Connection

DAVID G JOHNSON to Polymorphism, Single Nucleotide

This is a "connection" page, showing publications DAVID G JOHNSON has written about Polymorphism, Single Nucleotide.
  1. Genetic factors underlying the risk of thalidomide-related neuropathy in patients with multiple myeloma. J Clin Oncol. 2011 Mar 01; 29(7):797-804.
    View in: PubMed
    Score: 0.167
  2. Genetic associations with thalidomide mediated venous thrombotic events in myeloma identified using targeted genotyping. Blood. 2008 Dec 15; 112(13):4924-34.
    View in: PubMed
    Score: 0.142
  3. Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma. Nat Commun. 2018 09 13; 9(1):3707.
    View in: PubMed
    Score: 0.071
  4. Genetic Predisposition to Multiple Myeloma at 5q15 Is Mediated by an ELL2 Enhancer Polymorphism. Cell Rep. 2017 Sep 12; 20(11):2556-2564.
    View in: PubMed
    Score: 0.066
  5. Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma. Nat Commun. 2016 Jan 08; 7:10290.
    View in: PubMed
    Score: 0.059
  6. Implementation of genome-wide complex trait analysis to quantify the heritability in multiple myeloma. Sci Rep. 2015 Jul 24; 5:12473.
    View in: PubMed
    Score: 0.057
  7. FAAH genetic variation enhances fronto-amygdala function in mouse and human. Nat Commun. 2015 Mar 03; 6:6395.
    View in: PubMed
    Score: 0.056
  8. The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. Nat Genet. 2013 May; 45(5):522-525.
    View in: PubMed
    Score: 0.049
  9. Genetic factors underlying the risk of bortezomib induced peripheral neuropathy in multiple myeloma patients. Haematologica. 2011 Nov; 96(11):1728-32.
    View in: PubMed
    Score: 0.043
  10. Effects of MDM2 promoter polymorphisms and p53 codon 72 polymorphism on risk and age at onset of squamous cell carcinoma of the head and neck. Mol Carcinog. 2011 Sep; 50(9):697-706.
    View in: PubMed
    Score: 0.043
  11. Integration of global SNP-based mapping and expression arrays reveals key regions, mechanisms, and genes important in the pathogenesis of multiple myeloma. Blood. 2006 Sep 01; 108(5):1733-43.
    View in: PubMed
    Score: 0.030
  12. Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes. Hum Genomics. 2019 08 20; 13(1):37.
    View in: PubMed
    Score: 0.019
  13. Regions of homozygosity as risk factors for multiple myeloma. Ann Hum Genet. 2019 07; 83(4):231-238.
    View in: PubMed
    Score: 0.018
  14. Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology. Blood Cancer J. 2018 12 21; 9(1):1.
    View in: PubMed
    Score: 0.018
  15. Search for rare protein altering variants influencing susceptibility to multiple myeloma. Oncotarget. 2017 May 30; 8(22):36203-36210.
    View in: PubMed
    Score: 0.016
  16. Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci. Sci Rep. 2017 01 23; 7:41071.
    View in: PubMed
    Score: 0.016
  17. Multiple myeloma risk variant at 7p15.3 creates an IRF4-binding site and interferes with CDCA7L expression. Nat Commun. 2016 11 24; 7:13656.
    View in: PubMed
    Score: 0.016
  18. The 7p15.3 (rs4487645) association for multiple myeloma shows strong allele-specific regulation of the MYC-interacting gene CDCA7L in malignant plasma cells. Haematologica. 2015 Mar; 100(3):e110-3.
    View in: PubMed
    Score: 0.014
  19. Inherited genetic susceptibility to monoclonal gammopathy of unknown significance. Blood. 2014 Apr 17; 123(16):2513-7; quiz 2593.
    View in: PubMed
    Score: 0.013
  20. Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. Nat Genet. 2011 Nov 27; 44(1):58-61.
    View in: PubMed
    Score: 0.011
  21. Reductions in claudin-1 may enhance susceptibility to herpes simplex virus 1 infections in atopic dermatitis. J Allergy Clin Immunol. 2011 Jul; 128(1):242-246.e5.
    View in: PubMed
    Score: 0.011
  22. A high-frequency regulatory polymorphism in the p53 pathway accelerates tumor development. Cancer Cell. 2010 Sep 14; 18(3):220-30.
    View in: PubMed
    Score: 0.010
  23. A compendium of myeloma-associated chromosomal copy number abnormalities and their prognostic value. Blood. 2010 Oct 14; 116(15):e56-65.
    View in: PubMed
    Score: 0.010
  24. Homozygous deletion mapping in myeloma samples identifies genes and an expression signature relevant to pathogenesis and outcome. Clin Cancer Res. 2010 Mar 15; 16(6):1856-64.
    View in: PubMed
    Score: 0.010
  25. Enhanced skin carcinogenesis and lack of thymus hyperplasia in transgenic mice expressing human cyclin D1b (CCND1b). Mol Carcinog. 2009 Jun; 48(6):508-16.
    View in: PubMed
    Score: 0.009
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