Jenkins, V. Farewell, V. May, S. Catt, S. Matthews, L. Shilling, V. Dickson, J. Simcock, R. Fallowfield, L. Do drugs offering only PFS maintain quality of life sufficiently from a patient’s perspective? Results from AVALPROFS (Assessing the ‘VALue’ to patients of PROgression Free Survival) study. Support Care Cancer (2018). https://doi.org/10.1007/s00520-018-4273-3
Shilling, V. Starkings R, Jenkins, V. Fallowfield, L. The pervasive nature of uncertainty—a qualitative study of patients with advanced cancer and their informal caregivers. Journal of Cancer Survivorship. 2017, 1-14. doi: 10.1007/s11764-017-0628-x.
Catt, S. Starkings, R. Shilling, V. Fallowfield, L. Patient-reported outcome measures of the impact of cancer on patients’ everyday lives: a systematic review. Journal of Cancer Survivorship. 2017, 11(2), 211-232.
Fallowfield, L. Catt, S. May, S. Matthews, L. Shilling, V. Simcock, R. Westwell, S. Jenkins, V. Therapeutic aims of drugs offering only Progression Free Survival are misunderstood by patients, and oncologists may be overly optimistic about likely benefits. Supportive Care in Cancer. 2017; 25(1): 237–244.
Madden L, Shilling V, Woolfall K, Sowden E, Smyth R.L, Williamson P.R, Young B. Questioning assent: how are children's views included as families make decisions about clinical trials? Child: Care, Health and Development. 2016; 42(6), 900-908.
Shilling V, Matthews L, Jenkins V, Fallowfield L. Patient reported outcome measures for cancer caregivers: A systematic review. Quality of Life Research, 2016 25(8), 1859-1876.
Morris C, Janssens A, Shilling V, Allard A, Fellowes A, Tomlinson R, Williams J, Thompson Coon J, Rogers M, Beresford B, Green C, Jenkinson C, Tennant A, Logan S. Meaningful health outcomes for paediatric neurodisability: Stakeholder prioritisation and appropriateness of patient reported outcome measures. Health and Quality of Life Outcomes 2015, 13:87.
Shilling V, Bailey S, Logan S, Morris C. Peer support for parents of disabled children part 1: perceived outcomes of a one-to-one service, a qualitative study. Child: Care Health and Development 2015; 41(4) 537-546.
Shilling V, Bailey S, Logan S, Morris C. Peer support for parents of disabled children part 2: how organizational and process factors influenced shared experience in a one-to-one service, a qualitative study. Child: Care, Health and Development. 2015;41(4):537-546.
Morris C, Janssens A, Allard A, Thompson Coon J, Shilling V, Tomlinson R et al. Informing the NHS Outcomes Framework: evaluating meaningful health outcomes for children with neurodisability using multiple methods including systematic review, qualitative research, Delphi survey and consensus meeting. Health Services and Delivery Research. 2014;2(15):1-224.
Shilling V, Morris C, Thompson-Coon J, Ukoumunne O, Rogers M, Logan S. Peer support for parents of children with chronic disabling conditions: a systematic review of quantitative and qualitative studies. Dev Med Child Neurol. 2013;55(7):602-609.