Resultats de la cerca - Denise Syndercombe‐Court

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  1. 1
    Forensic genealogy: Some serious concerns

    Forensic genealogy: Some serious concerns per Denise Syndercombe Court

    Publicat 2018
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  2. 2
    Mitochondrial DNA in forensic use

    Mitochondrial DNA in forensic use per Denise Syndercombe Court

    Publicat 2021
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  3. 3
    The Y chromosome and its use in forensic DNA analysis

    The Y chromosome and its use in forensic DNA analysis per Denise Syndercombe Court

    Publicat 2021
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  4. 4
    Discovery of potential DNA methylation markers for forensic tissue identification using bisulphite pyrosequencing

    Discovery of potential DNA methylation markers for forensic tissue identification using bisulphite pyrosequencing per Athina Vidaki, Federica Giangasparo, Denise Syndercombe Court

    Publicat 2016
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  5. 5
    Increased platelet aggregate formation in patients with chronic airflow obstruction and hypoxaemia.

    Increased platelet aggregate formation in patients with chronic airflow obstruction and hypoxaemia. per JA Wedzicha, Denise Syndercombe‐Court, Kai Chah Tan

    Publicat 1991
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  6. 6
    Forensic identity SNPs: Characterisation of flanking region variation using massively parallel sequencing

    Forensic identity SNPs: Characterisation of flanking region variation using massively parallel sequencing per Lucinda Davenport, Laurence Devesse, Denise Syndercombe Court, David Ballard

    Publicat 2023
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  7. 7
    DNA methylation-based forensic age prediction using artificial neural networks and next generation sequencing

    DNA methylation-based forensic age prediction using artificial neural networks and next generation sequencing per Athina Vidaki, David Ballard, Anastasia Aliferi, Thomas H. Miller, Leon Barron, Denise Syndercombe Court

    Publicat 2017
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  8. 8
    Concordance of the ForenSeq™ system and characterisation of sequence-specific autosomal STR alleles across two major population groups

    Concordance of the ForenSeq™ system and characterisation of sequence-specific autosomal STR alleles across two major population groups per Laurence Devesse, David Ballard, Lucinda Davenport, Immy Riethorst, Gabriella Mason-Buck, Denise Syndercombe Court

    Publicat 2017
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  9. 9
    DNA methylation-based age prediction using massively parallel sequencing data and multiple machine learning models

    DNA methylation-based age prediction using massively parallel sequencing data and multiple machine learning models per Anastasia Aliferi, David Ballard, Matteo D. Gallidabino, Helen Thurtle, Leon Barron, Denise Syndercombe Court

    Publicat 2018
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  10. 10
    Combining current knowledge on DNA methylation-based age estimation towards the development of a superior forensic DNA intelligence tool

    Combining current knowledge on DNA methylation-based age estimation towards the development of a superior forensic DNA intelligence tool per Anastasia Aliferi, Sudha Sundaram, David Ballard, A. Freire-Aradas, Christopher Phillips, M.V. Lareu, Denise Syndercombe Court

    Publicat 2021
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  11. 11
    Human peripheral blood monocytes express protease receptor-2 and respond to receptor activation by production of IL-6, IL-8, and IL-1β

    Human peripheral blood monocytes express protease receptor-2 and respond to receptor activation by production of IL-6, IL-8, and IL-1β per Ulrika Johansson, Charlotte Lawson, Michael Dabare, Denise Syndercombe‐Court, Adrian C. Newland, Gareth L. Howells, Marion G. Macey

    Publicat 2005
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  12. 12
    The peopling of Greenland: further insights from the analysis of genetic diversity using autosomal and X-chromosomal markers

    The peopling of Greenland: further insights from the analysis of genetic diversity using autosomal and X-chromosomal markers per Vânia Pereira, Carmen Tomàs, Juan José Martínez Sánchez, Denise Syndercombe‐Court, António Amorim, Leonor Gusmão, Maria João Prata, Niels Morling

    Publicat 2014
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  13. 13
    Haplotype Combinations of Calpain 10 Gene Polymorphisms Associate With Increased Risk of Impaired Glucose Tolerance and Type 2 Diabetes in South Indians

    Haplotype Combinations of Calpain 10 Gene Polymorphisms Associate With Increased Risk of Impaired Glucose Tolerance and Type 2 Diabetes in South Indians per Paul G. Cassell, Alan E. Jackson, Bernard V. North, Julie Evans, Denise Syndercombe‐Court, Christopher Phillips, Ambady Ramachandran, Chamukuttan Snehalatha, Susan Gelding, Shanti Vijayaravaghan, David Curtis, G. A. Hitman

    Publicat 2002
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  14. 14
    A common epigenetic clock from childhood to old age

