Rehder, H.
Medical University of Vienna
2 papers on CoChatORCID 0000-0002-5215-623X
Most cited papers
- Verified
BRCA2 germline mutations in familial pancreatic carcinoma
Hahn, S. A., Greenhalf, B., Ellis, I., Sina-Frey, M., Rieder, H., Korte, B., Gerdes, B., Kress, R., Ziegler, A., Raeburn, J. A., et al. (2003) · JNCI Journal of the National Cancer Institute
BRCA gene mutations in cancerPancreatic and Hepatic Oncology Research
Cited by 480
- Verified
Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome)
Zenker, M., Mayerle, J., Lerch, M. M., Tagariello, A., Zerres, K., Durie, P. R., Beier, M., Hülskamp, G., Guzman, C., Rehder, H., et al. (2005) · Nature Genetics
Ubiquitin and proteasome pathwaysGenomics and Rare Diseases
Cited by 266
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