The DOI matches its Crossref record; 40 of the 40 references it cites were found in a registry or an index.
Will Genetics Revolutionize Medicine?
Abstract
On both sides of the Atlantic, revolutionary claims have been made about the ultimate impact of genetics on clinical medicine. John Bell at Oxford has asserted that “within the next decade genetic testing will be used widely for predictive testing in healthy people and for diagnosis and management of patients. . . . The excitement in the field has shifted to the elucidation of the genetic basis of the common diseases.”1 And in the United States the director of the National Human Genome Research Institute, Francis Collins, has stated that the good that would come from mapping the human genetic . . .
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Citations
Cites
Kessler, R. C. (1994) · Archives of General Psychiatry · doi:10.1001/archpsyc.1994.03950010008002 · Cited by 12,370
Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
Lander, E., & Kruglyak, L. (1995) · Nature Genetics · doi:10.1038/ng1195-241 · Cited by 5,239
Sick individuals and sick populations
Rose, G. (2001) · International Journal of Epidemiology · doi:10.1093/ije/30.3.427 · Cited by 3,736
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
Feder, J. N., Gnirke, A., Thomas, W., Tsuchihashi, Z., Ruddy, D. A., Basava, A., Dormishian, F., Domingo, R., Ellis, M. C., Fullan, A., et al. (1996) · Nature Genetics · doi:10.1038/ng0896-399 · Cited by 3,664
Sick individuals and sick populations
ROSE, G. (1985) · International Journal of Epidemiology · doi:10.1093/ije/14.1.32 · Cited by 2,701
The Risk of Cancer Associated with Specific Mutations of BRCA1 and BRCA2 among Ashkenazi Jews
Struewing, J. P., Hartge, P., Wacholder, S., Baker, S. M., Berlin, M., McAdams, M., Timmerman, M. M., Brody, L. C., & Tucker, M. A. (1997) · New England Journal of Medicine · doi:10.1056/nejm199705153362001 · Cited by 2,281
Current estimates from the National Health Interview Survey.
Ss, J. (1981) · PubMed · Cited by 1,866
Aaltonen, L. A., Salovaara, R., Kristo, P., Canzian, F., Hemminki, A., Peltomäki, P., Chadwick, R. B., Kääriäinen, H., Eskelinen, M., Järvinen, H., et al. (1998) · New England Journal of Medicine · doi:10.1056/nejm199805213382101 · Cited by 1,152
Current estimates from the National Health Interview Survey, 1990.
Adams, P. F., Hendershot, G. E., & Marano, M. A. (1987) · PubMed · Cited by 1,104
Colorectal Cancer: Molecules and Populations
Potter, J. D. (1999) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/91.11.916 · Cited by 881
Cited by
Potential Role of Pharmacogenomics in Reducing Adverse Drug Reactions: A Systematic Review
Phillips, K. A., Veenstra, D. L., Oren, E., Lee, J. K., & Sadee, W. (2001) · JAMA · doi:10.1001/jama.286.18.2270 · Cited by 705
The genetics and genomics of cancer
Balmain, A., Gray, J., & Ponder, B. (2003) · Nature Genetics · doi:10.1038/ng1107 · Cited by 573
Advanced sequencing technologies: methods and goals
Shendure, J., Mitra, R. D., Varma, C., & Church, G. M. (2004) · Nature Reviews Genetics · doi:10.1038/nrg1325 · Cited by 558
Evans, D. M., Visscher, P. M., & Wray, N. R. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp295 · Cited by 297
Janssens, A. C. J. W., Gwinn, M., Bradley, L. A., Oostra, B. A., van Duijn, C. M., & Khoury, M. J. (2008) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2007.12.020 · Cited by 278
Metadata
- Authors
- Holtzman, N. A., & Marteau, T. M.
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 2000-07-13
- Volume
- 343
- Issue
- 2
- Pages
- 141-144
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W2012014972
- Cited by
- 408
- References
- 40
- FWCI
- 30.98
- Type
- journal article
- Language
- en
- Open access
- closed
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- Holtzman, N. A., & Marteau, T. M. (2000). Will Genetics Revolutionize Medicine? New England Journal of Medicine. https://doi.org/10.1056/nejm200007133430213
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.