Название: Genetic Analysis of Complex Disease
Автор: Группа авторов
Издательство: John Wiley & Sons Limited
Жанр: Биология
isbn: 9781119104070
isbn:
70 Piegorsch, W.W., Weinberg, C.R., and Taylor, J.A. (1994). Non‐hierarchical logistic models and case‐only designs for assessing susceptibility in population‐based case‐control studies. Stat. Med. 13: 153–162.
71 Rice, T., Despres, J.P., Daw, E.W. et al. (1997). Familial resemblance for abdominal visceral fat: the HERITAGE family study. Int. J. Obes. Relat. Metab. Disord. 21: 1024–1031.
72 Risch, N. (1990a). Linkage strategies for genetically complex traits. I. Multilocus models. Am. J. Hum. Genet. 46: 222–228.
73 Risch, N. (1990b). Linkage strategies for genetically complex traits. II. The power of affected relative pairs. Am. J. Hum. Genet. 46: 229–241.
74 Risch, N. (1990c). Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs. Am. J. Hum. Genet. 46: 242–253.
75 Roses, A.D., Devlin, B., Conneally, P.M. et al. (1995). Measuring the genetic contribution of APOE in late‐onset Alzheimer disease (AD). Am. J. Hum. Genet. 57: A202.
76 Rothman, K.J. and Greenland, S. (1998). Modern Epidemiology. Philadelphia, PA: Lippincott‐Raven.
77 Rousseau, F., Heitz, D., Tarleton, J. et al. (1994). Higher rate of transition from fragile X permutations into full mutation in males than in females suggest post‐conceptional expansion of the CGG repeats. Am. J. Hum. Genet. 55: A240.
78 Rumble, B., Retallack, R., Hilbich, C. et al. (1989). Amyloid A4 protein and its precursor in down's syndrome and Alzheimer's disease. N. Engl. J. Med. 320: 1446–1452.
79 Seybolt, L.M., Vachon, C., Potter, K. et al. (1997). Evaluation of potential sources of bias in a genetic epidemiologic study of breast cancer. Genet. Epidemiol. 14: 85–95.
80 Sherman, S.L., Morton, N.E., Jacobs, P.A., and Turner, G. (1984). The marker (X) syndrome: a cytogenetic and genetic analysis. Ann. Hum. Genet. 48 (Pt 1): 21–37.
81 Shields, R. and Dell, H. (2001). Genes for HIV susceptibility. Trends Genet. 17: 19.
82 Speed, D., Cai, N., the UCLEB Consortium et al. (2017). Reevaluation of SNP heritability in complex human traits. Nat. Genet. 49: 986–992.
83 St George‐Hyslop, P.H., Tanzi, R.E., Polinsky, R.J. et al. (1987). The genetic defect causing familial Alzheimer's disease maps on chromosome 21. Science 235: 885–890.
84 Stene, J. (1989). The incomplete, multiple ascertainment model: assumptions, applications, and alternative models. Genet. Epidemiol. 6: 247–251.
85 Terwilliger, J.D. and Goring, H.H. (2000). Gene mapping in the 20th and 21st centuries: statistical methods, data analysis, and experimental design. Hum. Biol. 72: 63–132.
86 Turkmen, A.S. and Lin, S. (2020). Detecting X‐linked common and rare variant effects in family‐based sequencing studies. Genet. Epidemiol. 45 (1): 36–45. https://doi.org/10.1002/gepi.22352. Epub 2020 Aug 30.
87 Vieland, V.J. and Hodge, S.E. (1996). The problem of ascertainment for linkage analysis. Am. J. Hum. Genet. 58: 1072–1084.
88 Waller, D.K., Anderson, J.L., Lorey, F., and Cunningham, G.C. (2000). Risk factors for congenital hypothyroidism: an investigation of infant's birth weight, ethnicity, and gender in California, 1990–1998. Teratology 62: 36–41.
89 Weeks, D.E. and Lange, K. (1988). The affected‐pedigree‐member method of linkage analysis. Am. J. Hum. Genet. 42: 315–326.
90 Weinberg, W. (1912). Zur Verebung der Anlage der Bluterkrankheit mit methodol. Erganzungen meiner Geschwistermethode. Arch. Rass. Ges. Biol. 6: 694–709.
91 Wellcome Trust Case Control Consortium (2007). Genome‐wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447: 661–678.
92 Wilk, J.B., Djousse, L., Arnett, D.K. et al. (2000). Evidence for major genes influencing pulmonary function in the NHLBI family heart study. Genet. Epidemiol. 19: 81–94.
93 Wolpert, C.M., Menold, M.M., Bass, M.P. et al. (2000). Three probands with autistic disorder and isodicentric chromosome 15. Am. J. Med. Genet. 96: 365–372.
94 Yang, J., Benyamin, B., McEvoy, B.P. et al. (2010). Common SNPs explain a large proportion of the heritability for human height. Nat. Genet. 42 (7): 565–569.
95 Yang, J., Lee, S.H., Goddard, M.E., and Visscher, P.M. (2011). GCTA: a tool for genome‐wide complex trait analysis. Am. J. Hum. Genet. 88 (1): 76–82.
Конец ознакомительного фрагмента.
Текст предоставлен ООО «ЛитРес».
Прочитайте эту книгу целиком, купив полную легальную версию на ЛитРес.
Безопасно оплатить книгу можно банковской картой Visa, MasterCard, Maestro, со счета мобильного телефона, с платежного терминала, в салоне МТС или Связной, через PayPal, WebMoney, Яндекс.Деньги, QIWI Кошелек, бонусными картами или другим удобным Вам способом.