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 *

430 related articles for article (PubMed ID: 20027720)

  • 1. The role of genes in disease: beware of simplistic interpretations!
    Prescrire Int; 2009 Dec; 18(104):279-82. PubMed ID: 20027720
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Risk estimation for multifactorial diseases. A report of the International Commission on Radiological Protection.
    Ann ICRP; 1999; 29(3-4):1-144. PubMed ID: 11108911
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic mapping of complex traits: promises, problems, and prospects.
    Guo SW; Lange K
    Theor Popul Biol; 2000 Feb; 57(1):1-11. PubMed ID: 10708625
    [No Abstract]   [Full Text] [Related]  

  • 4. Approaches to identify genes for complex human diseases: lessons from Mendelian disorders.
    Dean M
    Hum Mutat; 2003 Oct; 22(4):261-74. PubMed ID: 12955713
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic basis of common diseases: the general theory of Mendelian recessive genetics.
    Hutchinson M; Spanaki C; Lebedev S; Plaitakis A
    Med Hypotheses; 2005; 65(2):282-6. PubMed ID: 15922101
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Multifactorial diseases: a nightmare for the geneticist].
    Feingold J
    Med Sci (Paris); 2005 Nov; 21(11):927-33. PubMed ID: 16274643
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The common variants/multiple disease hypothesis of common complex genetic disorders.
    Becker KG
    Med Hypotheses; 2004; 62(2):309-17. PubMed ID: 14962646
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases?
    Bourgain C; Génin E; Cox N; Clerget-Darpoux F
    Eur J Hum Genet; 2007 Mar; 15(3):260-3. PubMed ID: 17164797
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association mapping of complex diseases in linked regions: estimation of genetic effects and feasibility of testing rare variants.
    Wang WY; Cordell HJ; Todd JA
    Genet Epidemiol; 2003 Jan; 24(1):36-43. PubMed ID: 12508254
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Robustness of inference on measured covariates to misspecification of genetic random effects in family studies.
    Pfeiffer RM; Hildesheim A; Gail MH; Pee D; Chen CJ; Goldstein AM; Diehl SR
    Genet Epidemiol; 2003 Jan; 24(1):14-23. PubMed ID: 12508252
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Multifactorial disease].
    Hata A
    Nihon Rinsho; 2005 Dec; 63 Suppl 12():70-4. PubMed ID: 16416773
    [No Abstract]   [Full Text] [Related]  

  • 12. [Strategies and methods to identify genes for complex diseases].
    Zhang KX; Zhu DL; Huang W
    Sheng Li Ke Xue Jin Zhan; 2001 Jul; 32(3):215-9. PubMed ID: 12545792
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genes, environment, and cardiovascular disease.
    Sing CF; Stengård JH; Kardia SL
    Arterioscler Thromb Vasc Biol; 2003 Jul; 23(7):1190-6. PubMed ID: 12730090
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The genetic epidemiology of cancer: interpreting family and twin studies and their implications for molecular genetic approaches.
    Risch N
    Cancer Epidemiol Biomarkers Prev; 2001 Jul; 10(7):733-41. PubMed ID: 11440958
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Genetics of multifactorial diseases].
    Kere J; Ripatti S; Perola M
    Duodecim; 2010; 126(19):2305-10. PubMed ID: 21086688
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Predictive medicine - clinical genetics 2010].
    Blum HE
    Dtsch Med Wochenschr; 2010 Jun; 135(25-26):1334-8. PubMed ID: 20556694
    [No Abstract]   [Full Text] [Related]  

  • 17. Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies.
    Lin S; Chakravarti A; Cutler DJ
    Nat Genet; 2004 Nov; 36(11):1181-8. PubMed ID: 15502828
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic Analysis Workshop II: combined segregation, linkage, and association analysis.
    Morton NE; Sherman SL; MacLean S; Yee S; Lew R
    Genet Epidemiol; 1984; 1(2):195-9. PubMed ID: 14971374
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Strategy for detecting susceptibility genes with weak or no marginal effect.
    Kotti S; Bickeboller H; Clerget-Darpoux F
    Hum Hered; 2007; 63(2):85-92. PubMed ID: 17283437
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Lessons from studying monogenic disease for common disease.
    Peltonen L; Perola M; Naukkarinen J; Palotie A
    Hum Mol Genet; 2006 Apr; 15 Spec No 1():R67-74. PubMed ID: 16651371
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 22.