about
X-chromosome SNP analyses in 11 human Mediterranean populations show a high overall genetic homogeneity except in North-west Africans (Moroccans)Evaluation of Forensic DNA Traces When Propositions of Interest Relate to Activities: Analysis and Discussion of Recurrent ConcernsHigh frequencies of Y chromosome lineages characterized by E3b1, DYS19-11, DYS392-12 in Somali malesGenetic sub-structure in western Mediterranean populations revealed by 12 Y-chromosome STR lociTyping of 48 autosomal SNPs and amelogenin with GenPlex SNP genotyping system in forensic geneticsPeopling of the North Circumpolar Region – Insights from Y Chromosome STR and SNP Typing of GreenlandersA global analysis of Y-chromosomal haplotype diversity for 23 STR lociDetection 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.Data reduction in HLA-D typing with the primed lymphocyte typing (PLT) technique. the normalized median response (NMR).Population and forensic data for three sets of forensic genetic markers in four ethnic groups from Iran: Persians, Lurs, Kurds and Azeris.Statistical modelling of Ion PGM HID STR 10-plex MPS data.Determination of cis/trans phase of variations in the MC1R gene with allele-specific PCR and single base extension.Post-transfusion purpura (PTP) due to anti-Zwb (-PlA2): the significance of IgG3 antibodies in PTP.Genetic determinants of hair and eye colours in the Scottish and Danish populations.Increased prevalence of late stage T cell activation antigen (VLA-1) in active juvenile chronic arthritismiR-125b induces cellular senescence in malignant melanoma.Increasing the reference populations for the 55 AISNP panel: the need and benefitsHigh-throughput sequencing of core STR loci for forensic genetic investigations using the Roche Genome Sequencer FLX platform.Analysis of matches and partial-matches in a Danish STR data set.Toward male individualization with rapidly mutating y-chromosomal short tandem repeats.Multiplex PCR and minisequencing of SNPs--a model with 35 Y chromosome SNPs.Melanocortin-1 receptor, skin cancer and phenotypic characteristics (M-SKIP) project: study design and methods for pooling results of genetic epidemiological studiesY-chromosome STR haplotypes in Somalis.Introduction of an single nucleodite polymorphism-based "Major Y-chromosome haplogroup typing kit" suitable for predicting the geographical origin of male lineages.A multiplex assay with 52 single nucleotide polymorphisms for human identification.Carrier frequency of a nonsense mutation in the adenosine deaminase (ADA) gene implies a high incidence of ADA-deficient severe combined immunodeficiency (SCID) in Somalia and a single, common haplotype indicates common ancestry.A study of the peopling of Greenland using next generation sequencing of complete mitochondrial genomes.Founder effect in the Horn of Africa for an insulin receptor mutation that may impair receptor recyclingEvaluation of the iPLEX® Sample ID Plus Panel designed for the Sequenom MassARRAY® system. A SNP typing assay developed for human identification and sample tracking based on the SNPforID panel.The peopling of Greenland: further insights from the analysis of genetic diversity using autosomal and X-chromosomal markers.Brittle cornea syndrome associated with a missense mutation in the zinc-finger 469 gene.Building a forensic ancestry panel from the ground up: The EUROFORGEN Global AIM-SNP set.Massively parallel pyrosequencing of the mitochondrial genome with the 454 methodology in forensic genetics.Next-generation sequencing of multiple individuals per barcoded library by deconvolution of sequenced amplicons using endonuclease fragment analysis.Next-generation sequencing of 34 genes in sudden unexplained death victims in forensics and in patients with channelopathic cardiac diseases.Evaluation of DNA variants associated with androgenetic alopecia and their potential to predict male pattern baldness.Forensic ancestry analysis with two capillary electrophoresis ancestry informative marker (AIM) panels: Results of a collaborative EDNAP exercise.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.Pigmentary Markers in Danes--Associations with Quantitative Skin Colour, Nevi Count, Familial Atypical Multiple-Mole, and Melanoma SyndromeKinship Analysis with Diallelic SNPs - Experiences with the SNPforID Multiplex in an ISO17025 Accreditated Laboratory.
P50
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P50
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Niels Morling
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Niels Morling
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Niels Morling
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Niels Morling
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Niels Morling
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Niels Morling
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Niels Morling
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Niels Morling
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Niels Morling
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2000-01-01T00:00:00Z
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