Author

Giuseppe Floris

KU LeuvenORCID 0000-0003-2391-5425Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:deconvolution· 1 Assay:DNA methylation· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

ABCTB Investigators· 1 shared Adinda BateniD· 1 shared Adrienne L. MoreyiD· 1 shared Alexander FossåiD· 1 shared Alison M. DunningiD· 1 shared An CoosemansiD· 1 shared Angela CoxiD· 1 shared Angela R Brooks-WilsoniD· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetics

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2 papers

Recent·Most cited

Genetic & Genomic MedicineBioinformaticsPeer-reviewedAug 22, 2024

MetDecode: methylation-based deconvolution of cell-free DNA for non-invasive multi-cancer typing

Antoine Passemiers, Stefania Tuveri, Dhanya Sudhakaran…·Joris Robert Vermeesch

MetDecode uses methylation patterns to estimate tumor proportion and identify tissue origin in cell-free DNA samples from cancer patients.

15 citations

humanDNA methylation

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GeneticsBreast Cancer ResearchPeer-reviewedJan 4, 2022

Common variants in breast cancer risk loci predispose to distinct tumor subtypes

Thomas U. Ahearn, Haoyu Zhang, Kyriaki Michailidou…·Peter T. Simpson

The paper identifies breast cancer risk variants associated with tumor subtypes and shows their differential effects on luminal and non-luminal subtypes.

33 citations

humanGWAS summary statistics

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