Author

Chunxu Han

Technical University of Denmark

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:eQTL / molecular QTL mapping· 1 Research Focus:gene regulatory network inference· 1 Assay:long-read sequencing· 1 Assay:scRNA-seq· 1

Frequent Co-Authors

Kristoffer Vitting‐SeerupiD· 2 shared Dimitrios S. KanakoglouiD· 1 shared Elena Iriondo Delgado· 1 shared Jeppe Malthe Mikkelsen· 1 shared Jeroen GilisiD· 1 shared Lieven ClementiD· 1 shared Peter Wad SackettiD· 1 shared Simone TiberiiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 16 mutual co-author links

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2 shared papersBioinformatics

Kristoffer Vitting‐SeerupORCID

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2 papers

Recent·Most cited

IsoformSwitchAnalyzeR v2: Analysis of Functional Isoform Changes in Long-read and Single-cell Sequencing Data

Chunxu Han, Jeroen Gilis, Elena Iriondo Delgado, Lieven Clement, Kristoffer Vitting‐Seerup

IsoformSwitchAnalyzeR v2 identifies and analyzes functional isoform switches in long-read and single-cell sequencing data, showing disease-relevant changes in Alzheimer's and glioblastoma.

NAR Genomics and Bioinformatics · Jun 27, 2026Peer-reviewedBioinformatics

Beyond the Gene in Genetics: How Isoform-Resolved Analysis Empowers the Study of Both Common and Rare Genetic Variation

Jeppe Malthe Mikkelsen, Dimitrios S. Kanakoglou, Chunxu Han, Peter Wad Sackett, Simone Tiberi, Kristoffer Vitting‐Seerup

This study shows that analyzing genetic variants at the isoform level reveals significant associations with human phenotypes and rare variants, highlighting the importance of isoform-resolved analysis in genetics.

medRxiv · Mar 31, 2025 · PreprintGenetic & Genomic Medicine