Author

Deborah J. Morris-Rosendahl

Guy's and St Thomas' NHS Foundation TrustORCID 0000-0002-7780-4707Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Approach:statistical model· 3 Research Focus:differential expression· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Abhijit DixitiD· 1 shared Ajoy Sarkar· 1 shared Alicja Wilk· 1 shared Alistair T. PagnamentaiD· 1 shared Amit MandaliD· 1 shared Anca NăstaseiD· 1 shared Andrew Gordon NicholsoniD· 1 shared Andrew R. WoodiD· 1 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetic & Genomic Medicine

Abhijit DixitORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Lung adenocarcinoma WHO histological classes contain distinct immune cell profiles

Anca Năstase, Michael T. Olanipekun, E. Starren, Saffron A.G. Willis‐Owen, Amit Mandal, Clara Domingo‐Sabugo, Deborah J. Morris-Rosendahl, Eric Kian Saik Lim, Liming Liang, Andrew Gordon Nicholson, Miriam F. Moffatt, WO Cookson

The paper identifies distinct immune cell profiles in lung adenocarcinoma histological subtypes and links them to survival-associated transcripts.

medRxiv · Mar 26, 2026 · PreprintGenetic & Genomic Medicine

Utility of genome sequencing and group-enrichment to support splice variant interpretation in Marfan syndrome

Susan Walker, David J. Bunyan, Huw B. Thomas, Yeşim Kesim, Christopher J. Kershaw, John W. Holloway, Htoo A. Wai, Michael J. Day, Cassandra L. Smith, Gareth Hawkes, Andrew R. Wood, Michael N. Weedon, Ed Blair, Stephanie Curtis, Catherine Fielden, , Alistair T. Pagnamenta

The paper identifies non-canonical FBN1 splice variants in undiagnosed Marfan syndrome families using genome sequencing and RNA testing, finding 20 candidate variants with significant enrichment in FTAAD cases.

Genetics in Medicine · Jun 2, 2025Peer-reviewedGenetic & Genomic Medicine

CardioClassifier: demonstrating the power of disease- and gene-specific computational decision support for clinical genome interpretation

Nicola Whiffin, Roddy Walsh, Risha Govind, Matthew Edwards, Mian Ahmad, Xiaolei Zhang, Upasana Tayal, Rachel J. Buchan, William Midwinter, Alicja Wilk, Hanna Najgebauer, Catherine Francis, Sam Wilkinson, Thomas Monk, Laura Brett, , Stuart A. Cook

CardioClassifier is a decision-support tool for inherited cardiac conditions that improves variant interpretation by integrating disease-specific annotations and case data.

Genetics in Medicine · Jan 25, 2018Peer-reviewedGenomics