116 related articles for article (PubMed ID: 20707788)
1. Allele-sharing statistics using information on family history.
Callegaro A; Meulenbelt I; Kloppenburg M; Slagboom PE; Houwing-Duistermaat JJ
Ann Hum Genet; 2010 Nov; 74(6):547-54. PubMed ID: 20707788
[TBL] [Abstract][Full Text] [Related]
2. Tests for covariate-associated heterogeneity in IBD allele sharing of affected relatives.
Mirea L; Briollais L; Bull S
Genet Epidemiol; 2004 Jan; 26(1):44-60. PubMed ID: 14691956
[TBL] [Abstract][Full Text] [Related]
3. Appropriate use of information on family history of disease in recruitment for linkage analysis studies.
Wallace C; Clayton DG
Ann Hum Genet; 2006 May; 70(Pt 3):360-71. PubMed ID: 16674558
[TBL] [Abstract][Full Text] [Related]
4. Powerful allele sharing statistics for nonparametric linkage analysis.
Lange EM; Lange K
Hum Hered; 2004; 57(1):49-58. PubMed ID: 15133312
[TBL] [Abstract][Full Text] [Related]
5. The power of two-locus affected sib-pair linkage analysis to detect interacting disease loci.
Hallgrímsdóttir IB; Speed TP
Genet Epidemiol; 2008 Jan; 32(1):84-8. PubMed ID: 17654608
[TBL] [Abstract][Full Text] [Related]
6. Affected-sib-pair test for linkage based on constraints for identical-by-descent distributions corresponding to disease models with imprinting.
Knapp M; Strauch K
Genet Epidemiol; 2004 May; 26(4):273-85. PubMed ID: 15095387
[TBL] [Abstract][Full Text] [Related]
7. A new strategy for linkage analysis under epistasis taking into account genetic heterogeneity.
Bureau A; Mérette C; Croteau J; Fournier A; Chagnon YC; Roy MA; Maziade M
Hum Hered; 2009; 68(4):231-42. PubMed ID: 19622890
[TBL] [Abstract][Full Text] [Related]
8. Genetic heterogeneity in schizophrenia II: conditional analyses of affected schizophrenia sibling pairs provide evidence for an interaction between markers on chromosome 8p and 14q.
Chiu YF; McGrath JA; Thornquist MH; Wolyniec PS; Nestadt G; Swartz KL; Lasseter VK; Liang KY; Pulver AE
Mol Psychiatry; 2002; 7(6):658-64. PubMed ID: 12140791
[TBL] [Abstract][Full Text] [Related]
9. Comparison of allele-sharing statistics for general pedigrees.
Feingold E; Song KK; Weeks DE
Genet Epidemiol; 2000; 19 Suppl 1():S92-8. PubMed ID: 11055376
[TBL] [Abstract][Full Text] [Related]
10. Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 3, 5, 15, 16, 17, and 22.
Edenberg HJ; Foroud T; Conneally PM; Sorbel JJ; Carr K; Crose C; Willig C; Zhao J; Miller M; Bowman E; Mayeda A; Rau NL; Smiley C; Rice JP; Goate A; Reich T; Stine OC; McMahon F; DePaulo JR; Meyers D; Detera-Wadleigh SD; Goldin LR; Gershon ES; Blehar MC; Nurnberger JI
Am J Med Genet; 1997 May; 74(3):238-46. PubMed ID: 9184305
[TBL] [Abstract][Full Text] [Related]
11. Using family history information to distinguish true and false positive model-free linkage results.
Olson JM; Elston RC
Genet Epidemiol; 1998; 15(2):183-92. PubMed ID: 9554555
[TBL] [Abstract][Full Text] [Related]
12. Relative risks and effective number of meioses: a unified approach for general genetic models and phenotypes.
Kurbasic A; Hössjer O
Ann Hum Genet; 2006 Nov; 70(Pt 6):907-22. PubMed ID: 17044865
[TBL] [Abstract][Full Text] [Related]
13. Conditional multipoint linkage analysis using affected sib pairs: an alternative approach.
Chiu YF; Liang KY
Genet Epidemiol; 2004 Feb; 26(2):108-15. PubMed ID: 14748010
[TBL] [Abstract][Full Text] [Related]
14. HLA and susceptibility to juvenile idiopathic arthritis: a study of affected sibpairs in an isolated Finnish population.
Säilä H; Pitkäniemi J; Tuomilehto J; Savolainen A; Alakulppi N; Tuomilehto-Wolf E; Leirisalo-Repo M; Aho K
J Rheumatol; 2004 Nov; 31(11):2281-5. PubMed ID: 15517645
[TBL] [Abstract][Full Text] [Related]
15. Assessing the contribution family data can make to case-control studies of rare variants.
Curtis D
Ann Hum Genet; 2011 Sep; 75(5):630-8. PubMed ID: 21675965
[TBL] [Abstract][Full Text] [Related]
16. Comprehensive linkage and linkage heterogeneity analysis of 4344 sibling pairs affected with hypertension from the Family Blood Pressure Program.
Greenwood TA; Libiger O; Kardia S; Hanis C; Morrison AC; Gu CC; Rice T; Miller M; Turner ST; Myers RH; Grove J; Hsiao CF; Weder AB; Schork NJ
Genet Epidemiol; 2007 Apr; 31(3):195-210. PubMed ID: 17266112
[TBL] [Abstract][Full Text] [Related]
17. A class of tests for linkage using affected pedigree members.
Whittemore AS; Halpern J
Biometrics; 1994 Mar; 50(1):118-27. PubMed ID: 8086596
[TBL] [Abstract][Full Text] [Related]
18. A score test for linkage analysis of ordinal traits based on IBD sharing.
Feng R; Zhang H
Biostatistics; 2008 Jan; 9(1):114-27. PubMed ID: 17519391
[TBL] [Abstract][Full Text] [Related]
19. Optimal allele-sharing statistics for genetic mapping using affected relatives.
McPeek MS
Genet Epidemiol; 1999; 16(3):225-49. PubMed ID: 10096687
[TBL] [Abstract][Full Text] [Related]
20. Irish study on high-density schizophrenia families: field methods and power to detect linkage.
Kendler KS; O'Neill FA; Burke J; Murphy B; Duke F; Straub RE; Shinkwin R; Ni Nuallain M; MacLean CJ; Walsh D
Am J Med Genet; 1996 Apr; 67(2):179-90. PubMed ID: 8723045
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
