List of works - Denise Syndercombe-Court

"New turns from old STaRs": enhancing the capabilities of forensic short tandem repeat analysis

scientific article published on 16 July 2014

A global analysis of Y-chromosomal haplotype diversity for 23 STR loci

scientific article (publication date: September 2014)

A multiplex assay with 52 single nucleotide polymorphisms for human identification

scientific article

A novel application of real-time RT-LAMP for body fluid identification: using HBB detection as the model

scientific article published on 16 April 2015

An Israeli Arab patient with a de novo TNFRSF1A mutation causing tumor necrosis factor receptor-associated periodic syndrome

scientific article published on January 2002

Brief report: isogenic induced pluripotent stem cell lines from an adult with mosaic down syndrome model accelerated neuronal ageing and neurodegeneration

scientific article published on June 2015

Collaborative EDNAP exercise on the IrisPlex system for DNA-based prediction of human eye colour

scientific article published on 21 April 2014

Comprehensive Analysis of Pan-African Mitochondrial DNA Variation Provides New Insights into Continental Variation and Demography

scientific article

Concordance of the ForenSeq™ system and characterisation of sequence-specific autosomal STR alleles across two major population groups

scientific article published on 4 November 2017

DNA methylation-based age prediction using massively parallel sequencing data and multiple machine learning models

scientific article published on 08 September 2018

DNA methylation-based forensic age prediction using artificial neural networks and next generation sequencing

scientific article

Development and validation of a next generation STR ESS-pentaplex

article

Development of a multiplex PCR assay detecting 52 autosomal SNPs

Development of original donor cell leukemia after successful engraftment from a second donor

scientific article published on December 2007

Differentially methylated embryonal Fyn-associated substrate (EFS) gene as a blood-specific epigenetic marker and its potential application in forensic casework

scientific article

Discovery of potential DNA methylation markers for forensic tissue identification using bisulphite pyrosequencing

scientific article published on 8 September 2016

Evaluation of DNA variants associated with androgenetic alopecia and their potential to predict male pattern baldness

scientific article published on 22 May 2015

Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans

scientific article published on 14 September 2015

Forensic DNA methylation profiling—Potential opportunities and challenges ⬇️

scientific article published on June 28, 2013

Forensic DNA phenotyping legislation cannot be based on "Ideal FDP"-A response to Caliebe, Krawczak and Kayser (2017).

scientific article published on 9 February 2018

Forensic validation of the Genplex SNP typing system—Results of an inter-laboratory study

Forensic validation of the SNPforID 52-plex assay

scientific article published on 06 March 2007

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

scientific article published on 03 September 2018

Haplotype combinations of calpain 10 gene polymorphisms associate with increased risk of impaired glucose tolerance and type 2 diabetes in South Indians

scientific article published on May 2002

Human peripheral blood monocytes express protease receptor-2 and respond to receptor activation by production of IL-6, IL-8, and IL-1{beta}.

scientific article published on 6 July 2005

Increased proteasomal degradation of Bax is a common feature of poor prognosis chronic lymphocytic leukemia

scientific article

Introduction of an single nucleodite polymorphism-based "Major Y-chromosome haplogroup typing kit" suitable for predicting the geographical origin of male lineages

scientific article

Mixture analysis using SWaP™ SNPs and non-biallelic SNPs

Non-myeloablative bone marrow transplantation in an adult with Wiskott-Aldrich syndrome

scientific article published in February 2002

Population specific single nucleotide polymorphisms

Population studies using single nucleotide polymorphisms—how important is detailed sample origin information?

