Web-based genetics resources for clinicians, researchers, students, and patients: Online Mendelian Inheritance in Man (OMIM™) and GeneTests™

Journal of Electronic Resources in Medical Libraries

Volumn 3, Issue 2, 2006, Pages 1-22

  Tennant, Michele R ^a   Lyon, Jennifer A ^b  

^a UNIVERSITY OF FLORIDA HEALTH   (United States)

^b VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

Clinicians; GeneReviews; GeneTests; Genetic information resources; Genetic knowledge base; Genetic testing; Human genes; Human genetic disorders; OMIM; Patient information; Researchers; Students

Indexed keywords

EID: 33748657364     PISSN: 15424065     EISSN: 15424073     Source Type: Journal    
DOI: 10.1300/J383v03n02_01     Document Type: Review

References (19)

1. National Center for Biotechnology Information (NCBI). Available: . Accessed: October 6, 2005.
2. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University and National Center for Biotechnology Information, National Library of Medicine. Online Mendelian Inheritance in Man, OMIM™. Available: . Accessed: October 6, 2005.
3. University of Washington, Seattle. GeneTests: Medical Genetics Information Resource. Available: . Accessed: October 6, 2005.
4. McKusick, V.A. Mendelian Inheritance in Man: Catalogs of Autosomal Dominant, Autosomal Recessive, and X-linked Phenotypes. Baltimore: Johns Hopkins University Press, 1966.
5. "Classical Genetics." DNA from the Beginning. 2002. Available: . Accessed: October 6, 2005.
6. McKusick, V.A. Mendelian Inheritance in Man: A Catalog of Human Genes and Genetic Disorders. 12th ed. Baltimore: Johns Hopkins University Press, 1998.
7. Brandt, K.A. "The GDB Human Genome Data Base: A Source of Integrated Genetic Mapping and Disease Data." Bulletin of the Medical Library Association 81(July 1993): 285-92.
8. National Library of Medicine. "Multiple Endocrine Neoplasia (MEN) II." MedlinePlus Medical Encyclopedia. 2004. Available: . Accessed: October 6, 2005.
9. Hamosh, A.; Scott, A.F.; Amberger, J.S.; Bocchini, C.A.; and McKusick, V.A. "Online Mendelian Inheritance in Man (OMIM), a Knowledgebase of Human Genes and Genetic Disorders." Nucleic Acids Research 33, Database issue (January 1, 2005): D514-7. doi: 10.1093/nar/gki033.
10. Jablonski, S. Jablonski's Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes Database. 1999. Available: . Accessed: October 6, 2005.
11. Tarczy-Hornoch, P.; Shannon, P.; Baskin, P.; Espeseth, M.; and Pagon, R.A. "GeneClinics: A Hybrid Text/Data Electronic Publishing Model Using XML Applied to Clinical Genetic Testing." Journal of the American Medical Informatics Association 7(May-June 2000): 267-76.
12. National Center for Biotechnology Information. DbSNP: Single Nucleotide Polymorphism Database. Available: . Accessed: October 6, 2005.
13. Chattopadhyay, A., and Tennant, M.R. "Genetic Variations Resources." NCBI's Advanced Workshop for Bioinformatics Information Specialists (NAWBIS). 2001-2005. Available: . Accessed: October 6, 2005.
14. Pagon, R.A.; Tarczy-Hornoch, P.; Baskin, P.K. et al. "GeneTests-GeneClinics: Genetic Testing Information for a Growing Audience." Human Mutation 19(May 2002): 501-9. doi: 10.1002/humu.10069.
15. Health on the Net Foundation. HON Code of Conduct (HONCode) for Medical and Health Web Sites. Available: . Accessed: October 6, 2005.
16. Human Genome Organisation. HUGO Gene Nomenclature Committee. Available: . Accessed: October 6, 2005.
17. Centers for Medicare & Medicaid Services. CLIA Program Clinical Laboratory Improvement Amendments. Available: . Accessed: October 6, 2005.
18. Ohles, J.A. "Clinical Resources." NCBI's Advanced Workshop for Bioinformatics Information Specialists (NAWBIS). 2001-2005. Available: . Accessed: October 6, 2005.
19. Geer, R.C.; Messersmith, D.J.; Alpi, K. et al. NCBI Advanced Workshop for Bioinformatics Information Specialists. 2001-2005. Available: . Accessed: October 6, 2005.