Lista de obras - Denise Syndercombe-Court

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

artículo científico

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

artículo científico publicado en 2014

A multiplex assay with 52 single nucleotide polymorphisms for human identification

artículo científico publicado en 2006

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

artículo científico publicado en 2015

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

artículo científico publicado en 2002

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

artículo científico publicado en 2015

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

artículo científico publicado en 2014

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

artículo científico publicado en 2015

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

artículo científico publicado en 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

artículo científico publicado en 2017

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

artículo científico publicado en 2007

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

artículo científico publicado en 2017

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

artículo científico publicado en 2016

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

artículo científico publicado en 2015

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

artículo científico publicado en 2015

Forensic DNA methylation profiling—Potential opportunities and challenges ⬇️

artículo científico publicado el 28 de junio de 2013

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

artículo científico publicado en 2018

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

Forensic validation of the SNPforID 52-plex assay

artículo científico publicado en 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

artículo científico publicado en 2018

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

artículo científico publicado en 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}.

artículo científico publicado en 2005

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

artículo científico publicado en 2007

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

artículo científico publicado en 2005

Mixture analysis using SWaP™ SNPs and non-biallelic SNPs

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

artículo científico publicado en 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

artículo científico publicado en 2001

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

artículo científico publicado en 2004

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

artículo científico publicado en 2014

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

artículo científico publicado en 2011

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

artículo científico publicado en 2014

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.

artículo científico publicado en 2006

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

artículo científico publicado en 2018

Lista de obras de 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