Author

Iliana A. Chatzispyrou

Amsterdam UMC Location University of Amsterdam

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioinformatics· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Assay:proteomics· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Riekelt H. HoutkooperiD· 2 shared Sergio Guerrero‐CastilloiD· 2 shared Astrid S. PlompiD· 1 shared Frank BaasiD· 1 shared Hans R. WaterhamiD· 1 shared Janet Koster· 1 shared Joeri van StrieniD· 1 shared Johan H. AuwerxiD· 1 shared

Activity by Year

2017-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersBioinformatics

Riekelt H. HoutkooperORCID

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2 papers

Recent·Most cited

BioinformaticsBioinformaticsPeer-reviewedJan 10, 2019

COmplexome Profiling ALignment (COPAL) reveals remodeling of mitochondrial protein complexes in Barth syndrome

Joeri van Strien, Sergio Guerrero‐Castillo, Iliana A. Chatzispyrou…·Martijn A. Huynen

COPAL aligns complexome profiles to identify changes in mitochondrial protein complex abundance caused by Barth syndrome mutations.

42 citations

humanproteomics

𝕏 PostBluesky

GeneticsHuman Molecular GeneticsPeer-reviewedApr 20, 2017

A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndrome

Iliana A. Chatzispyrou, Marielle M. Alders, Sergio Guerrero‐Castillo…·Astrid S. Plomp

This study identifies a homozygous ERAL1 mutation as the cause of Perrault syndrome, showing it disrupts mitochondrial ribosome assembly and function.

79 citations

humanwhole-exome sequencing

𝕏 PostBluesky