Skip to main content
Val Sheffield, MD, Medical Genetics, Iowa City, IA

ValCSheffieldMD

Medical Genetics Iowa City, IA

Clinical Genetics, Clinical Molecular Genetics

Professor, Pediatrics, University of Iowa College of Medicine

Dr. Sheffield is on Doximity

As a Doximity member you'll join over two million verified healthcare professionals in a private, secure network.

  • Gain access to free telehealth tools, such as our “call shielding” and one-way patient texting.
  • Connect with colleagues in the same hospital or clinic.
  • Read the latest clinical news, personalized to your specialty.

See Dr. Sheffield's full profile

Already have an account?

  • Office

    200 Hawkins Dr
    Iowa City, IA 52242
    Phone+1 319-335-6898
    Fax+1 319-335-7588

Education & Training

  • University of California (San Francisco)
    University of California (San Francisco)Residency, Pediatrics, 1985 - 1988
  • University of Chicago Division of the Biological Sciences The Pritzker School of Medicine
    University of Chicago Division of the Biological Sciences The Pritzker School of MedicineClass of 1985

Certifications & Licensure

  • CA State Medical License
    CA State Medical License 1987 - Present
  • IA State Medical License
    IA State Medical License 1990 - 2025
  • American Board of Medical Genetics and Genomics Clinical Genetics

Awards, Honors, & Recognition

  • Elected Member Institute of Medicine, 2005
  • Investigator Howard Hughes Medical Institute

Publications & Presentations

PubMed

Lectures

  • A Novel Role for Neuronal Bardet-Biedl Syndrome 1 Protein in Glucose Homeostasis 
    Iowa City, IA - 6/14/2014

Press Mentions

  • Faulty Development of Immature Brain Cells Causes Hydrocephalus
    Faulty Development of Immature Brain Cells Causes HydrocephalusNovember 19th, 2012

Grant Support

  • Mechanisms Of Hypertension And Obesity In Mouse Models Of A Human Obesity SyndNational Heart, Lung, And Blood Institute2007–2011
  • Interdisciplinary Approach To Retinal Disease Gene IdentificationNational Eye Institute2007–2011
  • Evaluation Of Complex Inheritance Of Retinal Degeneration In Bardet-Biedl SyndromNational Eye Institute2007–2011
  • Molecular Genetics Of GlaucomaNational Eye Institute2006–2010
  • Molecular Biology Of Syndromic Retinal DegenerationNational Eye Institute1996–2006
  • Identification Of Genes Involved In Human HypertensionNational Heart, Lung, And Blood Institute2001–2005
  • Molecular Genetics Of Hereditary GlaucomaNational Eye Institute1994–2004
  • A Program For RAT Gene Discovery And MappingNational Heart, Lung, And Blood Institute2000–2001
  • Imaging Of Defects In Offspring Of Mutagenized MiceNational Center For Research Resources1998–2000
  • Core--Molecular GenotypingNational Heart, Lung, And Blood Institute1996–2000
  • Program For RAT Gene Discovery And MappingNational Heart, Lung, And Blood Institute1997–1999
  • Improved Mutation Detection &High Throughput GenotypingNational Human Genome Research Institute1994–1996
  • Identification Of Polymorphisms In Sequenced Tagged SiteNational Human Genome Research Institute1991–1993