Author

Anke A. Dijkstra

Amsterdam NeuroscienceORCID 0000-0003-2160-587XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Research Focus:fine-mapping· 1 Approach:statistical model· 1

Frequent Co-Authors

Alain NdayisabaiD· 1 shared Alan P. BoyleiD· 1 shared Alex SalazariD· 1 shared Amy Krans· 1 shared Andrea CorteseiD· 1 shared Andrea Suárez· 1 shared Betty Marije TijmsiD· 1 shared Camille MummiD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperNeuroscience

Alain NdayisabaORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintFeb 2, 2025

Fine-mapping reveals four TMEM106B haplotypes associated with neurodegenerative risk and preserved cognition at extreme age

Alex Salazar, Niccoló Tesi, Lydian Knoop…·Henne H. Holstege

DOI 10.1101/2025.02.02.25321330

humanwhole-genome sequencing

𝕏 PostBluesky

NeuroscienceScience AdvancesPeer-reviewedSep 4, 2024

AAGGG repeat expansions trigger RFC1-independent synaptic dysregulation in human CANVAS Neurons

Connor J. Maltby, Amy Krans, Samantha Grudzien…·Peter K. Todd

This study shows that AAGGG repeat expansions cause synaptic defects in CANVAS neurons independently of RFC1, with phenotypes corrected by repeat deletion.

23 citationstop 5%

humanbulk RNA-seq

𝕏 PostBluesky