L., Paulsen R.R., Børsting C., Niels Morling. Genetic analyses of the human eye colours using a novel objective method for eye colour classification. Forensic Sci. Int. Genet. (2013) 7, 508-515.

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77. Harder S., Christoffersen S., Johansen P., Andersen J., Børsting C., Dahl A.L., Morling N., Paulsen R.R. What Genes tell about Iris Appearance. Lecture notes in computer science (2013) 7766, 244-253. Proceedings of the 15th International conference on Medical Image Computing and Computer Assisted Intervention (France, October 2012).

78. Pereira V., Tomas C., Pietroni C., Andersen J.D., Fordyce S.L., Pinto N., Mikkelsen M., Børsting C., Amorim A., Gusmao L., Prata M., Morling N. Assessing the potential application of X-chromosomal haploblocks in population genetics and forensic studies. Prog. For. Genetics 15, Forensic Sci. Int. Genet. Suppl. 4 (2013), e9-e10. Proceedings of the 25’th congress of the International Society of Forensic Genetics (Australia, September 2013).

79. Pietroni C., Andersen J.D., Johansen P., Harder S., Paulsen R., Børsting C., Morling N. The genetics of eye colours in an Italian population measured with an objective method for eye colour quantification. Prog. For. Genetics 15, Forensic Sci. Int. Genet. Suppl. 4 (2013), e23-e24. Proceedings of the 25’th congress of the International Society of Forensic Genetics (Australia, September 2013).

80. Andersen J.D., Tvedebrink T., Mogensen H.S, Børsting C., Morling N. Drop-out probabilities of IrisPlex SNP alleles. Prog. For. Genetics 15, Forensic Sci. Int. Genet. Suppl. 4 (2013), e238-e239. Proceedings of the 25’th congress of the International Society of Forensic Genetics (Australia, September 2013).

81. Dalsgaard S., Rockenbauer E., Gelardi C., Børsting C., Fordyce S.L., Morling N. Characterization of mutations and sequence variations in complex STR loci by second generation sequencing. Prog. For. Genetics 15, Forensic Sci. Int. Genet. Suppl. 4 (2013), e218-e219. Proceedings of the 25’th congress of the International Society of Forensic Genetics (Australia, September 2013).

82. Rockenbauer E., Hansen S., Andersen M.R., Heerup E.F., Børsting C., Fordyce S., Morling N. Characterization of sequence variations in the D21S11 locus in Danes,

Somalis and Greenlanders by second generation sequencing. Prog. For. Genetics 15, Forensic Sci. Int. Genet. Suppl. 4 (2013), e302-e303. Proceedings of the 25’th congress of the International Society of Forensic Genetics (Australia, September 2013).

83. Lundsberg B., Johansen P., Børsting C., Morling N., EUROFORGEN-NoE Consortium. Development and optimisation of five multiplex assays with 117 of the AIM SNPs from the EUROFORGEN AIMs set on the Sequenom® MassARRAY® system. Prog. For. Genetics 15, Forensic Sci. Int. Genet. Suppl. 4 (2013), e182-e183. Proceedings of the 25’th congress of the International Society of Forensic Genetics (Australia, September 2013).

84. Olofsson J.K., Børsting C., Morling N. Distribution of Y chromosome haplogroup Q in Greenland. Prog. For. Genetics 15, Forensic Sci. Int. Genet. Suppl. 4 (2013), e220-e221. Proceedings of the 25’th congress of the International Society of Forensic Genetics (Australia, September 2013).

85. Rockenbauer E., Hansen S., Mikkelsen M., Børsting C., Morling N. Characterization of mutations and sequence variants in the D21S11 locus by next generation sequencing. Forensic Sci. Int. Genet. (2014) 8, 68-72.

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86. Dalsgaard S., Rockenbauer E., Buchard A., Mogensen H.S., Frank-Hansen R., Børsting C., Morling N. Non-uniform phenotyping of D12S391 resolved by second generation sequencing. Forensic Sci. Int. Genet. (2014) 8, 195-199.

