Author

Andreas Tzschach

Ghent University HospitalORCID 0000-0002-6840-965XUnclaimed 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:benchmarking· 1 Research Focus:database / resource· 1 Approach:experimental assay· 1 Assay:imaging· 1 Approach:statistical model· 1 Organism:zebrafish· 1

Frequent Co-Authors

Angela PeroniD· 2 shared Himanshu GoeliD· 2 shared Abbey Scott· 1 shared Agustí Rodríguez‐PalmeroiD· 1 shared Alejandro Iglesias· 1 shared Alessandro Mauro SpinelliiD· 1 shared Alexander HustinxiD· 1 shared Alexej KnausiD· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Angela PeronORCID

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2 papers

Recent·Most cited

Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder

María del Rocío Pérez Baca, María Palomares‐Bralo, Michiel Vanhooydonck, Lisa Hamerlinck, Eva D’haene, Sebastian Leimbacher, Eva Jacobs, Laurenz De Cock, Erika D’haenens, Annelies Dheedene, Zoë Malfait, Lies Vantomme, Ananilia Silva, Kathleen Rooney, Xiaonan Zhao, , Stephanie Baskin

This study identifies ZFHX4 loss-of-function variants as a cause of a neurodevelopmental disorder with distinctive facial features and brain abnormalities, supported by zebrafish models.

The American Journal of Human Genetics · May 13, 2025Peer-reviewedGenetic & Genomic Medicine

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases

Hellen Lesmann, Alexander Hustinx, Shahida Moosa, Hannah Klinkhammer, Elaine J. Marchi, Pilar Caro, Ibrahim M. Abdelrazek, Jean Tori Pantel, Merle ten Hagen, Meow‐Keong Thong, Rifhan Azwani Mazlan, Sok Kun Tae, Tom Kamphans, Wolfgang Meiswinkel, Jingmei Li, , Miray Karakoyun

The paper introduces the GestaltMatcher Database (GMDB), a global facial phenotypic reference for rare diseases, showing improved NGP performance with diverse ancestry data.

medRxiv · Jun 6, 2023 · PreprintGenetic & Genomic Medicine