Katharina T Schmid
7PUBLICATIONS
63CO-AUTHORS
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Publications (7)
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|Oct 02, 2025
Benchmarking scRNA-seq copy number variation callers.Katharina T Schmid, Aikaterini Symeonidi, Dmytro Hlushchenko
|Dec 09, 2024
Multiplexing cortical brain organoids for the longitudinal dissection of developmental traits at single-cell resolution.Nicolò Caporale, Davide Castaldi, Marco Tullio Rigoli
|Sep 20, 2023
epiAneufinder identifies copy number alterations from single-cell ATAC-seq data.Akshaya Ramakrishnan, Aikaterini Symeonidi, Patrick Hanel
|May 05, 2022
Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.Marie Loh, Weihua Zhang, Hong Kiat Ng
|Apr 08, 2022
Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.Marie Loh, Weihua Zhang, Hong Kiat Ng
|Jan 04, 2022
Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function.Johann S Hawe, Rory Wilson, Katharina T Schmid
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Frequent Collaborators
3 joint publications
Marie Loh
3 joint publications
Weihua Zhang
3 joint publications
Matthias Heinig
3 joint publications
John C Chambers
3 joint publications
Jaspal S Kooner
2 joint publications
Amel Lamri
2 joint publications
Cassandra N Spracklen
2 joint publications
Fumihiko Takeuchi
2 joint publications
Karen L Mohlke
2 joint publications
Guillaume Paré