87. Pietroni C., Andersen J.D., Johansen P., Andersen M.M., Harder S., Paulsen R., Børsting C., Morling N. The effect of gender on eye colour variation in European populations and an evaluation of the IrisPlex prediction model. Forensic Sci. Int. Genet. (2014) 11, 1-6.

88. Phillips C., Parson W., Lundsberg B., Santos C., Eduardoff M., Børsting C., Johansen P., Fondevila M., Morling N., Schneider P., Carrecedo A., Lareu M.V. Building a forensic ancestry panel from the ground up: The EUROFORGEN Global AIM-SNP set. Forensic Sci. Int. Genet. (2014) 11, 13-25.

89. Gelardi C., Rockenbauer E., Dalsgaard S., Børsting C., Morling N. Second generation sequencing of three STRs D3S1358, D12S391 and D21S11 in Danes and a new nomenclature for sequenced STR alleles. Forensic Sci. Int. Genet. (2014) 12, 38-41.

90. Børsting C., Fordyce S., Olofsson J., Mogensen H.S., Morling N. Evaluation of the Ion Torrent™ HID SNP 169-plex; A SNP typing assay developed for human identification by second generation sequencing. Forensic Sci. Int. Genet. (2014) 12, 144-154.

91. Andersen J.D., Pereira V., Pietroni C., Mikkelsen M., Johansen P., Børsting C., Morling N. Next-generation sequencing of multiple individuals per barcoded library by deconvolution of sequenced amplicons using endonuclease fragment analysis. Biotechniques (2014) 57, 91-94.

92. Børsting C., Pereira V., Andersen J.D., Morling N. Single nucleotide polymorphism. In: Jamieson A. and Moenssens A.A. (Eds.) Encyclopedia of Forensic Science (2014). John Wiley & Sons, Chichester, UK. DOI:10.1002/9780470061589.fsa1113 page 1-18.

93. Fordyce S.L., Mogensen H.S., Børsting C., Lagacé R.E., Chang C., Rajagopalan N., Morling N. Second-generation sequencing of forensic STRs using the Ion Torrent™ HID STR 10-plex and the Ion PGM™. Forensic Sci. Int. Genet. (2015) 14, 132-140.

94. Olofsson J.K., Pereira V., Børsting C., Morling N. Peopling of the North Circumpolar Region – Insights from Y chromosome STR and SNP typing of the Greenlanders. PLoS ONE (2015) 10, e0116573.

95. Tomas C., Skitsa I., Steinmeier E., Poulsen L., Ampati A., Børsting C., Morling N. Results for five sets of forensic genetic markers studied in a Greek population sample. Forensic Sci. Int. Genet. (2015)16, 132-137.

96. Olofsson J.K., Mogensen H.S., Buchard A., Børsting C. and Morling N. Forensic and population genetic analyses of Danes, Greenlanders and Somalis typed with the Yfiler®Plus PCR Amplification Kit. Forensic Sci. Int. Genet. (2015) 16, 232-236.

97. Poulsen L., Sharafi Farzad M., Børsting C., Tomas C., Pereira V. and Morling N. Population and forensic data for three sets of forensic genetic markers in four ethnic groups from Iran: Persians, Lurs, Kurds and Azeris. Forensic Sci. Int. Genet. (2015) 17, 43-46.

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98. Marcińska M., Pośpiech E., Andersen J.D., van den Berge M., Carracedo A., Eduardoff M., Marczakiewicz-Lustig A., Morling N., Sijen T., Skowron M., Söchtig J., Syndercombe-Court D., Weiler N., The EUROFORGEN-NoE Consortium, Ballard D., Børsting C., Parson W., Phillips C., and Branicki W. Evaluation of DNA variants associated with androgenetic alopecia and their potential to predict male pattern baldness. PLoS ONE (2015) 10, e0127852.

