Niels Morling

Niels Morling

Professor, Visiting professor

Member of:


    1. Published

      Semi-automatic preparation of biological database samples for STR typing

      Hansen, A. J., Simonsen, B. T., Børsting, Claus, Hallenberg, C. & Morling, Niels, 2006, Progress on Forensic Genetics 11. Elsevier, Vol. 1288. p. 663-665

      Research output: Chapter in Book/Report/Conference proceedingArticle in proceedingsResearchpeer-review

    2. Published

      Paternity testing with five VNTR systems in Danes

      Hansen, H. E. & Morling, Niels, 1992, Advances in Forensic Haemogenetics. Rittner, C. & Schneider, P. (eds.). Berlin, Heidelberg. New York: Springer: Springer, Vol. IV. p. 192-194

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

    3. Published

      Genetic investigations in immigration cases and frequencies of DNA fragments of the VNTR systems D2S44, D5S43, D7S21, D7S22, and D12S11 in Turks

      Hansen, H. E. & Morling, Niels, 1993, In: Forensic Science International. 60, 1-2, p. 23-35 12 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    4. Published

      Paternity testing with VNTR DNA systems. II. Evaluation of 271 cases of disputed paternity with the VNTR systems D2S44, D5S43, D7S21, D7S22, and D12S11

      Hansen, H. E. & Morling, Niels, 1993, In: International Journal of Legal Medicine (Print). 105, 4, p. 197-202 5 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    5. Published

      What Genes Tell about Iris Appearance

      Harder, S., Christoffersen, S. R., Johansen, P., Børsting, Claus, Morling, Niels, Andersen, J. D., L. Dahl, A. & R. Paulsen, R., 2013, In: Lecture notes in computer science. 7766, 244-253

      Research output: Contribution to journalConference articleResearchpeer-review

    6. Published

      Correlation of iris biometrics and DNA

      Harder, S., Clemmensen, L. H., Dahl, A. L., Andersen, Jeppe Dyrberg, Johansen, P., Christoffersen, Susanne, Morling, Niels, Børsting, Claus & Paulsen, R. R., 2013, 2013 International Workshop on Biometrics and Forensics, IWBF 2013. 6547325. (2013 International Workshop on Biometrics and Forensics, IWBF 2013).

      Research output: Chapter in Book/Report/Conference proceedingArticle in proceedingsResearchpeer-review

    7. Published

      The SNPforID Consortium. A sensitive issue: Pyrosequencing as a valuable forensic SNP typing platform

      Harrison, C., Musgrave-Brown, E., Bender, K., Carracedo, A., Morling, Niels, Schneider, P. & Syndercombe-Court, D., 2006, Progress on Forensic Genetics 11. Elsevier, Vol. 1288. p. 52-54

      Research output: Chapter in Book/Report/Conference proceedingArticle in proceedingsResearchpeer-review

    8. Published

      A sensitive issue: Pyrosequencing as a valuable forensic SNP typing platform

      Harrison, C., Musgrave-Brown, E., Bender, K., Carracedo, A., Morling, Niels, Schneider, P. M. & Syndercombe-Court, D., 2006, Progress in Forensic Genetics 11: Proceedings of the 21st International ISFG Congress. Elsevier, Vol. 1288. p. 52-54 (ICS - International Congress Series).

      Research output: Chapter in Book/Report/Conference proceedingArticle in proceedingsResearchpeer-review

    9. Published

      RNA analysis of tape strips to rule out melanoma in lesions clinically assessed as cutaneous malignant melanoma: A diagnostic study

      Heerfordt, I. M., Philipsen, P. A., Andersen, Jeppe Dyrberg, Langhans, Linnea, Schmidt, G., Morling, Niels & Wulf, H. C., 2023, In: Journal of the American Academy of Dermatology. 89, 3, p. 537-543

      Research output: Contribution to journalJournal articleResearchpeer-review

    10. Published

      Detection of cutaneous malignant melanoma using RNA sampled by tape strips: A study protocol

      Heerfordt, I. M., Andersen, Jeppe Dyrberg, Philipsen, P. A., Langhans, L., Tvedebrink, Torben, Schmidt, G., Poulsen, T., Lerche, Catharina Margrethe, Morling, Niels & Wulf, H. C., 2022, In: PLoS ONE. 17, 9 , 11 p., e0274413.

