Author

Imke Christiaans

University Medical Center GroningenORCID 0000-0001-5799-2344Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Approach:statistical model· 1

Frequent Co-Authors

Arie O. VerkerkiD· 2 shared Arthur A.M. WildeiD· 2 shared Connie R. BezzinaiD· 2 shared Elisabeth M. LodderiD· 2 shared Aafke A J Lommerse· 1 shared Alex Vincent PostmaiD· 1 shared Alexa M.C. VermeeriD· 1 shared Antonio M. A. MirandaiD· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Arie O. VerkerkORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJul 4, 2024

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy

Michele Nicastro, Alexa M.C. Vermeer, Pieter Gerard Postema…·Najim Lahrouchi

DOI 10.1101/2024.07.04.24309755

humanbulk RNA-seq

𝕏 PostBluesky

GeneticsHuman Molecular GeneticsPeer-reviewedOct 19, 2022

Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetrance

Jaël S. Copier, Marianne Bootsma, Chai‐Ann Ng…·Elisabeth M. Lodder

The paper reclassifies a variant in KCNH2 as a low penetrant likely pathogenic variant for LQTS2 based on biophysical effects and clinical variability.

6 citations

humanexperimental assay

𝕏 PostBluesky