The Internet offers many resources that may be useful to national, state and local public health professionals interested in learning more about genomics and public health. This chapter provides a selected list of sites that offer starting points. Many other online resources are available; this list is only a snapshot of some that may be useful for integrating genomics into health promotion and disease prevention programs. Please refer to the disclaimer at the end of this chapter.

CDC's National Office of Public Health Genomics (NOPHG)  

• CDC National Office of Public Health Genomics (NOPHG)
  This site provides information about ways that human genomic discoveries can be used to improve health and prevent disease. It provides links to activities in public health genomics across the lifespan, including links to programs throughout CDC.

• Weekly Update
  A weekly update on the impact of human genetic research on disease prevention and public health. To receive notification of this update by e-mail, please send the following message:
  To: listserv@listserv.cdc.gov
  Subject: (leave blank)
  Message: subscribe genetics

• Public Health Perspectives Series
  On the Highlights page of the NOPHG website, each Public Health Perspective focuses on a single topic and provides information relevant to public health practice. Past topics include family history, BRCA1/2 testing, obesity, and others.

• Genomics and Disease Prevention Information System (GDPInfo)
  The GDPInfo query tool allows you to define your search of the NOPHG website with a combination of genes, diseases/conditions, topics and other factors. The search provides a list of all related documents and links to other sites.

Human Genome Project (all links last accessed 2/2008)

• Human Genome Project Information from the US Department of Energy
  The U.S. Department of Energy and the National Institutes of Health formally initiated the Human Genome Project in 1990. The project originally was planned to last 15 years, but rapid technological advances allowed it to be completed in 2003. This site provides an overview of the Human Genome Project and links to other sites.

• National Human Genome Research Institute (NHGRI)
  The NHGRI supports genetic and genomic research, investigation into the ethical, legal and social implications surrounding genetics research, and educational outreach activities in genetics and genomics.

• The Human Genome—A Guide to Online Information Resources from the National Library of Medicine
  A comprehensive site that provides information and links to information about specific genes and genetic diseases.

• Selected articles:
  • Celebrating the 50th Anniversary of the Double Helix
    Articles from Annals of Internal Medicine 1 April 2003 Volume 138 Issue 7
  • Primer on Medical Genomics: History of Genetics and Sequencing of the Human Genome
  • A Vision for the Future of Genomics Research
  • New England Journal Of Medicine: Genomic Medicine Series (2002-2003)   The full text of all thirteen articles in this series is available free to all users.

Genomic Research (all links last accessed 2/2008)

• Human Genetics and Medical Research
  An online exhibit for the public providing information about the use of genetics in medicine sponsored by the National Institute of Health (NIH).

• Genes and Populations
  A series of questions and answers for patients considering participation in research studies from the National Institute of General Medical Sciences.

• August 2003 Issue Brief “Applied Public Health Research in Genomics”
  An issue brief released by ASTHO that outlines the importance of applied public health research in genomics and the types of research needed, the ethical, legal, and social issues that accompany this type of research, current public health genomics research activities, and future research directions.

Genetic Testing (all links last accessed 2/2008)

• GeneTests/GeneClinics
  A publicly-funded medical genetics information resource developed for physicians, other healthcare providers, researchers, and others needing information about existing genetic tests. This site includes expert-authored reviews, directories of laboratories and clinics offering genetic tests, and educational materials.

• National Academy of Sciences, Human Gene Testing
  A summary of human genetic testing that ranges from the unraveling of the nature of the gene to the social dilemmas posed by genetic testing.

• Understanding Gene Testing
  Provided by the National Cancer Institute, illustrates what genes are, explains how mutations occur and how they are identified within genes, and discusses the benefits and limitations of gene testing for cancer and other disorders.
  

Family History (all links last accessed 2/2008)

• Genetics & Your Practice
  A resource that provides practical information and resources to assist the busy professional in integrating genetics into their patient care.
  • Family Health and Social History
    A time-saving method of family history taking and sample family history questionnaires.

• The Genetic Family History in Practice newsletter for health care professionals from NCHPEG's Family History Working Group

• Your Family History
  A family history tool developed through the collaboration with the American Society of Human Genetics, the National Society of Genetic Counselors and Genetic Alliance.

Genes and Diseases (all links last accessed 2/2008)

• Disease InfoSearch™
  A tool to assist in finding specific and quality information about genetic conditions, provided by the Genetic Alliance.

• GeneReviews
  An online publication of expert authored disease reviews from GeneTests.

• Genetics Home Reference
  Provides consumer information about genetic conditions and associated genes from the National Library of Medicine.

• Office of Rare Diseases (ORD)
  This website provides information about ORD-sponsored scientific activities, an ORD cosponsored genetic and rare diseases information center, and a portal to databases that provide information on major topics of interest in rare diseases research.

• Genes and Diseases
  A collection of articles that discuss genes and the diseases that they cause from the National Center for Biotechnology Information (NCBI).

