Martina Wilke

Martina Wilke is a researcher in the Department of Clinical Genetics at Erasmus MC, a leading academic medical center in the Netherlands. Her work is centered on the application of genomic technologies to understand and diagnose rare genetic disorders, particularly those affecting neurodevelopment and prenatal development.

Her research interests span clinical genetics, exome sequencing, neurodevelopmental disorders, gene discovery, and prenatal genetic diagnostics. She actively contributes to expanding the phenotypic and genotypic understanding of rare Mendelian conditions through large-scale genomic analyses.

The recent trends in her publications indicate a strong focus on identifying novel genetic variants associated with intellectual disability, congenital malformations, and neurodegenerative diseases. Her work leverages exome sequencing in both prenatal and postnatal settings to improve diagnostic precision and inform clinical management.

She has contributed to significant studies published in high-impact journals such as American Journal of Human Genetics, Genetics in Medicine, and Prenatal Diagnosis, highlighting her role in collaborative, international research efforts.

• No scientific awards were mentioned in the provided text.

Martina Wilke participates in multi-center research collaborations, particularly in studies involving prenatal genomics and neurodevelopmental disorders. While no formal advisory role or grant leadership is indicated in the current data, her contributions to major publications suggest active involvement in funded research projects and scientific networks.

She is engaged in research within clinical genetics laboratories at Erasmus MC, contributing to diagnostic innovation and genomic medicine implementation, particularly in prenatal and pediatric contexts.