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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Joost P. H. Drenth

Department of Gastroenterology and Hepatology

Radboud University Nijmegen Medical Center




Name/email consistency: high



  • Department of Gastroenterology and Hepatology, Radboud University Nijmegen Medical Center, Nijmegen, Netherlands. 2001 - 2012
  • Cell Biology and Metabolism Branch, National Institute of Child Health and Human Development, National Institutes of Health, Building 18T, USA. 2004


  1. Rationale and design of the RESOLVE trial: lanreotide as a volume reducing treatment for polycystic livers in patients with autosomal dominant polycystic kidney disease. Gevers, T.J., Chrispijn, M., Wetzels, J.F., Drenth, J.P. BMC. Nephrol (2012) [Pubmed]
  2. Hepatitis C virus infection management in 2012. Van Gulick, J.J., Lamers, M.H., Drenth, J.P. Panminerva. Med (2012) [Pubmed]
  3. Primary erythermalgia as a sodium channelopathy: screening for SCN9A mutations: exclusion of a causal role of SCN10A and SCN11A. Drenth, J.P., Te Morsche, R.H., Mansour, S., Mortimer, P.S. Arch. Dermatol (2008) [Pubmed]
  4. Mutations in sodium-channel gene SCN9A cause a spectrum of human genetic pain disorders. Drenth, J.P., Waxman, S.G. J. Clin. Invest. (2007) [Pubmed]
  5. Do COX-2 inhibitors give enough gastrointestinal protection?. Drenth, J.P., Verheugt, F.W. Lancet (2007) [Pubmed]
  6. Chronic pancreatitis resulting from genetic mutations in trypsin and trypsin inhibitors. Drenth, J.P. Neth. J. Med (2007) [Pubmed]
  7. Polycystic liver disease is a disorder of cotranslational protein processing. Drenth, J.P., Martina, J.A., van de Kerkhof, R., Bonifacino, J.S., Jansen, J.B. Trends. Mol. Med (2005) [Pubmed]
  8. SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels. Drenth, J.P., te Morsche, R.H., Guillet, G., Taieb, A., Kirby, R.L., Jansen, J.B. J. Invest. Dermatol. (2005) [Pubmed]
  9. Abnormal hepatocystin caused by truncating PRKCSH mutations leads to autosomal dominant polycystic liver disease. Drenth, J.P., Tahvanainen, E., te Morsche, R.H., Tahvanainen, P., Kääriäinen, H., Höckerstedt, K., van de Kamp, J.M., Breuning, M.H., Jansen, J.B. Hepatology (2004) [Pubmed]
  10. Molecular characterization of hepatocystin, the protein that is defective in autosomal dominant polycystic liver disease. Drenth, J.P., Martina, J.A., Te Morsche, R.H., Jansen, J.B., Bonifacino, J.S. Gastroenterology (2004) [Pubmed]
  11. Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease. Drenth, J.P., te Morsche, R.H., Smink, R., Bonifacino, J.S., Jansen, J.B. Nat. Genet. (2003) [Pubmed]
  12. Genetic aspects of chronic pancreatitis, and the exploration of an association with keratin 8/18. Drenth, J.P., Verlaan, M. Dig. Liver. Dis (2003) [Pubmed]
  13. Mutations in serine protease inhibitor Kazal type 1 are strongly associated with chronic pancreatitis. Drenth, J.P., te Morsche, R., Jansen, J.B. Gut (2002) [Pubmed]
  14. Reduced diffusion in liver cirrhosis is related to impairment of protein liver synthesis. Drenth, J.P., Jansen, J.B., Dekhuijzen, P.N. Scand. J. Gastroenterol. (2002) [Pubmed]
  15. The primary erythermalgia-susceptibility gene is located on chromosome 2q31-32. Drenth, J.P., Finley, W.H., Breedveld, G.J., Testers, L., Michiels, J.J., Guillet, G., Taieb, A., Kirby, R.L., Heutink, P. Am. J. Hum. Genet. (2001) [Pubmed]
  16. Hereditary periodic fever. Drenth, J.P., van der Meer, J.W. N. Engl. J. Med. (2001) [Pubmed]
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