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- Genomische Pathologie - AG Hillmer
Genomische Pathologie
Cancer genomics to understand tumor characteristics and vulnerabilities
Genomic studies have identified new mechanisms that underlie the development of cancer and revealed targets for novel therapies. In addition, systematic genomics allow us to understand the context in which cancer driver mutations occur. Together with transcriptomic and epigenetic analyses, cancer entities are nowadays classified by their molecular features. In addition to the mutated cancer cells, other cellular compartments of solid tumors, including cancer associated fibroblasts and immune cells influence the clinical behavior of cancer patients.
Our lab uses next generation sequencing approaches to characterize cancer on the genomic, transcriptomic and epigenetic level. Using integrative analyses, we try to find molecular patterns that correlate with and potentially explain the different clinical categories of patients. We aim at identifying pathways that are altered in the different compartments of the tumor, including the stroma, that provide potential new targets for intervention.
Lab Members
Vanessa Richartz, technical assistant
Barbara Holz, technical assistant
Nastaran Biazar, scientific assistant
Hannah Demond, postdoctoral researcher
Dr. nat. med. Sonja Meemboor, postdoctoral researcher
Dr. (PhD) Ali Yazbeck, postdoctoral researcher
Dr. med. Sebastian Michels, Else Kröner fellow & clinician scientist
Julia Wiggeshoff, bioinformatician
Mohammad Ali (Shahrokh) Karimpour, PhD student
Marta Pistone, PhD student
Ruth Bakemeier, MD student
Hannah Kaiser, MD student
Patrizia Pauls, MD student
Marga und Walter Boll-Stiftung: „Sex chromosome-specific molecular alterations in esophageal adenocarcinoma“
Ministry for Education and Research (BMBF) CompLS Round 3 – Joint Research Project: “Deep Insight - Integrating germline and somatic genetic profiles through machine learning to understand esophageal cancer etiology”, Subproject B