Niels Morling researcher
Morling, Niels.
VIAF ID: 274765776 (Personal)
Permalink: http://viaf.org/viaf/274765776
Preferred Forms
- 100 1 _ ‡a Morling, Niels
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- 100 1 _ ‡a Morling, Niels
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- 100 1 _ ‡a Morling, Niels
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- 100 0 _ ‡a Niels Morling ‡c researcher
4xx's: Alternate Name Forms (4)
Works
Title | Sources |
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In vitro nickel binding to mononuclear cells in peripheral blood | |
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 | |
An investigation of the HUMVWA31A locus in British Caucasians. | |
Iron stores in blood donors evaluated by serum ferritin | |
ISFG: Recommendations on biostatistics in paternity testing | |
ISO 17025 validation of a next-generation sequencing assay for relationship testing | |
Kinship Analysis with Diallelic SNPs - Experiences with the SNPforID Multiplex in an ISO17025 Accreditated Laboratory | |
Lymphocyte transformation in vitro in dermatophytosis | |
Lymphocyte unresponsiveness to mitogens in vitro is not equivalent with severe immunodeficiency | |
Major inter-personal variation in the increase and maximal level of 25-hydroxy vitamin D induced by UVB. | |
Massively parallel pyrosequencing of the mitochondrial genome with the 454 methodology in forensic genetics | |
MDM2 inhibitor nutlin-3a induces apoptosis and senescence in cutaneous T-cell lymphoma: role of p53. | |
Melanocortin-1 receptor, skin cancer and phenotypic characteristics (M-SKIP) project: study design and methods for pooling results of genetic epidemiological studies | |
miR-125b induces cellular senescence in malignant melanoma. | |
A mitochondrial DNA SNP multiplex assigning Caucasians into 36 haplo- and subhaplogroups | |
MLC compatibility, HLA-D and DR typing in cadaver kidney transplantations | |
Modelling allelic drop-outs in STR sequencing data generated by MPS | |
Monozygotic twins discordant for narcolepsy type 1 and multiple sclerosis. | |
Multiplex PCR, amplicon size and hybridization efficiency on the NanoChip electronic microarray. | |
Multiplex PCR and minisequencing of SNPs--a model with 35 Y chromosome SNPs | |
Multiplex PCR detection of GSTM1, GSTT1, and GSTP1 gene variants: simultaneously detecting GSTM1 and GSTT1 gene copy number and the allelic status of the GSTP1 Ile105Val genetic variant | |
Multiplex PCR with minisequencing as an effective high-throughput SNP typing method for formalin-fixed tissue | |
Mutations and/or close relatives? Six case work examples where 49 autosomal SNPs were used as supplementary markers | |
New clues to the evolutionary history of the main European paternal lineage M269: dissection of the Y-SNP S116 in Atlantic Europe and Iberia. | |
New multiplexes for Europe-amendments and clarification of strategic development | |
Next-generation sequencing of 34 genes in sudden unexplained death victims in forensics and in patients with channelopathic cardiac diseases. | |
Next-generation sequencing of multiple individuals per barcoded library by deconvolution of sequenced amplicons using endonuclease fragment analysis | |
NGMSElect™ and Investigator(®) Argus X-12 analysis in population samples from Albania, Iraq, Lithuania, Slovenia, and Turkey. | |
Non-invasive prenatal paternity testing using a standard forensic genetic massively parallel sequencing assay for amplification of human identification SNPs | |
Non-uniform phenotyping of D12S391 resolved by second generation sequencing. | |
On the Bayesian approach to forensic age estimation of living individuals. | |
Paternity testing with VNTR DNA systems. II. Evaluation of 271 cases of disputed paternity with the VNTR systems D2S44, D5S43, D7S21, D7S22, and D12S11 | |
PCR typing of two short tandem repeat (STR) structures upstreams of the human myelin basic protein (MBP) gene; the genetic susceptibility in multiple sclerosis and monosymptomatic idiopathic optic neuritis in Danes | |
Peopling of the North Circumpolar Region – Insights from Y Chromosome STR and SNP Typing of Greenlanders | |
