Denise Syndercombe-Court
occupation: researcher
Articles 39
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Forensic DNA phenotyping legislation cannot be based on "Ideal FDP"-A response to Caliebe, Krawczak and Kayser (2017).
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UK and Irish Y-STR population data-A catalogue of variant alleles.
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Towards broadening Forensic DNA Phenotyping beyond pigmentation: Improving the prediction of head hair shape from DNA
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Global patterns of STR sequence variation: Sequencing the CEPH human genome diversity panel for 58 forensic STRs using the Illumina ForenSeq DNA Signature Prep Kit
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DNA methylation-based age prediction using massively parallel sequencing data and multiple machine learning models
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DNA methylation-based forensic age prediction using artificial neural networks and next generation sequencing
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Differentially methylated embryonal Fyn-associated substrate (EFS) gene as a blood-specific epigenetic marker and its potential application in forensic casework
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Concordance of the ForenSeq™ system and characterisation of sequence-specific autosomal STR alleles across two major population groups.
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Discovery of potential DNA methylation markers for forensic tissue identification using bisulphite pyrosequencing
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A novel application of real-time RT-LAMP for body fluid identification: using HBB detection as the model
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Evaluation of DNA variants associated with androgenetic alopecia and their potential to predict male pattern baldness
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Brief report: isogenic induced pluripotent stem cell lines from an adult with mosaic down syndrome model accelerated neuronal ageing and neurodegeneration
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Comprehensive Analysis of Pan-African Mitochondrial DNA Variation Provides New Insights into Continental Variation and Demography
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Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans.
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A global analysis of Y-chromosomal haplotype diversity for 23 STR loci
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Toward male individualization with rapidly mutating y-chromosomal short tandem repeats
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The peopling of Greenland: further insights from the analysis of genetic diversity using autosomal and X-chromosomal markers
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"New turns from old STaRs": enhancing the capabilities of forensic short tandem repeat analysis
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Collaborative EDNAP exercise on the IrisPlex system for DNA-based prediction of human eye colour.
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Forensic DNA methylation profiling--potential opportunities and challenges
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The recombination landscape around forensic STRs: Accurate measurement of genetic distances between syntenic STR pairs using HapMap high density SNP data
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Development and validation of a next generation STR ESS-pentaplex
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Forensic validation of the Genplex SNP typing system—Results of an inter-laboratory study
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Development of original donor cell leukemia after successful engraftment from a second donor
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Increased proteasomal degradation of Bax is a common feature of poor prognosis chronic lymphocytic leukemia.
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Forensic validation of the SNPforID 52-plex assay
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A multiplex assay with 52 single nucleotide polymorphisms for human identification
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Trinucleotide repeat dynamic mutation identifying susceptibility in familial and sporadic chronic lymphocytic leukaemia.
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Development of a multiplex PCR assay detecting 52 autosomal SNPs
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Mixture analysis using SWaP™ SNPs and non-biallelic SNPs
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Introduction of an single nucleodite polymorphism-based "Major Y-chromosome haplogroup typing kit" suitable for predicting the geographical origin of male lineages
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Human peripheral blood monocytes express protease receptor-2 and respond to receptor activation by production of IL-6, IL-8, and IL-1{beta}.
Human - wd:Q66360623