Gunnar Schmidt

2PUBLICATIONS
9CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseases
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Publications (2)

|Sep 21, 2022
GenOtoScope: Towards automating ACMG classification of variants associated with congenital hearing loss.

Damianos P Melidis, Christian Landgraf, Gunnar Schmidt

|Jan 21, 2022
Heterozygous DHTKD1 Variants in Two European Cohorts of Amyotrophic Lateral Sclerosis Patients.

Alma Osmanovic, Isabel Gogol, Helge Martens

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Frequent Collaborators

1 joint publications

Alma Osmanovic

1 joint publications

Helge Martens

1 joint publications

Olivia Schreiber-Katz

1 joint publications

Friedrich Feuerhake