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 *

145 related articles for article (PubMed ID: 19571035)

  • 1. Finding common susceptibility variants for complex disease: past, present and future.
    Panoutsopoulou K; Zeggini E
    Brief Funct Genomic Proteomic; 2009 Sep; 8(5):345-52. PubMed ID: 19571035
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic Epidemiology of Complex Phenotypes.
    O'Rielly DD; Rahman P
    Methods Mol Biol; 2021; 2249():335-367. PubMed ID: 33871853
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Do common variants play a role in risk for autism? Evidence and theoretical musings.
    Devlin B; Melhem N; Roeder K
    Brain Res; 2011 Mar; 1380():78-84. PubMed ID: 21078308
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Unraveling the genetics of common epilepsies: approaches, platforms, and caveats.
    Petrovski S; Kwan P
    Epilepsy Behav; 2013 Mar; 26(3):229-33. PubMed ID: 23103323
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genome-wide association studies.
    Yang TH; Kon M; DeLisi C
    Methods Mol Biol; 2013; 939():233-51. PubMed ID: 23192550
    [TBL] [Abstract][Full Text] [Related]  

  • 6. How important are rare variants in common disease?
    Saint Pierre A; Génin E
    Brief Funct Genomics; 2014 Sep; 13(5):353-61. PubMed ID: 25005607
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rare-variant genome-wide association studies: a new frontier in genetic analysis of complex traits.
    Wagner MJ
    Pharmacogenomics; 2013 Mar; 14(4):413-24. PubMed ID: 23438888
    [TBL] [Abstract][Full Text] [Related]  

  • 8. What will whole genome searches for susceptibility genes for common complex disease offer to clinical practice?
    Lango H; Weedon MN
    J Intern Med; 2008 Jan; 263(1):16-27. PubMed ID: 18088250
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The pursuit of genome-wide association studies: where are we now?
    Ku CS; Loy EY; Pawitan Y; Chia KS
    J Hum Genet; 2010 Apr; 55(4):195-206. PubMed ID: 20300123
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The overdue promise of short tandem repeat variation for heritability.
    Press MO; Carlson KD; Queitsch C
    Trends Genet; 2014 Nov; 30(11):504-12. PubMed ID: 25182195
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An evaluation of statistical approaches to rare variant analysis in genetic association studies.
    Morris AP; Zeggini E
    Genet Epidemiol; 2010 Feb; 34(2):188-93. PubMed ID: 19810025
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants.
    Bacchelli E; Cainazzo MM; Cameli C; Guerzoni S; Martinelli A; Zoli M; Maestrini E; Pini LA
    J Headache Pain; 2016 Dec; 17(1):114. PubMed ID: 27957625
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic susceptibility to SLE: new insights from fine mapping and genome-wide association studies.
    Harley IT; Kaufman KM; Langefeld CD; Harley JB; Kelly JA
    Nat Rev Genet; 2009 May; 10(5):285-90. PubMed ID: 19337289
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Recent advances in association studies of osteoarthritis susceptibility genes.
    Dai J; Ikegawa S
    J Hum Genet; 2010 Feb; 55(2):77-80. PubMed ID: 20075947
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The Genetics of Multiple Sclerosis: From 0 to 200 in 50 Years.
    Baranzini SE; Oksenberg JR
    Trends Genet; 2017 Dec; 33(12):960-970. PubMed ID: 28987266
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Genetic epidemiology--from gene to disease understanding].
    Andersen VC; Vogel U
    Ugeskr Laeger; 2010 Feb; 172(5):368-71. PubMed ID: 20122331
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-wide-associated variants in migraine susceptibility: a replication study from North India.
    Ghosh J; Pradhan S; Mittal B
    Headache; 2013; 53(10):1583-94. PubMed ID: 24266335
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rare variants and autoimmune disease.
    Massey J; Eyre S
    Brief Funct Genomics; 2014 Sep; 13(5):392-7. PubMed ID: 24817515
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic association of molecular traits: A help to identify causative variants in complex diseases.
    Vandiedonck C
    Clin Genet; 2018 Mar; 93(3):520-532. PubMed ID: 29194587
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rare variants and cardiovascular disease.
    Wain LV
    Brief Funct Genomics; 2014 Sep; 13(5):384-91. PubMed ID: 24771349
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.