119 related articles for article (PubMed ID: 8787983)
1. Screening for linkage and association in nuclear families.
Knapp M; Durner M; Baur MP
Genet Epidemiol; 1995; 12(6):619-23. PubMed ID: 8787983
[TBL] [Abstract][Full Text] [Related]
2. The TDT reveals linkage and linkage disequilibrium in a rare disease.
McGinnis RE; Ewens WJ; Spielman RS
Genet Epidemiol; 1995; 12(6):637-40. PubMed ID: 8787986
[TBL] [Abstract][Full Text] [Related]
3. Detection of vulnerability loci by association and sib-pair methods.
Levinson DF
Genet Epidemiol; 1995; 12(6):631-5. PubMed ID: 8787985
[TBL] [Abstract][Full Text] [Related]
4. Effects of marker information on sib-pair linkage analysis of a rare disease.
Korczak JF; Pugh EW; Premkumar S; Guo X; Elston RC; Bailey-Wilson JE
Genet Epidemiol; 1995; 12(6):625-30. PubMed ID: 8787984
[TBL] [Abstract][Full Text] [Related]
5. Sib-pair linkage analyses of nuclear family data: quantitative versus dichotomous disease classification.
Korczak JF; Goldstein AM
Genet Epidemiol; 1997; 14(6):827-32. PubMed ID: 9433585
[TBL] [Abstract][Full Text] [Related]
6. Interpretation of simultaneous linkage and family-based association tests in genome screens.
Chung RH; Hauser ER; Martin ER
Genet Epidemiol; 2007 Feb; 31(2):134-42. PubMed ID: 17123303
[TBL] [Abstract][Full Text] [Related]
7. Exact transmission-disequilibrium tests with multiallelic markers.
Cleves MA; Olson JM; Jacobs KB
Genet Epidemiol; 1997; 14(4):337-47. PubMed ID: 9271708
[TBL] [Abstract][Full Text] [Related]
8. Power calculations for a general class of tests of linkage and association that use nuclear families with affected and unaffected sibs.
Kaplan NL; Martin ER
Theor Popul Biol; 2001 Nov; 60(3):193-201. PubMed ID: 11855953
[TBL] [Abstract][Full Text] [Related]
9. Genotype relative-risks and association tests for nuclear families with missing parental data.
Schaid DJ; Li H
Genet Epidemiol; 1997; 14(6):1113-8. PubMed ID: 9433633
[TBL] [Abstract][Full Text] [Related]
10. Use of siblings as controls in case-control association studies.
Curtis D
Ann Hum Genet; 1997 Jul; 61(Pt 4):319-33. PubMed ID: 9365785
[TBL] [Abstract][Full Text] [Related]
11. Circumventing multiple testing: a multilocus Monte Carlo approach to testing for association.
McIntyre LM; Martin ER; Simonsen KL; Kaplan NL
Genet Epidemiol; 2000 Jul; 19(1):18-29. PubMed ID: 10861894
[TBL] [Abstract][Full Text] [Related]
12. Genome scan for association and linkage.
Holmans P; McGuffin P; Clayton D
Genet Epidemiol; 1995; 12(6):613-8. PubMed ID: 8787982
[TBL] [Abstract][Full Text] [Related]
13. Effectiveness of extreme discordant sib pairs to detect oligogenic disease loci.
Rogus JJ; Harrington DP; Jorgenson E; Xu X
Genet Epidemiol; 1997; 14(6):879-84. PubMed ID: 9433594
[TBL] [Abstract][Full Text] [Related]
14. Use of exact and adjusted liability scores to detect genes affecting common traits.
Goldin LR; Chase GA; King TM; Badner JA; Gershon ES
Genet Epidemiol; 1995; 12(6):765-9. PubMed ID: 8788006
[TBL] [Abstract][Full Text] [Related]
15. Randomization tests of disease-marker associations.
Morris AP; Curnow RN; Whittaker JC
Ann Hum Genet; 1997 Jan; 61(Pt 1):49-60. PubMed ID: 9066927
[TBL] [Abstract][Full Text] [Related]
16. Informative-transmission disequilibrium test (i-TDT): combined linkage and association mapping that includes unaffected offspring as well as affected offspring.
Guo CY; Lunetta KL; DeStefano AL; Ordovas JM; Cupples LA
Genet Epidemiol; 2007 Feb; 31(2):115-33. PubMed ID: 17123304
[TBL] [Abstract][Full Text] [Related]
17. Genome scanning for complex disease genes using the transmission/disequilibrium test and haplotype-based haplotype relative risk.
Matise TC
Genet Epidemiol; 1995; 12(6):641-5. PubMed ID: 8787987
[TBL] [Abstract][Full Text] [Related]
18. Optimal weighting scheme for affected sib-pair analysis of sibship data.
Sham PC; Zhao JH; Curtis D
Ann Hum Genet; 1997 Jan; 61(Pt 1):61-9. PubMed ID: 9066928
[TBL] [Abstract][Full Text] [Related]
19. High resolution T association tests of complex diseases based on family data.
Fan R; Knapp M; Wjst M; Zhao C; Xiong M
Ann Hum Genet; 2005 Mar; 69(Pt 2):187-208. PubMed ID: 15720300
[TBL] [Abstract][Full Text] [Related]
20. Statistical genetics of normal variation in family data for oligogenic diseases.
Mahaney MC; Jaquish CE; Comuzzie AG
Genet Epidemiol; 1995; 12(6):783-7. PubMed ID: 8788009
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
