Wanda Maria Gerding
10PUBLICATIONS
18CO-AUTHORS

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Publications (10)
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|Oct 16, 2024
Compound Heterozygous RYR1 Variants in a Patient with Severe Congenital Myopathy: Case Report and Comparison with Additional Cases of Recessive RYR1-Related Myopathy.Sören Janßen, Leoni S Erbe, Moritz Kneifel
|Jun 27, 2024
Optical Genome Mapping Reveals Disruption of the RASGRF2 Gene in a Patient with Developmental Delay Carrying a De Novo Balanced Reciprocal Translocation.Rosa Catalina Lederbogen, Sabine Hoffjan, Charlotte Thiels
|Mar 27, 2024
Optical Genome Mapping Reveals Genomic Alterations upon Gene Editing in hiPSCs: Implications for Neural Tissue Differentiation and Brain Organoid Research.Lucia Gallego Villarejo, Wanda M Gerding, Lisa Bachmann
|Oct 14, 2023
Exome Sequencing and Optical Genome Mapping in Molecularly Unsolved Cases of Duchenne Muscular Dystrophy: Identification of a Causative X-Chromosomal Inversion Disrupting the DMD Gene.Leoni S Erbe, Sabine Hoffjan, Sören Janßen
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Frequent Collaborators
9 joint publications
Huu Phuc Nguyen
5 joint publications
Deepak Ben Vangala
4 joint publications
Verena Nilius-Eliliwi
4 joint publications
Roland Schroers
2 joint publications
Marco Tembrink
2 joint publications
Maria Viktorovna Yusenko
2 joint publications
Ulrike Angelika Mau-Holzmann
2 joint publications
Matthias Vorgerd
2 joint publications
Charlotte Thiels
2 joint publications
Rosa Catalina Lederbogen