Anna Mantzouratou

Dr Anna Mantzouratou

  • Lecturer In Human Genetics
  • Christchurch House C213, Talbot Campus, Fern Barrow, Poole, BH12 5BB
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Journal Articles

  • Mania, A., Mantzouratou, A., Delhanty, J.D.A., Baio, G., Serhal, P. and Sengupta, S.B., 2014. Telomere length in human blastocysts. Reproductive BioMedicine Online, 28 (5), 624-637.
  • Xanthopoulou, L., Ghevaria, H., Mantzouratou, A., Serhal, P., Doshi, A. and Delhanty, J.D.A., 2012. Chromosome breakage in human preimplantation embryos from carriers of structural chromosomal abnormalities in relation to fragile sites, maternal age, and poor sperm factors. Cytogenetic and Genome Research, 136 (1), 21-29.
  • Xanthopoulou, L., Mantzouratou, A., Mania, A., Ghevaria, H., Ghebo, C., Serhal, P. and Delhanty, J.D.A., 2011. When is old too old for preimplantation genetic diagnosis for reciprocal translocations? Prenatal Diagnosis, 31 (10), 1002-1006.
  • Xanthopoulou, L., Delhanty, J.D.A., Mania, A., Mamas, T., Serhal, P., Sengupta, S.B. and Mantzouratou, A., 2011. The nature and origin of binucleate cells in human preimplantation embryos: Relevance to placental mesenchymal dysplasia. Reproductive BioMedicine Online, 22 (4), 362-370.
  • Mantzouratou, A. and Delhanty, J.D.A., 2011. Aneuploidy in the human cleavage stage embryo. Cytogenetic and Genome Research, 133 (2-4), 141-148.
  • Xanthopoulou, L., Mantzouratou, A., Mania, A., Cawood, S., Doshi, A., Ranieri, D.M. and Delhanty, J.D., 2010. Male and female meiotic behaviour of an intrachromosomal insertion determined by preimplantation genetic diagnosis. Molecular Cytogenetics, 3 (1).
  • Mantzouratou, A., Mania, A., Apergi, M., Laver, S., Serhal, P. and Delhanty, J., 2009. Meiotic and mitotic behaviour of a ring/deleted chromosome 22 in human embryos determined by preimplantation genetic diagnosis for a maternal carrier. Molecular Cytogenetics, 2 (1).
  • Finch, K.A., Fonseka, G., Ioannou, D., Hickson, N., Barclay, Z., Chatzimeletiou, K., Mantzouratou, A., Handyside, A., Delhanty, J. and Griffin, D.K., 2008. Nuclear organisation in totipotent human nuclei and its relationship to chromosomal abnormality. Journal of Cell Science, 121 (5), 655-663.
  • Mantzouratou, A. et al., 2007. Variable aneuploidy mechanisms in embryos from couples with poor reproductive histories undergoing preimplantation genetic screening. Human Reproduction, 22 (7), 1844-1853.
  • Simopoulou, M., Mantzouratou, A. et al., 2003. Preimplantation genetic diagnosis of chromosome abnormalities: Implications from the outcome for couples with chromosomal rearrangements. Prenatal Diagnosis, 23 (8), 652-662.

Conferences

  • Xanthopoulou, L., Mantzouratou, A., Mania, A., Ghevaria, H., Ghebo, C., Serhal, P. and Delhanty, J.D.A., 2011. When is old too old for preimplantation genetic diagnosis for reciprocal translocations? I106-I107.
  • Xanthopoulou, L., Ghevaria, H., Mantzouratou, A., Serhal, P., Doshi, A. and Delhanty, J.D., 2010. Fragile sites and chromosome breakage in embryos from carriers of structural chromosomal abnormalities determined by preimplantation genetic diagnosis. I325-I326.
  • Xanthopoulou, L., Mantzouratou, A., Mania, A., Harper, J. and Delhanty, J.D.A., 2007. The nature and origin of binucleate cells in human preimplantation embryos. I209.
  • Mania, A., Mantzouratou, A., Fragouli, E., Xanthopoulou, L., Tashkandi, S., Serhal, P., Harper, J. and Delhanty, J.D.A., 2007. Cytogenetic analysis of embryos from couples carrying balanced chromosomal translocations undergoing preimplantation genetic diagnosis. I92-I93.
  • Mantzouratou, A. et al., 2007. Evidence of different mechanisms of aneuploidy in embryos from couples with distinct indications for preimplantation genetic screening. I210.
  • Finch, K., Hickson, N., Barclay, Z., Chatzimeletiou, K., Handyside, A., Thornhill, A., Mantzouratou, A., Joy, D., Bridget, J. and Griffin, D., 2007. Genome organisation in spermatogenesis and preimplantation human development: Relationships to male infertility and aneuploidy. 82.
  • Delhanty, J.D.A., Fragouli, E., Mantzouratou, A., Wells, D., Serhal, P. and Faed, M.J.W., 2007. Comprehensive analysis of human oocytes and 1st polar bodies by comparative genomic hybridisation (CGH). 146.
  • Mantzouratou, A., Mania, A., Xanthopolou, L., Tashkandi, S., Doshi, A., Laver, S., Serhal, P., Ranieri, D.M., Harper, J.C. and Delhanty, J.D.A., 2007. Evidence for variable aneuploidy mechanisms in embryos from couples with distinct indications for preimplantaion genetic screening (PGS). 231.
  • Mania, A., Mantzouratou, A. and Delhanty, J., 2006. Telomere length analysis and Aneuploidy screening in human pre-implantation embryos using a quantitative FISH approach. S91.
  • Delhanty, J.D.A., Mantzouratou, A., Mania, A., Fordham, K., Doshi, A. and Serhal, P., 2006. Outcome of preimplantation aneuploidy screening for high risk couples. S111.

PhD Students

Profile of Teaching PG

  • Nutrition and the Brain

Profile of Teaching UG

  • Advanced Topics in Genetics Level 6
  • Pathophysiology Level 6
  • Introduction to Molecular Genetics Level 4
  • Biological Research skills

External Responsibilities

  • University College London, Visiting Lecturer (2018-)
  • UCL, Postgraduate Supervisor for Project Development (2018-)

Internal Responsibilities

  • Member, Clinical Governance Group
  • Member, Human Tissue License Working Group
  • Member, Phase 1 Christchurch House Lab development group
  • Member, Green Impact Group
  • Panel member, Teach BU assessment panel

Qualifications

  • MSc in Bioinformatics (University of Athens, 2021)
  • Postgraduate Certificate in Sequence analysis and Genomics (Johns Hopkins University, Baltimore, USA, 2018)
  • FHEA in Fellowship of Higher Education Academy (Higher Eucation Academy, 2018)
  • PhD in Human Preimplantation embryo and oocyte genetics (University College London, University of London, 2008)
  • MSc in Prenatal Genetics and Foetal Medicine (University College London, University of London, 2001)
  • BSc (Hons) in Genetics (Queen Mary University, University of London, 2000)

Memberships

  • Genetics Society, Local Ambassador for BU (2018-), http://www.genetics.org.uk/
  • Association of Clinical Genomic Science, Member (2017-),
  • British Society for Genetic Medicine, Member (2017-),
  • Clinical Genetics Society, Member (2017-),
  • European Society of Human Genetics, Member (2017-),
  • European Society of Human Reproduction and Embryology, Member (2017-),
The data on this page was last updated at 04:10 on April 3, 2020.