Katharina Eirich
Publications by Year
Research Areas
DNA Repair Mechanisms, BRCA gene mutations in cancer, Cytomegalovirus and herpesvirus research, CRISPR and Genetic Engineering, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype(2011)297 cited
- → WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects(2016)94 cited
- → Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families(2012)94 cited
- → Combined immunodeficiency develops with age in Immunodeficiency-centromeric instability-facial anomalies syndrome 2 (ICF2)(2014)43 cited
- → Mutations in PTRH2 cause novel infantile‐onset multisystem disease with intellectual disability, microcephaly, progressive ataxia, and muscle weakness(2014)37 cited
- → Hepatoblastoma in a 4‐year‐old girl with Fanconi anaemia(2010)24 cited
- → Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi Anemia(2012)18 cited
- → siRNA screening identifies differences in the Fanconi anemia pathway in BALB/c-Trp53+/− with susceptibility versus C57BL/6-Trp53+/− mice with resistance to mammary tumors(2013)8 cited
- → Germline RAD51C mutations confer susceptibility to ovarian cancer(2012)6 cited
- → Recurrent tendosynovitis as a rare manifestation of a lipid disorder(2018)5 cited