Annika Jacobsen
6PUBLICATIONS
29CO-AUTHORS
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Publications (6)
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|Sep 05, 2021
The de novo FAIRification process of a registry for vascular anomalies.Karlijn H J Groenen, Annika Jacobsen, Martijn G Kersloot
|Jan 16, 2021
A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration.Friederike Ehrhart, Annika Jacobsen, Maria Rigau
|May 15, 2019
The ability of transcription factors to differentially regulate gene expression is a crucial component of the mechanism underlying inversion, a frequently observed genetic interaction pattern.Saman Amini, Annika Jacobsen, Olga Ivanova
|Aug 08, 2018
Recommendations for Improving the Quality of Rare Disease Registries.Yllka Kodra, Jérôme Weinbach, Manuel Posada-de-la-Paz
|Apr 29, 2018
MECP2 variation in Rett syndrome-An overview of current coverage of genetic and phenotype data within existing databases.Gillian S Townend, Friederike Ehrhart, Henk J van Kranen
|May 25, 2016
Construction and Experimental Validation of a Petri Net Model of Wnt/β-Catenin Signaling.Annika Jacobsen, Nika Heijmans, Folkert Verkaar
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Frequent Collaborators
3 joint publications
Marco Roos
3 joint publications
Esther van Enckevort
2 joint publications
K Anton Feenstra
2 joint publications
Friederike Ehrhart
2 joint publications
Chris T Evelo
2 joint publications
Leopold M G Curfs
2 joint publications
Ronald Cornet
1 joint publications
Renée van Amerongen
1 joint publications
Gillian S Townend
1 joint publications
Henk J van Kranen
