M. Stephen Meyn
University of Wisconsin–Madison(US)
Publications by Year
Research Areas
Genomics and Rare Diseases, DNA Repair Mechanisms, Genomic variations and chromosomal abnormalities, BRCA gene mutations in cancer, Carcinogens and Genotoxicity Assessment
Most-Cited Works
- → Interaction of the Fanconi Anemia Proteins and BRCA1 in a Common Pathway(2001)1,204 cited
- → Targeted disruption of ATM leads to growth retardation, chromosomal fragmentation during meiosis, immune defects, and thymic lymphoma.(1996)835 cited
- → Comprehensive Analysis of Hypermutation in Human Cancer(2017)786 cited
- → Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test(2017)558 cited
- → Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers(2015)378 cited
- → Whole-genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine(2016)375 cited
- Ataxia-telangiectasia and cellular responses to DNA damage.