These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

229 related articles for article (PubMed ID: 7668275)

  • 1. Mapping disease genes: family-based association studies.
    Thomson G
    Am J Hum Genet; 1995 Aug; 57(2):487-98. PubMed ID: 7668275
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of complex human genetic traits: an ordered-notation method and new tests for mode of inheritance.
    Thomson G
    Am J Hum Genet; 1995 Aug; 57(2):474-86. PubMed ID: 7668274
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Partitioned association-linkage test: distinguishing "necessary" from "susceptibility" loci.
    Greenberg DA; Doneshka P
    Genet Epidemiol; 1996; 13(3):243-52. PubMed ID: 8797007
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Optimal ascertainment strategies to detect linkage to common disease alleles.
    Badner JA; Gershon ES; Goldin LR
    Am J Hum Genet; 1998 Sep; 63(3):880-8. PubMed ID: 9718337
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two-locus models of disease: comparison of likelihood and nonparametric linkage methods.
    Goldin LR; Weeks DE
    Am J Hum Genet; 1993 Oct; 53(4):908-15. PubMed ID: 8213819
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Bias of the estimated recombination fraction and lod score due to an association between a disease gene and a marker gene.
    Clerget-Darpoux F
    Ann Hum Genet; 1982 Oct; 46(4):363-72. PubMed ID: 6961885
    [No Abstract]   [Full Text] [Related]  

  • 7. Effect of genetic heterogeneity and assortative mating on linkage analysis: a simulation study.
    Falk CT
    Am J Hum Genet; 1997 Nov; 61(5):1169-78. PubMed ID: 9345086
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mapping genes that underlie ethnic differences in disease risk: methods for detecting linkage in admixed populations, by conditioning on parental admixture.
    McKeigue PM
    Am J Hum Genet; 1998 Jul; 63(1):241-51. PubMed ID: 9634509
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The haplotype-relative-risk (HRR) method for analysis of association in nuclear families.
    Knapp M; Seuchter SA; Baur MP
    Am J Hum Genet; 1993 Jun; 52(6):1085-93. PubMed ID: 8503442
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Finding genes influencing susceptibility to complex diseases in the post-genome era.
    Rannala B
    Am J Pharmacogenomics; 2001; 1(3):203-21. PubMed ID: 12083968
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Conclusion of LOD-score analysis for family data generated under two-locus models.
    Dizier MH; Babron MC; Clerget-Darpoux F
    Am J Hum Genet; 1996 Jun; 58(6):1338-46. PubMed ID: 8651311
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Adequacy of single-locus approximations for linkage analyses of oligogenic traits: extension to multigenerational pedigree structures.
    Vieland VJ; Greenberg DA; Hodge SE
    Hum Hered; 1993; 43(6):329-36. PubMed ID: 8288263
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Linkage analysis in nuclear families. 1: Optimality criteria for affected sib-pair tests.
    Knapp M; Seuchter SA; Baur MP
    Hum Hered; 1994; 44(1):37-43. PubMed ID: 8163290
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set.
    Field LL; Kaplan BJ
    Am J Hum Genet; 1998 Nov; 63(5):1448-56. PubMed ID: 9792873
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Two-locus disease models with two marker loci: the power of affected-sib-pair tests.
    Knapp M; Seuchter SA; Baur MP
    Am J Hum Genet; 1994 Nov; 55(5):1030-41. PubMed ID: 7977340
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Multipoint linkage analysis using sib pairs: an interval mapping approach for dichotomous outcomes.
    Olson JM
    Am J Hum Genet; 1995 Mar; 56(3):788-98. PubMed ID: 7887435
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Some epistatic two-locus models of disease. I. Relative risks and identity-by-descent distributions in affected sib pairs.
    Hodge SE
    Am J Hum Genet; 1981 May; 33(3):381-95. PubMed ID: 6941695
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Linkage and association to genetic markers.
    Elston RC
    Exp Clin Immunogenet; 1995; 12(3):129-40. PubMed ID: 8534500
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Admixture mapping using interval transmission/disequilibrium tests.
    Lee WC; Yen YC
    Ann Hum Genet; 2003 Nov; 67(Pt 6):580-8. PubMed ID: 14641245
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.