Citation: D. Gordon et al., A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data, AM J HU GEN, 69(2), 2001, pp. 371-380
Authors:
Knoblauch, H
Muller-Myhsok, B
Busjahn, A
Ben Avi, L
Bahring, S
Baron, H
Heath, SC
Uhlmann, R
Faulhaber, HD
Shpitzen, S
Aydin, A
Reshef, A
Rosenthal, M
Eliav, O
Muhl, A
Lowe, A
Schurr, D
Harats, D
Jeschke, E
Friedlander, Y
Schuster, H
Luft, FC
Leitersdorf, E
Citation: H. Knoblauch et al., A cholesterol-lowering gene maps to chromosome 13q, AM J HU GEN, 66(1), 2000, pp. 157-166
Authors:
Shmulewitz, D
Auerbach, SB
Lehner, T
Blundell, ML
Winick, JD
Youngman, LD
Skilling, V
Heath, SC
Ott, J
Stoffel, M
Breslow, JL
Friedman, JM
Citation: D. Shmulewitz et al., Epidemiology and factor analysis of obesity, type II diabetes, hypertension, and dyslipidemia (syndrome X) on the Island of Kosrae, Federated States of Micronesia, HUMAN HERED, 51(1-2), 2000, pp. 8-19
Authors:
Dansky, HM
Charlton, SA
Sikes, JL
Heath, SC
Simantov, R
Levin, LF
Shu, P
Moore, KJ
Breslow, JL
Smith, JD
Citation: Hm. Dansky et al., Genetic background determines the extent of atherosclerosis in ApoE-deficient mice, ART THROM V, 19(8), 1999, pp. 1960-1968
Citation: Sm. Leal et Sc. Heath, Searching for alcoholism susceptibility genes using Markov chain Monte Carlo methods, GENET EPID, 17, 1999, pp. S217-S222
Citation: D. Gordon et al., Power loss for multiallelic transmission/disequilibrium test when errors introduced: GAW11 simulated data, GENET EPID, 17, 1999, pp. S587-S592
Authors:
Johnson, WG
Stenroos, ES
Heath, SC
Chen, YP
Carroll, R
McKoy, VV
Chatkupt, S
Lehner, T
Citation: Wg. Johnson et al., Distribution of alleles of the methylenetetrahydrofolate reductase (MTHFR)C677T gene polymorphism in familial spina bifida, AM J MED G, 87(5), 1999, pp. 407-412
Citation: Ew. Daw et al., Multipoint oligogenic analysis of age-at-onset data with applications to Alzheimer disease pedigrees, AM J HU GEN, 64(3), 1999, pp. 839-851
Citation: D. Gordon et al., True pedigree errors more frequent than apparent errors for single nucleotide polymorphisms, HUMAN HERED, 49(2), 1999, pp. 65-70