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  • 2023

    A qualitative exploration of the older prisoner health and social care assessment and plan (OHSCAP) in a “dangerous” prison system

    Forsyth, K., Daker-White, G., Archer-Power, L., Senior, J., Edge, D., Webb, R. T. & Shaw, J., 13 May 2023, (E-pub ahead of print) In: The Journal of Forensic Psychiatry & Psychology. 34, 2, p. 275-293 19 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
  • 2021

    Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy

    Genomics England Research Consortium, Parry, D. A., Martin, C. A., Greene, P., Marsh, J. A., Ambrose, J. C., Arumugam, P., Baple, E. L., Bleda, M., Boardman-Pretty, F., Boissiere, J. M., Boustred, C. R., Brittain, H., Caulfield, M. J., Chan, G. C., Craig, C. E. H., Daugherty, L. C., de Burca, A., Devereau, A., Elgar, G., & 78 othersFoulger, R. E., Fowler, T., Furió-Tarí, P., Giess, A., Hackett, J. M., Halai, D., Hamblin, A., Henderson, S., Holman, J. E., Hubbard, T. J. B., Ibáñez, K., Jackson, R., Jones, L. J., Kasperaviciute, D., Kayikci, M., Kousathanas, A., Lahnstein, L., Lawson, K., Leigh, S. E. A., Leong, I. U. S., Lopez, F. J., Maleady-Crowe, F., Mason, J., McDonagh, E. M., Moutsianas, L., Mueller, M., Murugaesu, N., Need, A. C., Odhams, C. A., Orioli, A., Patch, C., Perez-Gil, D., Pereira, M. B., Polychronopoulos, D., Pullinger, J., Rahim, T., Rendon, A., Riesgo-Ferreiro, P., Rogers, T., Ryten, M., Savage, K., Sawant, K., Scott, R. H., Siddiq, A., Sieghart, A., Smedley, D., Smith, K. R., Smith, S. C., Sosinsky, A., Spooner, W., Stevens, H. E., Stuckey, A., Sultana, R., Tanguy, M., Thomas, E. R. A., Thompson, S. R., Tregidgo, C., Tucci, A., Walsh, E., Watters, S. A., Welland, M. J., Williams, E., Witkowska, K., Wood, S. M., Zarowiecki, M., Blyth, M., Cox, H., Donnelly, D., Greenhalgh, L., Greville-Heygate, S., Harrison, V., Lachlan, K., McKenna, C., Quigley, A. J., Rea, G., Robertson, L., Suri, M. & Jackson, A. P., 29 Jun 2021, In: Genetics in medicine : official journal of the American College of Medical Genetics. 23, 3, p. 408-414 7 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
  • 2020

    PRIM1 deficiency causes a distinctive primordial dwarfism syndrome

    The Scottish Genomes Partnership, Parry, D. A., Tamayo-Orrego, L., Carroll, P., Marsh, J. A., Greene, P., Murina, O., Uggenti, C., Leitch, A., Káposzta, R., Merő, G., Nagy, A., Orlik, B., Kovács-Pászthy, B., Quigley, A. J., Riszter, M., Rankin, J., Reijns, M. A. M., Szakszon, K. & Jackson, A. P., 15 Oct 2020, In: Genes & development. 34, 21-22, p. 1520-1533 14 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access