Jeremias Krause

8PUBLICATIONS
155CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesPharmacogenomicsNeurogeneticsGene mapping
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Publications (8)

|Sep 17, 2026
Genolator enables protein function interpretation using a multimodal large language model fusing genomic and structural interpretation with natural language interaction.

|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

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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