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

scientific article published on 01 June 2001

The EDNAP mitochondrial DNA population database (EMPOP) collaborative exercises: organisation, results and perspectives

scientific article

The peopling of Greenland: further insights from the analysis of genetic diversity using autosomal and X-chromosomal markers

scientific article

The recombination landscape around forensic STRs: Accurate measurement of genetic distances between syntenic STR pairs using HapMap high density SNP data

scientific article

Toward male individualization with rapidly mutating y-chromosomal short tandem repeats

scientific article

Towards broadening Forensic DNA Phenotyping beyond pigmentation: Improving the prediction of head hair shape from DNA

Trinucleotide repeat dynamic mutation identifying susceptibility in familial and sporadic chronic lymphocytic leukaemia.

scientific article

UK and Irish Y-STR population data-A catalogue of variant alleles

scientific article published on 2 March 2018

List of works by Denise Syndercombe-Court

"New turns from old STaRs": enhancing the capabilities of forensic short tandem repeat analysis

A global analysis of Y-chromosomal haplotype diversity for 23 STR loci

A multiplex assay with 52 single nucleotide polymorphisms for human identification

A novel application of real-time RT-LAMP for body fluid identification: using HBB detection as the model

An Israeli Arab patient with a de novo TNFRSF1A mutation causing tumor necrosis factor receptor-associated periodic syndrome

Brief report: isogenic induced pluripotent stem cell lines from an adult with mosaic down syndrome model accelerated neuronal ageing and neurodegeneration

Collaborative EDNAP exercise on the IrisPlex system for DNA-based prediction of human eye colour

Comprehensive Analysis of Pan-African Mitochondrial DNA Variation Provides New Insights into Continental Variation and Demography

Concordance of the ForenSeq™ system and characterisation of sequence-specific autosomal STR alleles across two major population groups

DNA methylation-based age prediction using massively parallel sequencing data and multiple machine learning models

DNA methylation-based forensic age prediction using artificial neural networks and next generation sequencing

Development and validation of a next generation STR ESS-pentaplex

Development of a multiplex PCR assay detecting 52 autosomal SNPs

Development of original donor cell leukemia after successful engraftment from a second donor

Differentially methylated embryonal Fyn-associated substrate (EFS) gene as a blood-specific epigenetic marker and its potential application in forensic casework

Discovery of potential DNA methylation markers for forensic tissue identification using bisulphite pyrosequencing

Evaluation of DNA variants associated with androgenetic alopecia and their potential to predict male pattern baldness

Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans

Forensic DNA methylation profiling—Potential opportunities and challenges ⬇️

Forensic DNA phenotyping legislation cannot be based on "Ideal FDP"-A response to Caliebe, Krawczak and Kayser (2017).

Forensic validation of the Genplex SNP typing system—Results of an inter-laboratory study

Forensic validation of the SNPforID 52-plex assay

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

Haplotype combinations of calpain 10 gene polymorphisms associate with increased risk of impaired glucose tolerance and type 2 diabetes in South Indians

Human peripheral blood monocytes express protease receptor-2 and respond to receptor activation by production of IL-6, IL-8, and IL-1{beta}.

Increased proteasomal degradation of Bax is a common feature of poor prognosis chronic lymphocytic leukemia

Introduction of an single nucleodite polymorphism-based "Major Y-chromosome haplogroup typing kit" suitable for predicting the geographical origin of male lineages

Mixture analysis using SWaP™ SNPs and non-biallelic SNPs

Non-myeloablative bone marrow transplantation in an adult with Wiskott-Aldrich syndrome

Population specific single nucleotide polymorphisms

Population studies using single nucleotide polymorphisms—how important is detailed sample origin information?

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

The EDNAP mitochondrial DNA population database (EMPOP) collaborative exercises: organisation, results and perspectives

The peopling of Greenland: further insights from the analysis of genetic diversity using autosomal and X-chromosomal markers

The recombination landscape around forensic STRs: Accurate measurement of genetic distances between syntenic STR pairs using HapMap high density SNP data

Toward male individualization with rapidly mutating y-chromosomal short tandem repeats

Towards broadening Forensic DNA Phenotyping beyond pigmentation: Improving the prediction of head hair shape from DNA

Trinucleotide repeat dynamic mutation identifying susceptibility in familial and sporadic chronic lymphocytic leukaemia.

UK and Irish Y-STR population data-A catalogue of variant alleles