Niels Morling
Professor, Visiting professor
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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
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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. 199-216Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Research
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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 journal › Journal article › Research › peer-review
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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. 947–948Research output: Contribution to journal › Comment/debate › Research
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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
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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 journal › Journal article › Research › peer-review
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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. 437–441Research output: Contribution to journal › Journal article › Research › peer-review
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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
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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
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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
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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. 536-545Research output: Contribution to journal › Journal article › Research › peer-review
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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 journal › Journal article › Research › peer-review
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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, , Jul 2016, In: Forensic Science International: Genetics. 23, p. 178-189 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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 journal › Journal article › Research › peer-review
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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 journal › Journal article › Research › peer-review
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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
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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 proceeding › Book chapter › Research › peer-review
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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. 817–822Research output: Contribution to journal › Journal article › Research › peer-review
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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. 1797–1802Research output: Contribution to journal › Journal article › Research › peer-review
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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 journal › Journal article › Research › peer-review
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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
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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 journal › Review › Research › peer-review
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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 journal › Journal article › Research › peer-review
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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. 698-704Research output: Contribution to journal › Journal article › Research › peer-review
ID: 6624
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A simple method for validation and verification of pipettes mounted on automated liquid handlers
Research output: Contribution to conference › Poster › Research
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4283
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Biomek®-3000 and GenPlex in Forensic Genetics
Research output: Contribution to conference › Poster › Research
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4118
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Evaluation of the Ion Torrent™ HID SNP 169-plex: A SNP typing assay developed for human identification by second generation sequencing
Research output: Contribution to journal › Journal article › Research › peer-review
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