Author

Richard J.E. Skipworth

Edinburgh Royal InfirmaryORCID 0000-0003-1349-9229Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cancer Biology· 1 Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Ahmad Miremadi· 2 shared Andrew David BeggsiD· 2 shared Andrew Davies· 2 shared Andrew HindmarshiD· 2 shared Anna M. GrabowskaiD· 2 shared Barbara Nutzinger· 2 shared Bhaskar KumariD· 2 shared Charles CrichtoniD· 2 shared

Activity by Year

2018-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersCancer Biology

Ahmad Miremadi

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3 papers

Recent·Most cited

Cancer BiologyNature CancerPeer-reviewedJan 3, 2025

Context-dependent effects of CDKN2A and other 9p21 gene losses during the evolution of oesophageal cancer

Piyali Ganguli, Celia De Los Angeles Colomina Basanta, Amelia Acha‐Sagredo…·Jo Spencer

The paper investigates how CDKN2A and other 9p21 gene losses influence oesophageal cancer progression, finding context-dependent effects on survival and immune infiltration.

28 citationstop 1%

humanbulk RNA-seq

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Genetic & Genomic MedicinemedRxivPreprintJul 24, 2023

A genome wide association study to identify germline variants associated with cancer-associated cachexia - a preliminary analysis

Ashok Narasimhan, Mahalakshmi Kumaran, Ioannis Gioulbasanis…·Sambasivarao Damaraju

This study conducts a GWAS to identify germline CNVs associated with weight loss in cancer cachexia, finding enriched pathways and overlapping genes with skeletal muscle expression.

1 citation

humanGWAS summary statistics

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GenomicsbioRxivPreprintAug 19, 2018

Low-cost and clinically applicable copy number profiling using repeat DNA

Sam Abujudeh, Sebastian S. Zeki, MCV van Lanschot…·Richard Calvin Turkington

The paper introduces conliga, a method for inferring high-resolution SCNA profiles from a low-cost and simple assay, addressing the need for affordable SCNA analysis in clinical settings.

2 citations

whole-genome sequencingstatistical model

𝕏 PostBluesky