BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

76 related articles for article (PubMed ID: 9723171)

  • 21. Novel linkage mapping approach using DNA pooling in human and animal genetics. I. Detection of complex disease loci.
    Pareek CS; Pareek RS; Walawski K
    J Appl Genet; 2002; 43(2):175-92. PubMed ID: 12080174
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Multipoint linkage analysis of quantitative traits on sex-chromosomes.
    Ekstrøm CT
    Genet Epidemiol; 2004 Apr; 26(3):218-30. PubMed ID: 15022208
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genetic mapping of a 17q chromosomal region linked to obesity phenotypes in the IRAS family study.
    Sutton BS; Langefeld CD; Campbell JK; Haffner SM; Norris JM; Scherzinger AL; Wagenknecht LE; Bowden DW
    Int J Obes (Lond); 2006 Sep; 30(9):1433-41. PubMed ID: 16520807
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Linkage mapping of ovine microphthalmia to chromosome 23, the sheep orthologue of human chromosome 18.
    Tetens J; Ganter M; Müller G; Drögemüller C
    Invest Ophthalmol Vis Sci; 2007 Aug; 48(8):3506-15. PubMed ID: 17652717
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Case-control single-marker and haplotypic association analysis of pedigree data.
    Browning SR; Briley JD; Briley LP; Chandra G; Charnecki JH; Ehm MG; Johansson KA; Jones BJ; Karter AJ; Yarnall DP; Wagner MJ
    Genet Epidemiol; 2005 Feb; 28(2):110-22. PubMed ID: 15578751
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Power of multipoint identity-by-descent methods to detect linkage using variance component models.
    Ekstrøm CT
    Genet Epidemiol; 2001 Dec; 21(4):285-98. PubMed ID: 11754465
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26.
    McAuley EZ; Blair IP; Liu Z; Fullerton JM; Scimone A; Van Herten M; Evans MR; Kirkby KC; Donald JA; Mitchell PB; Schofield PR
    Mol Psychiatry; 2009 May; 14(5):492-500. PubMed ID: 18227837
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Quantitative trait linkage analysis by generalized estimating equations: unification of variance components and Haseman-Elston regression.
    Chen WM; Broman KW; Liang KY
    Genet Epidemiol; 2004 May; 26(4):265-72. PubMed ID: 15095386
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Haplotype sharing analysis with SNPs in candidate genes: the Genetic Analysis Workshop 12 example.
    Fischer C; Beckmann L; Majoram P; te Meerman G; Chang-Claude J
    Genet Epidemiol; 2003 Jan; 24(1):68-73. PubMed ID: 12508257
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Analysis of genetic linkage data for Mendelian traits.
    Pericak-Vance MA
    Curr Protoc Hum Genet; 2001 May; Chapter 1():Unit 1.4. PubMed ID: 18428236
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A general method to assess the utility of the X-chromosomal markers in kinship testing.
    Pinto N; Silva PV; Amorim A
    Forensic Sci Int Genet; 2012 Mar; 6(2):198-207. PubMed ID: 21592877
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Allele-sharing among affected relatives: non-parametric methods for identifying genes.
    Shih MC; Whittemore AS
    Stat Methods Med Res; 2001 Feb; 10(1):27-55. PubMed ID: 11329690
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Crossing over...Markov meets Mendel.
    Mneimneh S
    PLoS Comput Biol; 2012; 8(5):1-12. PubMed ID: 22629235
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Pairwise Kinship Analysis by the Index of Chromosome Sharing Using High-Density Single Nucleotide Polymorphisms.
    Morimoto C; Manabe S; Kawaguchi T; Kawai C; Fujimoto S; Hamano Y; Yamada R; Matsuda F; Tamaki K
    PLoS One; 2016; 11(7):e0160287. PubMed ID: 27472558
    [TBL] [Abstract][Full Text] [Related]  

  • 36. From Mendel's factors to genes as functional units.
    Fincham JR
    Adv Sci; 1966 Jul; 23(109):124-8. PubMed ID: 5945335
    [No Abstract]   [Full Text] [Related]  

  • 37. Genetics of complex disease: approaches, problems, and solutions.
    Schork NJ
    Am J Respir Crit Care Med; 1997 Oct; 156(4 Pt 2):S103-9. PubMed ID: 9351588
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Extensions to pedigree analysis. IV. Covariance components models for multivariate traits.
    Lange K; Boehnke M
    Am J Med Genet; 1983 Mar; 14(3):513-24. PubMed ID: 6859102
    [No Abstract]   [Full Text] [Related]  

  • 39. Transmission-ratio distortion in the Framingham Heart Study.
    Paterson AD; Waggott D; Schillert A; Infante-Rivard C; Bull SB; Yoo YJ; Pinnaduwage D
    BMC Proc; 2009 Dec; 3 Suppl 7(Suppl 7):S51. PubMed ID: 20018044
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Sociability or association of the individuals of a species as 1 of the fundamental laws of the evolution of organisms].
    Novak V
    Zh Obshch Biol; 1967; 28(4):387-97. PubMed ID: 5621605
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.