Currently browsing: Items authored or edited by Lucy Wilde

Oliver, Chris; Ellis, Katherine; Agar, Georgie; Bissell, Stacey; Chung, Justin Cheuk Yin; Crawford, Hayley; Pearson, Effie; Wade, Kelly; Waite, Jane; Allen, Debbie; Deeprose, Lucy; Edwards, Georgina; Jenner, Lauren; Kearney, Breanne; Shelley, Lauren; Smith, Kayla; Trower, Hayley; Adams, Dawn; Daniel, Louise; Groves, Laura; Heald, Mary; Moss, Jo; Richards, Caroline; Royston, Rachel; Tarver, Joanne; Welham, Alice; Wilde, Lucy and Woodcock, Kate (2022). Distress and challenging behavior in people with profound or severe intellectual disability and complex needs: Assessment of causes and evaluation of intervention outcomes. In: Esbensen, Anna J. and Schworer, Emily K. eds. International Review of Research in Developmental Disabilities, Volume 62. Academic Press, pp. 109–189.

Bozhilova, Natali; Welham, Alice; Adams, Dawn; Bissell, Stacey; Bruining, Hilgo; Crawford, Hayley; Eden, Kate; Nelson, Lisa; Oliver, Christopher; Powis, Laurie; Richards, Caroline; Waite, Jane; Watson, Peter; Rhys, Hefin; Wilde, Lucy; Woodcock, Kate and Moss, Joanna (2023). Profiles of autism characteristics in thirteen genetic syndromes: a machine learning approach. Molecular Autism, 14(1), article no. 3.

• Download Published Version (PDF / 2MB)

Agar, Georgie and (2022). Caregivers’ experience of sleep management in Smith–Magenis syndrome: a mixed-methods study. Orphanet Journal of Rare Diseases, 17, article no. 35.

• Download Supplementary Material (PDF / 425kB)
• Download Published Version (PDF / 1MB)

Crawford, Hayley; Scerif, Gaia; Wilde, Lucy; Beggs, Andrew; Stockton, Joanne; Sandhu, Pria; Shelley, Lauren; Oliver, Chris and McCleery, Joseph (2021). Genetic modifiers in rare disorders: the case of fragile X syndrome. European Journal of Human Genetics, 29 pp. 173–183.

• Download Published Version (PDF / 646kB)