Wanda Maria Gerding

9PUBLICATIONS
15CO-AUTHORS
Respiratory diseasesDevelopmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Predictive and prognostic markers
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Publications (9)

|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

|Jun 10, 2023
Novel

Marco Tembrink, Wanda Maria Gerding, Stefan Wieczorek

|Mar 29, 2023
Optical Genome Mapping Reveals and Characterizes Recurrent Aberrations and New Fusion Genes in Adult ALL.

Lisa-Marie Vieler, Verena Nilius-Eliliwi, Roland Schroers

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Frequent Collaborators

8 joint publications

Huu Phuc Nguyen

5 joint publications

Deepak Ben Vangala

4 joint publications

Verena Nilius-Eliliwi

4 joint publications

Roland Schroers