Performance of the SNPforID 52 SNP-plex assay in paternity testing | |
Performance of two 17 locus forensic identification STR kits-Applied Biosystems's AmpFℓSTR® NGMSElect™ and Promega's PowerPlex® ESI17 kits. | |
Pigment genes not skin pigmentation affect UVB-induced vitamin D | |
Pigmentary Markers in Danes--Associations with Quantitative Skin Colour, Nevi Count, Familial Atypical Multiple-Mole, and Melanoma Syndrome | |
Plasma vitamin D-binding protein (GC) factors, immunoglobulin G heavy chain (GM) allotypes and immunoglobulin kappa light chain (KM1) allotype in patients with sarcoidosis and in healthy control subjects | |
Platelet alloimmunization after transfusion. A prospective study in 117 heart surgery patients | |
Post-mortem investigation of young deceased individuals with ischemic heart disease-outcome of supplementary genetic testing for dyslipidemia | |
Post-transfusion purpura (PTP) due to anti-Zwb (-PlA2): the significance of IgG3 antibodies in PTP. | |
Postmortem blood concentrations of R- and S-enantiomers of methadone and EDDP in drug users: influence of co-medication and p-glycoprotein genotype | |
Preface | |
Primed lymphocyte typing in man. | |
Progress in forensic genetics 10 : proceedings of the 20th International ISFG Congress held in Arcachon, France between 9 and 13 September 2003 | |
[Quality of antibodies and somatic hypermutation] | |
Quantification of massively parallel sequencing libraries - a comparative study of eight methods. | |
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). | |
Refining the genetic portrait of Portuguese Roma through X-chromosomal markers | |
Repeated extraction of DNA from FTA cards | |
A report of the 1997, 1998 and 1999 Paternity Testing Workshops of the English Speaking Working Group of the International Society for Forensic Genetics | |
Report of the European DNA profiling group (EDNAP)-an investigation of the hypervariable STR loci ACTBP2, APOAI1 and D11S554 and the compound loci D12S391 and D1S1656 | |
Restriction fragment length polymorphism of two HLA-B-associated transcripts genes in five autoimmune diseases. | |
Restriction fragment polymorphism (RFLP) of a "new" HLA-DP specificity, CDP-HEI. | |
Results for five sets of forensic genetic markers studied in a Greek population sample | |
Results of a collaborative study of the EDNAP group regarding the reproducibility and robustness of the Y-chromosome STRs DYS19, DYS389 I and II, DYS390 and DYS393 in a PCR pentaplex format | |
RNA/DNA co-analysis from human skin and contact traces--results of a sixth collaborative EDNAP exercise. | |
Sequence variants in muscle tissue-related genes may determine the severity of muscle contractures in cerebral palsy | |
Sequence variants of allele 22 and 23 of DYS635 causing different stutter rates. | |
Sequences of microvariant/“off-ladder” STR alleles | |
Sequencing of 231 forensic genetic markers using the MiSeq FGx™ forensic genomics system - an evaluation of the assay and software. | |
Sequencing strategy of mitochondrial HV1 and HV2 DNA with length heteroplasmy | |
Serum 25(OH)D levels after oral vitamin D3 supplementation and UVB exposure correlate | |
Severe hemolysis caused by graft-derived anti-B production after lung transplantation | |
A Simple Method for Validation and Verification of Pipettes Mounted on Automated Liquid Handlers | |
[Single cell sorting of human hematopoietic stem cells--why, how and with what consequences?] | |
Single Nucleotide Polymorphism | |
Skin pigmentation and genetic variants in an admixed Brazilian population of primarily European ancestry | |
A study of the peopling of Greenland using next generation sequencing of complete mitochondrial genomes | |
study on patterns of X-chromosomal diversity | |
Znaczenie czynników prenatalnych, środowiskowych oraz parametrów biochemicznych w kształtowaniu się proporcji i składu ciała oraz tempa rozwoju człowieka na różnych etapach ontogenezy progresywnej = The significance of the prenatal, environmental and biochemical factors in the forming of the body proportion and composition, as well as tempo of human development on the various stages of the progressive ontogenesis |