Niels Morling

Niels Morling

Professor


  1. 2016
  2. Published

    Importance of non-synonymous OCA2 variants in human eye colour prediction

    Andersen, Jeppe Dyrberg, Pietroni, Carlotta, Johansen, P., Andersen, M. M., Pereira, Vania, Børsting, Claus & Morling, Niels, Jul 2016, In: Molecular Genetics & Genomic Medicine. 4, 4, p. 420-430 11 p.

    Research output: Contribution to journalJournal articlepeer-review

  3. Published

    Evaluation of Forensic DNA Traces When Propositions of Interest Relate to Activities: Analysis and Discussion of Recurrent Concerns

    Biedermann, A., Champod, C., Jackson, G., Gill, P., Taylor, D., Butler, J., Morling, Niels, Hicks, T., Vuille, J. & Taroni, F., Dec 2016, In: Frontiers in Genetics. 7, 12 p., 215.

    Research output: Contribution to journalReviewpeer-review

  4. Published

    Recommendations of the DNA Commission of the International Society for Forensic Genetics (ISFG) on quality control of autosomal Short Tandem Repeat allele frequency databasing (STRidER)

    Bodner, M., Bastisch, I., Butler, J. M., Fimmers, R., Gill, P., Gusmão, L., Morling, Niels, Phillips, C., Prinz, M., Schneider, P. M. & Parson, W., Sep 2016, In: Forensic Science International: Genetics. 24, p. 97-102 6 p.

    Research output: Contribution to journalJournal articlepeer-review

  5. Published

    ISO 17025 validation of a next-generation sequencing assay for relationship testing

    Buchard, Anders, Kampmann, Marie-Louise, Poulsen, L., Børsting, Claus & Morling, Niels, Nov 2016, In: Electrophoresis. 37, 21, p. 2822-2831 10 p.

    Research output: Contribution to journalJournal articlepeer-review

  6. Published

    Genomic applications in forensic medicine

    Børsting, Claus & Morling, Niels, 1 Jul 2016, Medical and Health Genomics. Kumar, D. & Antonarakis, S. (eds.). Academic Press, p. 295-309 15 p.

    Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

  7. Published

    Single Nucleotide Polymorphism

    Børsting, Claus, Pereira, Vania, Andersen, Jeppe Dyrberg & Morling, Niels, 9 Mar 2016, A Guide to Forensic DNA Profiling . Jamieson, A. & Bader, S. (eds.). Chichester, UK: Wiley, p. 199-216

    Research output: Chapter in Book/Report/Conference proceedingBook chapterResearch

  8. Published

    Genetic investigation of 100 heart genes in sudden unexplained death victims in a forensic setting

    Christiansen, S. L., Hertz, C. L., Ferrero, L., Dahl, Morten, Weeke, P. E., LuCamp, Ottesen, G. L., Frank-Hansen, R., Bundgård, Henning & Morling, Niels, 2016, In: European Journal of Human Genetics. 24, p. 1797–1802

    Research output: Contribution to journalJournal articlepeer-review

  9. Published

    DNA Commission of the International Society for Forensic Genetics: Recommendations on the validation of software programs performing biostatistical calculations for forensic genetics applications

    Coble, M. D., Buckleton, J., Butler, J. M., Egeland, T., Fimmers, R., Gill, P., Gusmão, L., Guttman, B., Krawczak, M., Morling, Niels, Parson, W., Pinto, N., Schneider, P. M., Sherry, S. T., Willuweit, S. & Prinz, M., Nov 2016, In: Forensic Science International: Genetics. 25, p. 191-197 7 p.

    Research output: Contribution to journalJournal articlepeer-review

  10. Published

    Major inter-personal variation in the increase and maximal level of 25-hydroxy vitamin D induced by UVB

    Datta, P., Philipsen, P. A., Olsen, P., Petersen, B., Johansen, P., Morling, Niels & Wulf, H. C., 2016, In: Photochemical & Photobiological Sciences. 15, 4, p. 536-545

    Research output: Contribution to journalJournal articlepeer-review

  11. Published

    Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™

    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, Á., Lareu, M. V., Schneider, P. M., Parson, W., Phillips, C., EUROFORGEN-NoE Consortium & 2 others, Parson, W. & Phillips, C., Jul 2016, In: Forensic Science International: Genetics. 23, p. 178-189 12 p.

    Research output: Contribution to journalJournal articlepeer-review

  12. Published

    Frequencies of HID-ion ampliseq ancestry panel markers among greenlanders

    Espregueira Themudo, G., Mogensen, Helle Smidt, Børsting, Claus & Morling, Niels, 6 Jun 2016, In: Forensic Science International: Genetics. 24, p. 60-64 5 p.

    Research output: Contribution to journalJournal articlepeer-review

  13. Published

    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, S. L., Buchard, Anders, Rockenbauer, Eszter, Børsting, Claus & Morling, Niels, Mar 2016, In: Forensic Science International: Genetics. 21, p. 68-75 8 p.

    Research output: Contribution to journalJournal articlepeer-review

  14. Published

    Next-generation sequencing of 100 candidate genes in young victims of suspected sudden cardiac death with structural abnormalities of the heart

    Hertz, C. L., Christiansen, S. L., Ferrero-Miliani, L., Dahl, Morten, Weeke, P. E., Ottesen, G. L., Frank-Hansen, R., Bundgård, Henning, Morling, Niels & LuCamp, L., Jan 2016, In: International Journal of Legal Medicine. 130, 1, p. 91-102 12 p.

