Assessment of the effectiveness of the EUROFORGEN NAME and Precision ID Ancestry panel markers for ancestry investigations von Truelsen, D., Tvedebrink, T., Mogensen, H. S., Farzad, M. S., Shan, M. A., Morling, N., Pereira, V., Børsting, C.

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Non-uniform phenotyping of D12S391 resolved by second generation sequencing von Dalsgaard, S, Rockenbauer, E, Buchard, A, Mogensen, H.S, Frank-Hansen, R, Børsting, C, Morling, N

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NGMSElect™ and Investigator® Argus X-12 analysis in population samples from Albania, Iraq, Lithuania, Slovenia, and Turkey von Poulsen, L, Tomas, C, Drobnič, K, Ivanova, V, Mogensen, H.S, Kondili, A, Miniati, P, Bunokiene, D, Jankauskiene, J, Pereira, V, Morling, N

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Concordance study and population frequencies for 16 autosomal STRs analyzed with PowerPlex® ESI 17 and AmpFℓSTR® NGM SElect™ in Somalis, Danes and Greenlanders von Tomas, C, Mogensen, H.S, Friis, S.L, Hallenberg, C, Stene, M.C, Morling, N

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Amyloid β-peptide(25-35) changes [Ca2+] in hippocampal neurons von Mogensen, Helle S, Beatty, Diane M, Morris, Stephen J, Jorgensen, Ole Steen

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NMDAR1 mRNA expression and glutamate receptor stimulated increase in cytosolic calcium concentration in rat and mouse cerebellar granule cells von Mogensen, H.S., Jørgensen, O.S.

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Update of aims population data and test with the genogeographer admixture module von Mogensen, H.S., Tvedebrink, T., Pereira, V., Eriksen, P.S., Morling, N.

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Risk of fetal loss associated with invasive testing following combined first‐trimester screening for Down syndrome: a national cohort of 147 987 singleton pregnancies von Wulff, C. B., Gerds, T. A., Rode, L., Ekelund, C. K., Petersen, O. B., Tabor, A., Zingenberg, H., Jørgensen, F. S., Sundberg, K., Shalmi, A. ‐C., Näslund Thagaard, I., Skibsted, L., Fabricius, M., Sperling, L., Mogensen, H., Ibsen, M., Brendstrup, L., Petersen, O. B., Jensen, H. S., Kamper, C. H., Vase, L., Østergaard, M., Sørensen, A., Størup, B.

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Probabilistic SNP genotyping at low DNA concentrations von Nielsen, M.B., Andersen, M.M., Eriksen, P.S., Mogensen, H.S., Morling, N.

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Optimization of the collection and analysis of touch DNA traces von Haase, H.T., Mogensen, H.S., Petersen, C.B., Petersen, J.F., Holmer, A., Børsting, C., Pereira, V.

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The survival of cultured mouse cerebellar granule cells is not dependent on elevated potassium‐ion concentration von Mogensen, Helle S., Hack, Nicola, Balázs, Robert, Jørgensen, Ole Steen

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Test of Investigator ESSPLEX SE QS with quality sensors von Mogensen, H.S., Frank-Hansen, R., Morling, N.

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Typing of two Middle Eastern populations with the Precision ID Ancestry Panel von Truelsen, D.M., Farzad, M.S., Mogensen, H.S., Pereira, V., Tvedebrink, T., Børsting, C., Morling, N.

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Testing of the Illumina® ForenSeq™ kit von Hussing, C., Børsting, C., Mogensen, H.S., Morling, N.

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Comparison of techniques for quantification of next-generation sequencing libraries von Hussing, C., Kampmann, M.L., Mogensen, H.S., Børsting, C., Morling, N.

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Analysis of artificially degraded DNA using STRs and SNPs—results of a collaborative European (EDNAP) exercise von Dixon, L.A., Dobbins, A.E., Pulker, H.K., Butler, J.M., Vallone, P.M., Coble, M.D., Parson, W., Berger, B., Grubwieser, P., Mogensen, H.S., Morling, N., Nielsen, K., Sanchez, J.J., Petkovski, E., Carracedo, A., Sanchez-Diz, P., Ramos-Luis, E., Briōn, M., Irwin, J.A., Just, R.S., Loreille, O., Parsons, T.J., Syndercombe-Court, D., Schmitter, H., Stradmann-Bellinghausen, B., Bender, K., Gill, P.

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Template preparation of AmpliSeq™ libraries using the Ion Chef von Mogensen, H.S., Børsting, C., Morling, N.

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Performance of the RapidHIT™200 von Mogensen, H.S., Frank-Hansen, R., Simonsen, B.T., Morling, N.

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AMPA receptor subunit mRNAs and intracellular [Ca2+] in cultured mouse and rat cerebellar granule cells von Mogensen, Helle S., Jørgensen, Ole Steen

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First‐trimester screening for trisomy 21 in Denmark: implications for detection and birth rates of trisomy 18 and trisomy 13 von Ekelund, C. K., Petersen, O. B., Skibsted, L., Kjaergaard, S., Vogel, I., Tabor, A.

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