Should Scotland Provide Genome-Wide Sequencing for the Diagnosis of Rare Developmental Disorders?: A Cost-Effectiveness Analysis
Abbott, M., Ryan, M., Hernández, R. A., McKenzie, L., Heidenreich, S., Hocking, L., Clark, C., Ansari, M., Moore, D., Lampe, A., McGowan, R., Berg, J., Miedzybrodzka, Z.
European Journal of Health Economics, vol. 26, no. 3, pp. 503-512
The insula represents a key neurobiological pain hub in psoriatic arthritis
Sunzini, F., Stefanov, K., Al-Wasity, S., Kaplan, C., Schrepf, A., Waller, N., Harte, S., Harris, R., Clauw, D. J., McLean, J., Siebert, S., Goodyear, C. S., Waiter, G. D., Basu, N.
Cap-adjacent 2’-O-ribose methylation of RNA in C. elegans is required for postembryonic growth and germline development in the presence of the decapping exonuclease EOL-1
Clemens, E., Brivo, S., Al-Khafaji, M. I., Eijlers, P., Kurukulasuriya, M. S., Haussmann, I. U., MacLeod, D., Wenzel, M., Muller, B., Soller, M., Pettitt, J.
Statement on long-term cardiovascular consequences of maternal hypertension: Call for urgent action
Casey, H., Delles, C., Wilkinson, I. B., Banerjee, A., Andrews, M., Dawkes, S., Gatenby, K., Green, M., Head, C., Jenner, B., Lees, C., Lewis, P., MacLeod, M. J., McEniery, C., Mustafa, A., Working Group on Postpartum Care of Maternal Hypertension
Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy
Tadros, R., Zheng, S. L., Grace, C., Jordà, P., Francis, C., West, D. M., Jurgens, S. J., Thomson, K. L., Harper, A. R., Ormondroyd, E., Xu, X., Theotokis, P. I., Buchan, R. J., McGurk, K. A., Mazzarotto, F., Boschi, B., Pelo, E., Lee, M., Noseda, M., Varnava, A., Vermeer, A. M., Walsh, R., Amin, A. S., van Slegtenhorst, M. A., Roslin, N., Strug, L. J., Salvi, E., Lanzani, C., Marvao, A. d., Hypergenes InterOmics Collaborators, Roberts, J. D., Tremblay-Gravel, M., Giraldeau, G., Cadrin-Tourigny, J., L L'Allier, P., Garceau, P., Talajic, M., Gagliano Taliun, S. A., Pinto, Y. M., Rakowski, H., Pantazis, A., Bai, W., Baksi, J., Halliday, B. P., Prasad, S. K., Barton, P. J., O'Regan, D. P., Cook, S. A., de Boer, R. A., Christiaans, I., Michels, M., Kramer, C. M., Ho, C. Y., Neubauer, S., HCMR Investigators, Matthews, P. M., Wilde, A. A., Tardif, J., Olivotto, I., Adle, A., Goel, A., Ware, J. S., Bezzina, C. R., Watkins, H., Dawson, D.
Inhibiting disulphide bonding in truncated tau297-391 results in enhanced self-assembly of tau into seed-competent assemblies
Oakley, S. S., Marshall, K. E., Meisl, G., Copsey, A., Maina, M. B., Milton, R., Vorley, T., Storey, J., Harrington, C., Wischik, C., Xue, W., Serpell, L. C.
The genetic architecture of hip shape and its role in the development of hip osteoarthritis and fracture
Faber, B. G., Frysz, M., Zheng, J., Lin, H., Flynn, K. A., Ebsim, R., Saunders, F., Beynon, R., Gregory, J., Aspden, R. M., Harvey, N. C., Lindner, C., Cootes, T., Evans, D. M., Smith, G. D., Gao, X., Wang, S., Kemp, J. P., Tobias, J. H.
Human Molecular Genetics, vol. 34, no. 3, pp. 207-217
