Author

Eva M. M. Strijbis

Amsterdam NeuroscienceORCID 0000-0001-6705-5864Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 3

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:fine-mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alex SalazariD· 2 shared Daniel Álvarez Sirvent· 2 shared Henne H. HolstegeiD· 2 shared Marc HulsmaniD· 2 shared Natasja M. van SchooriD· 2 shared Niccoló TesiiD· 2 shared Sven J. van der LeeiD· 2 shared A.E.J. Slettenaar· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Alex SalazarORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintOct 9, 2026

Fine-mapping HLA-II haplotypes in Alzheimer's disease and healthy longevity reveals distinct associations with microglial HLA-II load and neuropathology

Daniel Álvarez Sirvent, Maruelle C. Luimes, Niccoló Tesi…·Henne H. Holstege

DOI 10.64898/2026.08.24.26361177

humanGWAS summary statistics

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Genetic & Genomic MedicinemedRxivPreprintMar 30, 2025

Cognitively healthy centenarians are characterized by lower frequencies of six disease-associated HLA alleles

Daniel Álvarez Sirvent, Niccoló Tesi, Marc Hulsman…·Henne H. Holstege

The paper identifies six HLA alleles associated with reduced likelihood of becoming a cognitively healthy centenarian, revealing pleiotropic effects on disease susceptibility and longevity.

DOI 10.1101/2025.03.30.25324899

humanstatistical model

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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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