The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Highly Parallel SNP Genotyping
Abstract
The genetic factors underlying common disease arelargely unknown. Discovery of disease-causing genes willtransform our knowledge of the genetic contribution tohuman disease, lead to new genetic screens, and underpinresearch into new cures and improved lifestyles. The sequencing of the human genome has catalyzed efforts tosearch for disease genes by the strategy of associating sequence variants with measurable phenotypes. In particular, the Human Genome Project and follow-on efforts tocharacterize genetic variation have resulted in the discovery of millions of single-nucleotide polymorphisms(SNPs) (Patil et al. 2001; Sachidanandam et al. 2001;Reich et al. 2003). This represents a significant fraction ofcommon genetic variation in the human genome and creates an unprecedented opportunity to associate genes withphenotypes via large-scale SNP genotyping studies...
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Cites
The Structure of Haplotype Blocks in the Human Genome
Gabriel, S. B., Schaffner, S. F., Nguyen, H., Moore, J. M., Roy, J., Blumenstiel, B., Higgins, J., DeFelice, M., Lochner, A., Faggart, M., et al. (2002) · Science · doi:10.1126/science.1069424 · Cited by 5,863
Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21
Patil, N., Berno, A. J., Hinds, D. A., Barrett, W. A., Doshi, J. M., Hacker, C. R., Kautzer, C. R., Lee, D. H., Marjoribanks, C., McDonough, D. P., et al. (2001) · Science · doi:10.1126/science.1065573 · Cited by 1,145
Chromosome-wide distribution of haplotype blocks and the role of recombination hot spots
Phillips, M. S., Lawrence, R., Sachidanandam, R., Morris, A. P., Balding, D. J., Donaldson, M. A., Studebaker, J. F., Ankener, W. M., Alfisi, S. V., Kuo, F.-S., et al. (2003) · Nature Genetics · doi:10.1038/ng1100 · Cited by 278
Cited by
A functional genetic link between distinct developmental language disorders
Vernes, S. C., Newbury, D. F., Abrahams, B. S., Winchester, L., Nicod, J., Groszer, M., Alarcón, M., Oliver, P. L., Davies, K. E., Geschwind, D. H., et al. (2008) · New England Journal of Medicine · doi:10.1056/nejmoa0802828 · Cited by 676
Multiple regions within 8q24 independently affect risk for prostate cancer
Haiman, C. A., Patterson, N., Freedman, M. L., Myers, S. R., Pike, M. C., Waliszewska, A., Neubauer, J., Tandon, A., Schirmer, C., McDonald, G. J., et al. (2007) · Nature Genetics · doi:10.1038/ng2015 · Cited by 663
High-throughput DNA methylation profiling using universal bead arrays
Bibikova, M., Lin, Z., Zhou, L., Chudin, E., Garcia, E. W., Wu, B., Doucet, D., Thomas, N. J., Wang, Y., Vollmer, E., et al. (2006) · Genome Research · doi:10.1101/gr.4410706 · Cited by 657
Self-citationAdmixture mapping identifies 8q24 as a prostate cancer risk locus in African-American men
Freedman, M. L., Haiman, C. A., Patterson, N., McDonald, G. J., Tandon, A., Waliszewska, A., Penney, K., Steen, R. G., Ardlie, K., John, E. M., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605832103 · Cited by 612
Genomic Selection in Plant Breeding
Lorenz, A. J., Chao, S., Asoro, F. G., Heffner, E. L., Hayashi, T., Iwata, H., Smith, K. P., Sorrells, M. E., & Jannink, J.-L. (2011) · Advances in Agronomy · doi:10.1016/b978-0-12-385531-2.00002-5 · Cited by 477
Metadata
- Authors
- FAN, J.-B., OLIPHANT, A., SHEN, R., KERMANI, B. G., GARCIA, F., GUNDERSON, K. L., HANSEN, M., STEEMERS, F., BUTLER, S. L., DELOUKAS, P., GALVER, L., HUNT, S., MCBRIDE, C., BIBIKOVA, M., RUBANO, T., CHEN, J., WICKHAM, E., DOUCET, D., CHANG, W., CAMPBELL, D., ZHANG, B., KRUGLYAK, S., BENTLEY, D., HAAS, J., RIGAULT, P., ZHOU, L., STUELPNAGEL, J., & CHEE, M. S.
- Venue
- Cold Spring Harbor Symposia on Quantitative Biology
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2003-01-01
- Volume
- 68
- Issue
- 0
- Pages
- 69-78
- ISSN
- 0091-7451 (ISSN-L)
- 1943-4456
- OpenAlex
- W2071199144
- Cited by
- 635
- References
- 3
- Type
- posted content
- Language
- en
- Open access
- closed
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- The paper
- FAN, J.-B., OLIPHANT, A., SHEN, R., KERMANI, B. G., GARCIA, F., GUNDERSON, K. L., HANSEN, M., STEEMERS, F., BUTLER, S. L., DELOUKAS, P., GALVER, L., HUNT, S., MCBRIDE, C., BIBIKOVA, M., RUBANO, T., CHEN, J., WICKHAM, E., DOUCET, D., CHANG, W., . . . CHEE, M. S. (2003). Highly Parallel SNP Genotyping. Cold Spring Harbor Symposia on Quantitative Biology. https://doi.org/10.1101/sqb.2003.68.69
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