Page 181 - Applied Probability

8. The Polygenic Model
166
[2] Barnholtz JS, de Andrade M, Page GP, King TM, Peterson LE, Amos
CI (1999) Assessing linkage of monoamine oxidase B in a genome-
wide scan using a variance components approach. Genet Epidemiol
17(Supplement 1):S49–S54
[3] Blangero J, Almasy L (1997) Multipoint oligogenic linkage analysis of
quantitative traits. Genet Epidemiol 14:959–964
[4] Boerwinkle E, Chakraborty R, Sing CF (1986) The use of measured
genotype information in the analysis of quantitative phenotypes in
man. I. Models and analytical methods. Ann Hum Genet 50:181–194
[5] Cannings C, Thompson EA, Skolnick MH (1978) Probability functions
on complex pedigrees. Adv Appl Prob 10:26–61
[6] Daiger SP, Miller M, Chakraborty R (1984) Heritability of quantitative
variation at the group-specific component (Gc) locus. Amer J Hum
Genet 36:663–676
[7] Dempster AP, Laird NM, Rubin DB (1977) Maximum likelihood esti-
mation with incomplete data via the EM algorithm (with discussion).
J Roy Stat Soc B 39:1–38

[8] Elston RC, Stewart J (1971) A general model for the genetic analysis
of pedigree data. Hum Hered 21:523–542

[9] Falconer DS (1965) The inheritance of liability to certain diseases,
estimated from the incidences among relatives. Ann Hum Genet 29:51–
79

[10] Falconer DS (1967) The inheritance of liability to diseases with vari-
able age of onset, with particular reference to diabetes mellitus. Ann
Hum Genet 31:1–20
[11] Fernando RL, Stricker C, Elston RC (1994) The finite polygenic mixed
model: An alternative formulation for the mixed model of inheritance.
Theor Appl Genet 88:573–580

[12] Fisher RA (1918) The correlation between relatives on the supposition
of Mendelian inheritance. Trans Roy Soc Edinburgh 52:399–433
[13] Goldgar DE (1990) Multipoint analysis of human quantitative genetic
variation.
Amer J Hum Genet 47:957–967

[14] Holt SB (1954) Genetics of dermal ridges: Bilateral asymmetry in fin-
ger ridge-counts. Ann Eugenics 18:211–231