Markus Schülke

49PUBLICATIONS
282CO-AUTHORS
Energy generation, conversion and storage (excl. chemical and electrical)Computational physiologyMedical virologyInfant and child healthNeurology and neuromuscular diseases
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Publications (49)

|May 05, 2026
Biallelic MCUR1 nonsense mutation associated with vacuolar myopathy and altered mitochondrial calcium signaling.

|Apr 20, 2026
Accelerating Leigh syndrome drug discovery through deep learning screening in brain organoids.

|Mar 17, 2026
Single-cell multi-omic analysis of mitochondrial mutational mosaicism and dynamics.

Yu-Hsin Hsieh, Pauline Kautz, Lena Nitsch

|Dec 23, 2025
The use of carbogen for interruption of febrile seizures - the randomized controlled CARDIF trial.

Claudia Weiß, Alice Hucko, Stephanie Müller-Ohlraun

|Jul 29, 2025
Novel Biallelic SQSTM1 Mutation Causing a Subacute-Onset Complex Movement Disorder with Oculomotor Abnormalities.

Ana Luísa de Almeida Marcelino, Nina-Maria Wilpert, Jonas Leubner

|Jun 24, 2025
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.

Axel Schmidt, Magdalena Danyel, Kathrin Grundmann

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Frequent Collaborators

7 joint publications

Heiko Krude

6 joint publications

Werner Stenzel

6 joint publications

Alessandro Prigione

5 joint publications

Angela M Kaindl