Author

Nicol Cornelia Voermans

Radboud University Medical CenterORCID 0000-0002-5837-7295Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:proteomics· 1

Frequent Co-Authors

Alex R. HastieiD· 1 shared Alexander HoischeniD· 1 shared Alice Flynn Ford· 1 shared Alide A. TielemaniD· 1 shared Anahit MehrabyaniD· 1 shared Andrzej KochańskiiD· 1 shared Andy Wing Chun PangiD· 1 shared Bart P. G. H. van der SandeniD· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperGenomics

Alex R. HastieORCID

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintApr 19, 2024

Optical genome mapping enables accurate repeat expansion testing

Bart P. G. H. van der Sanden, Kornelia Neveling, Syukri Shukor…·Alexander Hoischen

This study evaluates optical genome mapping (OGM) for detecting STR repeat expansions and somatic instability, showing high accuracy and efficiency compared to current methods.

2 citations

humanexperimental assay

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Genetic & Genomic MedicineJCI InsightPeer-reviewedJul 21, 2021

DEFINING THE DIVERSITY OF HNRNPA1 MUTATIONS IN CLINICAL PHENOTYPE AND PATHOMECHANISM

Danique Beijer, Hong Joo Kim, Lin E. Guo…·Jonathan Baets

The paper characterizes HNRNPA1 mutations in patients with neurodegenerative diseases, showing varied effects on fibrillization, phase separation, and stress granule dynamics.

72 citationstop 3%

humanproteomics

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