Important Links

• 23andMe
• Bioinformatics Web
• caBIG
• CDC Family Healthware
• Celera
• deCODEme
• DNAdirect
• Electronic Medical Records and Genomics (eMERGE) Network
• Framingham SNP Health Association Resource (SHARe)
• GenBank®
• Human Gene Mutation Database
• Human Genome Project
• Informatics for Integrating Biology & the Bedside
• Mayo Clinic Bipolar Disorder Biobank
• Metagenomics. Human Microbiome Project. The NIH Common Fund.
• My Family Health Portrait
• National Human Genome Research Institute
• National Institute of General Medical Sciences. The New Genetics.
• NCBI Human Genome Resources
• NCBI Online Mendelian Inheritance in Man (OMIM)
• Pharmacogenomics Knowledge Base
• The Human Variome Project
• The Pharmacogenomics Knowledge Base
• World Community Grid

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• Butte AJ, Shah NH. Computationally translating molecular discoveries into tools for medicine: translational bioinformatics articles now featured in JAMIA. J Am Med Inform Assoc. 2011;18(4):352-353
• caGrid 1.0: An Enterprise Grid Infrastructure for Biomedical Research []
• Cardiovascular Disease Risk Prediction With and Without Knowledge
  of Genetic Variation at Chromosome 9p21.3 []
• Genomic Medicine- An Updated Primer []
• Genotype Score in Addition to Common Risk Factors for Prediction of Type 2 Diabetes []
• Human Genetic Variation Primer []
• Keeping Pace with the Times- The Genetic Information Nondiscrimination Act of 2008 []
• Kmiecik, T. & Sanders, D. Integration of Genetic and Familial Data into Electronic Medical Records and Healthcare Processes []
• Kohane IS. Using EHRs to drive discovery in disease genomics. Nature reviews genetics. 2011;12:417-428
• Personalised Medicine and the Personal Genome
• Personalized Genetic Prediction: Too Limited, Too Expensive, or Too Soon?
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• Ten Years On - The Human Genome and Medicine []
• The New Genetics []
• Ullman MH, Matthew JP. Emerging landscape of genomics in the EHR for personalized medicine. 2011;32(8):512-516
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