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Distinguished Speaker Series | Val C. Sheffield, MD, PhD

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Location
https://ucihealth.zoom.us/j/94483669170?pwd=WUd1clg2aUM1bnpPVHd3MlkwTUN1Zz09
Event Type

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The Center for Translational Vision Research Distinguished Speaker Series, also known as "Friday Seminars" showcases innovative research across the world. The seminar series has now been expanded to include lectures by experts on topics ranging from Ophthalmology, Genetics, Biochemistry, Neurobiology, Imaging, Computational Sciences to Novel Ophthalmic Treatments.

All talks are hybrid. You can join us in person at the Gavin Herbert Eye Institute Building, 3d floor Conference Room.

You can also join us by zoom. Zoom link and information are on your right and in the calendar links above.

April 26, 2024 |  Val C. Sheffield, MD, PhD

The Molecular Genetics of a Syndromic Retinopathy (Bardet-Biedl Syndrome) and Treatment of Inherited Blindness

 

Learn More About the Distinguished Speaker Series

  • Agenda for the morning:

    • 8:15   am  Coffee and Bagels, GHEI, 3d Floor Cavanaugh Conference Room
    • 8:30   am  Start of the Seminar
    • 9:30   am  Questions and Discussion
    • 10:00 am  End of the Seminar

Featured


Val C. Sheffield, MD, PhD
Val C. Sheffield, MD, PhD
  • Professor of Pediatrics and Ophthalmology, Division of Medical Genetics, University of Iowa Carver College of Medicine, Iowa City, IA

Introduction

My laboratory is interested in identifying and understanding the function of genes which cause a variety of human disorders. Our research efforts have focused on the molecular genetics of monogenic disorders, as well as polygenic and multifactorial disorders. Our research efforts have resulted in the mapping of many different disease loci. In addition, we have used positional cloning methods to identify genes involved in a number of different diseases including hereditary blindness and deafness. Efforts are currently underway to use positional cloning strategies to identify additional disease-causing genes. Complex genetic disorders currently under investigation in the laboratory include hypertension, obesity, congenital heart disease and autism. In addition, we have worked on developing and improving techniques for disease mapping, positional cloning, and mutation detection. We have also had an active role in the human genome project and the rat genome project.