99. Børsting C and Morling N. Next generation sequencing and its applications in forensic genetics. Forensic Sci. Int. Genet. (2015) 18, 78-89.

100. Santos C., Fondevila M., Ballard D., Banemann R., Bento A.M., Børsting C., Branicki W., Brisighelli F., Burrington M., Capal T., Chaitanya L., Daniel R., Decroyer V., England R., Gettings K.B., Gross T.E., Haas C., Harteveld J., Hoff-Olsen P., Hoffmann A., Kayser M., Linacre A., Kohler P., Mayr-Eduardoff M., McGovern C., Morling N., Noe ̈l F., O'Donnell G., Parson W., Pascali V.L., Porto M.J., Roseth A., Schneider P.M., Sijen T., Stenzl V., Syndercombe Court D., Templeton J., Turanska M., Vallone P.M., van Oorschot R.A.H., Zatkalikova L., The EUROFORGEN-NoE Consortium; Carracedo A., and Phillips C. Forensic ancestry analysis with two capillary electrophoresis ancestry informative marker (AIM) panels: Results of a collaborative EDNAP exercise. Forensic Sci. Int. Genet. (2015) 19, 56-67.

101. Pośpiech E., Karłowska-Pik J., Marcińska M., Abidi S., Andersen J.D., van den Berge M., Carracedo A., Eduardoff M., Freire-Aradas A., Morling N., Sijen T., Skowron M., Söchtig J., Syndercombe-Court D., Weiler N., The EUROFORGEN-NoE Consortium, Schneider P.M., Ballard D., Børsting C., Parson W., Phillips C., Branicki W. Evaluation of the predictive capacity of DNA variants associated with straight hair in humans. Forensic Sci. Int. Genet. (2015) 19, 280-288.

102. Mogensen H.S., Børsting C., Morling N. Template preparation of AmpliSeq™ libraries using the Ion Chef™. Prog. For. Genetics 16, Forensic Sci. Int. Genet. Suppl. 5 (2015), e368-e369. Proceedings of the 26’th congress of the International Society of Forensic Genetics (Poland, September 2015).

103. Ribeiro J., Pereira V., Kondili A., Miniati P., Børsting C., Morling N., EUROFORGEN-NoE. Typing of 111 Ancestry Informative Markers in an Albanian Population. Prog. For. Genetics 16, Forensic Sci. Int. Genet. Suppl. 5 (2015), e124-e125. Proceedings of the 26’th congress of the International Society of Forensic Genetics (Poland, September 2015).

104. Hussing C., Børsting C., Mogensen H.S., Morling N. Testing of the Illumina® Forenseq™ kit. Prog. For. Genetics 16, Forensic Sci. Int. Genet. Suppl. 5 (2015), e449-e450. Proceedings of the 26’th congress of the International Society of Forensic Genetics (Poland, September 2015).

105. Hussing C., Kampmann M., Mogensen H.S., Børsting C., Morling N. Comparison of techniques for quantification of next-generation sequencing libraries. Prog. For. Genetics 16, Forensic Sci. Int. Genet. Suppl. 5 (2015), e276-e278. Proceedings of the 26’th congress of the International Society of Forensic Genetics (Poland, September 2015).

106. Friis S.L., Buchard A., Rockenbauer E., Børsting C., Morling N. Introduction of the Python script STRinNGS for analysis of STR regions in FASTQ or BAM files and

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expansion of the Danish STR sequence database to 11 STRs. Forensic Sci. Int. Genet. (2016) 21, 68-75.

107. Johansen P., Andersen J.D., Madsen L.N., Glud M., Børsting C., Gniadecki R., Morling N. Pigmentary markers in Danes – associations with quantitative skin colour, nevi count, familial atypical multiple-mole syndrome and melanoma syndrome. PLoS ONE (2016) 11, e0150381.

