Items where authors include "Smith, S.C."

Article

Niggl, E. orcid.org/0000-0002-5654-8425, Bouman, A., Briere, L.C. et al. (345 more authors) (2023) HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder. The American Journal of Human Genetics, 110 (8). pp. 1414-1435. ISSN 0002-9297

Robbe, P. orcid.org/0000-0002-0691-1126, Ridout, K.E., Vavoulis, D.V. orcid.org/0000-0002-3984-1507 et al. (142 more authors) (2022) Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features. Nature Genetics, 54. pp. 1675-1689. ISSN 1061-4036

Rowen, D. orcid.org/0000-0003-3018-5109, Mulhern, B., Banerjee, S. et al. (6 more authors) (2015) Comparison of general population, patient, and carer utility values for dementia health states. Medical Decision Making, 35 (1). pp. 68-80. ISSN 0272-989X

Monograph

Mulhern, B., Smith, S.C., Rowen, D. et al. (7 more authors) (2010) Improving the measurement of QALYs in dementia: Developing patient- and carer-reported health state classification systems using Rasch analysis. Discussion Paper. (Unpublished)