Jeremias Krause
7PUBLICATIONS
155CO-AUTHORS
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Publications (7)
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|Mar 30, 2026
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.Elsa Leitão, Amandine Santini, Benjamin Cogne
|Feb 04, 2026
The potential of whole genome sequencing in pharmacogenetics: a retrospective health record study in rare disease patients.Madeline Gorny, Katja S Just, Tim Krüger
|Sep 15, 2025
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.Elsa Leitão, Amandine Santini, Benjamin Cogne
|Jul 25, 2025
Utilizing protein structure graph embeddings to predict the pathogenicity of missense variants.Martin Danner, Matthias Begemann, Miriam Elbracht
|Dec 12, 2024
Diagnostic Use of Genome Sequencing in Patients With 11p15.5 Imprinting Disorder Features: A Pilot Study.Luise Kessler, Jeremias Krause, Florian Kraft
|Oct 31, 2024
Brain malformations and seizures by impaired chaperonin function of TRiC.Florian Kraft, Piere Rodriguez-Aliaga, Weimin Yuan
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Frequent Collaborators
5 joint publications
Florian Kraft
4 joint publications
Miriam Elbracht
4 joint publications
Ingo Kurth
4 joint publications
Miriam Elbracht
3 joint publications
Gael Nicolas
3 joint publications
Jean-Madeleine de Sainte Agathe
2 joint publications
Tobias B Haack
2 joint publications
Thomas Eggermann
2 joint publications
Yvonne Weber
2 joint publications
Cordula Knopp
