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 *

144 related articles for article (PubMed ID: 15682273)

  • 21. Identifying rare variants for genetic risk through a combined pedigree and phenotype approach: application to suicide and asthma.
    Darlington TM; Pimentel R; Smith K; Bakian AV; Jerominski L; Cardon J; Camp NJ; Callor WB; Grey T; Singleton M; Yandell M; Renshaw PF; Yurgelun-Todd DA; Gray D; Coon H
    Transl Psychiatry; 2014 Oct; 4(10):e471. PubMed ID: 25335167
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genome-wide linkage analysis of chromogranin B expression in the CEPH pedigrees: implications for exocytotic sympathochromaffin secretion in humans.
    Greenwood TA; Cadman PE; Stridsberg M; Nguyen S; Taupenot L; Schork NJ; O'Connor DT
    Physiol Genomics; 2004 Jun; 18(1):119-27. PubMed ID: 15138309
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Multipoint oligogenic linkage analysis of quantitative traits.
    Blangero J; Almasy L
    Genet Epidemiol; 1997; 14(6):959-64. PubMed ID: 9433607
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Attention-deficit/hyperactivity disorder (ADHD): feasibility of linkage analysis in a genetic isolate using extended and multigenerational pedigrees.
    Arcos-Burgos M; Castellanos FX; Lopera F; Pineda D; Palacio JD; Garcia M; Henao GC; Palacio LG; Berg K; Bailey-Wilson JE; Muenke M
    Clin Genet; 2002 May; 61(5):335-43. PubMed ID: 12081716
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Power to localize the major gene for disease liability is increased after accounting for the effects of related quantitative phenotypes.
    Arya R; Duggirala R; Williams JT; Almasy L; Blangero J
    Genet Epidemiol; 2001; 21 Suppl 1():S774-8. PubMed ID: 11793776
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Disentangling linkage disequilibrium and linkage from dense single-nucleotide polymorphism trio data.
    Clarke GM; Cardon LR
    Genetics; 2005 Dec; 171(4):2085-95. PubMed ID: 16118185
    [TBL] [Abstract][Full Text] [Related]  

  • 27. In silico method for inferring genotypes in pedigrees.
    Burdick JT; Chen WM; Abecasis GR; Cheung VG
    Nat Genet; 2006 Sep; 38(9):1002-4. PubMed ID: 16921375
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Estimating the power of a proposed linkage study for a complex genetic trait.
    Ploughman LM; Boehnke M
    Am J Hum Genet; 1989 Apr; 44(4):543-51. PubMed ID: 2929597
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Detecting dominant QTL with variance component analysis in simulated pedigrees.
    Rowe SJ; Pong-Wong R; Haley CS; Knott SA; De Koning DJ
    Genet Res (Camb); 2008 Aug; 90(4):363-74. PubMed ID: 18840310
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Linkage of body mass index to chromosome 20 in Utah pedigrees.
    Hunt SC; Abkevich V; Hensel CH; Gutin A; Neff CD; Russell DL; Tran T; Hong X; Jammulapati S; Riley R; Weaver-Feldhaus J; Macalma T; Richards MM; Gress R; Francis M; Thomas A; Frech GC; Adams TD; Shattuck D; Stone S
    Hum Genet; 2001 Sep; 109(3):279-85. PubMed ID: 11702208
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Allele frequency misspecification: effect on power and Type I error of model-dependent linkage analysis of quantitative traits under random ascertainment.
    Mandal DM; Sorant AJ; Atwood LD; Wilson AF; Bailey-Wilson JE
    BMC Genet; 2006 Apr; 7():21. PubMed ID: 16618369
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Accommodating chromosome inversions in linkage analysis.
    Chen GK; Slaten E; Ophoff RA; Lange K
    Am J Hum Genet; 2006 Aug; 79(2):238-51. PubMed ID: 16826515
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Restricted maximum likelihood analysis of linkage between genetic markers and quantitative trait loci for a granddaughter design.
    Van Arendonk JA; Tier B; Bink MC; Bovenhuis H
    J Dairy Sci; 1998 Sep; 81 Suppl 2():76-84. PubMed ID: 9777514
    [TBL] [Abstract][Full Text] [Related]  

  • 34. From linkage maps to quantitative trait loci: the history and science of the Utah genetic reference project.
    Prescott SM; Lalouel JM; Leppert M
    Annu Rev Genomics Hum Genet; 2008; 9():347-58. PubMed ID: 18544033
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The CEPH consortium linkage map of human chromosome 1.
    Dracopoli NC; O'Connell P; Elsner TI; Lalouel JM; White RL; Buetow KH; Nishimura DY; Murray JC; Helms C; Mishra SK
    Genomics; 1991 Apr; 9(4):686-700. PubMed ID: 2037294
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Linkage analysis of quantitative traits in randomly ascertained pedigrees: comparison of penetrance-based and variance component analysis.
    Göring HH; Williams JT; Blangero J
    Genet Epidemiol; 2001; 21 Suppl 1():S783-8. PubMed ID: 11793778
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Joint segregation and linkage analysis of a quantitative trait compared to separate analyses.
    Gauderman WJ; Faucett CL; Morrison JL; Carpenter CL
    Genet Epidemiol; 1997; 14(6):993-8. PubMed ID: 9433613
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A variance component approach to dichotomous trait linkage analysis using a threshold model.
    Duggirala R; Williams JT; Williams-Blangero S; Blangero J
    Genet Epidemiol; 1997; 14(6):987-92. PubMed ID: 9433612
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Power of variance component linkage analysis to detect quantitative trait loci.
    Williams JT; Blangero J
    Ann Hum Genet; 1999 Nov; 63(Pt 6):545-63. PubMed ID: 11246457
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A genome-wide linkage study of GAW15 gene expression data.
    Kan D; Cooper R; Zhu X
    BMC Proc; 2007; 1 Suppl 1(Suppl 1):S87. PubMed ID: 18466590
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.