Author

Joseph P. Dewulf

Cliniques Universitaires Saint-LucORCID 0000-0001-7223-2706Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1 Systems Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 3 Approach:experimental assay· 2 Organism:human· 2 Assay:proteomics· 2 Approach:statistical model· 2 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Vincent HaufroidiD· 2 shared Andrew D.H. Morgan· 1 shared Anja HolziD· 1 shared Arndt BorkhardtiD· 1 shared Benoît Kabamba· 1 shared Bradley WardiD· 1 shared Cécile LibioulleiD· 1 shared Clara van KarnebeekiD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersGenetics

Vincent HaufroidORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

GeneticsJCI InsightPeer-reviewedJun 2, 2026

A Slc5a6 Deficient Mouse Model Reveals a Metabolically Driven Dilated Cardiomyopathy with Therapeutic Potential for Vitamin-Based Intervention

Millie Fullerton, Lauren C. Phillips, Rachael E. Redgrave…·Helen M. Phillips

This study shows that SLC5A6 deficiency causes dilated cardiomyopathy in mice, which can be prevented by vitamin supplementation, mirroring clinical outcomes in patients.

1 citation

mouseproteomics

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Systems BiologybioRxivPreprintFeb 23, 2024

Deep plasma proteomics with data-independent acquisition: A fastlane towards biomarkers identification.

Bradley Ward, Sébastien Pyr dit Ruys, Jean‐Luc Balligand…·Laure Elens

This study introduces a method combining plasma prefractionation and DIA to improve proteome coverage and depth, enabling robust biomarker identification in a COVID-19 cohort.

2 citations

humanproteomics

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Genetic & Genomic MedicineJournal of Clinical InvestigationPeer-reviewedMay 4, 2021

A human multisystem disorder with autoinflammation, leukoencephalopathy and hepatopathy is caused by mutations in C2orf69

Eva Lausberg, Sebastian Gießelmann, Joseph P. Dewulf…·Florian Kraft

The paper identifies mutations in the C2orf69 gene as the cause of a human multisystem disorder characterized by autoinflammation, leukoencephalopathy, and hepatopathy.

23 citations

humanwhole-exome sequencing

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