Lucy Wilde

578 total citations
18 papers, 285 citations indexed

About

Lucy Wilde is a scholar working on Cognitive Neuroscience, Genetics and Clinical Psychology. According to data from OpenAlex, Lucy Wilde has authored 18 papers receiving a total of 285 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Cognitive Neuroscience, 11 papers in Genetics and 4 papers in Clinical Psychology. Recurrent topics in Lucy Wilde's work include Autism Spectrum Disorder Research (12 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Family and Disability Support Research (4 papers). Lucy Wilde is often cited by papers focused on Autism Spectrum Disorder Research (12 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Family and Disability Support Research (4 papers). Lucy Wilde collaborates with scholars based in United Kingdom, United States and South Africa. Lucy Wilde's co-authors include Chris Oliver, Joanna Moss, Alice Welham, Petrus J. de Vries, Paolo Curatolo, Romina Moavero, Deborah A. Pearson, Mary Heald, Jane Waite and Dawn Adams and has published in prestigious journals such as Journal of Autism and Developmental Disorders, Behavioural Brain Research and Developmental Medicine & Child Neurology.

In The Last Decade

Lucy Wilde

17 papers receiving 272 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Lucy Wilde United Kingdom 12 144 88 70 62 40 18 285
Griselda Gutierrez United States 5 265 1.8× 275 3.1× 149 2.1× 132 2.1× 37 0.9× 10 514
Ana Florencia Vega-Benedetti Italy 9 98 0.7× 109 1.2× 15 0.2× 128 2.1× 17 0.4× 13 338
Sanae Tanaka Japan 12 37 0.3× 111 1.3× 39 0.6× 46 0.7× 43 1.1× 49 404
Alessia Trovato Italy 6 131 0.9× 164 1.9× 41 0.6× 109 1.8× 82 2.0× 7 486
Alison Schwartz United States 8 75 0.5× 89 1.0× 20 0.3× 54 0.9× 68 1.7× 20 420
Petrus de Vries South Africa 7 49 0.3× 131 1.5× 112 1.6× 38 0.6× 96 2.4× 23 302
Loretta Thomaidis Greece 14 205 1.4× 84 1.0× 14 0.2× 128 2.1× 47 1.2× 40 452
Precilla D’Souza United States 11 114 0.8× 51 0.6× 21 0.3× 121 2.0× 111 2.8× 24 336
Laura Groves United Kingdom 5 166 1.2× 215 2.4× 16 0.2× 79 1.3× 64 1.6× 7 303
Leontine W. ten Hoopen Netherlands 12 186 1.3× 105 1.2× 166 2.4× 130 2.1× 91 2.3× 25 514

Countries citing papers authored by Lucy Wilde

Since Specialization
Citations

This map shows the geographic impact of Lucy Wilde's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Lucy Wilde with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lucy Wilde more than expected).

Fields of papers citing papers by Lucy Wilde

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lucy Wilde. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Lucy Wilde. The network helps show where Lucy Wilde may publish in the future.

Co-authorship network of co-authors of Lucy Wilde

This figure shows the co-authorship network connecting the top 25 collaborators of Lucy Wilde. A scholar is included among the top collaborators of Lucy Wilde based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Lucy Wilde. Lucy Wilde is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Scerif, Gaia, Chris Oliver, Andrew D. Beggs, et al.. (2025). Genetic determinants of longitudinal behavioural trajectories in rare conditions: The case of fragile X syndrome. Behavioural Brain Research. 485. 115527–115527.
2.
Bozhilova, Natali, Alice Welham, Dawn Adams, et al.. (2023). Profiles of autism characteristics in thirteen genetic syndromes: a machine learning approach. Molecular Autism. 14(1). 3–3. 15 indexed citations
3.
Wilde, Lucy, et al.. (2022). Caregivers’ experience of sleep management in Smith–Magenis syndrome: a mixed-methods study. Orphanet Journal of Rare Diseases. 17(1). 35–35. 7 indexed citations
4.
Crawford, Hayley, Gaia Scerif, Lucy Wilde, et al.. (2020). Genetic modifiers in rare disorders: the case of fragile X syndrome. European Journal of Human Genetics. 29(1). 173–183. 11 indexed citations
5.
Oliver, Chris, Dawn Adams, Hayley Crawford, et al.. (2020). The behaviour and wellbeing of children and adults with severe intellectual disability and complex needs: the Be-Well checklist for carers and professionals. Paediatrics and Child Health. 30(12). 416–424. 12 indexed citations
6.
Wilde, Lucy, et al.. (2019). Communication in Angelman syndrome: a scoping review. Developmental Medicine & Child Neurology. 61(11). 1266–1274. 25 indexed citations
7.
Wilde, Lucy, et al.. (2018). The behavioural phenotype of Potocki-Lupski syndrome: a cross-syndrome comparison. Journal of Neurodevelopmental Disorders. 10(1). 2–2. 14 indexed citations
8.
Wilde, Lucy, et al.. (2018). Persistence of self‐injury, aggression and property destruction in children and adults with tuberous sclerosis complex. Journal of Intellectual Disability Research. 62(12). 1058–1071. 8 indexed citations
9.
Vries, Petrus J. de, et al.. (2018). A clinical update on tuberous sclerosis complex‐associated neuropsychiatric disorders (TAND). American Journal of Medical Genetics Part C Seminars in Medical Genetics. 178(3). 309–320. 65 indexed citations
10.
Oliver, Chris, et al.. (2017). Service receipt of adults with rare genetic syndromes who engage in challenging behaviour. Journal of Intellectual & Developmental Disability. 43(3). 308–316. 3 indexed citations
11.
Wilde, Lucy, et al.. (2017). Self-injury and aggression in adults with tuberous sclerosis complex: Frequency, associated person characteristics, and implications for assessment. Research in Developmental Disabilities. 64. 119–130. 9 indexed citations
12.
Wilde, Lucy & Chris Oliver. (2017). Brief Report: Contrasting Profiles of Everyday Executive Functioning in Smith–Magenis Syndrome and Down Syndrome. Journal of Autism and Developmental Disorders. 47(8). 2602–2609. 11 indexed citations
13.
Waite, Jane, John Rose, Lucy Wilde, et al.. (2017). Associations between behaviours that challenge in adults with intellectual disability, parental perceptions and parental mental health. British Journal of Clinical Psychology. 56(4). 408–430. 5 indexed citations
14.
Wilde, Lucy, et al.. (2016). Differences in Social Motivation in Children with Smith–Magenis Syndrome and Down Syndrome. Journal of Autism and Developmental Disorders. 46(6). 2148–2159. 12 indexed citations
15.
Welham, Alice, Johnny King L Lau, Joanna Moss, et al.. (2015). Are Angelman and Prader‐Willi syndromes more similar than we thought? Food‐related behavior problems in Angelman, Cornelia de Lange, Fragile X, Prader‐Willi and 1p36 deletion syndromes. American Journal of Medical Genetics Part A. 167(3). 572–578. 15 indexed citations
16.
Welham, Alice, et al.. (2015). Behavioral characteristics associated with 19p13.2 microdeletions. American Journal of Medical Genetics Part A. 167(10). 2334–2343. 17 indexed citations
17.
Waite, Jane, Mary Heald, Lucy Wilde, et al.. (2014). The importance of understanding the behavioural phenotypes of genetic syndromes associated with intellectual disability. Paediatrics and Child Health. 24(10). 468–472. 37 indexed citations
18.
Wilde, Lucy, et al.. (2013). The nature of social preference and interactions in Smith–Magenis syndrome. Research in Developmental Disabilities. 34(12). 4355–4365. 19 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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