Anne Herkert

Anne Herkert is a Researcher with expertise in Genetics, Biochemistry, and Molecular Biology, particularly active in fields related to Intellectual Disability, Cardiomyopathy, and Pediatrics. Her work contributes to the United Nations Sustainable Development Goals (SDGs), focusing on health and well-being, and scientific advancement.

Her research interests include:

• Genetic Disorders: Studying variants in genes like CUL3, SOX11, and BRWD3 to understand their role in syndromic and non-syndromic conditions.
• Neurodevelopmental Disorders: Investigating the clinical and molecular characteristics of rare genetic syndromes, such as those linked to BRWD3 and CUL3 genes.
• Cardiomyopathy: Analyzing genetic variants like MYH7 and ALPK3 in cohort studies to assess penetrance, prognosis, and phenotypic presentation.

Her recent publications highlight her engagement with Exome Sequencing, Genetic Screening, and Missense Mutations. She collaborates across countries and institutions, with a focus on Dutch multicenter studies. Her work involves interdisciplinary approaches bridging Biomedical Research, Genomics, and Clinical Genetics.

Anne Herkert has contributed to 48 research outputs, including 32 peer-reviewed Articles, 6 Meeting Abstracts, and 4 Review Articles. Her publications are freely available through Open Access and have garnered significant citations and Mendeley readership.