I am a trained biomedical scientist with a focus on translational medicine and a passion for computer science and bioinformatics.
I am currently a doctoral candidate at the Institute of Human Genetics, University Hospital Erlangen and member of CRC1181.
My research focuses on the genetic and molecular mechanisms driving autoinflammatory skin and bone disorders, with particular emphasis on pustular psoriasis and chronic non-bacterial osteomyelitis (CNO)/SAPHO syndrome.
These conditions represent a spectrum of rare and severe inflammatory diseases characterized by dysregulated innate immune responses, neutrophil-driven inflammation, and aberrant cytokine and lipid-mediator signaling. Despite clinical overlap, their molecular underpinnings remain incompletely understood.
Using an integrated approach that combines human genetics, functional genomics, and molecular biology, my work aims to:
By linking genotype to mechanism, my research seeks to improve our understanding of autoinflammatory disease biology and contribute to the development of precision-based therapeutic strategies for rare inflammatory disorders.
Genetic underpinnings of the psoriatic spectrum
Hüffmeier, U., Klima, J., & Hayatu, M. (2023). Medizinische Genetik, 35, 46-54.
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