Prof D Gareth EvansMD FCRP

Professor in Med Genetics and Cancer Epi

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Publications

  1. 2019
  2. Published

    Incidence of mosaicism in 1055 de novo NF2 cases: Much higher than previous estimates with high utility of Next Generation Sequencing.

    Evans, D. G., Hartley, C., Smith, P. T., King, A. T., Bowers, N. L., Tobi, S., Wallace, A. J., Perry, M., Anup, R., Lloyd, S. K. W., Rutherford, S. A., Hammerbeck-Ward, C., Pathmanaban, O., Stapleton, E., Freeman, S., Kellett, M., Halliday, D., Parry, A., Gair, J. J., Axon, P. R. & 9 othersLaitt, R., Thomas, O., Afridi, S. K., Obholzer, R., Duff, C., Stivaros, S., Vassallo, G., Harkness, E. & Smith, M. J., 5 Jul 2019, In : Genetics in Medicine.

    Research output: Contribution to journalArticle

  3. Accepted/In press

    Should we offer multi-gene testing to all patients with breast cancer: a cost-effectiveness analysis

    Sun, L., Brentnall, A., Patel, S., Buist, D. S. M., Bowles, E. J. A., Evans, D. G., Eccles, D., Hopper, J., Li, S., Southey, M., Duffy, S., Cuzick, J., dos-Santos-Silva, I., Miners, A., Sadique, Z., Yang, L., Legood, R. & Manchanda, R., 21 Jun 2019, (Accepted/In press) In : JAMA oncology.

    Research output: Contribution to journalArticle

  4. Accepted/In press

    Cancer risks by gene, age and gender in 6,350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

    Evans, D. G., Crosbie, E., Hill, J. & et al., 18 Jun 2019, (Accepted/In press) In : Genetics in Medicine.

    Research output: Contribution to journalArticle

  5. Accepted/In press

    The genetic interplay between body mass index, breast size and breast cancer risk: a Mendelian randomization analysis

    Sern Ooi, B. N., Loh, H., Ho, P. J., Milne, R., Giles, G., Gao, C., Kraft, P., John, E. M., Swerdlow, A., Brenner, H., Wu, A. H., Haiman, C., Evans, D. G., Zheng, W., Fasching, P., Castelao, J. E., Kwong, A., Xia, S., Czene, K. & Hall, P., 10 Jun 2019, (Accepted/In press) In : International Journal of Epidemiology.

    Research output: Contribution to journalArticle

  6. Accepted/In press

    Multiple primary malignancies associated with a germline SMARCB1 pathogenic variant

    Eelloo, J., Smith, M. J., Bowers, N., Ealing, J., Hulse, P., Wylie, J., Shenjere, P., Clarke, N., Soh, C., Whitehouse, R., Jones, M., Duff, C. J., Freemont, T. & Evans, D. G., 3 Jun 2019, (Accepted/In press) In : Familial Cancer.

    Research output: Contribution to journalArticle

  7. Accepted/In press

    An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome

    Evans, D. G. & et al., 30 May 2019, (Accepted/In press) In : Genetics in Medicine.

    Research output: Contribution to journalArticle

  8. Accepted/In press

    Lynch Syndrome Screening in Gynecological Cancers: Results of an International Survey with Recommendations for Uniform Reporting Terminology for Mismatch Repair Immunohistochemistry Results

    Ryan, N., Wall, J., Crosbie, E., Arends, M., Bosse, T., Arif, S., Faruqi, A., Frayling, I., Ganesan, R., Hock, Y. L., Mcmahon, R., Manchanda, R., McCluggage, W. G., Mukonoweshuro, P., van Schalkwyk, G., Side, L., Smith, J. H., Tanchel, B., Evans, D. G., Gilks, C. B. & 1 othersSingh, N., 29 May 2019, (Accepted/In press) In : Pathology.

    Research output: Contribution to journalArticle

  9. Accepted/In press

    A case-control evaluation of 143 single nucleotide polymorphisms for breast cancer risk stratification with classical factors and mammographic density

    Brentnall, A. R., Van Veen, E., Harkness, E., Rafiq, S., Byers, H., Astley, S., Sampson, S., Howell, A., Newman, W., Cuzick, J. & Evans, D. G., 28 May 2019, (Accepted/In press) In : Int. J. Cancer.

    Research output: Contribution to journalArticle

  10. Accepted/In press

    Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

    Evans, D. G., Lalloo, F., Woodward, E. & et al., 22 May 2019, (Accepted/In press) In : Human Mutation.

    Research output: Contribution to journalArticle

  11. Accepted/In press

    Epithelial ovarian cancer risk: a review of the current genetic landscape

    Flaum, N., Crosbie, E., Edmondson, R., Smith, M. J. & Evans, D. G., 14 May 2019, (Accepted/In press) In : Clinical Genetics.

    Research output: Contribution to journalArticle

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