108. Børsting C., Pereira V., Andersen J.D., Morling N. Single nucleotide polymorphism. In: Jamieson, A. and Bader, S. (Eds) A Guide to Forensic DNA Profiling (2016). John Wiley & Sons Ltd, Chichester, UK, chapter 25, 205-222, ISBN: 978-1-118-75152-7.

109. Andersen J.D., Pietroni C., Johansen P., Andersen M.M., Pereira V., Børsting C., Morling N. Importance of non-synonymous OCA2 variants in human eye colour prediction. Mol. Genet. Genomic Med. (2016) 4, 420-430.

110. Børsting C., Morling N. Genomic applications in forensic medicine. In: Kumar D. and Antonarakis S. (Eds.) Medical and Health Genomics (2016). Elsevier, Maryland, USA, chapter 22, 295-309, ISBN: 978-0-12-420196-5.

111. Eduardoff M., Gross T.E., Santos C., de la Puente M., Ballard D., Strobl C., Børsting C., Morling N., Fusco L., Hussing C., Egyed B., Souto L., Uacyisrael J., Syndercombe Court D., Carracedo A., Lareu M.V., Schneider P.M., The EUROFORGEN-NoE Consortium, Parson W., Phillips C. Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™. Forensic Sci. Int. Genet. (2016) 23, 178-189.

112. Themudo G.E., Mogensen H.S., Børsting C., Morling N. Frequencies of HID-Ion Ampliseq Ancestry Panel markers among Greenlanders. Forensic Sci. Int. Genet. (2016) 24, 60-64.

113. Kampmann M., Buchard A., Børsting C., Morling N. High throughput sequencing of forensic genetic samples using punches of FTA cards with buccal swabs. Biotechniques (2016) 61, 149-151.

114. Tomas C., Poulsen L., Drobnič K., Ivanova V., Jankauskiene J., Bunokiene D., Børsting C., Morling N. Thirty autosomal insertion-deletion polymorphisms analyzed using the Investigator® DIPplex Kit in populations from Iraq, Lithuania, Slovenia, and Turkey. Forensic Sci. Int. Genet. (2016) 25, 142-144.

115. Lopopolo M., Børsting C., Pereira V., Morling N. A study of the peopling of Greenland using next generation sequencing of complete mitochondrial genomes. Am. J. Phys. Anthropol. (2016), in press.

116. Pingel J., Andersen J.D., Christiansen S.L., Børsting C., Morling N., Lorentzen J., Kirk H., Doessing S., Wong C. & Nielsen J.B. Sequence variants in muscle tissue related genes may determine the severity of muscle contractures in cerebral palsy. J. Physiol. (2016) submitted.

117. Jensen L., Børsting C., Dalhoff K., Morling N. Evaluation of the iPLEX® ADME PGx Pro Panel and Allele frequencies of Pharmacogenetic markers in Danes. Clin. Biochem. (2016) in press.

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118. Buchard A., Kampmann M., Poulsen L., Børsting C., Morling N. ISO17025 validation of a next generation sequencing assay for relationship testing. Electrophoresis (2016), in press.

119. Fondevila M., Børsting C., Phillips C., de la Puente M., Santos C., The EuroForGen-NoE Consortium, Carracedo A., Morling N., Lareu M.V. Forensic SNP genotyping with SNaPshot: Technical considerations for the development and optimisation of multiplexed SNP assays. Forensic Sci. Rev. (2016), submitted.

Posters/Oral presentations;

a. Børsting C . Oral presentation; Acyl-CoA binding protein in yeast. One-day meeting on Yeast genetics (Denmark, Marts 1994).

b. Kristiansen K ., Hummel R., Børsting C., Wogensen C., Skøtt H., Rose T. M. and Knudsen J. The role of acyl-CoA binding protein in yeast. 16’th International congress of biochemistry and molecular biology (India, September 1994).

c. Kristiansen K., Mandrup S., Hummel R., Børsting C., Elholm M., Krogsdam A., Madsen I., Nielsen C.A.F., Gøttlicher M., Gustafsson J., Wogensen C., Albrechtsen T., Larsen L.C.S. and Knudsen J. Lipid carrier proteins and lipids in regulation of gene expression. 16’th International congress of biochemistry and molecular biology (India, September 1994).

