Kraft Florian

27PUBLICATIONS
315CO-AUTHORS
Neurology and neuromuscular diseasesMolecular targetsCellular nervous systemPharmacogenomicsMedical molecular engineering of nucleic acids and proteins
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Publications (27)

|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

|Mar 27, 2026
The protein kinase DYRK1B is a p53 target gene and functions as a negative feedback regulator of the transcription factor RFX7.

Gerrit Wilms, Katharina Schwandt, Stefan Düsterhöft

|Feb 12, 2026
The chaperonin TRiC component Cct3 is required for axonal transport, myelination, and neuromuscular junction refinement.

Xiaomeng Zhang, Kamil Kajetan Zajt, Tayfun Palaz

|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

|Dec 01, 2025
Direct RNA sequencing enables improved transcriptome assessment and tracking of RNA modifications for medical applications.

Charlotte Hewel, Anna Wierczeiko, Johannes Miedema

|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

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Frequent Collaborators

11 joint publications

Miriam Elbracht

9 joint publications

Miriam Elbracht

9 joint publications

Ingo Kurth

6 joint publications

Thomas Eggermann