Author

Esther Zeinstra

IsalaORCID 0000-0002-2777-2313Unclaimed 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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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

A.E.J. Slettenaar· 1 shared 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 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

A.E.J. Slettenaar

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1 paper

Recent·Most cited

Genetic & Genomic MedicineInternational Journal of Molecular SciencesPeer-reviewedSep 28, 2022

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

Julia Horjus, Tineke van Mourik-Banda, Marco A. P. Heerings…·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.

14 citations

humanwhole-exome sequencing

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