Author

Angel Ashikov

Radboud University Medical CenterORCID 0000-0001-9679-7955Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Organism:human· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

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 Karin Huijben· 1 shared Katrin ÕunapiD· 1 shared Kimiyo RaymondiD· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Dirk J. LefeberORCID

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1 paper

Recent·Most cited

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