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Brandon L. Pierce to Genome-Wide Association Study

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This is a "connection" page, showing publications Brandon L. Pierce has written about Genome-Wide Association Study.
Brandon L. Pierce
Connection Strength
3.640
Genome-Wide Association Study
  1. 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: 0.336
  2. Mediation analysis demonstrates that trans-eQTLs are often explained by cis-mediation: a genome-wide analysis among 1,800 South Asians. PLoS Genet. 2014 Dec; 10(12):e1004818.
    View in: PubMed
    Score: 0.274
  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: 0.257
  4. 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: 0.230
  5. 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: 0.226
  6. 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: 0.204
  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: 0.195
  8. Genome-wide association study of prostate-specific antigen levels in 392,522 men identifies new loci and improves prediction across ancestry groups. Nat Genet. 2025 Feb; 57(2):334-344.
    View in: PubMed
    Score: 0.139
  9. DNA methylation correlates of chronological age in diverse human tissue types. Epigenetics Chromatin. 2024 Aug 08; 17(1):25.
    View in: PubMed
    Score: 0.134
  10. An integrative multi-context Mendelian randomization method for identifying risk genes across human tissues. Am J Hum Genet. 2024 Aug 08; 111(8):1736-1749.
    View in: PubMed
    Score: 0.133
  11. The Impact of Inherited Genetic Variation on DNA Methylation in Prostate Cancer and Benign Tissues of African American and European American Men. Cancer Epidemiol Biomarkers Prev. 2024 Apr 03; 33(4):557-566.
    View in: PubMed
    Score: 0.131
  12. The association of cigarette smoking with DNA methylation and gene expression in human tissue samples. Am J Hum Genet. 2024 04 04; 111(4):636-653.
    View in: PubMed
    Score: 0.130
  13. DNA methylation QTL mapping across diverse human tissues provides molecular links between genetic variation and complex traits. Nat Genet. 2023 01; 55(1):112-122.
    View in: PubMed
    Score: 0.119
  14. Primo: integration of multiple GWAS and omics QTL summary statistics for elucidation of molecular mechanisms of trait-associated SNPs and detection of pleiotropy in complex traits. Genome Biol. 2020 09 11; 21(1):236.
    View in: PubMed
    Score: 0.102
  15. Genetic Determinants of Reduced Arsenic Metabolism Efficiency in the 10q24.32 Region Are Associated With Reduced AS3MT Expression in Multiple Human Tissue Types. Toxicol Sci. 2020 08 01; 176(2):382-395.
    View in: PubMed
    Score: 0.101
  16. Co-occurring expression and methylation QTLs allow detection of common causal variants and shared biological mechanisms. Nat Commun. 2018 02 23; 9(1):804.
    View in: PubMed
    Score: 0.086
  17. Incorporation of Biological Knowledge Into the Study of Gene-Environment Interactions. Am J Epidemiol. 2017 Oct 01; 186(7):771-777.
    View in: PubMed
    Score: 0.083
  18. A unified set-based test with adaptive filtering for gene-environment interaction analyses. Biometrics. 2016 06; 72(2):629-38.
    View in: PubMed
    Score: 0.073
  19. Genome-wide association studies and heritability estimates of body mass index related phenotypes in Bangladeshi adults. PLoS One. 2014; 9(8):e105062.
    View in: PubMed
    Score: 0.067
  20. Practical barriers and ethical challenges in genetic data sharing. Int J Environ Res Public Health. 2014 Aug 15; 11(8):8383-98.
    View in: PubMed
    Score: 0.067
  21. 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
  22. 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
  23. Clinical assessment incorporating a personal genome. Lancet. 2010 Sep 11; 376(9744):869; author reply 869-70.
    View in: PubMed
    Score: 0.051
  24. Genetic susceptibility to type 2 diabetes is associated with reduced prostate cancer risk. Hum Hered. 2010; 69(3):193-201.
    View in: PubMed
    Score: 0.049
  25. Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances. Elife. 2019 01 15; 8.
    View in: PubMed
    Score: 0.046
  26. Integrative cross-omics and cross-context analysis elucidates molecular links underlying genetic effects on complex traits. Nat Commun. 2024 Mar 16; 15(1):2383.
    View in: PubMed
    Score: 0.033
  27. Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. Nat Genet. 2021 09; 53(9):1300-1310.
    View in: PubMed
    Score: 0.027
  28. The impact of sex on gene expression across human tissues. Science. 2020 09 11; 369(6509).
    View in: PubMed
    Score: 0.026
  29. Circulating vitamin D concentrations and risk of breast and prostate cancer: a Mendelian randomization study. Int J Epidemiol. 2019 10 01; 48(5):1416-1424.
    View in: PubMed
    Score: 0.024
  30. 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
  31. Circulating vitamin D concentration and risk of seven cancers: Mendelian randomisation study. BMJ. 2017 10 31; 359:j4761.
    View in: PubMed
    Score: 0.021
  32. 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
  33. Lessons Learned From Past Gene-Environment Interaction Successes. Am J Epidemiol. 2017 Oct 01; 186(7):778-786.
    View in: PubMed
    Score: 0.021
  34. 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
  35. 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
  36. Association between Adult Height and Risk of Colorectal, Lung, and Prostate Cancer: Results from Meta-analyses of Prospective Studies and Mendelian Randomization Analyses. PLoS Med. 2016 Sep; 13(9):e1002118.
    View in: PubMed
    Score: 0.019
  37. Genome-wide association study of parity in Bangladeshi women. PLoS One. 2015; 10(3):e0118488.
    View in: PubMed
    Score: 0.017
  38. Genome-wide association study of smoking behaviours among Bangladeshi adults. J Med Genet. 2014 May; 51(5):327-33.
    View in: PubMed
    Score: 0.016
  39. 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
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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.