Mrs Helen Byers

Research Assistant

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Publications

  1. 2017
  2. Published

    A synonymous variant in TREX1 is associated with systemic sclerosis and severe digital ischaemia

    Hughes, M., Little, J., Herrick, A., Pushpakom, S., Byers, H., Worthington, J. & Newman, W., 2017, In: Scandinavian Journal of Rheumatology. 46, 1, p. 77-78 2 p.

    Research output: Contribution to journalLetterpeer-review

  3. 2016
  4. Published

    Sensitivity of BRCA1/2 testing in high-risk breast/ovarian/male breast cancer families: little contribution of comprehensive RNA/NGS panel testing

    Byers, H., Yvonne Wallis, Van Veen, E., Lalloo, F., Kim Reay, Smith, P., Wallace, A. J., Bowers, N., Newman, W. & Evans, D., Nov 2016, In: European Journal of Human Genetics. 24, 11, p. 1591-1597 7 p.

    Research output: Contribution to journalArticlepeer-review

  5. Accepted/In press

    Use of multiple Single Nucleotide Polymorphism (SNP) testing to predict breast cancer risk in a familial screening clinic

    Evans, D., Brentnall, A. R., Byers, H., Harkness, E., Stavrinos, P., Howell, A., Newman, W. & Cuzick, J., 28 Oct 2016, (Accepted/In press) In: Journal of Medical Genetics.

    Research output: Contribution to journalArticlepeer-review

  6. Published

    Association of a promoter polymorphism in FSHR with ovarian reserve and response to ovarian stimulation in women undergoing assisted reproductive treatment

    Tohlob, D., Abo Hashem, E., Ghareeb, N., Ghanem, M., Elfarahaty, R., Byers, H., Pemberton, P., Roberts, S. A., Newman, W. G. & Mohiyiddeen, L., Sep 2016, In: Reproductive BioMedicine Online. 33, 3, p. 391-7 7 p.

    Research output: Contribution to journalArticlepeer-review

  7. Published

    Relationship of ZNF423 and CTSO with breast cancer risk in two randomised tamoxifen prevention trials

    Brentnall, A. R., Cuzick, J., Byers, H., Segal, C., Reuter, C., Detre, S., Sestak, I., Howell, A., Powles, T. J., Newman, W. G. & Dowsett, M., 1 Aug 2016, In: Breast Cancer Research and Treatment. 158, 3, p. 591-596 6 p.

    Research output: Contribution to journalArticlepeer-review

  8. Published

    AMH type II receptor and AMH gene polymorphisms are not associated with ovarian reserve, response, or outcomes in ovarian stimulation

    Cerra, C., Newman, W. G., Tohlob, D., Byers, H., Horne, G., Roberts, S. A. & Mohiyiddeen, L., Aug 2016, In: Journal of Assisted Reproduction and Genetics. 33, 8, p. 1085-91 7 p.

    Research output: Contribution to journalArticlepeer-review

  9. Published

    DMRTA2 (DMRT5) is mutated in a novel cortical brain malformation

    Urquhart, J. E., Beaman, G., Byers, H., Roberts, N. A., Chervinsky, E., O'Sullivan, J., Pilz, D., Fry, A., Williams, S. G., Bhaskar, S. S., Khayat, M., Simanovsky, N., Shachar, I. B., Shalev, S. A. & Newman, W. G., Jun 2016, In: Clinical Genetics. 89, 6, p. 724-7 4 p.

    Research output: Contribution to journalArticlepeer-review

  10. Published

    The Contribution of Whole Gene Deletions and Large Rearrangements to the Mutation Spectrum in Inherited Tumor Predisposing Syndromes.

    Smith, M. J., Urquhart, J., Harkness, E., Miles, E. K., Bowers, N. L., Byers, H., Bulman, M., Gokhale, C., Wallace, A. J., Newman, W. & Evans, G., Mar 2016, In: Human Mutation. 37, 3, p. 250–256

    Research output: Contribution to journalArticlepeer-review

  11. 2015
  12. Published

    Identification of a novel familial FGF16 mutation in two cases of MF4.

    Jones, B., Byers, H., Watson, S. & Newman, W., Jul 2015, In: Clinical dysmorphology. 23, 3

    Research output: Contribution to journalArticlepeer-review

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