      Research output: Contribution to journalJournal articleResearchpeer-review

    11. 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 articleResearchpeer-review

    12. 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/debateResearch

    13. Published

      A comparison of genetic findings in sudden cardiac death victims and cardiac patients: the importance of phenotypic classification

      Hertz, C. L., Ferrero-Miliani, L., Frank-Hansen, R., Morling, Niels & Bundgård, H., 1 Mar 2015, In: Europace. 17, 3, p. 350-357

      Research output: Contribution to journalJournal articleResearchpeer-review

    14. 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 articleResearchpeer-review

    15. Published

      Next-generation sequencing of 34 genes in sudden unexplained death victims in forensics and in patients with channelopathic cardiac diseases

      Hertz, C. L., Christiansen, S. L., Ferrero-Miliani, L., Fordyce, S. L., Dahl, M., Holst, A. G., Ottesen, G. L., Frank-Hansen, R., Bundgård, Henning & Morling, Niels, Jul 2015, In: International Journal of Legal Medicine. 129, 4, p. 793-800

      Research output: Contribution to journalJournal articleResearchpeer-review

    16. Stimulation in primary MLR caused by a PLT defined non-HLA-D/DR determinant, EP1

      Holter, W. & Morling, Niels, 1983, In: HLA. 22, 1, p. 42-8 6 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    17. Published

      Cord blood immunoglobulin E in like-sexed monozygotic and dizygotic twins

      Husby, S., Holm, N. V., Christensen, K., Skov, R., Morling, Niels & Petersen, P. H., 1996, In: Clinical Genetics. 50, 5, p. 332-8 6 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    18. Published

      The Danish STR sequence database: duplicate typing of 363 Danes with the ForenSeq™ DNA Signature Prep Kit

      Hussing, C., Bytyci, R., Huber, C., Morling, Niels & Børsting, Claus, Mar 2019, In: International Journal of Legal Medicine. 133, 2, p. 325–334

      Research output: Contribution to journalJournal articleResearchpeer-review

    19. Published

      Testing of the Illumina® ForenSeq™ kit

      Hussing, C., Børsting, Claus, Mogensen, Helle Smidt & Morling, Niels, 28 Dec 2015, In: Forensic Science International: Genetics Supplement Series. 5, p. e449-e450 2 p.

      Research output: Contribution to journalConference articleResearchpeer-review

    20. Published

      Sequencing of 231 forensic genetic markers using the MiSeq FGx™ forensic genomics system – an evaluation of the assay and software

      Hussing, C., Huber, C., Bytyci, R., Mogensen, Helle Smidt, Morling, Niels & Børsting, Claus, 9 Apr 2018, In: Forensic Sciences Research. 3, 2, p. 111-123

      Research output: Contribution to journalJournal articleResearchpeer-review

    21. Published

      Quantification of massively parallel sequencing libraries - a comparative study of eight methods

      Hussing, C., Kampmann, Marie-Louise, Mogensen, Helle Smidt, Børsting, Claus & Morling, Niels, 1 Dec 2018, In: Scientific Reports. 8, 9 p., 1110.

      Research output: Contribution to journalJournal articleResearchpeer-review

    22. Published

      Comparison of techniques for quantification of next-generation sequencing libraries

      Hussing, C., Kampmann, Marie-Louise, Mogensen, Helle Smidt, Børsting, Claus & Morling, Niels, Dec 2015, In: Forensic Science International: Genetics. Supplement Series. 5, p. e276-e278 3 p.

      Research output: Contribution to journalConference articleResearchpeer-review

    23. Published

      Characterization of a new HLA-G allele encoding a nonconservative amino acid substitution in the alpha3 domain (exon 4) and its relevance to certain complications in pregnancy

      Hviid, T. V., Christiansen, O. B., Johansen, J. K., Hviid, U. R., Lundegaard, C., Møller, C. & Morling, Niels, 2001, In: Immunogenetics. 53, 1, p. 48-53 6 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    24. Published

      Detection of fetal-specific DNA after enrichment for trophoblasts using the monoclonal antibody LK26 in model systems but failure to demonstrate fetal DNA in maternal peripheral blood

      Hviid, Thomas Vauvert F., Sørensen, S. & Morling, Niels, 1999, In: Prenatal Diagnosis. 19, 3, p. 271-278 8 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    25. Published

      Polymorphism in the regulatory region located more than 1.1 kilobases 5' to the start site of transcription, the promoter region, and exon 1 of the HLA-G gene

      Hviid, Thomas Vauvert F., Sørensen, S. & Morling, Niels, 1999, In: Human Immunology. 60, 12, p. 1237-1244 8 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

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