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Connection

Brandon L. Pierce to Genetic Predisposition to Disease

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This is a "connection" page, showing publications Brandon L. Pierce has written about Genetic Predisposition to Disease.
Brandon L. Pierce
Connection Strength
2.830
Genetic Predisposition to Disease
  1. Research Participants' Attitudes towards Receiving Information on Genetic Susceptibility to Arsenic Toxicity in Rural Bangladesh. Public Health Genomics. 2020; 23(1-2):69-76.
    View in: PubMed
    Score: 0.390
  2. Screening for gene-environment (G×E) interaction using omics data from exposed individuals: an application to gene-arsenic interaction. Mamm Genome. 2018 02; 29(1-2):101-111.
    View in: PubMed
    Score: 0.339
  3. Genetic susceptibility to accelerated cognitive decline in the US Health and Retirement Study. Neurobiol Aging. 2014 Jun; 35(6):1512.e11-8.
    View in: PubMed
    Score: 0.255
  4. Clinical assessment incorporating a personal genome. Lancet. 2010 Sep 11; 376(9744):869; author reply 869-70.
    View in: PubMed
    Score: 0.203
  5. Power and instrument strength requirements for Mendelian randomization studies using multiple genetic variants. Int J Epidemiol. 2011 Jun; 40(3):740-52.
    View in: PubMed
    Score: 0.202
  6. Genetic susceptibility to type 2 diabetes is associated with reduced prostate cancer risk. Hum Hered. 2010; 69(3):193-201.
    View in: PubMed
    Score: 0.196
  7. Case-only genome-wide interaction study of disease risk, prognosis and treatment. Genet Epidemiol. 2010 Jan; 34(1):7-15.
    View in: PubMed
    Score: 0.193
  8. The impact of patents on the development of genome-based clinical diagnostics: an analysis of case studies. Genet Med. 2009 Mar; 11(3):202-9.
    View in: PubMed
    Score: 0.182
  9. The effect of age on DNA methylation in whole blood among Bangladeshi men and women. BMC Genomics. 2019 Sep 10; 20(1):704.
    View in: PubMed
    Score: 0.095
  10. Genome-wide association study of telomere length among South Asians identifies a second RTEL1 association signal. J Med Genet. 2018 01; 55(1):64-71.
    View in: PubMed
    Score: 0.083
  11. Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study. Hum Mol Genet. 2015 Sep 15; 24(18):5356-66.
    View in: PubMed
    Score: 0.071
  12. Arsenic metabolism efficiency has a causal role in arsenic toxicity: Mendelian randomization and gene-environment interaction. Int J Epidemiol. 2013 Dec; 42(6):1862-71.
    View in: PubMed
    Score: 0.063
  13. The effect of non-differential measurement error on bias, precision and power in Mendelian randomization studies. Int J Epidemiol. 2012 Oct; 41(5):1383-93.
    View in: PubMed
    Score: 0.058
  14. Unidentified genetic variants influence pancreatic cancer risk: an analysis of polygenic susceptibility in the PanScan study. Genet Epidemiol. 2012 Jul; 36(5):517-24.
    View in: PubMed
    Score: 0.057
  15. Genome-wide association study identifies chromosome 10q24.32 variants associated with arsenic metabolism and toxicity phenotypes in Bangladesh. PLoS Genet. 2012; 8(2):e1002522.
    View in: PubMed
    Score: 0.056
  16. Genetic susceptibility to type 2 diabetes and breast cancer risk in women of European and African ancestry. Cancer Epidemiol Biomarkers Prev. 2012 Mar; 21(3):552-6.
    View in: PubMed
    Score: 0.056
  17. Genome-wide "pleiotropy scan" identifies HNF1A region as a novel pancreatic cancer susceptibility locus. Cancer Res. 2011 Jul 01; 71(13):4352-8.
    View in: PubMed
    Score: 0.053
  18. Association study of type 2 diabetes genetic susceptibility variants and risk of pancreatic cancer: an analysis of PanScan-I data. Cancer Causes Control. 2011 Jun; 22(6):877-83.
    View in: PubMed
    Score: 0.053
  19. Genomic scan of 12 hereditary prostate cancer families having an occurrence of pancreas cancer. Prostate. 2007 Mar 01; 67(4):410-5.
    View in: PubMed
    Score: 0.040
  20. HOXD10 M319K mutation in a family with isolated congenital vertical talus. J Orthop Res. 2006 Mar; 24(3):448-53.
    View in: PubMed
    Score: 0.037
  21. A meta-analysis approach with filtering for identifying gene-level gene-environment interactions. Genet Epidemiol. 2018 07; 42(5):434-446.
    View in: PubMed
    Score: 0.021
  22. Circulating vitamin D concentration and risk of seven cancers: Mendelian randomisation study. BMJ. 2017 10 31; 359:j4761.
    View in: PubMed
    Score: 0.021
  23. Identifying cis-mediators for trans-eQTLs across many human tissues using genomic mediation analysis. Genome Res. 2017 11; 27(11):1859-1871.
    View in: PubMed
    Score: 0.021
  24. Lessons Learned From Past Gene-Environment Interaction Successes. Am J Epidemiol. 2017 Oct 01; 186(7):778-786.
    View in: PubMed
    Score: 0.021
  25. Trans-ethnic predicted expression genome-wide association analysis identifies a gene for estrogen receptor-negative breast cancer. PLoS Genet. 2017 Sep; 13(9):e1006727.
    View in: PubMed
    Score: 0.021
  26. Telomere structure and maintenance gene variants and risk of five cancer types. Int J Cancer. 2016 Dec 15; 139(12):2655-2670.
    View in: PubMed
    Score: 0.019
  27. A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age. Cancer Epidemiol Biomarkers Prev. 2014 Apr; 23(4):658-69.
    View in: PubMed
    Score: 0.016
  28. Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCR. Hum Genet. 2005 Dec; 118(3-4):466-76.
    View in: PubMed
    Score: 0.009
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Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.