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Public Health Genomics Program
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O u r V i s i o n
Improved health outcomes and enhanced
quality of life for the people of
Michigan through appropriate use of genetic
information, technology and services
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The Genomics and Genetic Disorders Section provides assessment, policy development, and assurance related to newborn screening, birth defects, genetic disorders, and the use of genomics* in public health programs. Our mission is to:
- Facilitate early identification and treatment of individuals with birth defects, heritable disorders and genetic susceptibilities throughout the lifecycle;
- Coordinate educational activities that increase genetic literacy; and
- Foster collaboration to integrate advances in genomic science throughout public health and other systems of care
The Section is responsible for implementing the State Genetics Plan in collaboration with local, state and national partners. It also conducts newborn screening follow-up and provides support for a statewide network of genetic diagnosis and counseling services. The Genetics Resource Center includes directories of genetic service providers, state genetic support groups, and event calendar along with information on birth defects prevention, resources for families, and the role of family history in complex chronic diseases.
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National Links
2010 State Public Health Genomics Resource Guide
Multiple-State Genomics Data
Order materials
Contact us:
Genetics Information Line 1-866-852-1247
Email: genetics@michigan.gov
Genomics and Genetic Disorders Section
Lifecourse Epidemiology and Genomics Division
P.O. Box 30195
201 Townsend Street, CV 4th floor
Lansing, Michigan 48909-30195
Staff Directory
*The word GENOMICS refers to the functions and interactions of all the genes in the genome, including the interaction with environmental factors. GENETICS is the science of heredity and the study of single genes in the genome.
Last updated 01/13
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