Author

A.E.J. Slettenaar

Medisch Spectrum Twente

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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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Anne J. Jansen· 1 shared Barbara FrankeiD· 1 shared Brigit A. de JongiD· 1 shared Dorothea J. Heersema· 1 shared Erwin L.J. Hoogervorst· 1 shared Esther ZeinstraiD· 1 shared Eva M. M. StrijbisiD· 1 shared Geert PoelmansiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Anne J. Jansen

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1 paper

Recent·Most cited

Whole exome sequencing in multi-incident families identifies novel candidate genes for multiple sclerosis

Julia Horjus, Tineke van Mourik-Banda, Marco A. P. Heerings, Marina Hakobjan, Ward De Witte, Dorothea J. Heersema, Anne J. Jansen, Eva M. M. Strijbis, Brigit A. de Jong, A.E.J. Slettenaar, Esther Zeinstra, Erwin L.J. Hoogervorst, Barbara Franke, W. Kruijer, Peter Joseph Jongen, , Geert Poelmans

The paper uses whole exome sequencing in multi-incident families to identify rare genetic variants associated with multiple sclerosis, finding 12 candidate genes involved in myelination and auto-immunity.

International Journal of Molecular Sciences · Sep 28, 2022Peer-reviewedGenetic & Genomic Medicine