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 *

531 related articles for article (PubMed ID: 11525833)

  • 21. Allelic variation in human mitochondrial genes based on patterns of restriction site polymorphism.
    Whittam TS; Clark AG; Stoneking M; Cann RL; Wilson AC
    Proc Natl Acad Sci U S A; 1986 Dec; 83(24):9611-5. PubMed ID: 2432597
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Colorectal cancer susceptibility genetic variants in tumor free and colorectal carcinoma bearing Hungarian population. Individual predisposition to cancer].
    Szentirmay Z; Kurcsics J; Csernák E; Tándor I; Tóth E
    Orv Hetil; 2018 Oct; 159(40):1614-1623. PubMed ID: 30277414
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Searching for missing heritability: designing rare variant association studies.
    Zuk O; Schaffner SF; Samocha K; Do R; Hechter E; Kathiresan S; Daly MJ; Neale BM; Sunyaev SR; Lander ES
    Proc Natl Acad Sci U S A; 2014 Jan; 111(4):E455-64. PubMed ID: 24443550
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Hypertension genetics, single nucleotide polymorphisms, and the common disease:common variant hypothesis.
    Doris PA
    Hypertension; 2002 Feb; 39(2 Pt 2):323-31. PubMed ID: 11882567
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic analysis.
    Koornneef M; Alonso-Blanco C; Stam P
    Methods Mol Biol; 2006; 323():65-77. PubMed ID: 16739568
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Association mapping reveals the role of purifying selection in the maintenance of genomic variation in gene expression.
    Josephs EB; Lee YW; Stinchcombe JR; Wright SI
    Proc Natl Acad Sci U S A; 2015 Dec; 112(50):15390-5. PubMed ID: 26604315
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Identification of susceptibility loci contributing to a complex disease using conventional segregation, linkage, and association methods.
    Falk CT; Ashley A; Lamb N; Sherman SL
    Genet Epidemiol; 1995; 12(6):601-6. PubMed ID: 8787980
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Schizophrenia: the testing of genetic models by pedigree analysis.
    Stewart J; Debray Q; Caillard V
    Am J Hum Genet; 1980 Jan; 32(1):55-63. PubMed ID: 7361764
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Selection and mutation at a diallelic X-linked locus.
    Szucs JM
    J Math Biol; 1991; 29(7):587-627. PubMed ID: 1940662
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Obstruction of adaptation in diploids by recessive, strongly deleterious alleles.
    Assaf ZJ; Petrov DA; Blundell JR
    Proc Natl Acad Sci U S A; 2015 May; 112(20):E2658-66. PubMed ID: 25941393
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clines in polygenic traits.
    Barton NH
    Genet Res; 1999 Dec; 74(3):223-36. PubMed ID: 10689800
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disorders.
    Pesch K; Tomiuk J; Broghammer M; Zrenner E; Apfelstedt-Sylla E; Jacobi FK; Wissinger B; Pusch CM
    Int J Mol Med; 2001 Jul; 8(1):53-8. PubMed ID: 11408949
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The effect of subdivision on variation at multi-allelic loci under balancing selection.
    Schierup MH; Vekemans X; Charlesworth D
    Genet Res; 2000 Aug; 76(1):51-62. PubMed ID: 11006634
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The rise and fall of the common disease-common variant (CD-CV) hypothesis: how the sickle cell disease paradigm led us all astray (or did it?).
    Mayo O
    Twin Res Hum Genet; 2007 Dec; 10(6):793-804. PubMed ID: 18179390
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Association Mapping and Disease: Evolutionary Perspectives.
    Besenbacher S; Mailund T; Vilhjálmsson BJ; Schierup MH
    Methods Mol Biol; 2019; 1910():533-553. PubMed ID: 31278676
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Some properties of a variance components model for fine-mapping quantitative trait loci.
    Cardon LR; Abecasis GR
    Behav Genet; 2000 May; 30(3):235-43. PubMed ID: 11105397
    [TBL] [Abstract][Full Text] [Related]  

  • 37. On selecting markers for association studies: patterns of linkage disequilibrium between two and three diallelic loci.
    Garner C; Slatkin M
    Genet Epidemiol; 2003 Jan; 24(1):57-67. PubMed ID: 12508256
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The structure of linkage disequilibrium around a selective sweep.
    McVean G
    Genetics; 2007 Mar; 175(3):1395-406. PubMed ID: 17194788
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Epialleles and common disease.
    Peedicayil J
    Med Hypotheses; 2005; 64(1):215. PubMed ID: 15533644
    [No Abstract]   [Full Text] [Related]  

  • 40. The genetics of autism.
    Muhle R; Trentacoste SV; Rapin I
    Pediatrics; 2004 May; 113(5):e472-86. PubMed ID: 15121991
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 27.