| 1. |
Risch, N. and Merikangas, K. (1996) The future of genetic studies of complex diseases. Science
273, 1516–1517.
|
| |
| 2. |
Zondervan, K. T. and Cardon, L. R. (2004) The complex interplay among factors that influence allelic association. Nat. Rev. Genet.
5, 89–100.
|
| |
| 3. |
Kingman, J. F. C. (1982) The coalescent. Stoch. Proc. Appl.
13, 235–248.
|
| |
| 4. |
Nordborg, M. (2001) Coalescent theory. In: Handbook of Statistical Genetics (Balding, D. J., Bishop, M., and Cannings, C., eds.), Wiley, Chichester, UK, pp. 179–212.
|
| |
| 5. |
McPeek, M. S. and Strahs, A. (1999) Assessment of linkage disequilibrium by the decay of haplotype sharing, with application
to fine-scale genetic mapping. Am. J. Hum. Genet.
65, 858–875.
|
| |
| 6. |
Slatkin, M. (1996) Gene genealogies within mutant allelic classes. Genetics
143, 579–587.
|
| |
| 7. |
Wiuf, C. and Donnelly, P. (1999) Conditional genealogies and the age of a neutral mutant. Theor. Popul. Biol.
56, 183–201.
|
| |
| 8. |
Hudson, R. R. (1983) Properties of a neutral allele model with intragenic recombination. Theor. Popul. Biol.
23, 183–201.
|
| |
| 9. |
Griffiths, R. C. and Marjoram, P. (1996) Ancestral inference from samples of DNA sequences with recombination. J. Comput. Biol.
3, 479–502.
|
| |
| 10. |
Griffiths, R. C. and Marjoram, P. (1997) An ancestral recombination graph. In: Progress in Population Genetics and Human Evolution, (Donnelly, P. and Tavare, S., eds.), Springer-Verlag, New York, NY, pp. 257–270.
|
| |
| 11. |
Rannala, B. and Reeve, J. P. (2001) High-resolution multipoint linkage disequilibrium mapping in the context of a human genome
sequence. Am. J. Hum. Genet.
69, 159–178.
|
| |
| 12. |
Morris, A. P., Whittaker, J. C., and Balding, D. J. (2002) Fine-scale mapping of disease loci via coalescent modelling of
genealogies. Am. J. Hum. Genet.
70, 686–707.
|
| |
| 13. |
Liu, J. S., Sabatti, C., Teng, J., Keats, B. J. B., and Risch, N. (2001) Bayesian analysis of haplotypes for linkage disequilibrium
mapping. Genome Res.
11, 1716–1724.
|
| |
| 14. |
Strahs, A. L. and McPeek, M. S. (2003) Multipoint fine-scale linkage disequilibrium mapping: the importance of modeling background
LD. In: IMS Lecture Notes Monograph Series, Vol. 40 Science and Statistics, (Festschrift, A. and Goldstein, D. R., eds.), Institute of Mathematical Statistics, Beachwood, OH, pp. 343–366.
|
| |
| 15. |
Slatkin, M. and Rannala, B. (1997) Estimating the age of alleles by the use of intraallelic variability. Am. J. Hum. Genet.
60, 447–458.
|
| |
| 16. |
Metropolis, N., Rosenbluth, A. W., Rosenbluth, M. N., Teller, A. H., and Teller, E. (1953) Equation of state calculations
by fast computing machines. J. Chem. Phys.
21, 1087–1092.
|
| |
| 17. |
Hastings, W. K. (1970) Monte-Carlo sampling methods using Markov chains and their applications. Biometrika
57, 97–109.
|
| |
| 18. |
Gammerman, D. (1997) Markov Chain Monte Carlo: Stochastic Simulation for BayesianInference. Chapman and Hall, London, UK.
|
| |
| 19. |
Hartigan, J. A. (1975) Clustering Algorithms. Wiley, New York, NY.
|
| |
| 20. |
Zollner, S. and Pritchard, J. K. (2005) Coalescent-based association mapping and fine mapping of complex trait loci. Genetics
169, 1071–1092.
|
| |
| 21. |
Felsenstein, J. (1981) Evolutionary trees from DNA sequences: a maximum likelihood approach. J. Mol. Evol.
17, 368–376.
|
| |
| 22. |
Bertranpetit, J. and Calafell, F. (1996) Genetic and geographical variability in cystic fibrosis: evolutionary considerations.
In: Variation in the Human Genome, (Weiss, K., ed.), Wiley, Chichester, UK, pp. 97–114.
|
| |
| 23. |
Kerem, B., Rommens, J. M., Buchanan, J. A., et al. (1989) Identification of the cystic fibrosis gene: genetic analysis. Science
245, 1073–1080.
|
| |
| 24. |
Morris, A. P., Whittaker, J. C., and Balding, D. J. (2002) Little loss of information due to unknown phase for fine-scale
linkage disequilibrium mapping with single nucleotide polymorphism genotype data. Am. J. Hum. Genet.
74, 945–953.
|
| |
| 25. |
Stephens, M., Smith, N. J., and Donnelly, P. (2001) A new statistical method for haplotype reconstruction from population
data. Am. J. Hum. Genet.
68, 978–989.
|
| |
| 26. |
Stephens, M. and Donnelly, P. (2003) A comparison of Bayesian methods for haplotype reconstruction from population genotype
data. Am. J. Hum. Genet.
73, 1162–1169.
|
| |
| 27. |
Molitor, J., Marjoram, P., and Thomas, D. (2003) Application of Bayesian spatial statistical methods to the analysis of haplotype
effects and gene mapping. Genet. Epidemiol.
25, 95–105.
|
| |
| 28. |
Molitor, J., Marjoram, P., and Thomas, D. (2003) Fine-scale mapping of disease genes with multiple mutations via spatial clustering
techniques. Am. J. Hum. Genet.
73, 1368–1384.
|
| |
| 29. |
International Human Genome Sequence Consortium (2001) Initial sequencing and analysis of the human genome. Nature
409, 860–921.
|
| |
| 30. |
International SNP Map Working Group (2001) A map of the human genome sequence variation contains 1.42 million single nucleotide
polymorphisms. Nature
409, 860–921.
|
| |
| 31. |
International HapMap Consortium (2003) The international HapMap project. Nature
426, 789–795.
|
| |