Research
Profile (Community of Science)
Research: The research interests of Dr. Pagon focus
on the nosology and delineation of genetic disorders and syndromes,
and the development of electronic clinical genetics information resources.
Her clinical research is made possible through an extensive clinical
program involving in-patient and out-patient consultations at Childrens
Hospital and Regional Medical Center, the major tertiary-level pediatric
hospital in the WWAMI (Washington-Wyoming-Alaska-Montana-Idaho) region,
and a network of regional genetics clinics in Washington State. Genetic
eye diseases and the diagnosis and management of children with ambiguous
genitalia are special research interests. Dr. Pagon is interested in
the information needs of medical geneticists and genetic counselors
created by the discoveries of the Human Genome Project. She has developed
Helix: Genetic Testing Resource, a database of genetic testing laboratories
funded by the National Library of Medicine (NIH) and the Maternal Child
Health Bureau (HSRA), that serves as the "yellow pages" for
genetics laboratories (www.genetests.org).
With funding from the National Library of Medicine and the National
Human Genome Research Institute, she is developing GeneClinics, an electronic
expert-authored information resource that relates genetic testing information
to the diagnosis, management and risk assessment of patients and families
with inherited disorders (www.geneclinics.org).
Investigator: Dr. Pagon is Professor of Pediatrics
and Adjunct Professor of Ophthalmology and Medicine (Medical Genetics).
She is a consultant to the Regional Genetics Program of Washington State
and an attending physician in the Childrens Hospital and Regional
Medical Center Genetics Clinic. She is a member of the Board of Directors
of The American Board of Medical Genetics (ABMG) and a member of the
clinical practice committee of The American College of Medical Genetics
(ACMG).