Author

Spyridon Champeris Tsaniras

KU LeuvenORCID 0000-0002-4960-9314Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Assay:DNA methylation· 2 Research Focus:gene regulatory network inference· 2 Organism:mouse· 2 Approach:statistical model· 2 Approach:experimental assay· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Bernard K. van der VeeriD· 2 shared Colin CustersiD· 2 shared Kian Peng KohiD· 2 shared Qiuying CheniD· 2 shared Richard H. FinnelliD· 2 shared Steven S. GrossiD· 2 shared Wannes Brangers· 2 shared Bernard ThienpontiD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 43 mutual co-author links

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2 shared papersDevelopmental Biology

Bernard K. van der VeerORCID

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2 papers

Recent·Most cited

Developmental BiologybioRxivPreprintMay 27, 2025

Maternal Vitamin C Deficiency and Genetic Risk Factors Contribute to Congenital Defects through Dysregulation of DNA Methylation.

Bernard K. van der Veer, Colin Custers, Wannes Brangers…·Kian Peng Koh

This study shows maternal vitamin C deficiency in mice leads to DNA hypermethylation and congenital defects, suggesting VitC supplementation may prevent birth defects.

2 citations

mouseDNA methylation

𝕏 PostBluesky

Developmental BiologybioRxivPreprintFeb 21, 2024

Epigenetic regulation by TET1 in gene-environmental interactions influencing susceptibility to congenital malformations

Bernard K. van der Veer, Lehua Chen, Spyridon Champeris Tsaniras…·Kian Peng Koh

This study identifies TET1 as a key mediator of gene-environment interactions in congenital malformations, showing how maternal folate status and genetic background influence DNA methylation and NTD susceptibility.

2 citations

mouseDNA methylation

𝕏 PostBluesky