Author

Melissa Baerenfaenger

Radboud University Medical CenterORCID 0000-0002-2855-924XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Biochemistry· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:proteomics· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Approach:statistical model· 1

Frequent Co-Authors

Amalia Kontochristou· 1 shared Angel AshikoviD· 1 shared Anouk M. RijsiD· 1 shared Dirk J. LefeberiD· 1 shared Eveline C. F. GerretseniD· 1 shared Fokje Zijlstra· 1 shared Geert van den BogaartiD· 1 shared Kai MuruiD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperBiochemistry

Amalia Kontochristou

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Author profile →

2 papers

Recent·Most cited

Affinity Purification: From Interactome Analysis to Targeted Protein Enrichment

Amalia Kontochristou, Nika Šimičić, Anouk M. Rijs, Melissa Baerenfaenger

This study shows how adjusting purification conditions can direct affinity purification outcomes toward either interactome characterization or selective target enrichment for extracellular chaperones.

Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · Sep 28, 2026Peer-reviewedBiochemistry

Congenital disorder of glycosylation caused by starting site-specific variant in syntaxin-5

Peter T. A. Linders, Eveline C. F. Gerretsen, Angel Ashikov, Mari‐Anne Vals, Rinse de Boer, Natalia H. Revelo, Richard Arts, Melissa Baerenfaenger, Fokje Zijlstra, Karin Huijben, Kimiyo Raymond, Kai Muru, Olga Fjodorova, Sander Pajusalu, Katrin Õunap, , Geert van den Bogaart

This study identifies a congenital disorder of glycosylation caused by a missense variant in the second starting methionine of syntaxin-5, leading to loss of the short isoform and multisystem disease.

Nature Communications · Oct 28, 2021Peer-reviewedGenetic & Genomic Medicine