    Research output: Contribution to journalJournal articlepeer-review

  15. Published

    Post-mortem investigation of young deceased individuals with ischemic heart disease—outcome of supplementary genetic testing for dyslipidemia

    Hertz, C. L., Christiansen, S. L., Ottesen, G. L., Frank-Hansen, R., Bundgård, Henning & Morling, Niels, Jul 2016, In: International Journal of Legal Medicine (Print). 130, 4, p. 947–948

    Research output: Contribution to journalComment/debate

  16. Published

    Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases

    Hertz, C. L., Christiansen, S. L., Larsen, M. K., Dahl, M., Ferrero-Miliani, L., Weeke, P. E., Pedersen, Oluf Borbye, Hansen, Torben, Grarup, Niels, Ottesen, G. L., Frank-Hansen, R., Banner, Jytte & Morling, Niels, 2016, In: European Journal of Human Genetics. 24, p. 817–822

    Research output: Contribution to journalJournal articlepeer-review

  17. Published

    Monozygotic twins discordant for narcolepsy type 1 and multiple sclerosis

    Jennum, Poul, Kornum, Birgitte Rahbek, Issa, N. M., Gammeltoft, S., Tommerup, Niels, Morling, Niels, Tümer, Asuman Zeynep & Knudsen, S., Aug 2016, In: Neurology: Neuroimmunology & Neuroinflammation. 3, 4, 2 p., e249.

    Research output: Contribution to journalLetterpeer-review

  18. Published

    Evaluation of the iPLEX® ADME PGx Pro Panel and allele frequencies of pharmacogenetic markers in Danes

    Jensen, L., Børsting, Claus, Dalhoff, Kim & Morling, Niels, Nov 2016, In: Clinical Biochemistry. 49, 16-17, p. 1299–1301 3 p.

    Research output: Contribution to journalLetterpeer-review

  19. Published

    Pigmentary Markers in Danes – Associations with Quantitative Skin Colour, Nevi Count, Familial Atypical Multiple-Mole, and Melanoma Syndrome

    Johansen, P., Andersen, Jeppe Dyrberg, Madsen, L. N., Ullum, H., Glud, M., Børsting, Claus, Gniadecki, R. & Morling, Niels, 2016, In: PLOS ONE. 11, 3, 13 p., e0150381.

    Research output: Contribution to journalJournal articlepeer-review

  20. Published

    High-throughput sequencing of forensic genetic samples using punches of FTA cards with buccal swabs

    Kampmann, Marie-Louise, Buchard, Anders, Børsting, Claus & Morling, Niels, Sep 2016, In: BioTechniques. 61, 3, p. 149-151 3 p.

    Research output: Contribution to journalJournal articlepeer-review

  21. Published

    A study of the peopling of Greenland using next generation sequencing of complete mitochondrial genomes

    Lopopolo, M., Børsting, Claus, Pereira, Vania & Morling, Niels, Dec 2016, In: American Journal of Physical Anthropology. 161, 4, p. 698-704

    Research output: Contribution to journalJournal articlepeer-review

  22. Published

    Massively parallel sequencing of forensic STRs: Considerations of the DNA commission of the International Society for Forensic Genetics (ISFG) on minimal nomenclature requirements

    Parson, W., Ballard, D., Budowle, B., Butler, J. M., Gettings, K. B., Gill, P., Gusmão, L., Hares, D. R., Irwin, J. A., King, J. L., Knijff, P. D., Morling, Niels, Prinz, M., Schneider, P. M., Neste, C. V., Willuweit, S. & Phillips, C., May 2016, In: Forensic science international. Genetics. 22, p. 54-63 10 p.

    Research output: Contribution to journalJournal articlepeer-review

  23. Published

    NGMSElect™ and Investigator® Argus X-12 analysis in population samples from Albania, Iraq, Lithuania, Slovenia, and Turkey

    Poulsen, L., Tomas Mas, Carmen, Drobnic, K., Ivanova, V., Mogensen, Helle Smidt, Kondili, A., Miniati, P., Bunokiene, D., Jankauskiene, J., Pereira, Vania & Morling, Niels, May 2016, In: Forensic Science International: Genetics. 22, p. 110-112 3 p.

    Research output: Contribution to journalLetterpeer-review

  24. Published

    Thirty autosomal insertion-deletion polymorphisms analyzed using the Investigator(®) DIPplex Kit in populations from Iraq, Lithuania, Slovenia, and Turkey

    Tomas Mas, Carmen, Poulsen, L., Drobnič, K., Ivanova, V., Jankauskiene, J., Bunokiene, D., Børsting, Claus & Morling, Niels, Nov 2016, In: Forensic science international. Genetics. 25, p. 142-144 3 p.

    Research output: Contribution to journalLetterpeer-review

  25. Published

    New clues to the evolutionary history of the main European paternal lineage M269: dissection of the Y-SNP S116 in Atlantic Europe and Iberia

    Valverde, L., Illescas, M. J., Villaescusa, P., Gotor, A. M., García, A., Cardoso, S., Algorta, J., Catarino, S., Rouault, K., Férec, C., Hardiman, O., Zarrabeitia, M., Jiménez, S., Pinheiro, M. F., Jarreta, B. M., Olofsson, Jill Katharina, Morling, Niels & de Pancorbo, M. M., 2016, In: European Journal of Human Genetics. 24, p. 437–441

    Research output: Contribution to journalJournal articlepeer-review

ID: 6624