Author

Christian M. Korff

University Hospital of GenevaORCID 0000-0002-3328-7680Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:cell type annotation· 1 Approach:experimental assay· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Agnieszka CharzewskaiD· 1 shared Alessandro PorroiD· 1 shared Alexej KnausiD· 1 shared Allan BayatiD· 1 shared Amitav Parida· 1 shared Andrea SaponaroiD· 1 shared Anna Castellini· 1 shared Anna MoroniiD· 1 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetics

Agnieszka CharzewskaORCID

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2 papers

Recent·Most cited

Comprehensive classification of HCN1 variants linked to neurodevelopmental disorders with and without epilepsy

Roberta Castelli, Carla Marini, Alessandro Porro, Anna Castellini, Greta Fontana, Andrea Saponaro, Gianpiero L. Cavalleri, Susanna Rizzi, Carlo Fusco, Amitav Parida, Richard C. Caswell, Charlotte Sherlaw, Dario Pruna, Christopher A. Reid, Lauren E. Bleakley, , Anna Moroni

This study functionally classifies HCN1 variants in patients with neurodevelopmental disorders, finding genotype-phenotype correlations and potential therapeutic targets.

bioRxiv · Mar 20, 2026 · PreprintPathology

Characterization of Glycosylphosphatidylinositol Biosynthesis Defects by Clinical Features, Flow Cytometry, and Automated Image Analysis

Alexej Knaus, Jean Tori Pantel, Manuela Pendziwiat, Nurulhuda Hajjir, Max Zhao, Tzung‐Chien Hsieh, Max Schubach, Yaron Gurovich, Nicole Fleischer, Marten Jäger, Sebastian Köhler, Hiltrud Muhle, Christian M. Korff, Rikke Steensbjerre Møller, Allan Bayat, , Peter Michael Krawitz

The paper evaluates clinical features, flow cytometry, and facial image analysis to classify GPIBDs and identify gene-specific patterns, finding that facial recognition software is most effective for gene prediction.

Genome Medicine · Jan 5, 2018Peer-reviewedGenetics