Author

Cameron James Watson

King's College LondonORCID 0000-0003-2346-4636Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Assay:electronic health records· 1 Research Focus:gene regulatory network inference· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Cathryn M. LewisiD· 2 shared Oliver PainiD· 2 shared 23andMe Research Institute· 1 shared Abigail L. PfaffiD· 1 shared AGDS Research Team· 1 shared Alfredo IacoangeliiD· 1 shared AMBER Research Team· 1 shared Brittany L MitchelliD· 1 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 26 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Cathryn M. LewisORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintNov 12, 2026

Genetic architecture and polygenic prediction of self-reported response to selective serotonin reuptake inhibitors in individuals with depression: a genome-wide meta-analysis

Michelle Kamp, Madhurbain Singh, Ke Hu…·Cathryn M Lewis

This study identifies genetic factors associated with self-reported SSRI response in depression using genome-wide meta-analysis and polygenic scores, highlighting GABAergic and glutamatergic pathways.

DOI 10.64898/2026.11.11.26367161

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintAug 4, 2026

The Neuropsychiatry of 22q11.2 Deletion Syndrome: An Electronic Health Records Study.

Cameron James Watson, Maria Rogdaki, Katharine Lynch-Kelly…·Thomas Arthur Pollak

This study uses electronic health records to analyze the neuropsychiatric phenotype of 22q11.2 deletion syndrome at scale, revealing high prevalence of neurodevelopmental and psychiatric disorders.

DOI 10.64898/2026.08.03.26359320

humanelectronic health records

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Genetic & Genomic MedicinemedRxivPreprintMar 20, 2025

Using polygenic and transcriptional risk scores to investigate psychiatric and cognitive symptoms in Parkinson's disease

Lachlan Gilchrist, Oliver Pain, Heather Marriott…·Petroula Proitsi

This study uses polygenic and transcriptional risk scores to analyze psychiatric and cognitive symptoms in Parkinson's disease, finding distinct associations between genetic and transcriptional risks and symptom progression.

DOI 10.1101/2025.03.20.25324166

humanbulk RNA-seq

𝕏 PostBluesky