Elliott Rees

Cardiff University — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

42h-index11.7kcitations167works2.72yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(74), Genomics and Rare Diseases(69), Genetic Associations and Epidemiology(47), Genetics and Neurodevelopmental Disorders(37), Congenital heart defects research(23)

Publications167 total

W33. ANALYSIS OF WHOLE-GENOME SEQUENCING DATA FOR DE NOVO STRUCTURAL VARIANTS IN 81 BIPOLAR DISORDER TRIOS
European Neuropsychopharmacology·2025
T70. ANALYSIS OF WHOLE GENOME SEQUENCING DATA FOR DE NOVO CODING VARIANTS IN 118 BIPOLAR PROBAND-PARENT TRIOS
European Neuropsychopharmacology·2025
M78. RARE AND COMMON VARIANT CONTRIBUTIONS TO HOSPITAL ADMISSIONS AND SOCIAL AND FUNCTIONAL OUTCOMES IN SCHIZOPHRENIA
European Neuropsychopharmacology·2025
M77. GENETICS TO IMPROVE OUTCOMES IN SCHIZOPHRENIA (GENIOS): A WITHIN-CASE MOLECULAR GENETIC STUDY PROTOCOL
European Neuropsychopharmacology·2025
92. IDENTIFICATION OF NOVEL SCHIZOPHRENIA GENES THROUGH DEEP-LEARNING PRIORITISATION OF DELETERIOUS MISSENSE VARIANTS
European Neuropsychopharmacology·2025
Whole-exome sequencing analysis identifies risk genes for schizophrenia
Nature Communications·2025· 5 citedOpen Access
Large Language Model–Supported Identification of Intellectual Disabilities in Clinical Free-Text Summaries: Mixed Methods Study
JMIR AI·2025Open Access
Copy number variants and their implications for developmental and behavioural problems in cleft lip and/or palate
Human Molecular Genetics·2025· 2 citedOpen Access
The Effect of the Ketogenic Diet on Aggression and Violence in Patients with Severe Mental Illness: A Systematic Review
BJPsych Open·2025Open Access
The role of rare copy number variants in early-onset depression
2025· 1 citedOpen Access
Copy Number Variants and their Implications for Developmental and Behavioural Problems in Cleft Lip and/or Palate
2025Open Access
Clinical Free Text Summaries and LLMs: A Case Study on LLM-supported Identification of Intellectual Disabilities in Clinical Free Text Summaries (Preprint)
2025Open Access
Analysis of exome sequencing data implicates rare coding variants in <i>STAG1</i> and <i>ZNF136</i> in schizophrenia
2024· 1 citedOpen Access
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
UNC Libraries·2024Open Access
Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia
UNC Libraries·2024Open Access
Genetic Implication of Specific Glutamatergic Neurons of the Prefrontal Cortex in the Pathophysiology of Schizophrenia
Biological Psychiatry Global Open Science·2024· 2 citedOpen Access
Characterization of Single Gene Copy Number Variants in Schizophrenia
UNC Libraries·2024Open Access
Genetic and Phenotypic Features of Schizophrenia in the UK Biobank
JAMA Psychiatry·2024· 35 citedOpen Access
Rare variants in pharmacogenes influence clozapine metabolism in individuals with schizophrenia
European Neuropsychopharmacology·2024· 8 citedOpen Access
The Association of Hippocampal Long-Term Potentiation-Induced Gene Expression with Genetic Risk for Psychosis
International Journal of Molecular Sciences·2024Open Access
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Frequent Co-authors

Michael O’Donovan(41), George Kirov(39), Michael J. Owen(35), James Walters(32), Peter Holmans(22), Sophie E. Legge(16), Steven A. McCarroll(16), Antonio F. Pardiñas(14), Valentina Escott‐Price(14), Jennifer L. Moran(14), Andrew Pocklington(12), Alexander Richards(10), Pamela Sklar(8), Kimberley Kendall(8), Shaun Purcell(7), Kimberly D. Chambert(7), Noa Carrera(6), Derek W. Morris(6), Aiden Corvin(6), Stephan Ripke(5)