Author

Marcin Karpiński

AstraZeneca (United Kingdom)

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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Genetic & Genomic Medicine· 3

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:gene regulatory network inference· 2 Approach:machine learning (classical)· 2 Assay:whole-genome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Research Focus:GWAS / association mapping· 1

Frequent Co-Authors

Dimitrios VitsiosiD· 3 shared Quanli WangiD· 3 shared Slavé PetrovskiiD· 3 shared Fengyuan HuiD· 2 shared Jonathan MitchelliD· 2 shared Rafael Campos· 2 shared Rahul Sharma· 2 shared Ryan S. DhindsaiD· 2 shared

Activity by Year

2023-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Dimitrios VitsiosORCID

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3 papers

Recent·Most cited

The Impact of Non-coding G-quadruplex Variants on Human Traits and Disease Susceptibility

Rahul Sharma, Fengyuan Hu, Xiaoyin Li, Rafael Campos, Kousik Kundu, Santosh S. Atanur, Marcin Karpiński, Sebastian Wasilewski, Stewart MacArthur, Dimitrios Vitsios, Ryan S. Dhindsa, Ilias Georgakopoulos‐Soares, Oliver S. Burren, Slavé Petrovski, Anthony M. Mustoe, , Xueqing Zoe Zou

The paper identifies non-coding G-quadruplex variants associated with plasma proteins and clinical traits, showing stronger signals when considering G4 stability impacts and integrating with protein-truncating variants.

medRxiv · Jun 1, 2026 · PreprintGenetic & Genomic Medicine

Clonal haematopoiesis without identified genetic drivers: insights from analyses of 407,512 individuals

Sean Wen, Rafael Campos, Marcin Karpiński, Rahul Sharma, Veselin Manojlović, Sri V. V. Deevi, Sean O’Dell, Xiaoyin Li, Fengyuan Hu, Jared O’Connell, Abhishek Nag, Karyn Mégy, Stewart MacArthur, Sebastian Wasilewski, Xueqing Zoe Zou, , Jonathan Mitchell

This study identifies 26,963 individuals with clonal haematopoiesis without known genetic drivers (CH-UD) and finds strong genetic and phenotypic links to other forms of clonal haematopoiesis, implicating TCL1A and epigenetic changes.

medRxiv · May 21, 2026 · PreprintGenetic & Genomic Medicine

Applying Machine Learning on UK Biobank biomarker data empowers case-control discovery yield

Manik Garg, Marcin Karpiński, Dorota Matelska, Lawrence Middleton, Jonathan Mitchell, Amanda O’Neill, Quanli Wang, Andrew Robert Harper, Ryan S. Dhindsa, Slavé Petrovski, Dimitrios Vitsios

The paper uses machine learning to identify undiagnosed cases in UK Biobank data, improving gene-disease associations and discovering novel relationships.

medRxiv · Oct 10, 2023 · PreprintGenetic & Genomic Medicine