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 *

125 related articles for article (PubMed ID: 28980250)

  • 21. The affected-/discordant-sib-pair design can guarantee validity of multipoint model-free linkage analysis of incomplete pedigrees when there is marker-marker disequilibrium.
    Xing C; Sinha R; Xing G; Lu Q; Elston RC
    Am J Hum Genet; 2006 Aug; 79(2):396-401. PubMed ID: 16826532
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A statistical method for identification of polymorphisms that explain a linkage result.
    Sun L; Cox NJ; McPeek MS
    Am J Hum Genet; 2002 Feb; 70(2):399-411. PubMed ID: 11791210
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genetic linkage analysis of a large family identifies
    Puigdevall P; Piccari L; Blanco I; Barberà JA; Geiger D; Badenas C; Milà M; Castelo R; Madrigal I
    J Med Genet; 2019 Jul; 56(7):481-490. PubMed ID: 30894412
    [TBL] [Abstract][Full Text] [Related]  

  • 24. An Overview of Genome-Wide Association Studies.
    Chang M; He L; Cai L
    Methods Mol Biol; 2018; 1754():97-108. PubMed ID: 29536439
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Power-based, phase-informed selection of single nucleotide polymorphisms for disease association screens.
    Saccone SF; Rice JP; Saccone NL
    Genet Epidemiol; 2006 Sep; 30(6):459-70. PubMed ID: 16685721
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Properties and modeling of GWAS when complex disease risk is due to non-complementing, deleterious mutations in genes of large effect.
    Thornton KR; Foran AJ; Long AD
    PLoS Genet; 2013; 9(2):e1003258. PubMed ID: 23437004
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Gene finding strategies.
    Vink JM; Boomsma DI
    Biol Psychol; 2002 Oct; 61(1-2):53-71. PubMed ID: 12385669
    [TBL] [Abstract][Full Text] [Related]  

  • 28. QTL mapping using high-throughput sequencing.
    Jamann TM; Balint-Kurti PJ; Holland JB
    Methods Mol Biol; 2015; 1284():257-85. PubMed ID: 25757777
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13.
    Teltsh O; Kanyas K; Karni O; Levi A; Korner M; Ben-Asher E; Lancet D; Hamdan A; Lerer B; Kohn Y
    Am J Med Genet B Neuropsychiatr Genet; 2008 Mar; 147B(2):209-15. PubMed ID: 17823922
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Power of association and linkage tests when the disease alleles are unobserved.
    Tu IP; Whittemore AS
    Am J Hum Genet; 1999 Feb; 64(2):641-9. PubMed ID: 9973303
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Simulating autosomal genotypes with realistic linkage disequilibrium and a spiked-in genetic effect.
    Shi M; Umbach DM; Wise AS; Weinberg CR
    BMC Bioinformatics; 2018 Jan; 19(1):2. PubMed ID: 29291710
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Program update and novel use of the DESPAIR program to design a genome-wide linkage study using relative pairs.
    Ochs-Balcom HM; Guo X; Yonebayashi T; Wiesner G; Elston RC
    Hum Hered; 2010; 69(1):45-51. PubMed ID: 19797908
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular genetic studies of complex phenotypes.
    Marian AJ
    Transl Res; 2012 Feb; 159(2):64-79. PubMed ID: 22243791
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Joint modeling of linkage and association: identifying SNPs responsible for a linkage signal.
    Li M; Boehnke M; Abecasis GR
    Am J Hum Genet; 2005 Jun; 76(6):934-49. PubMed ID: 15877278
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Designs for linkage analysis and association studies of complex diseases.
    Cui Y; Li G; Li S; Wu R
    Methods Mol Biol; 2010; 620():219-42. PubMed ID: 20652506
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Japonica Array NEO with increased genome-wide coverage and abundant disease risk SNPs.
    Sakurai-Yageta M; Kumada K; Gocho C; Makino S; Uruno A; Tadaka S; Motoike IN; Kimura M; Ito S; Otsuki A; Narita A; Kudo H; Aoki Y; Danjoh I; Yasuda J; Kawame H; Minegishi N; Koshiba S; Fuse N; Tamiya G; Yamamoto M; Kinoshita K
    J Biochem; 2021 Oct; 170(3):399-410. PubMed ID: 34131746
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A comparison of different linkage statistics in small to moderate sized pedigrees with complex diseases.
    Flaquer A; Strauch K
    BMC Res Notes; 2012 Aug; 5():411. PubMed ID: 22862841
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis.
    Huang Q; Shete S; Amos CI
    Am J Hum Genet; 2004 Dec; 75(6):1106-12. PubMed ID: 15492927
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genotype Imputation in Genome-Wide Association Studies.
    Naj AC
    Curr Protoc Hum Genet; 2019 Jun; 102(1):e84. PubMed ID: 31216114
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Single-marker and two-marker association tests for unphased case-control genotype data, with a power comparison.
    Kim S; Morris NJ; Won S; Elston RC
    Genet Epidemiol; 2010 Jan; 34(1):67-77. PubMed ID: 19557751
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.