d. Kristiansen K., Mandrup S., Hummel R., Børsting C., Elholm M., Krogsdam A., Madsen I., Nielsen C.A.F., Gøttlicher M., Gustafsson J., Wogensen C., Albrechtsen T., Larsen L.C.S. and Knudsen J. Acyl-CoA binding protein and acyl-CoA esters in regulation of gene expression in yeast and mammels. 4’th international symposium on protein structure function relationship (Pakistan, January 1995).

e. Børsting C ., Hummel R., Knudsen J. and Kristiansen K. Saccharomyces carlsbergensis contains two functional ACB1 genes, one similar to the ACB1 gene from S. cerevisiae and one similar to the ACB1 gene from S. monacensis. 17’th international conference on yeast genetics and molecular biology (Portugal, June 1995).

f. Børsting C ., Hummel R., Knudsen J. and Kristiansen K. Acyl-CoA binding protein and acyl-CoA esters in regulation of gene expression in yeast. 17’th international conference on yeast genetics and molecular biology (Portugal, June 1995).

g. Schjerling C., Hansen J.K., Børsting C., Hummel R., Kristiansen K. and Knudsen J. The effect of deleting the acyl-CoA-binding protein gene (ACB1) on lipid metabolism in S. cerevisiae. 25’th annual meeting at the Biochemistry society (Denmark, October 1995).

h. Børsting C ., DiRusso C., and Black P.N. Uptake and activation of fatty acids in the yeast Saccharomyces cerevisiae. Gordon research conference (USA, June 1999).

i. Børsting C . Oral presentation: SNP’s in forensic science. Nanogen user group meeting (Denmark, May 2002).

j. Børsting C . Oral presentation: SNP typing strategies – Copenhagen. Nanogen SNP typing workshop (Germany, June 2002).

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k. Børsting C . Oral presentation: Analysis of Y chromosome SNP’s on the Nanogen Molecular Biology Workstation. Pre-meeting to The second bi-annual symposium on array technology in research and diagnostics (Denmark, October 2002).

l. Børsting C . Oral presentation: Analysis of Y chromosome SNP’s on the Nanogen Molecular Biology Workstation. III international forensic Y-user workshop (Portugal, November 2002).

m. Børsting C. Oral presentation: Multiplex PCR, amplicon size and hybridization efficiency on the NanoChip electronic microarray. The Y-chromosome SNPs as an example. Curso avanzado de Genetica Forense (Spain, May 2003).

n. Sanchez JJ , Børsting C., Hallenberg C., Hernandez A. and Morling N. Y chromosome analysis of the Somali population suggests the origin of the haplogroup E3b1. 2’nd international symposium on DNA polymorphisms in human populations (France, December 2003).

o. SNPforID consortium. Major Y-chromosome haplogroup typing by use of a 29-multiplex kit. IV international forensic Y-user workshop (Germany, November 2004).

p. Mengel-From J , Børsting C, Hallenberg C, Sanchez JJ and Morling N. Gene variations associated with hair and eye colours in humans. Pigment Cell Res. 19, 520 (2006). 13’th meeting of the European Society for Pigment Cell Research (Spain, September 2006).

q. Mengel-From J, Wächter A, Børsting C, Sanchez JJ, and Morling N. PCR and SBE multiplexes for determination of SNPs associated with hair and eye colours in humans. DNA in forensics (Austria, September 2006).

r. SNPforID consortium. Forensic validation of the SNPforID 52-plex SNP assay. DNA in forensics (Austria, September 2006).

s. Stangegaard M , Tomàs C, Hansen AJ, Frank-Hansen R, Børsting C, and Morling N. Biomek-3000 and GenPlex in forensic genetics. LabAutomation2008 (USA, January 2008).

