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Journal Abstract Search

140 related items for PubMed ID: 10597504

  • 1. Nonparametric linkage and family-based association studies of a simulated complex disorder.
    Koller DL, Balding J, Foroud T.
    Genet Epidemiol; 1999; 17 Suppl 1():S627-32. PubMed ID: 10597504
    [Abstract] [Full Text] [Related]

  • 2. Analysis of simulated data: evidence for genetic and environmental effects.
    Crockford GP, Iles MM, Durham LK, Bishop DT.
    Genet Epidemiol; 1999; 17 Suppl 1():S527-32. PubMed ID: 10597487
    [Abstract] [Full Text] [Related]

  • 3. Search for susceptibility genes, gene x gene interactions, and gene x environment interactions utilizing nonparametric linkage analysis.
    Ehm MG, Karnoub MC, St Jean P.
    Genet Epidemiol; 1999; 17 Suppl 1():S539-43. PubMed ID: 10597489
    [Abstract] [Full Text] [Related]

  • 4. Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12.
    Pericak-Vance MA, Bass MP, Yamaoka LH, Gaskell PC, Scott WK, Terwedow HA, Menold MM, Conneally PM, Small GW, Vance JM, Saunders AM, Roses AD, Haines JL.
    JAMA; 1997 Oct 15; 278(15):1237-41. PubMed ID: 9333264
    [Abstract] [Full Text] [Related]

  • 5. A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder.
    DeLisi LE, Shaw SH, Crow TJ, Shields G, Smith AB, Larach VW, Wellman N, Loftus J, Nanthakumar B, Razi K, Stewart J, Comazzi M, Vita A, Heffner T, Sherrington R.
    Am J Psychiatry; 2002 May 15; 159(5):803-12. PubMed ID: 11986135
    [Abstract] [Full Text] [Related]

  • 6. Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing.
    Boyles AL, Scott WK, Martin ER, Schmidt S, Li YJ, Ashley-Koch A, Bass MP, Schmidt M, Pericak-Vance MA, Speer MC, Hauser ER.
    Hum Hered; 2005 May 15; 59(4):220-7. PubMed ID: 16093727
    [Abstract] [Full Text] [Related]

  • 7. A generalized estimating equations approach to linkage analysis in sibships in relation to multiple markers and exposure factors.
    Thomas DC, Qian D, Gauderman WJ, Siegmund K, Morrison JL.
    Genet Epidemiol; 1999 May 15; 17 Suppl 1():S737-42. PubMed ID: 10597523
    [Abstract] [Full Text] [Related]

  • 8. Strategies for detecting susceptibility genes in a complex disease.
    Babron MC, Barillot E, Margaritte-Jeannin P, Clerget-Darpoux F.
    Genet Epidemiol; 1999 May 15; 17 Suppl 1():S479-83. PubMed ID: 10597479
    [Abstract] [Full Text] [Related]

  • 9. Summary of analyses of problem 2 simulated data for GAW11.
    Greenberg DA.
    Genet Epidemiol; 1999 May 15; 17 Suppl 1():S429-47. PubMed ID: 10597474
    [Abstract] [Full Text] [Related]

  • 10. Complete genomic screen for disease susceptibility loci in nuclear families.
    Anderson JL, Hauser ER, Martin ER, Scott WK, Ashley-Koch A, Kim KJ, Monks SA, Haynes CS, Speer MC, Pericak-Vance MA.
    Genet Epidemiol; 1999 May 15; 17 Suppl 1():S473-8. PubMed ID: 10597478
    [Abstract] [Full Text] [Related]

  • 11. Determining trait locus position from multipoint analysis: accuracy and power of three different statistics.
    Greenberg DA, Abreu PC.
    Genet Epidemiol; 2001 Dec 15; 21(4):299-314. PubMed ID: 11754466
    [Abstract] [Full Text] [Related]

  • 12. Generalization of the extended transmission disequilibrium test to two unlinked disease loci.
    Morris A, Whittaker J.
    Genet Epidemiol; 1999 Dec 15; 17 Suppl 1():S661-6. PubMed ID: 10597510
    [Abstract] [Full Text] [Related]

  • 13. Association between a genetic trait and a marker: discrimination between epistasis and gametic disequilibrium.
    Clerget-Darpoux F, Lathrop GM.
    Hum Genet; 1985 Dec 15; 69(2):188-9. PubMed ID: 3855838
    [Abstract] [Full Text] [Related]

  • 14. A study comparing precision of the maximum multipoint heterogeneity LOD statistic to three model-free multipoint linkage methods.
    Finch SJ, Chen CH, Gordon D, Mendell NR.
    Genet Epidemiol; 2001 Dec 15; 21(4):315-25. PubMed ID: 11754467
    [Abstract] [Full Text] [Related]

  • 15. Affected relative pairs and simultaneous search for two-locus linkage in the presence of epistasis.
    Schaid DJ, McDonnell SK, Carlson EE, Thibodeau SN, Ostrander EA, Stanford JL.
    Genet Epidemiol; 2007 Jul 15; 31(5):431-49. PubMed ID: 17410530
    [Abstract] [Full Text] [Related]

  • 16. Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A-I/C-III/A-IV locus. The NHLBI Family Heart Study.
    Coon H, Myers RH, Borecki IB, Arnett DK, Hunt SC, Province MA, Djousse L, Leppert MF.
    Arterioscler Thromb Vasc Biol; 2000 Oct 15; 20(10):2275-80. PubMed ID: 11031215
    [Abstract] [Full Text] [Related]

  • 17. Should we consider gene x environment interaction in the hunt for quantitative trait loci?
    Gauderman WJ, Morrison JL, Siegmund KD.
    Genet Epidemiol; 2001 Oct 15; 21 Suppl 1():S831-6. PubMed ID: 11793788
    [Abstract] [Full Text] [Related]

  • 18. Optimal ascertainment strategies to detect linkage to common disease alleles.
    Badner JA, Gershon ES, Goldin LR.
    Am J Hum Genet; 1998 Sep 15; 63(3):880-8. PubMed ID: 9718337
    [Abstract] [Full Text] [Related]

  • 19. Association tests using unaffected-sibling versus pseudo-sibling controls.
    Siegmund KD, Gauderman WJ, Thomas DC.
    Genet Epidemiol; 1999 Sep 15; 17 Suppl 1():S731-6. PubMed ID: 10597522
    [Abstract] [Full Text] [Related]

  • 20. Using linkage analysis to detect gene-gene interaction by stratifying family data on known disease, or disease-associated, alleles.
    Corso B, Greenberg DA.
    PLoS One; 2014 Sep 15; 9(4):e93398. PubMed ID: 24690899
    [Abstract] [Full Text] [Related]

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