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Richard Smith

Professor,  Otolaryngology Head Neck Surg

Contact Information

Phone: +1 319 356 3612
Email: richard-smith@uiowa.edu



Primary: Otolaryngology Head Neck Surg
Secondary: Anatomy and Cell Biology
Secondary: Physiology
Secondary: Internal Medicine
Secondary: Pediatrics

Centers and Program Affiliations

Interdisciplinary Graduate Program in Genetics
Interdisciplinary Graduate Program in Informatics

Research Interests

MeSH Terms from Publications

Research Summary

Dr. Smith's research interests include branchio-oto-renal (BOR) syndrome and complement-mediated glomerular diseases with a focus on membranoproliferative glomerulonephritis type II (MPGN II). The Clinical Diagnostics Division of his laboratory offers mutation screening of EYA1 in persons with a BOR phenotype and Factor H screening in persons with atypical hemolytic uremic syndrome or biopsy proven MPGN II.

Recent Publications

Show publications
  1. Tailored eculizumab therapy in the management of complement factor h-mediated atypical hemolytic uremic syndrome in an adult kidney transplant recipient: a case report. Transplant Proc 44(10):3037-40, 2012. [PubMed]
  2. Sialoendoscopy for the treatment of pediatric salivary gland disorders. Arch Otolaryngol Head Neck Surg 138(10):912-5, 2012. [PubMed]
  3. Determination of crystallographic orientation of large grain metals with surface acoustic waves. J Acoust Soc Am 132(2):738-45, 2012. [PubMed]
  4. Eculizumab for dense deposit disease and C3 glomerulonephritis. Clin J Am Soc Nephrol 7(5):748-56, 2012. [PubMed]
  5. Association between red blood cell distribution width and macrovascular and microvascular complications in diabetes. Diabetologia 55(1):226-35, 2012. [PubMed]
  6. Evidence for separatrix formation and sustainment with steady inductive helicity injection. Phys Rev Lett 107(16):165005, 2011. [PubMed]
  7. Indication of electron neutrino appearance from an accelerator-produced off-axis muon neutrino beam. Phys Rev Lett 107(4):041801, 2011. [PubMed]
  8. Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4). Proc Natl Acad Sci U S A 108(10):4218-23, 2011. [PubMed]
  9. Microdeletion of 17q22q23.2 encompassing TBX2 and TBX4 in a patient with congenital microcephaly, thyroid duct cyst, sensorineural hearing loss, and pulmonary hypertension. Am J Med Genet A 155A(2):418-23, 2011. [PubMed]
  10. Reducing the exome search space for mendelian diseases using genetic linkage analysis of exome genotypes. Genome Biol 12(9):R85, 2011. [PubMed]