Author

David Kavanagh

Newcastle UniversityORCID 0000-0003-4718-0072Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

David Kavanagh1 paper

Biology Disciplines

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Cell Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Approach:experimental assay· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aarno V. PalotieiD· 1 shared Aaron R. WoleniD· 1 shared Abraham ReichenbergiD· 1 shared Agata L. Rozanska· 1 shared Alexander L. RichardsiD· 1 shared Andrew J. ChessiD· 1 shared Andrew J. PocklingtoniD· 1 shared Aniket ShettyiD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aarno V. PalotieORCID

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2 papers

Recent·Most cited

Cell BiologybioRxivPreprintJun 19, 2026

Oxidative Stress Susceptibility, Complement Dysregulation, and Metabolic Reprogramming in CFH Y402H Patient-Derived Choriocapillaris Endothelial Cells

Agata L. Rozanska, Jasenka Guduric‐Fuchs, Varun Pathak…·Majlinda Lako

This study shows that the CFH Y402H variant makes choriocapillaris endothelial cells more susceptible to oxidative stress and complement dysregulation, linking these factors to AMD pathogenesis.

DOI 10.64898/2026.06.18.733111

humanbulk RNA-seq

𝕏 PostBluesky

Genetic & Genomic MedicineCell GenomicsPeer-reviewedJul 6, 2023

Schizophrenia-associated somatic copy number variants from 12,834 cases reveal contribution to risk and recurrent, isoform-specific NRXN1 disruptions

Eduardo A. Maury, Maxwell A. Sherman, Giulio Genovese…·Brandon K. Wormley

This study identifies somatic copy number variants (sCNVs) in schizophrenia cases, revealing their contribution to risk and specific NRXN1 disruptions.

47 citationstop 2%

humanwhole-genome sequencing

𝕏 PostBluesky