t. Mengel-From J , Børsting C, Johansen P, Eiberg H, and Morling N. Genetic determinations of hair and eye colours in Danes. DNA in forensics (Italy, May 2008).

u. Mikkelsen M , Rockenbauer E, Sørensen E, Børsting C, and Morling N. A mitochondrial DNA SNP multiplex PCR assay assigning Caucasians into 41 haplo- and subhaplogroups. DNA in forensics (Italy, May 2008).

v. Børsting C . Oral presentation: Experiences with SNP analyses in forensic cases. English Speaking Working Group of the International Society of Forensic Genetics (Sweden, September 2010).

w. Børsting C . Oral presentation: SNP typing of low template DNA. English Speaking Working Group of the International Society of Forensic Genetics (Denmark, May 2012).

x. Hvilsom C, Siegismund H, Frandsen P, Børsting C, Carlsen F, Sallé B, Simonsen BT. Out of Africa we presume? Ancestry assignment of chimpanzees in

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conservation programmes based on genetic structure in the natural distribution range. English Speaking Working Group of the International Society of Forensic Genetics (Denmark, May 2012).

y. Andersen JD , Johansen P, Børsting C, Morling N. The genetics of human eye colour and application to forensic genetic case work. English Speaking Working Group of the International Society of Forensic Genetics (Denmark, May 2012).

z. Andersen JD , Mogensen HS, Børsting C, Morling N. Implementation of the IrisPlex assay in forensic genetic case work. English Speaking Working Group of the International Society of Forensic Genetics (Denmark, May 2012).

aa. Delgado MC , Børsting C, Andersen JD, Johansen P, Morling N. Genetics of eye and skin colour in Swedes. English Speaking Working Group of the International Society of Forensic Genetics (Denmark, May 2012).

bb. Johansen P , Andersen JD, Delgado MC, Christoffersen SR, Harder S, Paulsen RR, Børsting C and Morling N. The genetics of human eye colour using a novel eye colour classification method. Pigment Cell Melanoma Res. (2012) 25, 651. 17’th meeting of the European Society for Pigment Cell Research (Switzerland, September 2012).

cc. Harder S. , Clemmensen L., Dahl A., Andersen J., Johansen P., Christoffersen S., Morling N., Børsting C., Paulsen R.R. Correlation of iris biometrics and DNA. Proceedings of the International Workshop on Biometrics and Forensics (Portugal, april 2013), 10.1109/IWBF.2013.6547325.

dd. Phillips C. , Parson W., Børsting C.,EUROFORGEN-NoE Consortium. A global ancestry SNP panel for next generation sequencing technologies. The 25’th congress of the International Society of Forensic Genetics (Australia, September 2013).

ee. Phillips C. , Santos C., Fondevila M., Parson W., Ballard D., Børsting C., Branicki W., Eduardoff M., Gross T., Kohler P., EUROFORGEN-NoE Consortium. The EUROFORGEN forensic ancestry marker exercise. The 25’th congress of the International Society of Forensic Genetics (Australia, September 2013).

ff. Børsting C. Oral presentation: Experiences with SNP and STR typing using second generation sequencing (SGS). 34. Spurenworkshop: 2014 Future trends in forensic DNA technology (Austria, February 2014).

gg. Pereira V. , Børsting C., Morling N. Further insights on the peopling of Greenland through the analysis of complete mtDNA sequences. DNA in forensics (Belgium, May 2014).

hh. Olofsson J.K., Børsting C., Morling N. Fine scale Y chromosome analysis in Danes. DNA in forensics (Belgium, May 2014).

ii. Børsting C. Oral presentation: Next generation sequencing of STRs: New possibilities and new challenges for forensic genetics. DNA in forensics, Future trends in forensic DNA technology (Belgien, Maj 2014).

jj. Rockenbauer E. , Manninen J., Dalsgaard S., Gelardi C., Mogensen H.S., Børsting C., Fordyce S.L., Morling N. STR sequencing on second generation sequencing

