Author

Dexin Dong

Heidelberg University

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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Biochemistry· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Organism:Drosophila· 1 Approach:experimental assay· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Aidin ForoutaniD· 1 shared Alice S. BrooksiD· 1 shared Alison M. R. CastleiD· 1 shared Alysia Kern LovgreniD· 1 shared Andi Lewis· 1 shared Andreas JanshoffiD· 1 shared Annelies DheedeneiD· 1 shared Annick Raas‐RothschildiD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aidin ForoutanORCID

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Author profile →

2 papers

Recent·Most cited

Membrane curvature regulates Ups1 dependent phosphatidic acid transfer across lipid bilayers

Fereshteh Sadeqi, Dexin Dong, Kai Steffen Stroh, Marian Vache, Jutta Metz, Dietmar Riedel, Andreas Janshoff, Herre Jelger Risselada, Caroline Kolenda, Michael Meinecke

The paper shows Ups1 preferentially binds to positively curved membranes, facilitating phosphatidic acid transfer between mitochondrial membranes.

bioRxiv · Apr 3, 2025 · PreprintBiochemistry

A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene

María del Rocío Pérez Baca, Eva Jacobs, Lies Vantomme, Pontus Leblanc, Elke Bogaert, Annelies Dheedene, Laurenz De Cock, Sadegheh Haghshenas, Aidin Foroutan, Michael A. Levy, Jennifer Kerkhof, Haley McConkey, Chun‐An Chen, Nurit Assia Batzir, Xia Wang, , Dorothea Wand

This paper identifies loss-of-function variants in ZFHX3 as a cause of syndromic intellectual disability and describes its role in chromatin remodeling and DNA methylation.

The American Journal of Human Genetics · Feb 26, 2024Peer-reviewedGenetic & Genomic Medicine