225 related articles for article (PubMed ID: 10677324)
21. HAPLORE: a program for haplotype reconstruction in general pedigrees without recombination.
Zhang K; Sun F; Zhao H
Bioinformatics; 2005 Jan; 21(1):90-103. PubMed ID: 15231536
[TBL] [Abstract][Full Text] [Related]
22. TreeDT: tree pattern mining for gene mapping.
Sevon P; Toivonen H; Ollikainen V
IEEE/ACM Trans Comput Biol Bioinform; 2006; 3(2):174-85. PubMed ID: 17048403
[TBL] [Abstract][Full Text] [Related]
23. Transmission/disequilibrium test meets measured haplotype analysis: family-based association analysis guided by evolution of haplotypes.
Seltman H; Roeder K; Devlin B
Am J Hum Genet; 2001 May; 68(5):1250-63. PubMed ID: 11309689
[TBL] [Abstract][Full Text] [Related]
24. Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified.
Göring HH; Terwilliger JD
Am J Hum Genet; 2000 Apr; 66(4):1310-27. PubMed ID: 10731466
[TBL] [Abstract][Full Text] [Related]
25. Bayesian fine-scale mapping of disease loci, by hidden Markov models.
Morris AP; Whittaker JC; Balding DJ
Am J Hum Genet; 2000 Jul; 67(1):155-69. PubMed ID: 10835299
[TBL] [Abstract][Full Text] [Related]
26. Localization of psoriasis-susceptibility locus PSORS1 to a 60-kb interval telomeric to HLA-C.
Nair RP; Stuart P; Henseler T; Jenisch S; Chia NV; Westphal E; Schork NJ; Kim J; Lim HW; Christophers E; Voorhees JJ; Elder JT
Am J Hum Genet; 2000 Jun; 66(6):1833-44. PubMed ID: 10801386
[TBL] [Abstract][Full Text] [Related]
27. Maximum-likelihood estimation of gene location by linkage disequilibrium.
Hill WG; Weir BS
Am J Hum Genet; 1994 Apr; 54(4):705-14. PubMed ID: 8128969
[TBL] [Abstract][Full Text] [Related]
28. Anonymous marker loci within 400 kb of HLA-A generate haplotypes in linkage disequilibrium with the hemochromatosis gene (HFE).
Yaouanq J; Perichon M; Chorney M; Pontarotti P; Le Treut A; el Kahloun A; Mauvieux V; Blayau M; Jouanolle AM; Chauvel B
Am J Hum Genet; 1994 Feb; 54(2):252-63. PubMed ID: 8304342
[TBL] [Abstract][Full Text] [Related]
29. Detection of disease genes by use of family data. I. Likelihood-based theory.
Whittemore AS; Tu IP
Am J Hum Genet; 2000 Apr; 66(4):1328-40. PubMed ID: 10739758
[TBL] [Abstract][Full Text] [Related]
30. Significant admixture linkage disequilibrium across 30 cM around the FY locus in African Americans.
Lautenberger JA; Stephens JC; O'Brien SJ; Smith MW
Am J Hum Genet; 2000 Mar; 66(3):969-78. PubMed ID: 10712211
[TBL] [Abstract][Full Text] [Related]
31. HLA-A3-B14 and the origin of the haemochromatosis C282Y mutation: founder effects and recombination events during 12 generations in a Scandinavian family with major iron overload.
Olsson KS; Ritter B; Raha-Chowdhury R
Eur J Haematol; 2010 Feb; 84(2):145-53. PubMed ID: 19912313
[TBL] [Abstract][Full Text] [Related]
32. A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a heterozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA association.
Simon M; Le Mignon L; Fauchet R; Yaouanq J; David V; Edan G; Bourel M
Am J Hum Genet; 1987 Aug; 41(2):89-105. PubMed ID: 3475981
[TBL] [Abstract][Full Text] [Related]
33. On selecting markers for association studies: patterns of linkage disequilibrium between two and three diallelic loci.
Garner C; Slatkin M
Genet Epidemiol; 2003 Jan; 24(1):57-67. PubMed ID: 12508256
[TBL] [Abstract][Full Text] [Related]
34. Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: implications for mapping the hemochromatosis gene (HFE).
Gandon G; Jouanolle AM; Chauvel B; Mauvieux V; le Treut A; Feingold J; Le Gall JY; David V; Yaouanq J
Hum Genet; 1996 Jan; 97(1):103-13. PubMed ID: 8557248
[TBL] [Abstract][Full Text] [Related]
35. The role of hemochromatosis susceptibility gene mutations in protecting against iron deficiency in celiac disease.
Butterworth JR; Cooper BT; Rosenberg WM; Purkiss M; Jobson S; Hathaway M; Briggs D; Howell WM; Wood GM; Adams DH; Iqbal TH
Gastroenterology; 2002 Aug; 123(2):444-9. PubMed ID: 12145797
[TBL] [Abstract][Full Text] [Related]
36. Haplotype sharing correlation analysis using family data: a comparison with family-based association test in the presence of allelic heterogeneity.
Qian D
Genet Epidemiol; 2004 Jul; 27(1):43-52. PubMed ID: 15185402
[TBL] [Abstract][Full Text] [Related]
37. Testing linkage disequilibrium in sibships.
Siegmund KD; Langholz B; Kraft P; Thomas DC
Am J Hum Genet; 2000 Jul; 67(1):244-8. PubMed ID: 10831398
[TBL] [Abstract][Full Text] [Related]
38. Joint Linkage and Association Analysis Using GENEHUNTER-MODSCORE with an Application to Familial Pancreatic Cancer.
Brugger M; Lutz M; Müller-Nurasyid M; Lichtner P; Slater EP; Matthäi E; Bartsch DK; Strauch K
Hum Hered; 2024; 89(1):8-31. PubMed ID: 38198765
[TBL] [Abstract][Full Text] [Related]
39. Bayesian model selection for multiple QTLs mapping combining linkage disequilibrium and linkage.
Jiang D; Ma G; Yang R; Li K; Fang M
Genet Res (Camb); 2014 Sep; 96():e10. PubMed ID: 25579473
[TBL] [Abstract][Full Text] [Related]
40. HLA class I haplotype diversity is consistent with selection for frequent existing haplotypes.
Alter I; Gragert L; Fingerson S; Maiers M; Louzoun Y
PLoS Comput Biol; 2017 Aug; 13(8):e1005693. PubMed ID: 28846675
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]