Waanders, Esmé
St. Jude Children's Research Hospital · University Medical Center Utrecht · Princess Máxima Center
3 papers on CoChatORCID 0000-0002-2466-953X
Most cited papers
- Verified
Relapse-Fated Latent Diagnosis Subclones in Acute B Lineage Leukemia Are Drug Tolerant and Possess Distinct Metabolic Programs
Dobson, S. M., García-Prat, L., Vanner, R. J., Wintersinger, J., Waanders, E., Gu, Z., McLeod, J., Gan, O. I., Grandal, I., Payne-Turner, D., et al. (2020) · Cancer Discovery
Acute Lymphoblastic Leukemia researchAcute Myeloid Leukemia Research
Cited by 94
- Verified
Extensive mutational analysis ofPRKCSH andSEC63 broadens the spectrum of polycystic liver disease
Waanders, E., te Morsche, R. H. M., de Man, R. A., Jansen, J. B. M. J., & Drenth, J. P. H. (2006) · Human Mutation
Genetic and Kidney Cyst DiseasesTuberous Sclerosis Complex Research
Cited by 64
- Verified
Congenital disorders of glycosylation in hepatology: The example of polycystic liver disease
Janssen, M. J., Waanders, E., Woudenberg, J., Lefeber, D. J., & Drenth, J. P. H. (2010) · Journal of Hepatology
Genetic and Kidney Cyst DiseasesGlycogen Storage Diseases and Myoclonus
Cited by 54
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