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

Laurence J. Egan

Division of Gastroenterology and Hepatology

Mayo Clinic


Minnesota 55905



Name/email consistency: high



  • Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota 55905, USA. 1999 - 2004
  • Clinical Pharmacology Unit, Division of Gastroenterology and Hepatology and Division of Biostatistics, Mayo Clinic, Rochester, USA. 2003


  1. Advances in the treatment of Crohn's disease. Egan, L.J., Sandborn, W.J. Gastroenterology (2004) [Pubmed]
  2. Drug interactions in gastroenterology: mechanisms, consequences, and how to avoid. Egan, L.J. Clin. Gastroenterol. Hepatol. (2004) [Pubmed]
  3. CYP2C19 pharmacogenetics in the clinical use of proton-pump inhibitors for gastro-oesophageal reflux disease: variant alleles predict gastric acid suppression, but not oesophageal acid exposure or reflux symptoms. Egan, L.J., Myhre, G.M., Mays, D.C., Dierkhising, R.A., Kammer, P.P., Murray, J.A. Aliment. Pharmacol. Ther. (2003) [Pubmed]
  4. Inhibition of interleukin-1-stimulated NF-kappaB RelA/p65 phosphorylation by mesalamine is accompanied by decreased transcriptional activity. Egan, L.J., Mays, D.C., Huntoon, C.J., Bell, M.P., Pike, M.G., Sandborn, W.J., Lipsky, J.J., McKean, D.J. J. Biol. Chem. (1999) [Pubmed]
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