Edinburgh Research Explorer

Dinesh Soares, PhD

(Former employee or visitor)

  1. Article › Research › Peer-reviewed
  2. In silico structure-function analysis of pathological variation in the HSD11B2 gene sequence

    Manning, J., Bailey, M. A., Soares, D. C., Dunbar, D. R. & Mullins, J. J., Aug 2010, In: Physiological Genomics. 42, 3, p. 319-330 12 p.

    Research output: Contribution to journalArticlepeer-review

  3. Large-scale modelling as a route to multiple surface comparisons of the CCP module family

    Soares, D. C., Gerloff, D. L., Syme, N. R., Coulson, A. F. W., Parkinson, J. & Barlow, P. N., 2005, In: Protein engineering, design & selection : PEDS. 18, 8, p. 379-88 10 p.

    Research output: Contribution to journalArticlepeer-review

  4. Molecular evolution of the human SRPX2 gene that causes brain disorders of the Rolandic and Sylvian speech areas

    Royer, B., Soares, D. C., Barlow, P. N., Bontrop, R. E., Roll, P., Robaglia-Schlupp, A., Blancher, A., Levasseur, A., Cau, P., Pontarotti, P. & Szepetowski, P., 2007, In: BMC Genetics. 8, 72, p. 1-9 9 p.

    Research output: Contribution to journalArticlepeer-review

  5. Monoallelic and Biallelic Mutations in MAB21L2 Cause a Spectrum of Major Eye Malformations

    Rainger, J., Pehlivan, D., Johansson, S., Bengani, H., Sanchez-Pulido, L., Williamson, K. A., Ture, M., Barker, H., Rosendahl, K., Spranger, J., Horn, D., Meynert, A., Floyd, J. A. B., Prescott, T., Anderson, C. A., Rainger, J. K., Karaca, E., Gonzaga-Jauregui, C., Jhangiani, S., Muzny, D. M. & 16 others, Seawright, A., Soares, D. C., Kharbanda, M., Murday, V., Finch, A., Gibbs, R. A., van Heyningen, V., Taylor, M. S., Yakut, T., Knappskog, P. M., Hurles, M. E., Ponting, C., Lupski, J. R., Houge, G., FitzPatrick, D. R. & UK10K, 5 Jun 2014, In: American Journal of Human Genetics. 94, 6, p. 915-23 9 p.

    Research output: Contribution to journalArticlepeer-review

  6. NDE1 and NDEL1: Multimerisation, alternate splicing and DISC1 interaction

    Bradshaw, N. J., Christie, S., Soares, D. C., Carlyle, B. C., Porteous, D. J. & Millar, J. K., Jan 2009, In: Neuroscience Letters. 449, 3, p. 228-233 6 p.

    Research output: Contribution to journalArticlepeer-review

  7. NDE1 and NDEL1: twin neurodevelopmental proteins with similar ‘nature’ but different ‘nurture’

    Bradshaw, N., Hennah, W. & Soares, D., Sep 2013, In: BioMolecular Concepts. 4, 5, p. 447-464 18 p.

    Research output: Contribution to journalArticlepeer-review

  8. Novel de novo EEF1A2 missense mutations causing epilepsy and intellectual disability

    DDD study & Abbott, C. M., Jul 2016, In: Molecular Genetics & Genomic Medicine.

    Research output: Contribution to journalArticlepeer-review

  9. Novel pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degeneration

    Stanton, C. M., Borooah, S., Drake, C., Marsh, J. A., Campbell, S., Lennon, A., Soares, D. C., Vallabh, N. A., Sahni, J., Cideciyan, A. V., Dhillon, B., Vitart, V., Jacobson, S. G., Wright, A. F. & Hayward, C., 22 Sep 2017, In: Scientific Reports. 7, 1, p. 12147

    Research output: Contribution to journalArticlepeer-review

  10. Opportunities for new therapies based on the natural regulators of complement activation

    Brook, E., Herbert, A. P., Jenkins, H. T., Soares, D. C. & Barlow, P. N., 2005, In: Annals of the New York Academy of Sciences. 1056, p. 176-188 13 p.

    Research output: Contribution to journalArticlepeer-review

  11. Oxovanadium(IV) Cyclam and Bicyclam Complexes: Potential CXCR4 Receptor Antagonists

    Ross, A., Soares, D. C., Covelli, D., Pannecouque, C., Budd, L., Collins, A., Robertson, N., Parsons, S., De Clercq, E., Kennepohl, P. & Sadler, P. J., 1 Feb 2010, In: Inorganic Chemistry. 49, 3, p. 1122-1132 11 p.

    Research output: Contribution to journalArticlepeer-review