Miss Elisavet Fotiou

Laboratory Manager

Affiliations:
Links:
ORCID: 0000-0002-9789-2599
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Publications

1 - 5 out of 5Page size: 10
  1. 2019
  2. Published

    IDENTIFICATION OF THE MAJOR GENETIC CONTRIBUTORS TO TETRALOGY OF FALLOT

    Page, D. J., Miossec, M. J., Williams, S. G., Monaghan, R. M., Fotiou, E., Cordell, H. J., Sutcliffe, L., Topf, A., Bourgey, M., Bourque, G., Eveleigh, R., Dunwoodie, S. L., Winlaw, D. S., Bhattacharya, S., Breckpot, J., Devriendt, K., Gewillig, M., Brook, D., Setchfield, K., Bu'Lock, F. A. & 14 others, O'Sullivan, J., Stuart, G., Bezzina, C., Mulder, B. J. M., Postma, A. V., Bentham, J. R., Baron, M., Bhaskar, S. S., Black, G. C., Newman, W. G., Hentges, K. E., Lathrop, M., Santibanez-Koref, M. & Keavney, B. D., May 2019, In: Heart. 105, p. A182-A183

    Research output: Contribution to journal › Meeting Abstract › peer-review

    DOI: 10.1136/heartjnl-2019-BCS.226
  3. Published

    Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot

    Page, D. J., Miossec, M. J., Williams, S. G., Monaghan, R. M., Fotiou, E., Cordell, H. J., Sutcliffe, L., Topf, A., Bourgey, M., Bourque, G., Eveleigh, R., Dunwoodie, S. L., Winlaw, D. S., Bhattacharya, S., Breckpot, J., Devriendt, K., Gewillig, M., Brook, J. D., Setchfield, K. J., Bu'Lock, F. A. & 14 others, O'Sullivan, J., Stuart, G., Bezzina, C. R., Mulder, B. J. M., Postma, A. V., Bentham, J. R., Baron, M., Bhaskar, S. S., Black, G. C., Newman, W. G., Hentges, K. E., Lathrop, G. M., Santibanez-Koref, M. & Keavney, B. D., 15 Feb 2019, In: Circulation research. 124, 4, p. 553-563 11 p.

    Research output: Contribution to journal › Article › peer-review

    DOI: 10.1161/CIRCRESAHA.118.313250
  4. Published

    Integration of Large-Scale Genomic Data Sources With Evolutionary History Reveals Novel Genetic Loci for Congenital Heart Disease

    Fotiou, E., Williams, S., Martin-Geary, A., Robertson, D., Tenin, BSc, MSc, PhD, G., Hentges, K. & Keavney, B., 2019, In: Circulation.

    Research output: Contribution to journal › Article › peer-review

    DOI: 10.1161/CIRCGEN.119.002694
  5. 2018
  6. Published

    Deleterious genetic variants in NOTCH1 are a major contributor to the incidence of non-syndromic Tetralogy of Fallot

    Page, DJ., Miossec, MJ., Williams, SG., Fotiou, E., Monaghan, RM., Cordell, HJ., Sutcliffe, L., Topf, A., Bourgey, M., Bourque, G., Eveleigh, R., Dunwoodie, SL., Winlaw, DS., Keavney, BD. & Newman, W., Apr 2018

    Research output: Other contribution › peer-review

    DOI: 10.1101/300905
  7. Published

    Using zebrafish larval models to study brain injury, locomotor and neuroinflammatory outcomes following intracerebral haemorrhage

    Crilly, S., Njegic, A., Laurie, S. E., Fotiou, E., Hudson, G., Barrington, J., Webb, K., Young, H. L., Badrock, A. P., Hurlstone, A., Rivers-Auty, J., Parry-Jones, A. R., Allan, S. M. & Kasher, P. R., 2018, In: F1000Research. 7, p. 1617

    Research output: Contribution to journal › Article › peer-review

    DOI: 10.12688/f1000research.16473.1 10.12688/f1000research.16473.2

Research Explorer downloads

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Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot

Research output: Contribution to journal › Article › peer-review