• Online Mendelian Inheritance of Man (OMIM)
  A database providing a catalog of human genes and genetic disorders authored by the Johns Hopkins University Medical School and developed by the National Center for Biotechnology Information (NCBI)  at the National Library of Medicine. 

Genes and Diseases: Cancer (all links last accessed 2/2008)

• National Cancer Institute 
  • Cancer Genetics
    A comprehensive list of cancer genetics information ranging from general to specific cancer information, policy, and cancer genetics research and information.

Genes and Diseases: Birth Defects (all links last accessed 2/2008)

• March of Dimes Birth Defects Foundation
  A not-for-profit organization with the mission to improve health of babies by preventing birth defects and infant mortality.
  • Birth Defects and Genetic Conditions

• National Birth Defects Prevention Network
  A group with the mission to establish and maintain a national network of state and population-based programs for birth defects surveillance and research to assess the impact of birth defects upon children, families, and health care; to identify factors that can be used to develop primary prevention strategies; and to assist families and their providers in secondary disabilities prevention.

Genes and Diseases: Newborn Screening (all links last accessed 2/2008)

• National Newborn Screening and Genetics Resource Center (NNSGRC)
  Provides information and resources in the area of newborn screening and genetics to benefit health professionals, the public health community, consumers, and government officials:
  • a report on the characteristics of state NBS programs,
  • state newborn screening program resources,   and
  • resources for state genetics planning.

• Association of Public Health Laboratories (APHL) Newborn Screening and Genetics Program

• March of Dimes Newborn Screening Recommendations

Public Health Ethical, Legal and Social Issues (PHELSI) (all links last accessed 2/2008)

• Human Genome Project Information - Ethical, Legal and Social Issues
  Information on the ethical, legal and social issues surrounding the availability of genetic information. This is a publication of the U.S. Department of Energy Human Genome Project.

• Genetics Education and Counseling Program
  A public health initiative for community and professional education and awareness on genetics. This website is sponsored by the University of Pittsburgh.

• Public Health Genetics from University of Sheffield-School of Health and Related Research (Scharr)
  A catalogued series of articles on various topics including technical issues, genetic testing in the workplace, and experiences of individuals affected by genetic diseases from the U.K.

• Michigan Centers for Genomics and Public Health
  The Michigan Center for Genomics & Public Health seeks to integrate genomic discoveries into public health practice, with consideration of the ethical, legal, and social issues associated with the application of these discoveries, as well as the involvement of the community at large.

• Genetics and Ethics Page
  A clearinghouse for information on the social, ethical and policy issues associated with genetic and genomic knowledge and technology.

Policy (all links last accessed 2/2008)

• National Conference of State Legislatures (NCSL) Genetic Technologies Project website
  A group commissioned to provide state legislators and other policymakers with objective, comprehensive, and scholarly information from a non-partisan source to facilitate the drafting of sound genetics-related legislation.

• Secretary’s Advisory Committee on Genetics, Health and Society
  “A forum for expert discussion and deliberation and the formulation of advice and recommendations on the range of complex and sensitive medical, ethical, legal and social issues raised by new technological developments in human genetics.”

• Genetics and Public Policy Center
  Information on genetic technologies and genetic policies for the public, media and policymakers. The Genetics and Public Policy Center is funded through a grant from The Pew Charitable Trusts.

Public Health Resources (all links last accessed 2/2008)

• Coalition of State Genetic Coordinators
  An organization of state and territorial genetics coordinators and others who support the mission to promote core public health functions as they apply to genetics.

• Genomics and Chronic Disease Summit Report, 2002
  A report from the Association of State and Territorial Chronic Disease Directors.

• Harnessing Genetics to Prevent Disease & Improve Health (95.7KB)
  A guide to help states shape genetics policies for the purpose of advancing individual and collective health. The report highlights recommendations for policymakers to address the social, legal and ethical implications of genetics in their states.

• Centers for Genomics and Public Health 
  • University of Washington Center for Genomics and Public Health
  • University of Michigan Center for Genomics and Public Health
  • University of North Carolina Center for Genomics and Public Health, the Genomics Revolution and Public Health

• Public Health Genetics Unit, U.K.
  “Providing news and information about advances in genetics and their impact on public health and the prevention of disease.”

• The WHO Genetics Programme
  Information about activities undertaken by the WHO Human Genetics Program to help control the “most common hereditary diseases and those having a genetic predisposition.”

Educational Resources (all links last accessed 2/2008)

• National Coalition for Health Professional Education in Genetics (NCHPEG)
  A national effort to promote health professional education and access to information about advances in human genetics:
  • Genetic Resources on the Web (GROW),
  • Genetic Family History Resources,   and
  • Educational Resources.

• Genetic Educational Materials Database (GEMS)
  Searchable listing of public health genetics policy documents and clinical genetics educational materials from the National Newborn Screening and Genetics Resource Center (NNSGRC).

• NOPHG List of Training Tools 
  A list of available training tools, courses, and multi-media educational materials designed to assist public health professionals and educators integrate genomics into public health practice.

Provides link to non-governmental sites and does not necessarily represent the views of the Centers  for Disease Control and Prevention.