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http://dx.doi.org/10.1109/IWBF.2013.6547325


platforms. English Speaking Working Group of the International Society of Forensic Genetics (Greece, May 2014).

kk. Skitsa I. , Tomas C., Steinmeier E., Børsting C., Morling N. Analyses of autosomal insertion/deletion makers using the DIPplex kit in a Greek population. English Speaking Working Group of the International Society of Forensic Genetics (Greece, May 2014).

ll. Børsting C. Oral presentation: Sequencing of SNPs and STRs with MPS for forensic genetics. The 26’th congress of the International Society of Forensic Genetics (Poland, September 2015).

mm. Buchard A. , Kampmann M., Børsting C., Morling N. Next generation sequencing of reference samples with the HID-Ion AmpliSeq™ Identity Panel using single punches from FTA cards. The 26’th congress of the International Society of Forensic Genetics (Poland, September 2015).

nn. Marcinska M. , Pospiech E., Abidi S., Andersen J.D., van den Berge M., Carracedo A., Eduardoff M., Freire-Aradas A., Morling N., Sijen T., Skowron M., Söchtig J., Court D.S., Weiler N., EUROFORGEN-NoE, Ballard D., Børsting C., Parson W., Phillips C., Branicki W. Frequency differences of SNP alleles associated with male pattern baldness in Africa, Asia and Europe. The 26’th congress of the International Society of Forensic Genetics (Poland, September 2015).

oo. Børsting C. Oral presentations: Human Identification Ion PGM™ Forensic Schools (Germany, September 2015).

pp. Møller L., Rockenbauer E., Børsting C., Morling N. Sequence variations in the short tandem repeat SE33 discovered by next generation sequencing. English Speaking Working Group of the International Society of Forensic Genetics (Hungary, September 2016).

qq. Rockenbauer E. , Buchard A., Friis S.L. Manninen J., Børsting C. Morling N. Analysis of next generation sequencing data of 11 STRs in 208 Somalis using the STRinNGS v1.0 software. English Speaking Working Group of the International Society of Forensic Genetics (Hungary, September 2016).

rr. Hussing C. , Huber C., Bytyci R., Mogensen H.S., Børsting C., Morling N. Sequencing of 58 STRs using the Illumina® ForenSeqTM workflow and analysis of the data with the STRinNGS v.1.1 software. English Speaking Working Group of the International Society of Forensic Genetics (Hungary, September 2016).

ss. Buchard A. , Kampmann M.L., Børsting C. Morling N. Validation of the HID-Ion Ampliseq™ Identity Panel for relationship testing and reflections on the first 10 months of experience with MPS in real case work. English Speaking Working Group of the International Society of Forensic Genetics (Hungary, September 2016).

Courses taken after the PhD;

1. GL-introduction to management. Dansk International Efteruddannelse (DIEU) (Denmark, January 2002).

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2. MALDI-tof Voyager DE-PRO Course. Applied Biosystems in-house training (England, May 2003).

3. Management. Personaleudvikling og metodeudvikling indenfor administration (PUMA), University of Copenhagen (Denmark, May 2006).

4. Population genetic data analysis. Scandinavian Institute in Statistical Genetics, University of Århus (Denmark, July 2006).

5. Association mapping and clinical trials. Scandinavian Institute in Statistical Genetics, University of Århus (Denmark, July 2006).

6. MUS course for the Department of Forensic Medicine. Personaleudvikling og metodeudvikling indenfor administration (PUMA), University of Copenhagen (Denmark, April 2007).

7. Disaster Victim Identification, mtDNA and Y-chromosome DNA in forensic genetics. ISFG summer school. University of Copenhagen (Danmark, June 2010).

8. Management at University of Copenhagen. Personaleudvikling og metodeudvikling indenfor administration (PUMA), University of Copenhagen (Denmark, Fall 2010).

9. HID PGM training course. Applied Biosystems in-house training (Denmark, December 2014).

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