Niels Morling

Niels Morling

Professor, Visiting professor

Member of:

    ORCID: 0000-0002-9463-5087

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    1. 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 journal › Journal article › Research › peer-review

    2. 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 journal › Letter › Research › peer-review

    3. 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 journal › Letter › Research › peer-review

    4. 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 journal › Journal article › Research › peer-review

    5. 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 journal › Journal article › Research › peer-review

    6. 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 journal › Journal article › Research › peer-review

    7. 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 journal › Journal article › Research › peer-review

    8. 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 journal › Letter › Research › peer-review

    9. 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 journal › Letter › Research › peer-review

    10. 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 journal › Journal article › Research › peer-review

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    ID: 6624