Lucy Wilde
Milton Keynes, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 14 publications
Genetic determinants of longitudinal behavioural trajectories in rare conditions: The case of fragile X syndrome.
Journal: Behavioural brain research
Published: September 18, 2024
Profiles of autism characteristics in thirteen genetic syndromes: a machine learning approach.
Journal: Molecular autism
Published: September 20, 2022
Caregivers' experience of sleep management in Smith-Magenis syndrome: a mixed-methods study.
Journal: Orphanet journal of rare diseases
Published: October 01, 2021
Genetic modifiers in rare disorders: the case of fragile X syndrome.
Journal: European journal of human genetics : EJHG
Published: January 08, 2020
Communication in Angelman syndrome: a scoping review.
Journal: Developmental medicine and child neurology
Published: March 27, 2019
A clinical update on tuberous sclerosis complex-associated neuropsychiatric disorders (TAND).
Journal: American journal of medical genetics. Part C, Seminars in medical genetics
Published: May 06, 2018
Brief Report: Contrasting Profiles of Everyday Executive Functioning in Smith-Magenis Syndrome and Down Syndrome.
Journal: Journal of autism and developmental disorders
Published: May 14, 2017
The behavioural phenotype of Potocki-Lupski syndrome: a cross-syndrome comparison.
Journal: Journal of neurodevelopmental disorders
Published: November 17, 2016
Self-injury and aggression in adults with tuberous sclerosis complex: Frequency, associated person characteristics, and implications for assessment.
Journal: Research in developmental disabilities
Published: October 11, 2016
Associations between behaviours that challenge in adults with intellectual disability, parental perceptions and parental mental health.
Journal: The British journal of clinical psychology
Published: July 05, 2016
Differences in Social Motivation in Children with Smith-Magenis Syndrome and Down Syndrome.
Journal: Journal of autism and developmental disorders
Published: March 18, 2016
Behavioral characteristics associated with 19p13.2 microdeletions.
Journal: American journal of medical genetics. Part A
Published: June 10, 2014
Last Updated: 09/26/2026