    A common epigenetic clock from childhood to old age per A. Freire-Aradas, Lorena Girón-Santamaría, Ana Mosquera‐Miguel, A. Ambroa-Conde, Christopher Phillips, Magdalena Cal, Antonio Gómez‐Tato, José Antonio Álvarez‐Dios, Ewelina Pośpiech, Anastasia Aliferi, Denise Syndercombe Court, Wojciech Branicki, M.V. Lareu

    Publicat 2022
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  15. 15
    A collaborative European exercise on mRNA-based body fluid/skin typing and interpretation of DNA and RNA results

    A collaborative European exercise on mRNA-based body fluid/skin typing and interpretation of DNA and RNA results per M. van den Berge, Ángel Carracedo, Iva Gomes, Eleanor A. M. Graham, Cordula Haas, B. Hjort, P. Hoff-Olsen, Olalla Maroñas, B. Mevåg, Niels Morling, Harald Niederstätter, Walther Parson, Peter M. Schneider, Denise Syndercombe Court, Athina Vidaki, Titia Sijen

    Publicat 2014
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  16. 16
    Evaluation of DNA Variants Associated with Androgenetic Alopecia and Their Potential to Predict Male Pattern Baldness

    Evaluation of DNA Variants Associated with Androgenetic Alopecia and Their Potential to Predict Male Pattern Baldness per Magdalena Marcińska, Ewelina Pośpiech, Sarah Abidi, Jeppe Dyrberg Andersen, M. van den Berge, Ángel Carracedo, Mayra Eduardoff, Anna Marczakiewicz-Lustig, Niels Morling, Titia Sijen, Małgorzata Skowron, Jens Söchtig, Denise Syndercombe‐Court, Natalie Weiler, Peter M. Schneider, David Ballard, Claus Børsting, Walther Parson, Christopher Phillips, Wojciech Branicki

    Publicat 2015
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  17. 17
    Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™

    Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™ per Mayra Eduardoff, T.E. Gross, Carla Santos, M. de la Puente, David Ballard, Christina Strobl, Claus Børsting, Niels Morling, L. Fusco, Christian Hussing, Balázs Egyed, L. Souto, J. Uacyisrael, Denise Syndercombe Court, Ángel Carracedo, M.V. Lareu, Peter M. Schneider, Walther Parson, Christopher Phillips, Walther Parson, Christopher Phillips

    Publicat 2016
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  18. 18
    A Comparison of Forensic Age Prediction Models Using Data From Four DNA Methylation Technologies

    A Comparison of Forensic Age Prediction Models Using Data From Four DNA Methylation Technologies per A. Freire-Aradas, Ewelina Pośpiech, Anastasia Aliferi, Lorena Girón-Santamaría, Ana Mosquera‐Miguel, Aleksandra Pisarek, A. Ambroa-Conde, Christopher Phillips, María Ángeles Casares De Cal, Antonio Gómez‐Tato, Magdalena Spólnicka, Anna Woźniak, José Antonio Álvarez‐Dios, David Ballard, Denise Syndercombe Court, Wojciech Branicki, Ángel Carracedo, M.V. Lareu

    Publicat 2020
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  19. 19
    Brief Report: Isogenic Induced Pluripotent Stem Cell Lines From an Adult With Mosaic Down Syndrome Model Accelerated Neuronal Ageing and Neurodegeneration

    Brief Report: Isogenic Induced Pluripotent Stem Cell Lines From an Adult With Mosaic Down Syndrome Model Accelerated Neuronal Ageing and Neurodegeneration per Aoife Murray, Audrey Letourneau, Claudia Canzonetta, Elisavet Stathaki, Stefania Gimelli, Frédérique Sloan‐Béna, Robert Abrehart, Pollyanna Goh, Shuhui Lim, Chiara Baldo, Franca Dagna‐Bricarelli, Saad Hannan, Martin Mortensen, David Ballard, Denise Syndercombe Court, Noemi Fusaki, Mamoru Hasegawa, Trevor G. Smart, Cleo L. Bishop, Stylianos E. Antonarakis, Jürgen Groet, Dean Nižetić

    Publicat 2015
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  20. 20
    Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans

    Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans per Ewelina Pośpiech, Joanna Karłowska-Pik, Magdalena Marcińska, Sarah Abidi, Jeppe Dyrberg Andersen, M. van den Berge, Ángel Carracedo, Mayra Eduardoff, A. Freire-Aradas, Niels Morling, Titia Sijen, Małgorzata Skowron, Jens Söchtig, Denise Syndercombe‐Court, Natalie Weiler, Peter M. Schneider, David Ballard, Claus Børsting, Walther Parson, Christopher Phillips, Wojciech Branicki

    Publicat 2015
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