參考文獻
何世屏 (2009)。遺傳學:分子探索。臺中市:五南圖書出版股份有限公司。
吳性慧 (2006)。利用親子二元體資料建立尋找疾病基因的相關分析。國立台灣大學流行病學研究所碩士論文,臺北市。
邱文雍 (2008)。合併親子三元體資料標識基因下傳/不下傳訊息與相似度訊息之相關分析方法。國立台灣大學流行病學研究所碩士論文,臺北市。武光東、劉權章 (1998)。遺傳諮詢。臺北市:合記圖書出版社。
范文穎 (2008)。利用家族資料不同型式相關訊息建立家族相關檢定方法。天主教輔仁大學應用統計研究所碩士論文,新北市。
鄭又綸 (2009)。家族資料相關檢定之遺傳訊息萃取與合併方法探討。天主教輔仁大學應用統計研究所碩士論文,新北市。戴政 (2002)。遺傳流行病學:基因定位之遺傳設計與分析方法。新北市:藝軒圖書文具有限公司。
Abel, L., Alcais, A., & Mallet, A. (1998). Comparison of four sib-pair linkage methods for analyzing sibships with more than two affecteds: interest of the binomial maximum likelihood approach. Genetic Epidemiology, 15(4), 371-390.
Bhattacharya, N. (1961). Sapling experiments on the combination of independent -tests. Sankhya Ser. A, 23(2), 191-196.
Blackwelder, W. C., & Elston, R. C. (1985). Acomparison of sib-pair linkage tests for disease susceptibility loci. Genetic Epidemiology, 2(1), 85-97.
Bourgain, C., Genin, E., Quesneville, H., & Clerget-Darpoux, F. (2000). Search for multifactorial disease susceptibility genes in founder populations. Annals of Human Genetics, 64(3), 255-265.
Camp, N. (1997). Genomewide transmission/disequilibrium testing- consideration of the genotypic relative risks at disease loci. The American Journal of Human Genetics, 61(6), 1424-1430.
Falk, C. T., & Rubinstein, P. (1987). Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculations. Annals of Human Genetics, 51(3), 227-233.
Gibson, G., & Muse, S. V. (2002). A primer of Genome Science. MA: Sinauer Associates, INC.
Hershey, A. D., & Chase, M. (1952). Independent functions of viral protein and nucleic acid in growth of bacteriophage. The Journal of General Physiology, 36(1), 39-56.
Holmans, P. (1993). Asymptotic properties of affected-sib-pair linkage analysis. The American Journal of Human Genetics, 52(2), 362-374.
Li, C. C. (1996). Population genetics of coincidental DNA matches. Human Biology, 68(2), 167-184.
Martin, E. R., Monks, S. A., Warren, L. L., & Kaplan, N. L. (2000). A test for linkage and association in general pedigrees: the pedigree disequilibrium test. The American Journal of Human Genetics, 67(1), 146-154.
Martin, E. R., Bass, M. P., & Kaplan, N. L. (2001). Correcting for a potential bias in the pedigree disequilibrium test. The American Journal of Human Genetics, 68(4), 1065-1067.
McNemar, Q. (1947). Note on the sampling error of the difference between correlated proportions or percentages. Psychometrika, 12(2), 153-157.
Ott, J. (1989). Statistical properties of the haplotype relative risk. Genetic Epidemiology, 6(1), 127-130.
Schaid, D. J., McDonnell, S. K., Hebbring, S. J., Cunningham, J. M., & Thibodeau, S. N. (2005). Nonparametric tests of association of multiple genes with human disease. The American Journal of Human Genetics, 76(5), 780-793.
Spielman, R. S., McGinnis, R. E., & Ewens, W. J. (1993). Transmission test for linkage disequilibrium: the insulin gene region and insulin- dependent diabetes mellitus (IDDM). The American Journal of Human Genetics, 52(3), 506-516.
Tai, J. J., & Hou, C. D. (2006). On the combination of transmission /disequilibrium test and mean test for linkage detection using affected sib pairs. Computational Statistics & Data Analysis, 50, 1072-1089.
Wei, L. J., & Johnson, W. E. (1985). Combining dependent tests with incomplete repeated measurements. Biometrika, 72(2), 359-364.
Wicks, J., & Wilson, S. R. (2000). Evaluating linkage and linkage disequilibrium: use of excess sharing and transmission disequilibrium methods in affected sib pairs. Annals of Human Genetics, 64(5), 419-432.
Xu, X., Weiss, S., Xu, X., & Wei, L. J. (2000). A unified haseman-elston method for testing linkage with quantitative traits. The American Journal of Human Genetics, 67(4), 1025-1028.