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

David S. Geller

Section of Nephrology

Howard Hughes Medical Institute

Yale University School of Medicine

New Haven

USA

[email]@yale.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Section of Nephrology, Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, USA. 2001 - 2008

References

  1. A novel form of human mendelian hypertension featuring nonglucocorticoid-remediable aldosteronism. Geller, D.S., Zhang, J., Wisgerhof, M.V., Shackleton, C., Kashgarian, M., Lifton, R.P. J. Clin. Endocrinol. Metab. (2008) [Pubmed]
  2. Autosomal dominant pseudohypoaldosteronism type 1: mechanisms, evidence for neonatal lethality, and phenotypic expression in adults. Geller, D.S., Zhang, J., Zennaro, M.C., Vallo-Boado, A., Rodriguez-Soriano, J., Furu, L., Haws, R., Metzger, D., Botelho, B., Karaviti, L., Haqq, A.M., Corey, H., Janssens, S., Corvol, P., Lifton, R.P. J. Am. Soc. Nephrol. (2006) [Pubmed]
  3. Mineralocorticoid resistance. Geller, D.S. Clin. Endocrinol. (Oxf) (2005) [Pubmed]
  4. A mineralocorticoid receptor mutation causing human hypertension. Geller, D.S. Curr. Opin. Nephrol. Hypertens. (2001) [Pubmed]
 
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